Benzi Gar 2018

Featuring work from the research group of Professor As featured in:
Ajayan Vinu, The University of Newcastle, Australia.
Recent advances in functionalized micro and mesoporous

carbon materials: synthesis and applications
The team is actively working in the field of ordered micro and

mesoporous carbon materials, which can offer solutions for
solving many issues that our universe is facing.
See Ajayan Vinu et al.,

Chem. Soc. Rev., 2018, 47, 2680.
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Recent advances in functionalized micro and

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mesoporous carbon materials: synthesis

Cite this: Chem. Soc. Rev., 2018,
47, 2680 and applications
Mercy R. Benzigar,†a Siddulu Naidu Talapaneni,†ab Stalin Joseph, ab
Kavitha Ramadass,ab Gurwinder Singh,a Jessica Scaranto,c Ugo Ravon,c
Khalid Al-Bahilyc and Ajayan Vinu *ab
Functionalized nanoporous carbon materials have attracted the colossal interest of the materials science
fraternity owing to their intriguing physical and chemical properties including a well-ordered porous
structure, exemplary high specific surface areas, electronic and ionic conductivity, excellent accessibility to
active sites, and enhanced mass transport and diffusion. These properties make them a special and unique
choice for various applications in divergent fields such as energy storage batteries, supercapacitors, energy
conversion fuel cells, adsorption/separation of bulky molecules, heterogeneous catalysts, catalyst supports,
photocatalysis, carbon capture, gas storage, biomolecule detection, vapour sensing and drug delivery.
Because of the anisotropic and synergistic effects arising from the heteroatom doping at the nanoscale,
these novel materials show high potential especially in electrochemical applications such as batteries,
supercapacitors and electrocatalysts for fuel cell applications and water electrolysis. In order to gain the
optimal benefit, it is necessary to implement tailor made functionalities in the porous carbon surfaces as
well as in the carbon skeleton through the comprehensive experimentation. These most appealing
nanoporous carbon materials can be synthesized through the carbonization of high carbon containing
molecular precursors by using soft or hard templating or non-templating pathways. This review
Received 15th November 2017 encompasses the approaches and the wide range of methodologies that have been employed over the
DOI: 10.1039/c7cs00787f last five years in the preparation and functionalisation of nanoporous carbon materials via incorporation
of metals, non-metal heteroatoms, multiple heteroatoms, and various surface functional groups that
rsc.li/chem-soc-rev mostly dictate their place in a wide range of practical applications.
1. Introduction (micro and mesoporous) carbons have been widely applied for
energy and environmental applications including as adsorbents
The design of carbon materials with ordered porous structure is for the purification of water and capture of greenhouse gases.5,6
one of the hot topics in the area of materials chemistry. The However, the complex synthesis methods required for the
high specific surface area, large pore volume, well-ordered and fabrication of carbon nanotubes or fullerenes place a hurdle
controllable porous structure, unique morphologies of carbons in the path of exploiting their full potential in various applica-
and their excellent chemical, mechanical and thermal stability tions. On the other hand, the preparation of highly ordered
make them attractive for various applications including energy nanoporous carbons is quite simple and the properties of these
storage and conversion, catalysis and sensing.1–4 Generally, materials are much better than those of other carbon materials
carbon nanotubes, fullerenes and ordered nanoporous owing to their ordered porous structure. Most importantly,
the well-ordered porous structures support the addition of
a
Future Industries Institute, Division of Information Technology Energy and
new functionalities including organic or inorganic or bio-
Environment, University of South Australia, Adelaide, SA 5095, Australia materials inside the porous channels or on the surface of the
b
Global Innovative Center for Advanced Nanomaterials (GICAN), carbon walls, which significantly enhance their performances
School of Engineering, Faculty of Engineering and Built Environment, in various applications.
The University of Newcastle, Callaghan, NSW 2308, Australia.
Highly ordered nanoporous carbon materials have been
E-mail: [email protected]
c
SABIC Corporate Research and Development Center at KAUST,
traditionally used for many years in a large number of practical
Saudi Basic Industries Corporation, Thuwal 23955, Saudi Arabia applications including catalysis, energy storage and conversion,
† These authors contributed equally. adsorption and separation and biomedical engineering.
2680 | Chem. Soc. Rev., 2018, 47, 2680--2721 This journal is © The Royal Society of Chemistry 2018
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Review Article Chem Soc Rev
The first report on the preparation of highly ordered meso- of these nanoporous materials can be controlled by varying the
porous carbon (CMK-1) via the nanocasting approach led to a structure of the templates used for the synthesis. For example,
new class of ordered mesoporous carbons (OMCs), with large several mesoporous silica materials with different structures
specific surface areas and tunable pore diameters between 2 including MCM-48, SBA-1, SBA-15, SBA-16, KIT-6 and KIT-5 have
and 50 nm.1,7 This invention has led to the discovery of many been used as templates for the fabrication of mesoporous carbon
useful porous materials including carbons, polymers, metal materials (CMK-x) with different mesoporous structures.8–12
oxides, silicas and metals which are considered as potential A similar nano-hard templating approach was also used by
game changers for various current technologies.1,7 The structure Hyeon et al. for the preparation of ordered porous carbon using
Mrs Mercy R. Benzigar is a final Dr Siddulu Naidu Talapaneni is a

year PhD student at Future Research Associate at Global
Industries Institute, University of Innovative Center for Advanced
South Australia. She received her Nanomaterials (GICAN), The
Bachelor’s and Master’s degrees University of Newcastle, Australia.
in biotechnology and genetic He received his MS degree in
engineering from Satyabhama Chemistry from NIT-Warangal,
University, Chennai, India. She India, in 2007. From 2007 to
was then awarded the prestigious 2009 he worked as a Research
NIMS (National Institute for Associate in GVK Biosciences
Materials Science), Japan intern- Private Limited, Hyderabad, India.
ship for developing new hydroxy- He moved to Japan in 2009 and
Mercy R. Benzigar apatite mesoporous materials. Siddulu Naidu Talapaneni completed his PhD in 2012 at the
During her PhD, under the National Institute for Materials
supervision of Professor Ajayan Vinu, she has developed a new Science (NIMS) in collaboration with Hokkaido University, Japan.
class of ‘‘Mesoporous Fullerene’’ based energy materials. Her He then worked as a postdoctoral researcher at the Laboratory of
current research interest is focussed on developing multifunctional Catalysis and Spectrochemie (LCS), ENSICAEN, France, Korea
nanoporous fullerenes for energy applications. Advanced Institute of Science and Technology (KAIST), South
Korea and Future Industries Institute (FII), University of South
Australia, Australia. His research work mainly focuses on the
design of nanoporous materials to tackle the energy and
environmental issues. He has authored 440 original research
papers in high impact factor peer reviewed journals.
Dr Stalin Joseph is a Research Dr Kavitha Ramadass is a

Associate at the Global Innovative Research Associate at the Global
Center for Advanced nanomaterials Innovative Centre for Advanced
(GICAN), The University of Nanomaterials (GICAN), The
Newcastle, Australia. He received University of Newcastle. She
his PhD degree (2018) from the received her MSc degree (2004)
Department of Environmental from Tamil Nadu Agricultural
Engineering at the University of University, India and PhD degree
South Australia. He received his (2011) from Centre for Environ-
Bachelor’s degree in Chemistry mental Risk Assessment and
from Kerala University, India. He Remediation at the University of
completed MSc in Chemistry from South Australia. She worked as a
Stalin Joseph Vels University, Chennai, India. In Kavitha Ramadass post-doctoral research associate
2012, during his MSc, he was at Future Industries Institute,
awarded the University of Queensland (UQ) summer internship to University of South Australia. Her research interests focus on the
work on ‘‘synthesis of novel nanoporous carbon nitride materials from design of multifunctional nanoporous materials for energy and
MOF templates’’. His research interests focus on the conversion of environmental applications. She has won the International
industrial wastes into functional nanoporous carbon based materials Postgraduate Scholarship (IPRS) award for PhD Studies, and the
for energy storage devices such as supercapacitors and batteries, and Research Encouragement award by IUMRS-ICAM held at Kyoto,
CO2 capture and conversion. Japan, in 2017.
This journal is © The Royal Society of Chemistry 2018 Chem. Soc. Rev., 2018, 47, 2680--2721 | 2681
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Chem Soc Rev Review Article
phenolic resin as the source of carbon.13,14 OMCs having sur- properties and application of pristine and functionalized OMCs
face areas of more than 2000 m2 g 1, a higher pore volume of (Table 1). Much emphasis will be given on the relatively new
up to 3.0 cm3 g 1 and tuneable pore diameters along with high and exciting discoveries of nanoporous carbon materials with
conductivity can be achieved through a nano-hard templating different organic or inorganic functional moieties such as B, N,
approach using mesoporous silica hard-templates. Because of O, S and P, amines, complexes and hybrid OMCs incorporated
their excellent textural characteristics, physical properties and with metal nanoparticles, metal oxides, metal chalcogenides
chemical stability, OMCs have been productively utilized in and graphene. We also address how these added functionalities
carbocatalysis, adsorption and separation of toxic molecules, gas may affect the final performance of the materials in various
storage, selective sensing, energy conversion fuel and solar cells, applications including sensing, drug delivery, carbon capture,
batteries, super(ultra)capacitors, and biomedical devices.4,15–17 energy storage and conversion and adsorption and separation
The properties and the performance of these OMCs can be (Fig. 1). New developments in the improvement of the proper-
controlled by modification of the porous structure with organic ties and performance of a variety of functionalized nanoporous
or inorganic moieties. For example, the introduction of foreign carbons reported during the last five years are also described in
atoms such as B, N, O, S and P in the carbon framework can tune detail with the aim of demonstrating the uniqueness and the real
not only the specific surface area and electronic properties of the academic and market potential of these materials. Finally, new
materials but also their performance in catalysis or sensing. directions and the development of these nanostructures and the
These factors are critical for various applications including extension of the application of these materials to various fields
semiconductors, field emission devices, optical and electronic are described in the conclusion and future prospects section.
devices and fuel cells. Therefore, research on the development of
ordered nanoporous carbons with different functional groups is
actively progressing for energy and electrocatalytic applications. 2. Synthesis methods
Several review articles have been reported on the preparation of
pure mesoporous carbons and their applications.4,18–21 However, OMCs and heteroatom doped OMCs are generally prepared by
review papers on the recent development in the preparation, using templating strategies. Two well-established templating
functionalization and applications of nanoporous carbon materials techniques such as hard and soft templating methods are
are quite limited.21 For instance, much progress has been made employed for the synthesis of OMCs and heteroatom doped
recently in the conversion of metal organic frameworks (MOFs) into OMCs. In the soft-templating method, the ordered mesoporous
highly dispersed metal/metal oxide functionalized nanoporous framework structure is achieved by the cooperative assembly of
carbons without any external sacrificial templates for energy amphiphilic surfactant molecules and precursor moieties. In this
related applications.21–23 case, mesoporosity is generated upon removing the surfactants
In this review, we give an overview of the latest advances through the calcination process at high temperatures. The nano-
in the synthesis, structural characteristics, physicochemical casting method is rather a conventional templating process,
Dr Khalid Al-Bahily has been the Prof. Ajayan Vinu is a Global

director of SABIC CRD at KAUST, Innovation Chair and Director
Saudi Arabia, since 2014. Prior to at Global Innovative Centre for
this, he worked as a senior manager Advanced Nanomaterials, The
for polypropylene catalysis section, University of Newcastle. During
SABIC, Saudi Arabia. He received his 18 years of research, Prof.
his MSc from Texas A & M Vinu has made a tremendous
University, United States, in 2004 contribution in the field of
and a PhD in chemistry from the nanoporous materials and their
University of Ottawa in 2011. application in sensing, energy
Dr Albahily was awarded the storage, fuel cells, adsorption
Pierre Laberge Prize by University and separation, and catalysis.
Khalid Al-Bahily of Ottawa for the best PhD thesis Ajayan Vinu His contribution in nanoporous
and was also the winner of IUPAC materials is also clearly reflected
prize for outstanding academic achievements. Dr Albahily has by Science Watch international ranking as one of the top 15
published in top quality journals such as JACS and Angewandte researchers in the field and has led to 330 original research
Chemie and authored more than 20 patents. Dr Ravon has been a papers in high impact factor journals with ca. 15 000 citations
senior scientist in SABIC CRD since 2015. His research expertise is in and an H-index of 62.
porous materials and catalysis. Dr Scaranto has been a Lead Scientist
in SABIC since 2013 and an expert in computational chemistry for
understanding heterogeneous catalytic processes.
Table 1 Summary of the synthesis conditions, heteroatom contents and textural parameters of the functionalized nanoporous carbons and their application possibilities
Template and Heteroatom dpore SABET VTotal

Material porogen Precursor T (1C) content Structure and morphology (nm) (m2 g 1) (cm3 g 1) Applications Ref.
Review Article
OMC spheres Silica inverse Phenol and formaldehyde 900 — Spherical shaped 3.1 2445 2.63 Li–S battery 24
opal spheres nanoparticles
2D hexagonal mesostructure 6.0
P6mm symmetry
TC-Y1 Zeolite Y Formaldehyde and 900 — Fd3m symmetry 0.7–4 3519 1.3 CO2 adsorption 27
propylene Nanoparticles
TC-Y2 Zeolite Y Propylene 900 — Fd3m symmetry 0.7–4 1815 1.8 CO2 adsorption 27
Nanoparticles
TC-EMC Zeolite EMC-2 Formaldehyde and 900 — P63/mmc symmetry 0.7–4 3840 1.8 CO2 adsorption 27, 48
propylene Retained EMC-2 zeolite and 49
morphology
HR-ZTC Hierarchical Ethanol 600–700 Nanoparticles 1.2 2220 2.45 Supercapacitor 29
zeolite beta Zeolite morphology
This journal is © The Royal Society of Chemistry 2018

P7 Zeolite Y Acetylene 900 Core–shell structure 1.0 2100 — Supercapacitor 30
FA-ZTC Zeolite 13X FA and ethylene 700 Zeolite particle type 1.2 3332 1.66 H2 storage 31
morphology
CB-700 ZIF FA and acetonitrile 700 Nanoparticles (50–100 nm) 0.8 970 0.66 H2 uptake 32
ZIF morphology
HPCMs Hierarchical Furfuryl alcohol and 850 — Positive replicas of SBA-15- 3.36 729–1354 1.6 Cleaning/recycling 26
SBA-15-monolith trimethyl benzene monolith spilled oils or organic
solvents.
Rod shaped morphology Bilirubin adsorption
OMCs Pluronic F127 and Resorcinol and 700– — Graphitic tubules morphology 4.8 603–808 0.55– Supercapacitors 50
Fe(NO3)39H2O formaldehyde 1000 P6mm symmetry 0.66
OMCs Pluronic F127, Resorcinol and 800 — Fm3m symmetry 10.1– 212–780 0.19– Stabilization of Ag 51
TEOS and AgNO3 formaldehyde Hexagonal arrangement of 11.0 0.65 nanoparticles
pores
Monolithic Pluronic F127 and Resorcinol and 600 — 2D hexagonal p6mm symmetry 4.7–5.1 675–758 0.14– Dehydrogenation of 52
mesoporous citric acid formaldehyde 0.16 propane to propylene
carbons
OMC films Pluronic F127 Phenol and formalin 350–800 — Cage type cubic Im3m Kr sorption 53
2-D hexagonal p6mm
Face centered orthorhombic
Fmmm
NMC-G SBA-15 Gelatin 600– N: 4.5 to 2D hexagonal mesostructure 3.54– 764–846 1.14– Sensing of acetic acid 54 and
1000 14.46 at% P6mm symmetry 6.41 1.50 CO2 adsorption 55
Rod shaped morphology Electrocatalyst for
ORR
OMFLC-N SBA-15 FA and dicyandiamide 1000 N: 8.2 to 2D hexagonal ‘‘crystal’’ 1.8–4.0 1580 2.2 Supercapacitrors 56
10.6 at% P6mm symmetry
NOMC and SBA-15 Honey 650–950 N: 1.0 to SBA-15 replicated structure 621–1273 0.73– Metal-free catalyst for 57 and
HNMC 3.5 at% 1.16 ORR 58
Rod shaped morphology Li and Na ion
batteries
P6mm symmetry
N-OMC and Crab shells and Resole and dicyandiamide 750 N: 4.6 to 2D hexagonal 4.1–15.0 516–1030 0.3–2.35 Supercapacitors 59
N-OMCNFA Pluronic F127 6.7 at% P6m symmetry
Nano fibre morphology
NONC SBA-15 Dopamine 800 N: 5 at% Successful SBA-15 replication 3.8 1013 1.14 Supercapacitors 60
P6mm symmetry
Rod shaped morphology
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Chem Soc Rev
Table 1 (continued)

Chem Soc Rev
G-OMC Mesoporous NiO Dopamine 900 N: 1.6 at% 2D morphology 3.5 269 0.35 Electrochemical 61
Ordered graphitic mesopores double layer capacitors
N-HMCs KIT-6 (1-Methyl-1H-pyrrole-2- 850 N: 0.5 to Well-ordered mesopores 3.4–4.0 780–1150 0.91– Electrocatalyst for 62
yl)methanol 10.0 at% Successful transformation of 1.02 ORR towards H2O2
KIT-6 type structure production
Ia3d symmetry
N-HMCSs Mesoporous silica Polystyrene/ 700 N: 3.6 at% Hollow structure 4.1 807 0.87 Supercapacitors 63 and
spheres polyacrylonitrile Mesopores on the shells 64
NHPCM Amine grafted Furfuryl alcohol 700– N: 1.1 to Carbon rod replicas 3.8 744–796 1.31– Electrocatalyst for 65
hierarchically 1000 1.5 at% Well retention of monolith 1.53 ORR
porous silica morphology
monolith Highly regular arrays of
2684 | Chem. Soc. Rev., 2018, 47, 2680--2721

branched morphology
N-MC Amine Sucrose 900 N: 0.6 to Hexagonally ordered cylind- 5.14 749–790 0.65– Supercapacitors 66
functionalized 1.5 at% rical mesopores 0.86
SBA-15 Negative replica of SBA-15
NOMC and SBA-15 Pyrrole or aniline 800– N: 0.5 to Inverse replica of the SBA-15 3.7–7.4 591–886 0.52– Electrocatalyst for 67–69
C-PY 1400 10.7 at% template 0.93 ORR
Highly ordered mesopores Supercapacitors
P6mm symmetry
NOMC SBA-15 D(+)-Glucose and 900 N: 2.5 to Stripe like mesopores 3.9–7.3 352–1152 0.59– Supercapacitors 70
D-glucosamine 3.9 at% Rod shaped morphology 0.97
P6mm symmetry
N-OMCs SBA-15 m-Aminobenzoic acid and 700 N: 7.8 to Pore channels arranged in a 5.0 1058– 1.0–1.8 Ibuprofen (drug) 71
p-aminobenzoic acid 8.3 at% bidimensional ordered array 1322 release
P6mm hexagonal symmetry
HPC-Ns Hierarchically FA, oxalic acid and urea 750–900 N: 1.8– Disordered hierarchically 3.5–3.6 1571– 1.5–2.2 Electrocatalyst for 72
porous silica 6.4 at% porous structure 2473 ORR
monolith Rod shaped morphology
NHPC-3D Silica spheres Dopamine 800 N: 7.4 at% Interconnected and layered 2.5 1056 2.56 Supercapacitors 73
Macroporous structure
N-OMCs SBA-15 Iron phthalocyanine 900 N: 3.5– Rugby ball or rice grain-like 3.1 1122– 1.6–2.1 Electrocatalyst for 74
3.7 at% ellipsoidal shaped nanoparticles 1720 ORR
Mesoporous channels run
parallel to the rod shaped
direction
P6mm hexagonal symmetry
N-MCHSs Silica hollow Dopamine 600–900 N: 2.2– Sponge like shells with 5.0 375–438 0.40– Anode for Li-ion 75
spheres and 4.5 at% interconnection of hollow cores 0.43 batteries
Pluronic P123 Carbon shells are inter-
connected by ‘‘carbon bridges’’
NMMC Pluronic F127 and Resol and dicyandiamide 700 N: 4.6– 2D hexagonal meso-structure 4.6 1344 0.90 Supercapacitors 76
titanium-carbide 7.8 at% Highly ordered, stripe-like
pores
NMCs SBA-15 Amino acids 700–900 N: 3.6– Ordered nanowire arrays 4.27– 694–1280 0.89– CO2 uptake 77
9.4 at% Rod like ‘‘wheats’’ shaped 5.72 2.48 Electrocatalyst for
morphology ORR
Ordered and disordered
mesoporous structure
NMC SBA-15 Resol and cyandiamide 800 N: 5.1– 2D hexagonal mesostructure 2.4–4.1 1095– 0.73– Supercapacitors 78
15.1 at% Shuttle-like morphology 1722 1.81
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Review Article
P6mm symmetry
Table 1 (continued)

Review Article
NNCM 3D continuous Polyacrylo nitrile (PAN) 900 N: 6.1– 3D continuous nano 30 391–663 0.9–2.1 Volumetric capacitors 79
skeleton silica 6.5 at% framework
particles Numerous continuous
mesopores
meso-BMP Ludox HS40 Ionic liquids 900 N: 5.0– Long-range ordered structure 5–20 320–1380 0.75–3.6 Electrocatalyst for 80–82
17 wt% H2O2 production
3DOm carbon Slilica spheres BMP-dca Pores are less well defined Electrochemical
double-layer capacitors
EMI-dca
EMI-tfsi
RF-1 and RF-2 Pluronic F127 and Resorcinol and hexa- 350–900 N: 1.1– Body-centred cubic (Im3m) to 3.1–6.7 659–870 0.33– Adsorption 83
trimethylbenzene methylene tetramine (HMT) 6.5 at% 2D hexagonal (p6m) structure 0.49
Ammonia Irregular polyhedral particles

PHMT — Resorcinol and hexa- 600– N: 1.3– Interconnected spherical 0.6–1.3 528–936 0.19– CO2 capture 84
methylene tetramine (HMT) 1000 6.9 at% particles 0.33
HMT Ammonia Nitrogen containing micro-
porous carbon
ACMP-N
NOMC Pluronic F127 Resorcinol–melamine– 600–800 N: 2.4– Body-centred cubic Im3m 2.71– 583–631 0.30– CO2 adsorption 85
formaldehyde resin 2.9 at% symmetry 3.02 0.33
Irregular polyhedral particles
Nitrogen- Pluronic F127 Resorcinol formaldehyde, 700–850 N: 7.1– Highly ordered mesoporous 6.6–7.0 643–1415 0.57–1.2 Supercapacitors 86
enriched NH3 gas 9.1 at% structure
OMCs P6m symmetry
H-NMC Pluronic F127 Resol and dicyandiamide 600 N: 0.09 to Tunable mesostructures 3.1–17.6 494–586 0.14– CO2 capture 87
13.1 wt% (p6m and Im3m symmetry) 0.17
C-NMC Mesostructure formed in a Supercapacitors
layer-by-layer fashion
N-OMCs Pluronic F127 Resorcinol formaldehyde 600 N: 0.23 to Parallel mesoporous channels 5.5–9.3 376–718 0.42– Dehydrochlorination 88–90
and Na2CO3 dicyandiamide 4.2 wt% Well retention of mesoporous 0.78 of 1,2-dichloroethane
structure
2D P6mm hexagonal symmetry
N-OMCs Pluronic F127 Urea–phenol–formaldehyde 600 N: 0.38 to Spherical morphology 2.1 446–566 0.24– Adsorbent for acidic 91–93
1.41 wt% 0.31 gases
Cubic Im3m mesostructure Electrochemical
capacitors
om-MR Pluronic F127 Phenolic-functionalized 400 N: 18.16 wt% Ordered mesostructures of 2.9 385.9 0.17 CO2 adsorption 94 and
melamine resin Im3m symmetry 95
Polyhedron shaped Supercapacitors
morphology
NPGC Pluronic F127 Glucose and melamine 800– N: 2.9– Nanosheet-like structure 4.8–6.3 579–1116 0.38– Supercapacitors 96
TEOS, nickel nitrate 1000 6.96 wt% Interconnected nanoporous 0.79
structure
N-Doped Pluronic F127 Resol and dicyandiamide 700 N: 5.74– Hexagonal pore arrangement 5.1–7.4 631–1374 0.4–1.5 Supercapacitors 97
OMC TEOS 8.1 wt% Stripe like 2D mesostructure
NMNC — Glucose and NH3 800– N: 2.6– Sphere structure 2.3–2.8 1154– 0.67– Electrocatalyst for 98
1000 4.7 wt% Network-like morphology 2588 1.71 ORR
NMC5 Pluronic F127 and Resorcinol formaldehyde 700– N: 5.5– Sphere shaped morphology 5.0 307–484 0.30– Electrocatalyst for 99
fluorocarbon Melamine 1000 25.7 wt% Ordered porous structure 0.41 ORR
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Chem Soc Rev
Table 1 (continued)

Chem Soc Rev
NOMC Pluronic F127 3-Aminophenol hexa- 800 N: 3.4– Polyhedral crystal like 3.6–5.4 72–1159 0.05– Supercapacitors 100
methylene tetramine (HMT) 5.4 wt% morphology 0.72
Ammonia Rhombic dodecahedron shape
m3m symmetry
NMC Pluronic P123 Melamine–formaldehyde 600–900 N: 5.5– Disordered porous structure 5.0 252–794 0.31– Electrocatalyst for 101
Sodium silicate resin 27.1 wt% 1.15 ORR
NHCSs Pluronic P123 2,4-Dihydroxybenzoic acid 800– N: 3.6– Ruptured spherical particles 3.9 738–820 0.5–0.56 Electrocatalyst for 102
Sodium oleate and hexamethylene tetra- 1000 7.8 at% Hollow spherical structures ORR
mine (HMT)
BOMCs SBA-15 Sucrose and 4- 900 B: 0.64– 2D hexagonal mesoporous 6.4–7.2 778–1040 1.18– Electrocatalyst for 103
hydroxyphenylboronicacid 2.11 at%structure 1.52 ORR and
P6mm symmetry 104
2686 | Chem. Soc. Rev., 2018, 47, 2680--2721

Rod-like particles
Mesoporous Pluronic F127 Phenol, formalin and boric 400–700 B: 3.6 at% 2D hexagonal mesoporous 3.6–4.1 475–551 0.45– Proton exchange 105
CB film acid structure 0.53 membrane fuel cells
Hierarchical Pluronic F127 Resorcinol and boric acid 800 B: 0.42– Hierarchically mesoporous 5.0 547–643 0.49– Supercapacitors 106
carbons with boron 2.37 at% structure 0.73
Ordered pores
POMCs SBA-15 Phenol and 900 P: 1.36 at% Spherical carbon 3.5 814–1182 1.4–1.87 Electrocatalyst for 107
triphenylphosphine microstructures ORR
Highly ordered uniform pore
distribution
POMCs SBA-15 Glucose and 900 P: 0.64 at% Rod shaped morphology 3.8–4.3 1117– 1.24– Pt nanoparticles 108
triphenylphosphine 1338 1.37 stabilization
P6mm symmetry Methanol
electrooxidation
SN-OMCs SBA-15 Thiophene and pyrimidine 700 N: 6.2 at% 2D hexagonal mesoporous 3.5 750–1100 0.53– Electrocatalyst for 109
structure 0.83 ORR
S: 0.25 to Rod like morphology
0.68 at%
P6mm symmetry
NSOMC SBA-15 Pyrrole and H2SO4 650–950 N: 4.8 to 2D hexagonal mesoporous 3.24 978–1021 1.1–1.2 Electrochemical 110
10.0 at% structure double-layer capacitor
2.6 at%
P6mm symmetry
SNOMC SBA-15 Pyrrole and thiophene 800 N: 1.2 to 2D hexagonal mesoporous 6.2 601 1.0 Electrocatalyst for 111
5.7 at% structure ORR
8.7 at%
P6mm symmetry
SN-OMC SBA-15 Diphenylthiocarbazone 800– N: 3.2 at% 2D hexagonal mesoporous 5.1 647–816 0.5–0.75 Electrocatalyst for 112
1000 structure ORR
S: 0.8 at% Rod like morphology
P6mm symmetry
OMC-S SBA-15 Sucrose and benzyl 900 S: 1.4 to 2D hexagonal mesoporous 4.5–5.4 1099– 1.37– Electrocatalyst for 113
disulfide 1.5 at% structure 1244 1.61 ORR
Rod like morphology
P6mm symmetry
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Review Article
View Article Online
but the scale of production is of a nanoscale order. In the nano
Ref.
114
templating approach, highly ordered inorganic mesoporous
solid materials are used to replicate their structure into nano-
porous carbon materials with well-ordered mesoporosity. There
Supercapacitors
are several review articles outlining the details of these synthetic
processes including history, different synthetic strategies, and
(cm3 g 1) Applications
the formation mechanism for obtaining ordered nanoporous
carbons.2,4,7,15 However, in the present review, we will discuss the
recently reported synthesis methods and templating strategies

applicable to OMCs from the last five years.
0.59–
VTotal
2.1 Hard templating method for OMCs

0.67
The hard templating approach is considered as one of the most

(m2 g 1)
straightforward ways for synthesizing OMCs.7 Ordered meso-

590–659
SABET
porosity in carbon materials can be easily introduced by the

nanocasting technique using mesoporous inorganic materials
such as mesoporous silica and zeolites as hard templates.
(nm)
dpore
Various mesoporous carbons with different textural properties

6.2
have been prepared by using different porous templates through

this simple technique and the details of the materials and the
structural parameters are given in Table 1. Although many
Structure and morphology
Ordered mesostructures
materials have been prepared, the control of structure and

morphology of the materials has been gaining significant atten-
tion owing to the correlation with their final textural parameters.
To control the morphology of the final OMCs, it is necessary to
control the morphology of the template materials. Schuster et al.
reported that spherical OMC nanoparticles with bimodal pore
size distribution having mean pore sizes centred at 6 and 3.1 nm
and having 300 nm kinetic diameter can be prepared via the
Heteroatom
nano templating approach by using the phenol and formalde-

10.0 at%
O: 8.1 to
B: 0.8 to
P: 2.3 to
1.6 at%
3.6 at%
content
hyde mixture precursor and spherical silica as a hard template.24

The material showed a high specific surface area of 2445 m2 g 1
and the highest inner pore volumes up to 2.32 cm3 g 1. In this
case, the shape of silica hard templates has been achieved by
T (1C)
Resorcinol, boric acid and 600
using 400 nm PMMA spheres with a close packed opal structure.

This unique structure has been replicated into the final nano-
porous carbon samples. The typical spherically ordered opal
structures of OMCs with large domains of nanoparticles are
shown in the TEM images and DLS measurements. Seo et al.
phosphoric acid
demonstrated the preparation of OMCs by using furfuryl alcohol

(FA) as a carbon source and phosphoric acid or sulfuric acid
Precursor
impregnated acidified mesoporous silica as a precursor.25 This

work was aimed at preventing the generation of external carbon
by selecting a moderately weak acid that would slowly catalyze
the polymerization of FA. However, the obtained OMCs exhibited
a lower surface area than OMCs prepared by using unmodified
Pluronic F127
Template and
mesoporous silicas.
The hard templating approach can also be used to prepare
porogen
nanoporous carbon in the form of monoliths. Hierarchically

porous carbon monoliths (HPCMs) with both ordered hexagonal
(continued)
mesoporosity and three-dimensionally connected macroporosity,

and controlled morphologies have been synthesized via a simple
nanocasting pathway by using hierarchically macro/mesoporous
silica with tunable morphologies as a hard template and the FA
Material
Table 1
HTBP
and trimethyl benzene (TMB) mixture as a carbon source. These

monoliths exhibit high pore volumes (1.6 cm3 g 1) and specific
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Fig. 1 Schematic illustration of the synthesis, functionalisation and applications of micro and mesoporous carbons.
surface areas (1354 m2 g 1) and a strong hydrophobicity due to three dimensional graphene based ordered microporous carbon
the nature of the precursor used in the synthesis.26 These with a surface area of 2100 m2 g 1 in the confined nanochannels
results reveal that the selection of the precursors is the key to of zeolite Y by using acetylene gas through a pulsed chemical
control the surface characteristics of the final carbon materials. vapour deposition technique.30
OMCs with various surface areas of 1361 to 3840 m2 g 1 and Mokaya et al. introduced an elegant approach to synthesise
tunable micropores have been prepared by using zeolite Y and porous carbons with an ultra high surface area of 3332 m2 g 1
zeolite EMC-2 as sacrificial hard templates and FA as the and a specific pore volume of 1.66 cm3 g 1 through the simple
precursor.27,28 Although FA was used as the precursor for impregnation of zeolite13X with FA followed by chemical vapour
zeolite templated porous carbons, the pores of the zeolites deposition (CVD) of ethylene gas.31 This unique double filling
are too small to accommodate bulky molecular precursors. approach introduced graphene sheets with a large number of
Ryoo et al. have tackled this problem by using ethanol as a edges within the nanochannels, which are responsible for
carbon source and hierarchically meso-/microporous zeolite enhancing the specific surface area of the final carbons. The
beta as a template for the synthesis of hierarchically nano- same group also demonstrated a pressure assisted strategy to
porous carbons with mesopore–micropore hierarchy.29 The hier- create microporosity within the porous carbons derived from
archically porous carbons exhibited a high BET surface area of zeolitic imidazolate framework (ZIF) templates.32–34 This simple
2220 m2 g 1, a large micropore volume of 0.62 cm3 g 1 and compaction technique can be used as an effective method to
a mesopore volume of 1.48 cm3 g 1. The authors concluded either increase or decrease the textural properties of the acti-
that the ethanol precursor is more suitable for hierarchical vated ZIF-templated carbons as it has the potential to create new
carbon synthesis, as compared with propylene or acetylene gas micropores or decrease the size of the large mesopores into
precursors, which is mainly because of the formation of water micropores. The properties of the OMCs can also be significantly
vapour due to the decomposition of ethanol during the heat altered with the external agents such as metal oxides.
treatment. It is also assumed that this process assisted in Ryoo and his co-workers realized this wonderful opportunity
delaying the deposition of carbons at the exterior. Nueangnoraj and demonstrated a ground breaking lanthanum-catalysed zeolite
et al. reported on the formation of cross linked fullerene like templated synthesis process of microporous 3D graphene-like
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commercialization is the removal of the mesoporous silica

and zeolite hard templates by highly toxic HF. Therefore, the
researchers found eco and environmentally friendly soft tem-
plating approaches to prepare OMCs without compromising
the textural parameters.
2.2 Soft templating method for OMCs

The soft-templating approach has been widely applied for the
synthesis of various mesoporous materials including zeolites,

silica, inorganic metal oxides and mesoporous carbons.38–44
Preparation procedures for silica, zeolites and metal oxides
have been well established.45,46 However, the direct synthesis of
OMCs by the soft-templating approach is not straightforward.
Various factors including the functionalization of templates
with polymeric units, hydrogen bonding between the template
and the precursors, organic–organic composites, organic–organic
self-assembly, and hydrogen bonding induced organic–organic
self-assembly have been optimized to obtain OMCs with excellent
textural parameters.15,41,47
Among these strategies, the direct synthesis of OMCs using
organic–organic self-assembly involving the combination of
Fig. 2 (A and B) Electron-density map of zeolite FAU after carbon deposi-
polymerizable precursors and block copolymer templates is
tion. (C) X-ray crystallographic analysis of the carbon structure formed in a expected to be more flexible than other soft templating methods
single crystal of La3+-ion-exchanged zeolite FAU. Reproduced with per- and the traditional hard templating nanocasting methods.47
mission from ref. 35. Copyright 2016, Nature Publishing Group. Li et al. reported a series of hexagonally ordered mesoporous
carbons (OMC-Ts) by adjusting the pyrolysis temperature of
the resorcinol and formaldehyde mixture via a soft templating
carbon materials using ethylene as a carbon precursor, which and catalytic graphitization approach by using the Pluronic
have two times higher conductivity than that of CMK-3 (Fig. 2).35 F127, EO106PO70EO20 triblock copolymer as the template and
This is an energy efficient synthesis process as it requires a Fe(NO3)39H2O as a catalyst.50 The structure of OMC-Ts has a
carbonization temperature of only 600 1C, whereas the conven- two-dimensional hexagonal ( p6mm) mesostructure with tubule
tional microporous graphene synthesis requires a temperature like morphology. The OMC-700 sample synthesized at 700 1C
in the range of 900 to 1000 1C. Noteworthily, microporous carbon showed a high specific surface area of 808 m2 g 1 and a pore
deposition in lanthanum modified zeolite Y occurs more than 20 volume of 0.55 cm3 g 1 with a uniform mean pore size of 4.8 nm.
times faster than in an acidic HY zeolite. Acetylene gas can also Sterk et al. described a soft-templating synthesis procedure
be used instead of ethylene to construct carbon frameworks by to prepare OMCs with BET surface area up to 780 m2 g 1 using
using modified zeolites. As acetylene gas is more reactive than triblock copolymer F127 and phenolic resin precursors in the
ethylene, carbon deposition can be accomplished even at lower presence of tetraethyl orthosilicate (TEOS). In this case, silver
temperatures as low as 340 1C.35 If the realized microporous nitrate was added in the synthesis mixture to increase the
carbon materials possess a poorly ordered porous structure, microporosity as well the metal nanoparticles in the porous
they can be converted to highly ordered materials after heat channels of OMCs.51 Monolithic mesoporous carbons were also
treatment of 900 1C.36 The same group has also developed a prepared from resorcinol–formaldehyde resin through a simple
large scale (70 g batch) synthesis of 3D graphene-like ordered autoclaving method using citric acid as a catalyst and triblock
microporous carbon with 2770 m2 g 1 BET surface area and copolymer F127 as a structure directing agent. The obtained
1.32 cm3 g 1 pore volume by using the cost effective calcium mesoporous carbons have a hexagonal pore system, a uniform pore
modified zeolite X template and ethylene gas under the same size of B5.0 nm and a high BET surface area of B758 m2 g 1.52
conditions.37 These zeolite templated carbons (ZTCs) have A similar strategy was also adopted to prepare highly ordered
a higher particle density and a higher surface area (around OMC films with controllable mesostructures and highly accessible
3000 m2 g 1) than CMK-3. The gravimetric and volumetric surfaces. A simple direct carbonization of phenolic resin and
surface areas of ZTCs are the highest among all the carbon the conventional Pluronic F127 and EO106PO70EO20 triblock
materials, and therefore they exhibit a superior capacity for copolymer as a template afforded the highly ordered OMC
energy storage. These approaches demonstrated that the pre- films (Fig. 3).53 The structure of the films can be controlled
paration strategy is the key to control the final properties of the by adjusting the amount of the surfactant in the synthesis
OMC which ultimately determine their performances in various mixture. The unique concept of mesostructural transformation of
applications. Although these materials have interesting proper- cage-type to tubular frameworks via anisotropic shrinkage upon
ties, the main issue that places a hurdle in the path of their increasing the carbonization temperature was also demonstrated.40
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Thus, nitrogen doping into the OMCs could change their

electronic structures while minimizing the lattice mismatch,
leading to unique electronic properties. Great efforts have been
paid to introduce nitrogen atoms into OMCs as the incorpora-
tion of nitrogen atoms into the nanoporous carbon matrix can
significantly enhance their conducting, field emission, catalytic,
and energy storage properties.118–132
3.1.1 Hard templating approach. The precursors contain-
ing N atoms including polymeric compounds, acetonitrile,

urea, aromatic or aliphatic amines are generally used in combi-
nation with the hard-templating method for the incorporation
of nitrogen in the carbon framework of OMCs.133,134 Recently,
Vinu et al. demonstrated the synthesis of highly ordered
nitrogen-containing mesoporous carbon (NMC-G) with well-
Fig. 3 TEM and FFT images of phenol resin films after carbonisation and ordered mesopores and various pore diameters and also high
the schematic illustration of variation in their mesostructure. Reproduced basicity using a low-cost, naturally occurring gelatin biomole-
with permission from ref. 53. Copyright 2013, Royal Society of Chemistry. cule as a single-molecule precursor and 2D hexagonal SBA-15
with different pore diameters prepared at different hydrother-
mal temperatures as the hard template (Fig. 4).54,55
Anisotropic shrinkage upon increasing the carbonization
The realized NMC-G materials have excellent textural prop-
temperature has been observed for thin film samples and the
erties such as high specific surface areas (764–804 m2 g 1),
process changes the space group of the obtained films. On the
huge pore volumes (1.14–1.40 cm3 g 1), and mesoporous
other hand, only unit cell parameters were reduced for the
diameters (3.54–4.89 nm). Recently, Huang et al. made a
powder samples upon alteration of carbonization temperature
ground-breaking discovery of the synthesis of self-supported
while keeping the original space groups by isotropic shrinkage
N-doped ordered mesoporous few-layer carbon (OMFLC-N)
with condensation of the framework. This unique approach
superstructures catalysed by Ni catalyst through chemical
involving a simple adjustment of the preparation conditions,
vapour deposition using simple and environmentally friendly
the amount of Pluronic F127, and the carbonization tempera-
precursors such as FA and dicyandiamide (DCDA) and meso-
ture is found to be an effective tool for controlling the structure
porous SBA-15 silica as the template.56 The OMFLC-N sample
of OMC films.
exhibited a high conductivity (360 S cm 1) with mesoscopically
ordered few-layers and also possessed the largest surface area
3. Heteroatom doped OMCs (1580 m2 g 1), a high total pore volume (2.20 cm3 g 1), the
smallest average pore width (2.25 nm), and the most prominent
Heteroatom doping is the replacement of some of the carbon pores smaller than 2 nm. A graphene-like structure with r5 layers
atoms in the uniform graphitic carbon structure with other and minimum number of defects in OMFLC-N were verified by
foreign atoms which significantly changes the electronic,
electrical and surface charge properties of the final materials.
The introduction of heteroatoms such as boron, nitrogen,
sulphur, and phosphorus into the OMCs could cause electron
modulation due to their different electronegativity. This also
tunes their charge distribution, optoelectronic properties and/
or defect induced chemical functionalities, which are useful for
many technological applications.115,116 Heteroatom-doped OMCs
can be prepared either by in situ doping during the preparation
of nanoporous carbon materials or through post-treatment of
preformed carbon nanomaterials with heteroatom-containing
precursors.117 The post treatment procedure often leads to only
surface functionalization without altering their bulk properties
whereas the in situ doping of heteroatoms can help to homo-
geneously incorporate the heteroatoms into the entire nano-
porous carbon matrix. Fig. 4 (A) Synthesis scheme for the fabrication of ordered mesoporous
carbon with nitrogen (NMC-G) prepared through the nano templating
3.1 Nitrogen doped OMCs approach. (B) N2 adsorption–desorption patterns of NMC-G samples
replicated from SBA-15-x templates: (a) NMC-G-100, (b) NMC-G-130,
Nitrogen is one of the neighbour elements next to carbon in the and (c) NMC-G-150. (C) Pore size distribution of the same. Reproduced
periodic table and it has an atomic radius similar to that of carbon with permission from ref. 54. Copyright 2012, Wiley-VCH Verlag GmbH &
but has different electronic configuration and electronegativity.117 Co. KGaA, Weinheim.
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Raman spectroscopy. The introduction of transition metal ions Although natural biomasses used for heteroatom doped
helps in the formation of a highly graphitic structure along the nanoporous carbons are cost effective, the control of the degree
walls whereas N doping changes the electronic structure of the of polymerization is highly difficult. This has been addressed by
formed carbons. The combination of these factors significantly the judicious choice of easily polymerisable precursors. A facile
enhances the conductivity of the final materials. synthesis route has been developed to prepare nitrogen-doped
Natural honey which contains 80–85% carbohydrates, ordered nanoporous carbons (NONCs) by Wu et al. based on
15–17% water, 0.3% proteins, 0.2% ashes and minor quantities in situ polydopamine coating onto the SBA-15 pore surface.60
of amino acids and vitamins has also been utilized as the The dopamine was quickly self-polymerized onto the pore wall
source of nitrogen and carbon for the fabrication of nitrogen- of SBA-15, forming polydopamine/silica nanocomposites in
doped ordered mesoporous carbons (NOMCs). Guo et al. and the presence of Tris-buffer solution. The carbonization of the
Xiao et al. have independently demonstrated the synthesis polydopamine/silica nanocomposite in N2 and then removal of
of NOMCs by the nanocasting method using SBA-15 as the the silica template eventually led to the formation of NONC
template and natural honey as the source of nitrogen and carbon material with a BET surface area of 1013 m2 g 1. However, these
(Fig. 5). The structure of NOMCs exhibited a two-dimensional materials suffered from poor crystallinity which suppresses the
hexagonal mesoporous framework, composed of ordered nitrogen conductivity of the materials. This was overcome by the discovery
doped carbon nano rods. The BET specific surface areas of NOMCs of Yuan et al., who reported the synthesis of nitrogenated
were in the range of 600 to 1100 m2 g 1 but varied significantly with graphitic ordered mesoporous carbon (G-OMC) by using meso-
the change of carbonization temperature. It should be noted that porous nickel oxide as a template as well as the catalyst and
the pore size of NOMCs is 4.0 nm, which is less than half of the dopamine as a precursor. The results revealed that G-OMC
mesoporous silica template SBA-15 (9.1 nm) but similar to the wall materials had a higher degree of graphitization compared to
thickness, revealing the transformation of silica walls into pores those prepared from dopamine and pure SBA-15 as the template,
and the pores of the templates into N-doped carbon walls.57,58 which was mainly because of the catalytic graphitization induced
A NOMC nanofiber array was prepared by the combination of a by the nickel oxide catalyst. The ID/IG value of the G-OMC was
soft templating method and a hard-templating approach using a 0.69, which was much less than the ID/IG value of CMK-3 (0.84),
well-mixed solution of calcined crab shells, Pluronic F127, dicyan- revealing the high graphitic nature of G-OMC.61
diamide (DCDA) and resole.59 NOMC nanofiber arrays possessed For many applications, not only the conductivity but also the
four resolved SAXS scattering peaks, which were indexed as the amount of nitrogen doping in the carbon framework is also
100, 110, 200, and 210 planes of a 2D hexagonal mesostructure crucial as it sometimes dictates the final performance of the
with the space group of p6m. The obtained NOMC nanofiber materials. For instance, Park et al. demonstrated the synthesis
material also exhibited a high surface area (1030 m2 g 1) and a of mesoporous nitrogen-doped carbon with tunable nitrogen
large pore volume (2.35 cm3 g 1), with uniform mesopores of ca. content by the simple adjustment of the amount of the pre-
15.0 nm which was much larger than that of CMK-3s, OMFLC-N, cursor, (1-methyl-1H-pyrrole-2-yl) methanol (MPM), which is
and NOMCs.1,56–58 These reports clearly reveal that the natural structurally similar to FA, using 3D body centred cubic KIT-6
biomasses are unique and low cost sources for the in situ intro- as a template. The nitrogen content of the resulting carbon was
duction of nitrogen atoms in the carbon framework of OMCs controlled in the range of 0–10 at% and all prepared samples
which could offer exciting electronic properties. had well-ordered mesopores with diameters of 3.4–4.0 nm and
BET specific surface areas of 780–1150 m2 g 1.62
Nitrogen atoms have also been doped with OMCs with
different morphologies using different techniques. For
example, monodispersed nitrogen-doped hollow mesoporous
carbon spheres (N-HMCSs) have been synthesized using a novel
‘‘dissolution-capture’’ method wherein the polystyrene/
polyacrylonitrile composite nanospheres (PS@PAN) were used
as the carbon and nitrogen resource, which were uniformly
coated by a layer of mesoporous silica. After organic solvent
treatment, the PS@PAN were dissolved and then captured
in the confined nanospace of the mesoporous silica shell. The
N-HMCSs with a surface area and pore volume of 807 m2 g 1 and
0.87 cm3 g 1 were produced after carbonization followed by the
removal of the template through HF etching.63,64 The orientation
of the formed carbon nanorods can be controlled by the simple
modification of the surface of the sacrificial template. Wang
Fig. 5 (a) Schematic illustration of the synthesis procedure of NOMCs
et al. reported an in situ source-template-interface reaction
prepared from honey and SBA-15. (b) FESEM and HRTEM images of NOMCs
synthesized at 800 1C. (c) Nitrogen sorption isotherms of NOMCs prepared at
route to prepare a 3D N-doped hierarchically porous carbon
different temperatures along with the mesoporous silica SBA-15 hard template. monolith (NHPCM) composed of branched mesoporous rods
Reproduced with permission from ref. 58. Copyright 2016, Elsevier. by the nanocasting method with the amine functionalized
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hierarchically porous silica monolith (NHPSM) scavenger and FA of nitrogen-doped micro-mesoporous carbon material with a
as the carbon source.65 It has been demonstrated that this unique surface area of 789–1367 m2 g 1 by employing urea–formalde-
approach helped to anchor a high density of N atoms on the hyde resin as carbon and nitrogen sources, zinc chloride as a
surface of the NHPCM as a simple solid–solid interface reaction porogen and SBA-15 as a hard template.137 Nitrogen doped
between the carbon precursors and amine functionalized NHPSM three dimensionally ordered microporous carbon (N-ZTC) was
favoured the doping on the surface. Asefa et al. also described the also synthesized by using aqueous acetonitrile as a nitrogen-
NOMC synthesis by using the amine group functionalized meso- containing carbon source and zeolite beta as a template. The
porous silica SBA-15 but glucose was used instead of FA as a obtained materials possess a nitrogen content of approximately
carbon precursor.66 By varying the nature of the solvents (polar or 4 wt% and a large surface area and pore volume of 1860 m2 g 1
non-polar) used for grafting amines on the surface of the tem- and 1.4 cm3 g 1, respectively.138 Ling et al. reported on the
plates, the amount of N doping on the final NOMC was controlled. hard-templating synthesis of pristine and functionalized
Liang and Tsiakaras et al. reported a novel impregnation CMK-3 materials having BET surface areas in the range of 1152
method, namely vaporization-capillary condensation process, to 1760 m2 g 1 with various functionalities, including micropore
to synthesize NOMC via the nano hard templating method development, nitrogen doping by using SBA-15 as the mesopore
using SBA-15 as the template and pyrrole as the precursor in template, and silicate oligomer as the micropore template,
the presence of FeCl3 catalyst. This new impregnation method low-molecular-weight phenolic resins as the carbon precursors
yielded a much larger surface area (661 m2 g 1) and pore volume and nitrogen-rich hexamethoxymethylmelamine (HMMM) as a
than the wet incipient method (292 m2 g 1).67,68 With the nitrogen precursor.139
adjustment of the pore diameter of the SBA-15 template and the Ahn et al. synthesized a series of ladder type nitrogen-doped
carbonization temperature, the textural parameters and nitrogen mesoporous carbons (CPANs), which were found to have high
content of NOMCs prepared from the pyrrole precursor were stability, by using SBA-15 and in situ polymerization of poly-
controlled, respectively.69 NOMCs have also been synthesized by acrylonitrile (PAN) inside the mesochannels of the template
using a mixture of D(+)-glucose and D-glucosamine hydrochloride at different carbonization temperatures. Among the materials
as carbon precursors and SBA-15 as the template. The as-prepared prepared, CPAN-800, synthesized at the carbonization tempera-
products showed large pore volumes (0.59–0.97 cm3 g 1), high ture of 800 1C, was found to be the best one with many desirable
surface areas (352.72–1152.67 m2 g 1) and rational nitrogen properties such as high specific surface area (1182 m2 g 1) and
content (ca. 2.5–3.9 wt%).70 In another study, Sanchez et al. pore volume (1.54 cm3 g 1), a moderate nitrogen content of
demonstrated the NOMC synthesis by using SBA-15 and two 9.52%, and a highly ordered mesoporous structure with uniform
aromatic polyaramids, namely m-aminobenzoic acid (MABA) and pore sizes of 4.34 nm.140 Zhao et al. adopted a similar strategy
p-aminobenzoic acid (PABA), as the precursors for C and N.71 but used a low molecular weight phenolic resin (resol) as a
NOMCs with different morphologies and a nitrogen content of carbon source and a high nitrogen-containing cyanamide as the
3.5–3.7 at% were also prepared by Yu et al. through the pyrolysis nitrogen dopant. The prepared NOMCs exhibited a high surface
of iron phthalocyanine infiltrated in SBA-15 with different area of 1741 m2 g 1 and nitrogen content up to 15 wt% by the
mesochannel lengths. The BET surface area was found to nanocasting approach. It was also demonstrated that the BET
be decreased with increasing mesopore channel length of the surface area (1397–1741 m2 g 1), pore size (3.6–4.1 nm) and
SBA-15 template.74 Transition metal containing precursors not pore volume (1.05–1.81 cm3 g 1) were easily tailored by con-
only act as the source of porous carbons, but also as catalysts in trolling the cyanamide-to-resol mass ratio or the carbonization
improving the graphitic nature and conductivity of the resulting temperature in the range of 600–900 1C.78 Yang et al. used a
materials. silica gel template with a 3D continuous skeleton and PAN in
Aniline, pyrrole and phenanthroline were also indepen- DMF solution for the synthesis of nitrogen-doped mesoporous
dently used as nitrogenated carbon precursors to synthesize carbon (NNCM) with a tunable pore volume (1.22 to 2.11 cm3 g 1)
NOMCs by the nanocasting method with SBA-15 template. The but a fixed pore size in order to control the coating density for
NOMC materials derived from pyrrole (C-PY-900: 765 m2 g 1) miniaturized energy devices. This was achieved by the simple
and phenanthroline (C-Phen-900: 746 m2 g 1) exhibited higher adjustment of the quantity of PAN in DMF in the mesochannels
specific surface areas compared to the aniline analogue but of the 3D template.79 3D NOMCs having a BET surface area up to
the nitrogen content of these samples was almost constant 1131 m2 g 1 have been prepared by using three dimensionally
(3.1–3.3 at%) for the three carbon sources, except for a slight ordered silica as the template and FA and oxalic acid as the
difference in the nitrogen configuration.135 NOMC catalyst was carbon source and an acid catalyst, respectively, under ammonia
directly synthesized using SBA-15 as a hard template, sucrose pyrolysis.141
as a carbon source and urea as a nitrogen source. A 3.6 wt% Nitrogen doped hierarchically porous carbon materials
nitrogen doping in the NOMC was achieved with more than 70% (HPC-Ns) have been successfully synthesized by Shi et al. by
of the nitrogen incorporated as quaternary nitrogen species.136 applying a simple N-doping procedure using the FA, oxalic acid
This is one of the best ways of controlling the nature of the and urea mixture in ethanol solution as a carbon and nitrogen
nitrogen species on the wall structure of the NOMCs. precursor and hierarchically macro/mesoporous silica as a template.
Nitrogen doping was also tried in porous carbons with The synthesized HPC-N samples demonstrated 3D connected
different pore diameters. Chen et al. reported on the synthesis ordered mesoporosity with an extremely large specific surface
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area (2473 m2 g 1) and relatively high content of pyridinic N.72 Nitrogen doped mesoporous carbon (meso-BMP) was synthe-
It was clear that when the nitrogen precursor was combined sized by Hasche et al. with the pyrolysis of high nitrogen
with an organic polar solvent, the specific surface area was (17 wt%) containing N-butyl-3-methylpyridinium dicyanamide
significantly enhanced. (BMP-dca) and commercial silica nanoparticles (Ludox HS40) as
3D interconnected nitrogen-doped hierarchically porous a template. The N2 adsorption derived BET surface area of the
carbons (NHPC-3D) were also prepared via a hard-templating meso-BMP was around 320 m2 g 1 and the total pore volume
method with colloidal silica spheres (80 nm) and dopamine as derived from the NLDFT method was 0.749 cm3 g 1.80 NOMC
the template and precursor, respectively. One of the interesting with a 2D hexagonal symmetry structure was synthesized via a
features of this study was the use of dopamine as the nitrogen facile solid–solid grinding/templating route, in which the ionic
precursor and the utilization of large sized colloidal silica liquids (ILs) 1-cyanoethyl-3-methylimidazolium chloride and
nanoparticles as templates. Dopamine has several advantages SBA-15 were employed as the precursor and hard template,
such as self and low temperature polymerization, easy inter- respectively. The as-synthesized NOMC featured a uniform
action with the surface of any templates and the final total mesoporous size (3.5 nm), rope-like morphology (0.4–1 mm in
carbon yield after carbonization. In addition, the templates length) and a high surface area (803 m2 g 1) with a nitrogen
with large nanoparticles offered a 3D structure with macro- content of 5.5 at%.82 Mesoporous nitrogen doped carbon
pores. The obtained NHPC-3D also exhibited a high surface with surface area up to 325 m2 g 1 was produced through the
area of 1056 m2 g 1, a large pore volume of 2.56 cm3 g 1, and a nano hard template method using resorcinol, melamine, and
high nitrogen content of 8.2 wt%, which also revealed the formaldehyde as the carbon precursors catalyzed by the alkaline
presence of a large quantity of micropores in the samples.73 medium and mesoporous silica as a hard template.144–147 It was
Huo et al. also used the dopamine precursor and the meso- believed that nitrogen doping sometimes results in the collapse
porous silica hollow sphere template to prepare nitrogen doped of the pore structure of the final porous carbons or creates a lot
mesoporous carbon hollow spheres (NMCHSs) with a specific of defects. Stein et al. used an elegant approach in which a novel
surface area of 411.6 m2 g 1.75 Tang et al. developed an ionic liquid (IL), 1-ethyl-3-methylimidazolium dicyanamide
innovative method based on sublimation and capillary con- (EMI-DCA), based precursor which not only acts as a nitrogen
densation assisted nanocasting for the fabrication of Fe and N source but also provides structural stabilization was used. In this
dual-doped mesoporous carbon catalyst with 988 m2 g 1 BET approach, silica spheres were used as templates which generated
surface area and 0.87 cm3 g 1 pore volume. Easily sublimable NOMC with a high specific surface area and a large pore volume
iron phthalocyanine was used as the source of iron, nitrogen of 1393 m2 g 1 and 4.5 cm3 g 1, respectively.81,148,149 Ionic
and carbon, while mesoporous silica SBA-15 was used as the liquid based precursors are found to be the best sources for
hard template.142 stabilising the porous structures of NOMC which resulted in a
Nitrogen-doped mesoporous carbon spheres (NMCS) were high specific pore volume owing to their good affinity and
prepared by a nanocasting route using benzoxazine resins as adhesion on silica surfaces.150–155
the precursor of nitrogen and carbon, and ordered mesoporous Most of these fabricated materials were made in the form
silica spheres as the hard template. The prepared NMCS of powder, which may not be useful for making devices for
exhibited amorphous spherical nanoparticles with worm-like electrochemical sensing applications. Therefore, researchers
mesoporous channels, and the specific surface area, pore turned their attention to fabricate these NOMCs in the form of
volume and nitrogen contents were 634 m2 g 1, 0.91 cm3 g 1 films. For instance, free-standing nitrogen-doped mesoporous
and 3.50 (wt%), respectively.143 Nitrogen-doped hierarchically carbon films were prepared by Peng et al. by carbonization of
mesoporous/microporous carbon (NMMC) was also prepared gelatin/HKUST-1 composite films, which were fabricated from
by using the nitrogen-doped mesoporous titanium-carbide/carbon gelatin/copper hydroxide nanostrand composite films. Gelatin
composite, followed by removal of carbides with chlorination. was the source of both carbon and nitrogen whereas the copper
The obtained NMMC gave a high surface area of 1344 m2 g 1 hydroxides offered porosity. The formation of HKUST-1 crystals
and exhibited micropores that were drilled on the mesopore expanded the gelatin matrix and produced porous structures
walls with the size of 0.70, 0.97 and 1.61 nm.76 which were retained during the carbonization process.156
Although the solvents play an important role in controlling 3.1.2 Soft templating approach. As hard templating proce-
the pore filling which is critical not only for controlling the dures require the removal of the inorganic materials using toxic
nitrogen content but also the structural order of the materials acids or strong bases, there has been significant attention to
sometimes they significantly increase the total cost of the the development of NOMCs using methods other than hard
production of the materials. Gao et al. described the synthesis templating. Soft-templating is considered as one of the viable
of NOMCs with improved yields of up to 25% by direct heating options to avoid the complex and toxic procedure involved in
of amino acids inside the porous channels of SBA-15 without hard templating. In the soft-templating synthesis of NOMCs,
using any solvent and metal catalysts. The diverse types of two key issues should be kept in mind for the generation of
amino acids, their variable interactions with SBA-15 and different ordered mesoporous frameworks. The first and the most
pyrolytic behaviours led to nitrogen-doped mesoporous carbons important point to consider before using the soft templating
with tunable surface areas (700–1400 m2 g 1), pore volumes approach is the interaction between the structure directing
(0.9–2.5 cm3 g 1), and pore sizes (4.3–10 nm).77 agents and the nitrogenated precursor as it is a key parameter
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which supports the formation of highly ordered structures. The

other factor is the condensation/polymerization kinetics of
intermolecular precursor species. It has been realized that
phenolic resins as the carbon source, nitrogen precursors,
and polyethylene oxide (PEO)-containing block copolymers as
structure directing soft templates, are a good combination for
the direct self-assembly synthesis of NOMCs. For example, Liu
et al. reported a one-pot route to prepare NOMCs having Ia3d
and p6m symmetry with BET surface areas in the range of 500
to 870 m2 g 1 in an aqueous medium by dissolving resorcinol,
hexamethylenetetramine (HMT) and Pluronic F127 in dilute
aqueous ammonia. It is worth mentioning that the symmetry
of NOMCs changed from Ia3d to P6m upon increasing the
carbonization temperature and also by the simple introduction
of trimethylbenzene (TMB) during the synthesis.83–85,157
Direct synthesis of NOMCs with a high nitrogen content Fig. 6 (A) Schematic representation of the N-OMC nanosphere synthesis
based on an aqueous-phase approach. Reproduced with permission from
through the soft templating approach remains a significant
ref. 91. Copyright 2014, Elsevier. (B) Schematic representation of the
challenge due to the limited availability of nitrogen precursors preparation of the NOMC/SiO2 nanocomposite using organic–organic
capable of co-polymerizing with phenolic resins without polymer co-assembly followed by polymerization. Reproduced with
deterioration of the order of mesostructural arrangement permission from ref. 93. Copyright 2015, Royal Society of Chemistry.
and a significant diminishment of nitrogen content during
carbonization. Dai et al. reported on the direct synthesis of
NOMCs through the self-assembly of phenolic resins and a self-assembly and condensation in the second step.88–90 Soluble
Pluronic block copolymer via the soft-template method under precursors such as urea–phenol–formaldehyde resin have been
pyrolysis of ammonia.86 This approach did not require any used as the nitrogen source for the preparation of NOMC
nitrogen-containing carbon precursors or post-treatment, but had spheres with a mean diameter of 240 nm and Im3m symmetry
the advantage of the preferential reaction and/or replacement through a simple co-assembly with the polymeric surfactants
of oxygen with nitrogen species, generated by decomposition of under highly acidic conditions (Fig. 6). By adjusting the ratio
ammonia at elevated temperatures, in oxygen-rich polymers of urea to phenol, the nitrogen content of the NOMCs was
during pyrolysis. This method used different steps including controlled.91–93
carbonization, nitrogen functionalization, and activation in a An aqueous cooperative assembly route has also been
simple one step process and generated NOMCs with a uniform employed for the fabrication of NOMC with body centred cubic
pore size, a large surface area (up to 1400 m2 g 1), and a high Im3m symmetry using resorcinol and hexamethylenetetramine
nitrogen content (up to 9.3 at%). The nitrogen atoms are mostly (HMT) precursors and copolymer F127 as the soft template.158
bound in the form of pyridinic and pyrrolic forms. Xue et al. and Choi et al. separately reported on a co-assembly
The evaporation-induced self-assembly (EISA) process has approach based on Pluronic F127 mediated micelles to convert
also been tried for the preparation of NOMCs. Zhao et al. made non-porous melamine and phenolic resin to a highly ordered
tremendous contribution to the direct synthesis of NOMCs and mesoporous polymeric network (space group: Im3% m) with a
established different methods for producing the same. Recently, high nitrogen content of 18 at% (Fig. 7).94,95 An amino-acid
this group has reported a controllable one-pot method to based cooperative assembly route has been introduced by
synthesize NOMC with a high N content up to 13.1 wt% by Liu et al. In this process, basic amino acids such as L-lysine
using F127, resol and dicyandiamide as a soft template, a carbon and L-arginine, as polymerization catalysts, and two phenol
source, and a nitrogen source, respectively. It was assumed that derivatives, resorcinol and 3-aminophenol, were used as carbon
the resol molecules not only assisted in the coordination of the and nitrogen sources and block copolymers F127 and P123
template and the nitrogen precursors through simple hydrogen as the soft templates. The NOMCs exhibited a BET surface area
bonding and electrostatic interactions but also provided stability up to 256 m2 g 1 with cubic Im3m and hexagonal p6m symmetry
to the final NOMCs. The obtained NOMCs possess tunable meso- depending on the template used in the synthesis process.159
structures ( p6m and Im3m symmetry) and pore size (3.1–17.6 nm) Yang et al. prepared nitrogen-doped carbon aerogels (NCAs)
and high surface areas of 494–586 m2 g 1.87 Later, NOMCs were by direct chemical synthesis by using an organic sol–gel process
prepared via a two-step approach by using the resorcinol (R), with different mole ratio of tripolycyanamide (T) and resorcinol (R).
formaldehyde (F) and dicyandiamide (DCD) mixture as the Then, the organic aerogels were pyrolyzed to obtain NCAs. The
precursor. In this approach, dicyandiamide, formaldehyde and N2 adsorption isotherms of the NCAs exhibit a typical type IV
resorcinol were pre-polymerized in the presence of Na2CO3 base isotherm with an obvious hysteresis loop at high relative
catalyst to produce DCD-RF resol. The DCD-RF resol was mixed pressure, which indicates that the prepared material has a mean
with a solution of triblock copolymer Pluronic F127 followed pore diameter of 12.6 nm.160 The pore diameter of the NCAs
by the addition of 2 M aqueous HCl solution to facilitate was controlled by tuning the concentration of the N precursors
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assembly of a triblock copolymer F127, resols and prehydro-

lyzed tetraethoxysilane on natural silk followed by pyrolysis.163
Nitrogen-doped hollow mesoporous carbon spheres (NHCSs)
were also prepared from 2,4-dihydroxybenzoic acid and hexa-
methylenetetramine as precursors and a mixture of Pluronic
P123 and sodium oleate as a template, followed by thermal
treatment at 650 1C in an ammonia atmosphere and subsequent
high temperature annealing at 800–1000 1C in nitrogen.102
Instead of POSS, TiO2 nanostructures were also used as inorganic

templates in order to ease the synthesis process and obtain the
hierarchically micro/mesoporous framework. Nitrogen-doped
hierarchically micro/mesoporous carbon nets were fabricated
via supramolecular assemblies of the block copolymer P123
with the assistance of dicyandiamide and TiO2 nanostructures.
Fig. 7 (A) Synthesis of mesoporous nitrogen doped carbon (MNC) with
The as-obtained carbon nets had the combination of both micro
various percentages of mixture of precursors. (B–D) HRTEM images of and mesopores that gave a specific surface area of approximately
MNCs of different compositions of precursors. Reproduced with permis- 2144 m2 g 1 and a high-level nitrogen doping with a nitrogen
sion from ref. 94. Copyright 2015, American Chemical Society. content of approximately 8.25 wt%.164
The microwave technique which is considered as an eco-
friendly and energy saving approach for the preparation of
with a concomitant increase of the mesoporous fraction. nanomaterials has been used for the synthesis of NOMCs.
Mesoporous carbon aerogels with 0–4% nitrogen content and a Hung et al. used this technique and prepared NOMCs with a
surface area of 798 m2 g 1 were also prepared from 3D resorcinol high specific surface area of 794 m2 g 1 from carbon–silicate
(R)–melamine (M)–formaldehyde (F) aerogels by tuning the M/R (C–Si) composites via the co-condensation method using a
ratio during the polymerization process.161 melamine–formaldehyde resin oligomer as the precursor and
The dual soft templating technique, the combination of the P123 triblock copolymer surfactant and sodium silicate as the
inorganic and organic templates, has been recently receiving soft and hard template, respectively.101 Although the technique
much attention for the synthesis of NOMCs with tunable proposed was eco-friendly, it was found to be not suitable to
morphologies and pore diameters. Qiao et al. demonstrated obtain NOMCs with excellent textural parameters which are
the synthesis of a series of nitrogen-doped mesoporous carbon needed for enhancing the performance of these materials in
spheres (NMCs) via a facile dual soft-templating procedure many applications including energy storage and conversion.
using a resorcinol–formaldehyde resin and melamine as carbon NOMC with a cubic Im3m symmetry and rhombic dodecahedral
and nitrogen precursors, and a mixture of Pluronic F127 and single-crystal morphology was also prepared via the organic–
fluorocarbon (FC4) surfactants at different carbonization tem- organic self-assembly of triblock copolymer F127, 3-aminophenol,
peratures. The surface area (307–483 m2 g 1), pore volume and hexamethylenetetramine (HMTA) in aqueous base solution
(0.3–0.4 cm3 g 1), conductivity, and nitrogen-doping (25–5.5 wt%) and it had a specific surface area up to 1159 m2 g 1.100
concentration of the synthesized NMC were tuned by adjusting the Guo et al. demonstrated the preparation of nitrogen-doped
nitrogen content and pyrolysis temperature.99 Porogens combined mesoporous network-like carbon (NMNC) via hydrothermal
with the Ni metal catalyst and melamine were added to control the reaction of glucose solution followed by pyrolysis under an
graphitic nature and the porosity of the nitrogen doped porous ammonia atmosphere without using any external template. In
graphitic carbon (NPGC) with a high surface area of 1027 m2 g 1 this work, the self-polymerization reaction of glucose molecules
and a nitrogen content of 7.7 wt%.96 On the other hand, in aqueous solution occurred under hydrothermal conditions
Xia et al. used resol and dicyandiamide as the carbon and at 200 1C. During this step, carbonaceous spheres were pro-
nitrogen precursor together with the porogen TEOS to increase duced via aromatization and carbonization of glucose, due to
the specific surface area and the pore size of the NOMC to the abundant functional groups (such as –OH, –CHO, –COOH,
1374 m2 g 1 and 7.4 nm, respectively.97 etc.) on their surfaces. These spheres colluded to form colloidal
Polyhedraloligosilsesquioxanes (POSS) were also used as network-like carbonaceous spheres through intermolecular
the carbon source and assembled into hierarchically porous dehydration and cross-linking with the dehydration reaction
carbon structures by a block copolymer-assisted method using among the carbonaceous spheres. The obtained NMNC sample
Pluronic P123 and F127 as the soft templates. The structure of synthesized at 1000 1C (NMNC-1000) exhibited an extremely
the materials was tuned from hexagonal to cubic by changing high specific surface area (2588 m2 g 1), well defined spherical
the nature of the templates. The prepared NOMCs from POSS shape morphology and a mesoporous structure which are
exhibited a specific surface area of over 2000 m2 g 1 and a large critical for mass transport and electrochemical applications.98
pore volume of 1.19 cm3 g 1.162 Nitrogen-doped mesoporous This elegant approach presents a unique way of improving the
carbon microfibers (NMCMFs) having a surface area of 230 m2 g 1 specific surface area and the functional groups of porous
were prepared via an evaporation-induced tri-consistent carbon materials. It can be expected that different combinations
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of carbon precursors with inorganic metal or metal oxides will

offer a new family of porous carbon nanostructures.
3.2 B doped ordered mesoporous carbons

Boron is one of the interesting elements which can not only
change the electronic and electrical properties of carbon nano-
structures but also the thermal stability under nitrogen or air
after substitution in the graphitic framework. Boron-doped
ordered mesoporous carbons (B-OMCs) were prepared using

an in situ approach via organic–inorganic co-assembly, in
which boron-modified phenolic resins were used as the carbon
precursor, tetraethyl orthosilicate was used as the inorganic
precursor and a reverse amphiphilic triblock copolymer
(PO97EO186PO97) was used as the soft template. B-OMCs with
BET surface areas of 1040 to 1255 m2 g 1 and a pore volume of
1.55 cm3 g 1 were also prepared by co-impregnation and Fig. 8 (A) Schematic representation of the synthesis of Pt/POMCs. Histo-
carbonization of sucrose and 4-hydroxyphenylboronic acid into grams of particle size distribution of (a) Pt/OMCs and (b) Pt/P7 OMCs.
the SBA-15 silica template.103,104 The EISA method has also Reproduced with permission from ref. 108. Copyright 2014, Elsevier.
been used for the preparation of B-OMCs in which resorcinol
and boric acid were used as the precursors and Pluronic F127 4. Binary atom doped OMC
as the soft template by combining the soft-templating and
hydrothermal techniques.106 The content of boron was easily 4.1 N and S co-doped ordered mesoporous carbons
tuned by the simple adjustment of the boric acid to resorcinol Incorporation of dual heteroatoms in the OMCs provides
ratio. Dense, continuous and amorphous boron-containing unique chemical and electronic properties due to the creation
ordered mesoporous carbon (CB) films were also synthesized of defects and uneven charge distribution in the carbon frame-
by using resols as a precursor for carbon, boric acid as a work structure. This will also change the hydrophobic or
heteroatom precursor, and amphiphilic triblock copolymer hydrophilic nature of the surface of the framework. In this
F127 as a template. In this case, the evaporation-induced section, we will show the methods used for different types of
triconstituent co-assembly method was used to obtain highly OMCs with dual heteroatom dopants and their effect on the
uniform films which were found to have high chemical inert- structure and properties of the materials. Guan et al. reported sulfur
ness. This unique property of these films made them attractive and nitrogen doped ordered mesoporous carbons (SN-OMCs) by
for corrosion resistance applications.105 using SBA-15 as a scavenger under CVD conditions with ferro-
cene, pyrimidine and thiophene precursors. After etching away
3.3 P doped ordered mesoporous carbons the iron and the SBA-15 silica template, the resulting SN-OMC
Phosphorus belongs to group V in the periodic table and has the material featured a distinctive bimodal mesoporous structure
same number of valence electrons as the nitrogen atom. Although with a high BET specific surface area (B1100 m2 g 1) and
it has lower electronegativity than the N atom, it exhibits almost uniform distribution of sulfur and nitrogen dopants.109 Different
similar chemical and electronic properties. However, phosphorus mixed precursors such as pyrrole–sulfuric acid and polythio-
has a larger atomic radius and higher electron releasing ability phene–polypyrrole (PPy) were also used for the preparation of
than nitrogen, which make it an excellent choice as dopant for SN-OMC which had a well-ordered porous structure and tunable
carbon materials. Yu et al. reported on the first synthesis of N and S contents.110 Instead of dual precursors, a single mole-
micron sized phosphorus-doped ordered mesoporous carbons cular precursor that contains both S and N was also used for the
(POMCs) with different lengths through the nanocasting method synthesis of SN-OMC. For example, SN-OMCs were synthesized
using SBA-15 mesoporous silica with different sizes as the tem- by the nano-casting method using a novel fluidic precursor,
plate and triphenylphosphine and phenol as the phosphorus and acrylonitrile telomer (ANT), and mesoporous silica SBA-15 as a
carbon sources, respectively. The realized POMCs exhibited a high hard template. SN-OMC contained both nitrogen and sulfur
BET specific surface area of 1182 m2 g 1 and a large pore volume atom dopants with 4 and 0.6 at% and also a high specific surface
of 1.87 cm3 g 1 with a mean pore diameter centred at 3.4 nm.107 area of 1012 m2 g 1.165 The one step nanocasting technique in
The content of P in POMCs can be varied by tuning the amount of which diphenylthiocarbazone was used as a precursor of carbon,
triphenylphosphine. The amount of P in the carbon nanostruc- sulphur and nitrogen and SBA-15 was used as a nano hard
tures also controls the micropores in the samples. The specific template was also developed for the synthesis of SN-OMC.112
surface area of the POMCs can be increased to 1338.8 m2 g 1 by a Sulfur-doped ordered mesoporous carbon (OMC-S) with 1.5 wt%
simple adjustment of the P content as it creates a lot of micro- sulphur and a BET surface area up to 1261 m2 g 1 was prepared
pores in the walls (Fig. 8).108 Through a careful adjustment of P in by using SBA-15 as the template and different amounts of
the synthesis mixture, porous carbons with different pore para- sucrose and benzyl disulphide as the carbon and sulfur sources,
meters and tunable electronic properties could be obtained. respectively (Fig. 9).113
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the OMCs. N, B, and P-doped ordered mesoporous carbons

with a surface area up to 550 m2 g 1 were prepared by applying
SBA-15 as a nano hard template and a mixture of aniline,
triphenylborane and triphenylphosphine as precursors through
the nano templating approach.169 First nitrogen was introduced
into the carbon matrix using aniline at 900 1C using Fe as a
catalyst but the B and P atoms were incorporated into the N doped
carbon matrix during the carbonization step.
4.4 Ordered mesoporous carbons with N and P doping

N and P co-doped 3D cubic ordered mesoporous carbons
(NP-OMCs) with bimodal mesoporosity and a surface area of
1968 m2 g 1 were prepared using saccharide as a carbon source
along with urea and phytic acid (PA) as precursors for N, P and
carbon, respectively, and cubic ordered Ia3d mesoporous silica
KIT-6 as a hard template.170 2D N and P doped ordered meso-
porous carbons (NP-OMCs) were also prepared by using sucrose,
Fig. 9 (A) Schematic representation for the preparation of metal free cyanamide and phosphoric acid mixtures and SBA-15 as the
OMC-S catalyst. The N2 sorption analysis (B) isotherms of OMCs and template. The prepared materials had a high BET surface area
(C) their pore size distribution. Reproduced with permission from ref. 113. (1300 m2 g 1) and a large total pore volume of 1.64 cm3 g 1.171
Copyright 2013, Elsevier.
4.2 N and O co-doped ordered mesoporous carbons

5. Functionalised nanoporous carbon
Polyamides have been used as precursors for the synthesis The functionalization of the porous structures with organic
of nitrogen- and oxygen-doped ordered mesoporous carbons molecules or inorganic metal or metal oxide nanoparticles can
(NOOMCs) by applying 3-aminobenzoic acid (MABA) and SBA-15 introduce new properties to the parent materials. This will
mesoporous silica as a precursor and template through the liquid expand the application potential of the OMCs in various fields
infiltration and thermal polymerization method. The obtained including adsorption, separation, sensing, energy storage and
NOOMCs showed a specific surface area up to 1084 m2 g 1 with a conversion, and catalysis. The highly ordered porous structure
narrow pore size distribution and a mean pore diameter centred with uniform pores and high specific surface area will provide
at 4.0 nm and nitrogen and oxygen contents as large as 6 and enough space for the decoration of the surface with different
6.4–11.5 wt%, respectively.166,167 A mixture of molten fructose functionalities which will enhance the properties that will be
and urea, which are low cost and environmental friendly helpful for various applications. However, the fabrication of
precursors, has also been used for the fabrication of NOOMCs these functionalities inside the mesochannels without any
with a 3D porous structure using mesoporous silica KIT-6 as a agglomeration is quite challenging as the uniform distribution
template. The obtained NOOMCs exhibited enhanced surface of these functionalities is the key to elevate the performance of
polarity and a high specific surface area and pore volume of these materials in several specific applications. Several reports
1197 m2 g 1 and 1.16 cm3 g 1 and heteroatom (O, N) contents have been published in the literature on metal, metal oxide,
of up to 19.1 wt%. However, the content of the dopants can be alloy, metal complex, graphene, metal chalcogenide, and amine
varied by tuning the quantity of the precursors.168 or amine complex, and protein functionalized OMCs. In this
section, we will highlight the different methods used for the
4.3 Ordered mesoporous carbons with B, P and/or N doping immobilization of these functionalities in OMCs and how these
The combination of P and B doping is another interesting dual functionalities create new properties in the final materials.
dopant which afforded interesting structural and chemical
properties. The hydrothermal doping strategy has been applied 5.1 Metal nanoparticle immobilized nanoporous carbons
for the doping of boron and phosphorus into OMCs (HTBP) via Li et al. described the immobilization of ultra-small size Pd
a facile aqueous self-assembly using resorcinol as the carbon nanoparticles (PdNPs) of 3.0 to 5.0 nm in size having a uniform
source, and boric acid and phosphoric acid as the heteroatom shape and without agglomeration in OMCs. In this method,
source. In this method, Pluronic F127 was employed as the soft nitrogen doped OMCs were used in order to provide anchoring
template structure-directing agent. By varying the hydrothermal support that would avoid the agglomeration of the small sized
synthesis temperature, the concentration of B and P introduced PdNPs. The incorporation of PdNPs in the OMC-N was performed
in the OMCs can be controlled from 0.8 to 1.6 wt% and from in a two-step process, immobilization followed by reduction
2.3 to 3.6 wt%, respectively.52 This was due to the different using an aqueous solution of NaBH4. The OMC-N used in this
interaction of B and P with C precursors at a high hydrothermal study had 8.6 wt% nitrogen which was introduced by post-
temperature. Triple heteroatom doping was also carried out on synthesis treatment either with NH3 or melamine over FDU type
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OMC materials.172 Pd supported CMK-3 (Pd/CMK-3) and 568, 387, and 239 m2 g 1, respectively. These values were much
N-doped CMK-3 (Pd/N-CMK-3) materials were also prepared higher than that of VB12/C (134 m2 g 1). The mesopore size
by impregnating CMK-3 powder with aqueous solutions of 1,10- distributions of the above samples were centred at 12.0, 3.5, and
phenanthroline and H2PdCl4 in two steps via the ultrasound- 4.5 nm, respectively, according to the BJH model.180 Mesoporous
assisted impregnation strategy followed by reduction using C–N–Fe material was also prepared by using poly(4-vinylpyridine)
30 vol% H2/N2 carrier gas at 200 1C.173 The N2 sorption analysis and iron chloride as the precursors and SBA-15 as a template.181
of Pd/CMK-3 and Pd/NCMK-3 showed typical type IV isotherms The combination of metal and heteroatom doping provides
with clear hysteresis loops of H1-type, indicating that the meso- much better chemical and electrical properties compared to
porous structure and the relatively uniform mesopores of CMK-3 that of OMCs doped with either heteroatom or metal nano-
were still preserved in Pd/CMK-3 and Pd/N-CMK-3 samples. particles. A series of Fe–Nx doped ordered hierarchically micro-
Mesoporous carbon (MC-8) and nitrogen doped mesoporous and mesoporous carbon (Fe–N-GC) materials were prepared
carbon (NMC-8) which were prepared based on Zr–SBA-15 as through the nanomoulding synthesis procedures by direct
the template were also used as supports to get the Pd NPs of pyrolysis of the various nitrogen containing heterocyclic com-
4.0 and 2.5 nm. NMC-8 and MC-8 supports with surface areas of pounds such as 2,2-bipyridine, p-aminotoluene, p-nitroaniline,
1054 m2 g 1 and 1489 m2 g 1 were prepared by carbonization and 2-amino pyridine, respectively, and iron chlorides in the
of a mixture of xylene/furfuryl alcohol/oxalic acid with and confined mesoporous channels of SBA-15 (Fig. 10).182 Fe–N-GC
without ammonia gas nitridation and the hard template method had a high specific surface area of up to 929 m2 g 1, which was
using large pore Zr–SBA-15. Zr atoms were introduced into the composed of a mesopore surface area of 499 m2 g 1 and a
template to obtain large pore size in the template which would be micropore surface area of 430 m2 g 1, corresponding to their
beneficial for the decoration of highly dispersed Pd nanoparticles narrow mesopore size distributions centred at 6.3 nm and micro-
which were prepared by a wet-chemical reduction method.174 pore size centred at 0.37 nm. Li et al. used the ‘‘task-specific’’
As the post-synthetic approach was considered as a time approach by using ferrocene-based ionic liquid [FcN][NTf2] (Fe-IL)
consuming process, Ye et al. used a one-step co-calcination as a metal-containing feedstock with a nitrogen-enriched ionic
approach to prepare Pd NPs budded on NOMC (Pd/N-MCN) by liquid [MCNIm][N(CN)2] (N-IL) as a compatible nitrogen content
using phenol, formaldehyde, melamine, and PdCl2 as precursors modulator and SBA-15 template to prepare mesoporous iron–
for C, N and Pd and F127 through the soft templating method.175 nitrogen-doped carbon (FeX@NOMC).183 FeX@NOMC had a
The in situ synthesis approach was also adopted for the prepara- nitrogen content up to 11.9 wt% and a highly ordered meso-
tion of Pd NPs supported on nitrogen doped mesoporous carbon porous structure, a high surface area (411–506 m2 g 1), and high
(Pd/N-C) by direct pyrolysis of the palladium dimethylglyoximate pore volumes (0.71–1.05 cm3 g 1) and pore size distribution was
complex at 400 1C under 10% hydrogen gas.176 However, highly uniform centred at 5.6 nm.
the obtained Pd/N-C exhibited a relatively low surface area and Ordered hierarchically porous carbon co-doped with N and
pore volume of 124.1 m2 g 1 and 0.158 cm3 g 1, respectively. An Fe (Fe–NOHPC) was prepared by Deng et al. through an EISA
in situ spray-drying method followed by the calcination route was process followed by carbonization under ammonia by using
used to fabricate 3.8 to 4.5 nm sized Pt nanoparticles supported resol, F127 and FeSO4 as the carbon precursor, soft template
on nitrogen-doped porous carbon microspheres (Pt/CN). This and iron source, respectively.184 Fe–NOHPC possessed N and Fe
study showed that the size of the Pt NPs and N-doping into
conventional carbon black were simultaneously controlled via
the spray-drying method and also by adjusting the precursor
pH using ammonium hydroxide.177 A nano-Sn/mesoporous
carbon parasitic composite was prepared by Duan et al. using
immobilization of Sn2+ solution and followed by H2 gas assisted
reduction.178 Mesoporous carbon used to anchor Sn nano-
particles has an open porous structure with less than 10 nm
filmy pore walls, and the pore diameter is about 30–70 nm,
which has been prepared using sucrose as the carbon source and
the CaCO3 template. The open porous structure of mesoporous
carbon was highly favourable for the filling of tin nanoparticles
of 10–30 nm which were uniformly distributed in the pores of
the carbon matrix.
Cobalt and iron doped NOMCs (C–N–Co and C–N–Fe) with
tunable nitrogen content (up to 9.5%) were prepared from the
direct carbonization of vitamin B12 and the polyaniline–Fe Fig. 10 (A) SEM image of Fe–N-GC-900. (B) EDS for Fe, N, C, Cl and O.
(C and D) Elemental mapping of Fe and N respectively. (E) The nitrogen
(PANI–Fe) complex,179 respectively, and silica nanoparticles,
adsorption–desorption isotherm of Fe–N-GC-900. (F) Schematic illustra-
SBA-15, and montmorillonite were used as templates. The tion of the synthesis of micro and mesoporous Fe–N-GC with an ordered
specific surface areas of these C–N–Co samples obtained by structure. Reproduced with permission from ref. 182. Copyright 2014,
using silica nanoparticles, SBA-15, and montmorillonite were American Chemical Society.
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concentrations of 3.54 and 0.18 at%, with an ordered hier-

archically porous structure, a high surface area (1172.5 m2 g 1)
and a pore volume of 1.03 cm3 g 1. Ahn et al. reported on the
preparation of well dispersed Fe nanoparticles within N-doped
mesoporous carbon nanofibers (Fe–NMCNF) with a surface area
and pore volume up to 468.9 m2 g 1 and 0.95 cm3 g 1 from a
polyacrylonitrile (PAN) and iron(II) phthalocyanine mixture using
electrospinning followed by reduction of H2 gas.185
Cobalt nanoparticles of 6.7 to 12.8 nm in size were immo-

bilized on the OMC-N materials through the excessive wetness
impregnation method using the Co(NO3)2 precursor by an auto
reduction process without using any external reductant. The
size of the Co nanoparticles was reduced from 12.8 to 6.7 nm
with an increase in the nitrogen content in the NOMC samples
from 5.8 to 10.4 wt%. However, the size of the particles was
increased to 19.4 nm when OMC without any N dopant was used,
confirming the anchoring role of N functionalities in OMCs.186
The soft-templating method was also used for the in situ pre-
paration of Co nanoparticles in NOMCs. 3D cobalt–nitrogen-
doped ordered macro-/mesoporous carbons (Co–N-OMMCs)
with 9.64 wt% nitrogen and 1.52 wt% Co were prepared from
a mixture of resol/dicyandiamide (DCDA)/Co(NO3)2 through a
dual-templating approach using opal colloidal silica spheres as
Fig. 11 (A) Schematic representation of the core–shell structure of
a macroporous mold and triblock copolymer Pluronic F127 as a
NiFe@MNCS prepared by pyrolysis. (B) N2 sorption isotherms of MNCS
mesoporous template. In the synthesis process, an aqueous/ and MNCS–NiFe. The inset shows their pore size distribution. Reproduced
ethanolic solution containing resol, DCDA, Co(NO3)26H2O with permission from ref. 190. Copyright 2016, Elsevier.
and F127 was infiltrated into the void spaces of the silica
opal template, and the mesostructure was formed during an
EISA process.187 The nitrogen adsorption/desorption isotherms based wet chemical reduction method.188 The noble metals
of Co–N-OMMCs samples were of type IV with a high specific were co-doped with transition metal nanoparticles inside the
surface area and a total pore volume of 679 m2 g 1 and mesochannels of OMCs in order to reduce the total cost of
1.71 cm3 g 1, respectively, with an average pore size centred these catalytic systems. Wang et al. described the synthesis of
at 11.2 nm. Direct polymerization of a reverse copolymer PtCo bimetallic nanoparticles with a molar ratio of Pt : Co of
PPO–PEO–PPO/[Ni(H2O)6](NO3)2/phenolic resin self-assembled about 1 : 1.1 supported on the NOMC framework with ultrafine
in ethanol medium yielded highly decorated Ni nanoparticles dispersion and uniform particle size distribution (ca. 1.5 nm)
in the OMCs. During the pyrolysis process, Ni2+ was reduced into through the wet impregnation method followed by reduction at
metallic Ni nanoparticles which were uniformly distributed on 500 1C in a flow of 5% H2 in Ar.189 The surface area, pore volume
the surface of OMCs. and pore size of PtCo/NOMC were 507 m2 g 1, 0.41 cm3 g 1 and
6.5 nm, respectively. NiFe alloy nanoparticles encapsulated in
5.2 Alloy nanoparticle incorporated nanoporous carbons the mesoporous nitrogen-doped carbon sphere (MNCS) were
The combination of metals can introduce unique electrical and also synthesized using direct thermal pyrolysis of nickel hexa-
electronic properties as it tunes the electronic structure of cyanoferrate at 500 1C without using any external template
the nanoparticles. In addition, alloy systems have also been (Fig. 11).190 Pd3Cu alloy nanoparticles were also encapsulated
employed in many catalytic systems owing to their ability to inside the mesochannels of NOMCs using PdCl2 and cupric
lower the activation barrier. Most importantly, the concept of acetate as precursors for Pd and Cu, and sodium citrate as a
alloying can also significantly reduce the cost of the materials. reducing agent via the wet chemistry method.191
By decorating these alloy systems on highly ordered support
systems, the active specific surface area or the properties of the 5.3 Metal oxide and metal chalcogenide functionalized
alloy nanoparticles can be significantly altered. In this section, nanoporous carbons
we will summarise the different methods employed for the Metal oxide nanoparticles have been widely used in various
fabrication of various alloy or bimetallic doped OMCs and how applications. However, the textural properties of these oxides are
these nanoparticles affect the properties of the final materials. the limiting factors which affect the final performance of the
Maiyalagan et al. reported on the deposition of Pt–Ru alloy materials in different applications. On the other hand, metal
nanoparticles of 3.8 nm size with a Pt/Ru atomic ratio of 1 : 1 chalcogenides are unique semiconducting materials and they
and 20 wt% metal loading (Pt–Ru) in the highly ordered complement semi metallic graphene. They are widely employed
mesoporous carbon CMK-8 by using the sodium borohydride in electronic and optoelectronic applications owing to their
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small energy band gap. By functionalizing these metal chalco- can be rolled to form nanotubes or spherical fullerenes.
genide or metal oxide nanostructures inside the mesochannels Although graphene is a fascinating material with an effective
of OMCs, new advanced porous materials with improved prop- surface area, the undeveloped porous structure limits the
erties can be realized. Shen et al. reported on the synthesis of opportunity of developing graphene into a useful multi-
the mesoporous Li4Ti5O12/C nanocomposite by post function- dimensional flexible material. Recently, various constructive
alization of acid treated CMK-3 through the sintering of lithium ideas have been executed to build graphene with nanoporous
acetate and tetra butyl titanate precursors at 750 1C for 6 h in a structures and to utilize the surface defects originated from
nitrogen atmosphere.192 The small Li4Ti5O11 nanocrystals were imperfections of the crystal lattice for immobilisation and
nicely interconnected in the mesochannels of OMCs which anchoring of various nanoparticles or for fabricating hybrid
significantly increased the ionic and electronic conductivity of graphene materials. Noteworthily, the chemically synthesised
the composite system. These factors are critical for energy storage graphene through coupling reactions is usually said to be
applications, especially in batteries. A significant reduction of nanographene and nanoporous graphene which is the hot topic
the specific surface area from 1138 m2 g 1 to 127 m2 g 1 in the development of new generation materials.
confirmed the formation of these Li4Ti5O12 nanocrystals inside Despite graphene being one of the highest surface area
the mesochannels of OMCs. materials, graphene derived materials possess a very low surface
Meso-porous C–TiO2 nanocomposites with anatase TiO2 area when compared with the single layer graphene especially
whose contents ranged from 40 wt% to 87 wt% were prepared due to the p stacking exhibited by the graphene sheets. There-
through the EISA strategy by using TiCl4 and/or Ti(OC4H9)4 as fore, it is wise to create porosity in graphene based materials to
titanium sources, phenolic resin as the carbon source, and increase the specific surface area, and so far there have been
triblock copolymer F127 or P123 as the structure-directing four effective ways to achieve this, namely the exfoliation
agent.193 Nitrogen-doped urchin-like Fe3O4@C–N composites were technique, templating methods, stacking/aggregation and
prepared by a simple hydrothermal carbonization of hydroxyferric reduction of graphene oxide to form the core or hydrogels
oxide (a-FeOOH) coated with polydopamine (PDA) at 400 1C and finally integrating graphene using spacers. In this section,
under an Ar atmosphere.194 Cobalt oxide particles of 30–50 nm we will focus on the functionalization of graphene on the
encapsulated in nitrogen co-doped carbon (Co–N/C) bi-catalysts mesoporous channels of OMCs.
were prepared via a one-pot approach by using dopamine Porous and non-porous carbon nanofibers (PCNF and CNF)
hydrochloride (DA) and formaldehyde (F) as nitrogen containing were prepared and used as spacers to synthesise high surface
carbon sources, P123 as a soft template and cobalt acetate as area 2D graphene (G) prepared at 900 1C.199 In the typical
a precursor for Co.195 Iron sulphides (Fe1 xS) embedded in synthesis, graphite powder was chemically modified through
nitrogen and sulfur dual-doped mesoporous graphitic carbon acidification in two steps to get oxidized graphite and on
spheres (Fe1 xS/N, S-MGCSs) were synthesized via a two-step exfoliation and lyophilisation through the ultra-sonication
pyrolysis followed by the acid leaching process. The preparation process, the graphene oxide (GO) powder was obtained. The
of Fe1 xS/N, S-MGCSs involved the coordination of Fe2+ with resulting GO powder was mixed with PCNF and CNF to obtain
PDA followed by carbonization and leaching of iron oxides and G-PCNF and G-CNF. The 2D graphene sheets were further
finally vulcanization under thiourea. The prepared Fe1 xS/N, functionalised by Pt to form Pt/G-PCNF and Pt/G-CNF through
S-MGCS materials had a specific surface area and pore volume magnetic stirring and the Pt was reduced by refluxing, follow-
up to 371.4 m2 g 1 and 0.41 cm3 g 1, respectively.196 ing the polyol reduction method. The difference between the
N-Doped mesoporous carbon capped with MoO2 nanobelts porous and non-porous 2D graphene materials was demon-
(MoO2@NC) was prepared by in situ thermal reduction of strated through the FESEM, where the G/PCNF showed a
MoO3 nanobelts and the one-step annealing of polypyrrole mesoporous structure and the rough surface of the porous
precursor.197 Sun et al. described a facile melt-impregnation material provided more active sites for the catalyst deposition.
method for the confinement of Se2S6 ultra small nanocrystals Like spacers, other bridging molecules were also used to bridge
in the nitrogen-doped mesoporous carbons (Se2S6/NMCs).198 In the graphene sheets. For example, the synthesis of porous
the synthesis of Se2S6/NMCs, selenium and sulphur melts carbon nanosheets by using asparagine, which is an amino
are miscible with each other at 500 1C and then infiltrated into acid and is used as a bridging molecule to connect the GO,
the mesopores of NMCs. The composite Se2S6/NMCs had a and the electrostatically connected GO, which served as the
considerable amount of mesoporosity with a specific surface structure directing agent to form porous nanosheets, was
area of 159 m2 g 1 and a pore volume of 0.8 cm3 g 1. reported.200 The GO was also exfoliated into discrete sheets
through ultrasound and the individual sheets were then con-
5.4 Graphene functionalised nanoporous carbon verted into the 3D graphene composite (GN) by depositing Au
Graphene, a two-dimensional form of carbon layers with a nanoparticles and reduced by using PEG. The thus-prepared
crystalline honeycomb lattice and with the layers connected 3D-AuNPsGN had increased active surface area for electro-
by relatively weak forces, has gained substantial importance chemical sensing of antibodies.201
due to the open porous structure accrued from the stacking. It is well known that the multilayer graphene (MLG) has
Graphene tends to exhibit exclusive physical and chemical higher mechanical strength and at the same time has lesser
properties due to the ease of stacking to form graphite and it properties compared to that of single layer graphene. With the
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objective of allowing a wide range of applications of MLGs, the G-mC to form G-mC–Pd/SnO2. The metal functionalised porous
MLG was combined with porous carbon (PC) through a CVD graphene exhibited a decrease in the surface area and pore
process to form hybrid MLG/PC core–shell films, where their volume, suggesting that the Pd/SnO2 were located inside the
structure was controlled by nickel gauze which was used as the pores of G-mC. This was confirmed by TEM images that show
template and their pore sizes were controlled by the CVD only a few large Pd and SnO2 nanoparticles found outside
reaction time and by tuning the methane feeding rate. Since the surface of CMK-3. It was found that the particle size of the
the hybrid MLG has both the characteristics of graphene and G-mC was close to the particle size of the Pd/SnO2 nano-
porous carbon, the film was able to maintain an intact struc- particles and was conductive compared to the CMK-3–Pd/SnO2.
ture of the material with MLG shell and PC core.306 Since the PC Graphene oxide was also coated on the polyacrylonitrile
materials have shown tremendous advantage owing to their derived porous carbon (PAN) that is rich in nitrogen and oxygen
excellent structural and textural properties, Hongbo et al. prepared species. By heating the coated PAN (PAN/GO) followed by
hybrid films by combining graphene with PC microspheres.202 activation and washing with acid produced the final product.
They followed three conventional steps, namely reduction, The oxygen present in the final product inhibited the graphene
leavening and compression, to fabricate the hybrid flexible layer stacking and provided strong interactions between the
porous film. The porous carbon microspheres moved between sheets.205 A simplified strategy of synthesising graphene/
the pore walls of the flexible graphene nanosheet (GNS), pre- porous carbon was reported earlier in 2015, where the CNT
vented the stacking of the GNS and kept the open porous system was coated with activated porous carbon (CNT@AC) and was
in confinement facilitating electrochemical performance. used as a spacer dispatched in-between the graphene sheets
Although porous carbons are fascinating, they relatively have (RGO/CNT@AC). The coated CNTs played a vital role in inhibiting
poor electrical conductivity. For example, CMK-3 has a poor the restacking of the graphene layers displaying a better
electrical conductivity and cyclability compared to graphene. electrochemical performance compared to that of pure CNT/
To combine the bright side of porous carbon (CMK-3) and graphene.206 The specific surface area was lower and the porous
graphene, in 2015 Nan et al. synthesised graphene based 2D structure of the coated CNT was not controlled through this
porous carbon which was used as a support for the function- method. In another study, the restacking of graphene
alization of Pt nanoparticles.203 In the following year, the same nanosheets was inhibited by adding highly ordered porous
group demonstrated the functionalization of graphene based carbons prepared from SiO2 colloidal crystals with high specific
mesoporous carbon with Pd and SnO2 nanoparticles as shown surface area as a spacer. This simple approach not only helped
in Fig. 12. They used the SBA-15 silica template and graphene to to increase the specific surface area but also facilitated the
prepare graphene mesoporous carbon (G-mC).204 By following diffusion of electrons in the hybrid nanostructures. Their
the electroless plating method, Pd/SnO2 were introduced to the fabrication process involved ultra-sonication of the PC and
graphene oxide (GO) suspensions and after the hydrothermal
process at 180 1C, graphene/porous carbon hydrogels were
obtained. Interestingly these aerogels exhibited enhanced rate
performance when compared with the individual GN and
PC.305 Similar to the previous report, the pore structure of the
graphene materials was simply controlled by assembling the
graphene into a three-dimensional structure by hydrothermal
treatment. The colloidal suspension was hydrothermally trea-
ted at 150 1C to produce a black graphene hydrogel. This was
further impregnated with melted sulphur which was uniformly
anchored to the graphene sheets. The porous structure thus
produced was used as a model to study the influence of pores
on electrochemical performances.207 The graphene treated with
PC was also doped with nitrogen and activated by adding KOH
via in situ polymerisation and was used as an anode.208 N-Doping
was also done through the in situ carbonisation technique where
glucose was mixed with GO to form RGO–HTC carbon on a large
scale and was activated using NH3 to form nano-sandwich
N-doped carbon materials (NNCMs)209 as shown in Fig. 13.
Among the various NNCMs synthesised at 850, 900, 950 and
1050 1C, NNCMs prepared at 1050 1C exhibited a high surface
of about 1959 m2 g 1.
Fig. 12 (A) Schematic representation of the synthesis of CMK-3–Pd/SnO2
and G-mC–Pd/SnO2. (a and b) High resolution SEM and (c and d) TEM images 5.5 Fullerene based porous carbons
and (e and f) histograms of particle size distribution of CMK-3–Pd/SnO2
and G-mC–Pd/SnO2 respectively. Reproduced with permission from Fullerenes are the purest form of carbons connected by
ref. 204. Copyright 2016, Royal Society of Chemistry. hexagonal and pentagonal rings. The structure of fullerene
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pressure treatment. Finally, to understand the structural trans-

formation, theoretical calculations were applied. It was proved
that high temperatures and pressures favor the formation and
breaking of the interfullerene bonds which is the key for
the transformation of 0D fullerene nanostructures into 2D
graphitic nanostructures.211 The exfoliated graphite was used
as a carbon adsorbent and the polycrystalline C60 powder
was mixed along to be adsorbed by the exfoliated graphite.
The adsorbed C60 on thermal treatment evaporated and the

remaining particles were cold pressed.212 The porous carbon
based on fullerene and graphite was studied for electrical,
optical and various other properties. As one step further in
the development of fullerene based porous carbon, Tan et al.213
activated the fullerene using KOH and doped the fullerene
based porous carbon by nitrogen to form N–aC60 through thermal
annealing as shown in Fig. 14A. Interestingly the surface area of
the activated fullerene based porous carbon was 1457 m2 g 1
while that of the N-doped fullerene based porous carbon was
1274 m2 g 1. The nanoporous fullerene is a new area and the
discussion on the fullerene based porous carbon signifies that
a wide knowledge is necessary to understand the bonding
Fig. 13 (A) Schematic representation of the synthesis of NNCMs. (a and b)

The N2 adsorption–desorption isotherms of NNCMs and (c and d) the pore
size distribution of NNCMs. Reproduced with permission from ref. 209.
Copyright 2016, Royal Society of Chemistry.
differs from each other based on their number of carbon atoms

or the number of hexagons and pentagons in the fullerene ring.
The major difference between graphene and fullerene is that,
the fullerenes have very high thermal and mechanical stability
but have a very poor surface area and electrical conductivity. In
contrast to fullerenes, graphene has very poor stability but has a
high surface area and high electrical conductivity. However, the
high symmetrical structure of fullerenes is unique compared to
any other existing carbon materials so far, which provides
opportunities to the scientific world to explore their structural
properties for various applications. At the same time, the rigid
structure of fullerenes could only be modified organically but
due to its high thermal and mechanical stability, it is not very
easy to fabricate it into a nanoporous fullerene structure. The
rare reports on fullerene nanoporous carbons are discussed
in this section.
Considering the effect of templating methods, Duncan et al.
tried to self-assemble the fullerene by immobilising the
fullerenes on the graphite surface, where the pores were
generated by 1,3,5-benzenetricarboxylic acid to form a fullerene
monolayer.210 Inspired by the concept of the self-assembling Fig. 14 (A) Schematic illustration of KOH activation on fullerene
process, the single crystal C60 (FNR) and single crystal C60- C60 molecules. (a) Pore size distribution of C60, aC60 and N7.5% aC60.
(b) N2 adsorption–desorption isotherms of C60, aC60 and N7.5% aC60.
nanotubes (FNT) were synthesised through the liquid–liquid
(B) Schematic representation of the first successful synthesis of poly-
interfacial precipitation technique. These nanostructures can merised highly ordered nanoporous fullerene C60 with crystalline wall
be transformed into nanoporous carbon (HT-FNR and HT-FNT) structures. Reproduced with permission from ref. 213 and 214. Copyright
with random graphitic nature after the high temperature and 2016 and 2017, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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nature between the self-assembled fullerenes. In addition, the structure to the resultant amine functionalised MCM-41 carbon
polymerization between the solvent and the fullerene precur- material. The advantage of the bimodal porous structure to amine
sors and the formation of ordered porous structure in fullerene functionalisation is the increase in the adsorption phenomena.221
are yet unknown. Very recently, a striking report by Vinu et al. The trendy way of fabricating amine functionalised porous
proved the successful fabrication of highly ordered mesoporous polymers222 and organic polymers223 which did not require
fullerene (Fig. 14B), with crystalline walls using nano-hard any activation process was also reported. However, the cost was
templating approach wherein 2D mesoporous silica, SBA-15 is comparatively higher that limits the large-scale production.
used as a template and highly concentrated C60 solution in
5.7 Nanoporous carbon with metal nanoparticles from metal
chlorinated naphthalene as a fullerene precursor. This simple

strategy consists of the combination of several steps including complexes
high temperature collision of fullerenes in a nano-confined Metal complexes, generally known as coordination compounds,
matrix, polymerization, cross-linking of fullerenes with the are complexes that form intermolecular bonds between the
aromatic molecules and nanotemplating. It has been demon- metal acting as an electron accepter and the ligand acting as an
strated that chlorinated naphthalene plays a key role here as it electron donor. The ligands are also termed as mono, di, tri,
not only contributes the tight packing of the pores of the or poly-dentate depending on the number of electrons they
template but also helps to cross-link the C60 molecule at a high donate. For instance, if the ligand donates more than one pair
temperature. The prepared material showed excellent energy of electrons, the bonding between the metal ion and the ligand
storage and conversion properties. This discovery is going to will be more stable. The ability of the porous carbons to allow
make a huge impact on the field of fullerene. We believe that the accessibility of small ions or metals due to their open
this research would attract many researchers to work in this channels makes them excellent candidates to fabricate nano-
new area of research as they would be useful for a wide range of porous carbons with metal complexes.224
applications in the near future.214 Copper(II) acetate225 and copper(II)/silver(I) carboxylates were
immobilised in the nanoporous carbons and their combination
5.6 Amine functionalised nanoporous carbon was used to study the dihydrogen complexion.226 Foley et al.
Nanoporous carbons are unique due to their high surface area also reported the preparation of simple complexes of copper
and large pore volume with highly ordered porous structure. and silver loaded nanoporous carbon which showed highly
Regardless of their excellent features, the strong hydrophobic selective adsorption of 1–3 mol of hydrogen per metal center.
nature of their surface highly hinders them from various applica- It was assumed that the cooperative interactions between
tions like sensing, separation, physisorption and chemisorption, hydrogen, the nanoporous structure, and the highly dispersed
catalysis, etc. The hydrophobicity of these carbons can be tuned metal centers of the complexes in the mesochannels supported
by functionalisation, especially with organic groups rather the enhancement of hydrogen adsorption.225 It was also
than using metal or metal oxides for functionalisation. In the reported that highly ordered nanoporous carbons with metal
following, the functionalization using amines is discussed, since nanoparticles were prepared through a simple carbonization of
amines have relatively high affinity to bond with carbon. So far, the magnesium polyacrylate complex227 and benzoate metal
two main strategies such as grafting and impregnation have been complexes228 and exhibited a high specific surface area of ca
adopted for introducing amines to the porous materials. 1050 m2 g 1. However, the surface area of the materials was
CMK-3 was functionalised by more than one amine group significantly enhanced (1466.4 m2 g 1) when the composite was
likely 1,2-diaminopropane, trans-1,2-diaminocyclohexane and activated using KOH. By using the same carbonisation method,
o-phenylenediamine through C–N cross-coupling reaction. The the cobalt ion absorbed polyaniline (PANI) was converted into
aliphatic, cyclic and aromatic amines formed amide bonds on the Co–C–N complex, which showed excellent electrocatalytic
the surface of the CMK-3 material offering the catalytic sites to activity.73 The metal complex derived porous carbon was
produce carbonyl compounds, without any destruction of the also functionalised with selenium and the selenium interacted
long-range ordering of the CMK-3 material.215 To increase the with the metal complex porous framework through Se–O and
heterogenicity of the carbon, Zakova et al. used five different C–O bonds.94
sources of amine to work on amine–amide combinations. The
carbon nanoparticles (CNP) were modified with amides to 5.8 Protein functionalised nanoporous carbon
manifest COOH groups and refluxed with SOCl2 to yield –COCl Biomolecules are organic molecules derived from living tissues
groups to start the reaction of CNP with amines.216 Although composed mainly of carbon and hydrogen. Among the four
the XPS and Raman spectra confirmed the modification of the class of biomolecules, namely carbohydrates, proteins, lipids
CNP surface with the expected bonding, the N2 adsorption– and nucleic acids, the proteins are of great interest due to their
desorption showed a tremendous decrease in the surface area polymeric structure since they are natural heteropolymers
after the grafting process.217 Amine grafting was also carried out containing the carboxyl group and the amino group connected
in porous polymeric networks,218 carbonaceous nanomaterials,219 by peptide bonds. But, the common drawback of proteins is
porous carbon monoliths220 and MCM-41. their denaturation,229 physical instability and side reactions
Among these amine functionalised materials, MCM-41 caused by the hydrogen bonds. Therefore, the importance of
invigorated with carbon nanoparticles fetched bimodal porous trapping the proteins for useful applications has been realized
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since centuries and various methods have been developed to

serve the purpose. However, the approaches adopted so far to
immobilise the proteins can be split into three categories,
namely, immobilisation through covalent bonds, immobilisa-
tion through non-covalent bonds which includes hydrogen
bonds, electrostatic interactions and van der Waals interactions
and finally encapsulation. Immobilisation can also be described
as an adsorption process where a molecule can be entrapped or
adsorbed on to a support through the three types of interactions

mentioned above.
The nanoporous carbon can serve as an excellent substrate
for the immobilisation of proteins230,231 owing to its high
surface area, narrow pore size distribution and tuneable pore
sizes that can be suitable for the proteins to entangle into the
pores. Moreover, the hydrophobicity of the nanoporous carbon
protects the immobilised protein from solubility and various
other factors like mechanical and thermal instability and can
even cease the denaturation of proteins.232 The commercially Fig. 15 (A) Schematic illustration of the fabrication of the MNTP NCs/
MWCNTs intermediate and self-supporting MNTP C MWCNTs electrodes.
available microporous carbon with small mesopores (Norit (a and b) N2 isotherm and pore size distribution of MNTP C MWCNTs
DLC super 50) was investigated for adsorption of angiotensin electrodes and (c) their TGA/DSC curves. Reproduced with permission
converting enzyme (ACE) to inhibit the peptides233 and food from ref. 241. Copyright 2017, Royal Society of Chemistry.
protein234 and was monitored through the N2 adsorption
desorption process. Likewise, two different types of aprotinin
namely bovine serum albumin and bovine pancreatic trypsin From the above reports on protein assisted templating
inhibitor were adsorbed in an open structured hydrophobic methods, it could be noticed that the bare protein needs a
carbon aerogel (C1) consisting of mesopores and their adsorption templating substrate which otherwise would result in the
capacity was compared with that of the commercially available collapse of the protein. Moreover, the proteins being used as
hydrophilic nanoporous carbon (C2) having higher surface area a carbon precursor also have the major drawback of denatura-
than C1. Interestingly, the C1 exhibited the highest adsorption tion during the carbonisation process. As an alternate way, the
capacity for both the proteins. This clearly shows that the meso- hydrothermal method was employed to carbonise egg-protein
porous carbon has a superior capacity over other porous carbons using graphene nanosheets which play the role of template as
due to its pore size and allows the migration of the proteins inside well as catalyst. By this method, the protein can be avoided
the porous channels due to the hydrophobic nature of the carbon from any physical or chemical damage through the strong
compared with the commercially available hydrophilic carbon bonding between the GO and protein, which was further
which favors the agglomeration of proteins.235,236 activated using KOH to yield a heteroatom doped highly porous
Apart from immobilisation, proteins were also used as carbon carbon material.243
precursors to fabricate 3D porous carbon237,238 and activated
nanoporous carbon with a high surface area and different func-
tional groups such as sulphur239 or metal oxides like MnO2240 6. Applications of functionalized
to impose electrical conductivity. Since the proteins can be nanoporous carbon materials
denatured easily by physical factors like pH, high temperature
and acidic conditions, instead of proteins being used as carbon As nanoporous carbons with different functional groups can
source, alternatively protein themselves were used as templates offer interesting chemical and physical properties, these mate-
to fabricate mesoporous nanocrystals as shown in Fig. 15, rials were effectively utilized for various applications.150,244,245
wherein the mesoporous NaTiO2 (MNTP NC) was coated with Many investigations have focused on the usage of functionalized
BSA and was dispersed in the oxidised multiwalled carbon nanoporous carbon materials for a range of potential applica-
nanotube solution (MWCNTs). Finally, the MWCNT and MNTP tions including conventional Li-ion and post Li batteries,
NC were assembled through electrostatic interaction and supercapacitors, electrocatalysts for oxygen reduction reaction
thermally annealed to form MNTP/MWCNT film.241 This film (ORR), fuel cell supports, hydrogen storage, CO2 capture
exhibited a surface area of only 88.7 m2 g 1 with the typical type and field emission devices. This is mainly due to the fact that
IV isotherm and it was found to be composed of 63 wt% MNTP these fascinating materials can offer highly ordered porous
and 30 wt% MWCNT. structures, high specific surface areas, large pore volumes and a
In another report, the interaction of plasma or the blood uniform pore size distribution. In this section, we will address
proteins with graphitic carbon modified SBA-15 was also inves- the importance of the functionalization of nanoporous carbons
tigated and it was concluded that the graphitic domains and how these functionalities and excellent properties can
influence the interactions of complex protein–nanoparticles.242 elevate the application possibilities in various fields.
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6.1 Nanoporous carbon for sensing ability to generate superoxide ions that change the electrical
The application of carbon based materials for sensing has signals due to the formation of charge carriers.248 The sensing of
been widely studied and the demand for selective sensing is heavy metal ions249 and toxic chemicals like hydrogen peroxide250
changing day-by-day for various reasons including environmental was also studied by using nitrogen doped porous carbon and
monitoring and safety, medical diagnostics, etc. A majority of nanoporous carbon fibres. The ordered nanoporous carbon was
sensing materials exhibit high sensitivity, but high selectivity is also fabricated in a film form by Jia et al., who were successful in
the key and a new component that is now added as a trend to the creating a high surface area with tunable pore sizes. These porous
sensing materials. The non-porous materials like graphene, carbon films exhibited enough space for the immobilisation of glucose
nanotubes and porous materials like activated carbon, etc. fall under oxidase that exhibited an excellent bio sensing performance at a
the high sensitivity materials. On the other hand, the functionalized detection limit of 1.5 mM,251 as shown in Fig. 16. The nanoporous
nanoporous materials can offer both high sensitivity and selectivity carbon films with nickel for selectively sensing glucose were also
towards sensing which is discussed below. demonstrated.252 Nanoporous carbon was also functionalized
The nanoporous carbon can be used for selective sensing with copper to have an active surface area that showed enhanced
by various methodologies like functionalising NC with metal or sensitivity for the detection of biochemicals.253 Nanoporous
metal oxides, surface modification and doping, to sense the carbons were also employed as sensors for selectively detecting
toxic gases, heavy metals, biomolecules, etc. The selective various biomolecules like DNA bases, acids like ascorbic acid
sensing of NH3 gas was performed by heteroatom doping by and uric acid, and NADH.254,255
Travlou et al. where the interaction of NH3 with humidity (H2O)
played a major role in sensing through hydrogen bonding and 6.2 Nanoporous carbon for drug delivery
transport of proton through ionic conductivity.246 A similar The effective drug carrier/drug vehicle is the most demanding
sensing mechanism was followed to sense NH3 gas using the component in drug delivery applications. The addition of the
polymer derived nanoporous carbon. It was found that the specific targeting in the drug delivery system is also an impor-
weak interaction between the surface functional groups of tant factor for deciding on the efficacy of the drug delivery
nanoporous carbon and ammonia caused the protonation of system. Many carriers like nanoporous silica, polymers,
NH3 to NH4+ that resulted in the electrochemical performance micelles, nanotubes, nanoporous carbon, etc. have been employed
towards gas sensing.247 Travlou et al. also demonstrated that for this purpose. However, the biocompatibility of these materials
the doping of nanoporous carbon with N, S or O makes a great is still under research and recently the nanoporous carbon or
influence on their final sensing performance for toxic gases the functionalised nanoporous carbons are of interest in the
including ammonia and H2S as the functionalization has the field of drug delivery.
ability to control the electronic and transport properties of the Clarithromycin, a drug normally used for the treatment of
nanoporous carbons. It was reported that the reversible sensing tonsillitis, sinusitis and pharyngitis, causes side effects like
of ammonia with a high selectivity can be achieved over the swelling of mucosal tissues. In order to reduce the side effects
heteroatoms functionalized nanoporous carbons owing to their of clarithromycin, the nanoporous carbon functionalised with
amine groups was used as a carrier molecule (Fig. 17). It was
Fig. 16 FESEM image of the fabricated porous carbon film, (a) low
magnification, (b) high magnification and (c) the response of the biosensor Fig. 17 (A) Schematic representation of loading of clarithromycin drug in
corresponding to different GOD concentrations, curve a, 1 mg ml 1; curve b, the amine-functionalised nanoporous carbon. (a) Effect of pH on loading
5 mg ml 1; and curve c, 10 mg ml 1. Reproduced with permission from the drug and (b) effect of pH on drug release. Reproduced with permission
ref. 251. Copyright 2014, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. from ref. 256. Copyright 2013, Springer.
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reported that the amine modified nanoporous carbon was

completely biocompatible.256 The nanoporous carbon derived
from MOF was also examined through cytotoxicity assay and the
narrow pore size distribution was found to be suitable for the
controlled release of cisplatin.257 The dissolution and the poor
solubility of the valsartan drug in water was also addressed by
Zhang et al., who used porous carbon monoliths possessing
ordered macropores and uniform mesopores of about 5.2 nm as
a drug carrier.258 It has been reported that the material exhibited

a higher release rate compared with the pure valsartan.
6.3 Nanoporous carbon for catalysis

The increasing demand in the consumption of fossil fuels has
almost depleted the fossil fuel sources; hence renewable energy
sources must be found and developed to prevent the environ- Fig. 18 (A) Schematic representation of the NaOH assisted reduction
mental pollution caused by fossil fuels and to mitigate green- method of Pd/MSC-30 catalyst and gas evolution from the dehydrogenation
of FA–SF. (B) Volume of CO2 + H2 generated versus time. (C) Corresponding
house gasses. As an alternate source, many renewable energy TOF values of H2 generation. The inset of (B) Arrhenius plot (ln(TOF) vs. 1/T).
sources are emerging and being developed with the aim of Reproduced with permission from ref. 259. Copyright 2013, Royal Society
replacing the depleting sources. Among them, the hydrogen of Chemistry.
fuel is a blooming area in catalysis due to its non-toxic nature,
fast recharging ability and high stability. To produce hydrogen,
two well-known pathways have been used, namely dehydrogenation carbon owing to its high surface area and tunable and uniform
and dehydration. However, the latter pathway gives out the toxic pore size distribution. Despite the advantage of the nanopo-
carbon monoxide (CO), which is highly dangerous to the environ- rosity, apparently, the purification process which is otherwise
ment and immense control should be taken during the production called separation remains a difficult task so far. Hence, there is
of hydrogen. The main problem persisting in the field of catalysis is a clear need for developing advanced nanostructures for the
the separation of the product and the reusability of catalysts. efficient adsorption and separation applications.
Hence, it is necessary to fabricate efficient heterogeneous catalysts The neonicotinoid insecticides extracted from water and
which are highly cooperative with the reaction temperature and the fatmelon samples by the magnetic MOF derived nanoporous
pH of the reaction medium. carbon was reported by Hao et al.262 In their typical synthesis,
The synthesis of nanoporous carbon deposited with Pd the magnetic nanoporous carbon was prepared by one step
nanoparticles to synthesise heterogeneous catalysts with the direct carbonisation of ZIF-67 and the embedded Co nano-
strategy of sodium hydroxide assisted reduction was reported particles offered the magnetic property to the material which
by Zhu et al. Sodium hydroxide was used here for the reason of could demonstrate the adsorption and removal of insecticides
uniform dispersion of the metal on the surface of the nanoporous through liquid chromatography. Mesoporous carbon derived
carbon and the reduction assisted by sodium hydroxide resulted from MOF was also reported later for the separation of CO2 and
in the generation of hydrogen from formic acid decomposition CH4 from the mixture.263 On the other hand, the magnetic
without the CO side reaction. Interestingly, the turnover fre- mesoporous carbon (Ni–CMK-3) was also reported for the
quency (TOF) was 2623 h 1 with 100% hydrogen selectivity,259 adsorption and removal of sulfur from oil264 and the pure
as shown in Fig. 18. The N-doped nanoporous carbon was also CMK-3 with a high surface area of 1268 m2 g 1 was employed
surface functionalised with the AgPd zeolite framework for the for the adsorption and recovery of 2-phenylethanol which is a
decomposition of formic acid and the TOF reported was 936 h 1 rose oil component.265 Following the use of mesoporous carbon
at 353 K.260 These two reports clearly showed the advantage of in adsorption and separation, Ma et al. functionalised nano-
nanoporous carbon over the zeolite framework decorated with porous carbon with highly uniform MgO nanoparticles through
nanoporous carbon. Oxidation had a key role in the surface the EISA process for the separation of methanol. The largest
modification of the nanoporous carbons. Velasco et al. demon- adsorption capacity of 11.90 mmol g 1 was observed.266
strated that the oxygen functional groups on the surface Perreault et al. functionalised and grafted mesoporous carbon
of nanoporous carbons can enhance the photoelectrochemical with diglycolyl chloride (DGCI) and N,N1-bis-chloropropyl diglycol-
conversion of light inside the pores. The enhancement in the amide (CI-PDGA) to form CMK-8–DGO and CMK-8–PDGA. These
photoactivity is due to the surface active oxygen groups which two grafted CMK-3 materials were used as adsorbents to study
favor the splitting of the exciton in the nanoconfined space and the adsorption of lanthanides. Although both the components
its efficient use in photochemical reactions.261 showed a type IV isotherm, at lower pH the CMK-8–DGO
exhibited excellent reusability of Ln (Fig. 19).267
6.4 Nanoporous carbon in adsorption and separation An interesting report on the role of different pore structures
Adsorption is the most conventional application of nanoporous in the adsorption and separation of CO2 from the mixture of
carbon compared to various other applications of nanoporous CO2 and hydrogen was presented by Kumar et al. The molecular
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Fig. 19 (A) Schematic illustration of the synthesis of functional meso-

porous carbons. (a) N2 adsorption–desorption isotherms for pristine and
modified mesoporous carbons and (b) pore size distributions of CMK-8.
Reproduced with permission from ref. 267. Copyright 2017, American
Chemical Society.
stimulation studies clearly showed that adsorption and separa- Fig. 20 (A) Charge–discharge curves of HMNC-700 at 0.1 A g 1.
tion were quite sensitive to the pore structure and the composi- (B) Cycling performance and corresponding Coulombic efficiency at a
tion of nanoporous carbon nanostructures. It was found that current density of 1 A g 1. Reproduced with permission from ref. 58.
Copyright 2016, Elsevier. (C) The charge–discharge profiles of Se S/NMC.
the porous carbon with a tube like structure was the best for the
(D) Cycling performance of Se S/NMC at 250 mA g 1. Reproduced with
highly selective adsorption of CO2 molecules from the CO2 and permission from ref. 198. Copyright 2016, American Chemical Society.
hydrogen mixture. Although nanoporous carbons with slit, (E) The galvanostatic charge–discharge curves of bulk Li4Ti5 O12/C.
foam like and random porous structure showed adsorption (F) Specific capacity and Coulombic efficiency of mesoporous Li4Ti5 O12/C.
the selectivity was much inferior to that of porous carbon with Reproduced with permission from ref. 192. Copyright 2012, Wiley-VCH
Verlag GmbH & Co. KGaA, Weinheim.
tube like structures.268
6.5 Nanoporous carbon for batteries of 0.2 mV s 1 and at a potential window of 1.0–2.5 V (vs. Li/Li+)
Modified nanoporous carbon materials have been extensively showed a pair of well-defined redox peaks at 1.65/1.50 V, which
utilized as electrode materials in the lithium ion and post was attributed to the redox reaction of Ti4+/Ti3+, respectively.192
Li-ion batteries such as Li–S, Na-ion and Na–S batteries owing These features revealed that the nanocomposite electrode had
to their superior textural properties together with high con- fast lithium ion insertion and extraction kinetics that was
ductivity and stability. Duan et al. reported on the usage of Sn attributed to the highly ordered mesoporous structure with
nanoparticle incorporated mesoporous carbon as an anode enhanced electrical conductivity. The Li4Ti5O12/C nanocompo-
material for Li-ion batteries.178 The charge/discharge voltage site possessed superior cycling stability performance of more
curves observed for nano-Sn/mesoporous carbon showed a than 1000 cycles at the discharge capacity of 103.1 mA h g 1 at a
typical sloping voltage profile associated with lithium alloy- high rate of 20C with only 5.6% capacity loss (Fig. 20E and F).
ing–dealloying with nano-sized Sn in the sample. The initial Tan et al. reported that the N-doped mesoporous carbon-
columbic efficiency was 60%, which was calculated according capped MoO2 nanobelts (MoO2@NC) electrode delivered
to the discharge capacity of 1246 mA h g 1 and charge capacity high first-cycle discharge and charge capacities of 942.3 and
of 747 mA h g 1. The columbic efficiency increases to 85% 690.7 mA h g 1, respectively, with a Coulombic efficiency (CE)
during the 2nd cycle, to 90% in the 3rd cycle, and to above 97% of 73.3%. In the second cycle, the CE of the anode sample
after 7 cycles. Urchin-like Fe3O4@C–N composites displayed an increased to 94.6%, indicating a good lithium ion insertion/
excellent electrochemical performance with a reversible specific extraction performance during the cycling process. The discharge
capacity of 800 mA h g 1 after 100 cycles at 500 mA h g 1 in the capacity of the MoO2@NC electrode remained at 692.4 mA h g 1
0.01–3 V voltage range at room temperature.194 This significant after 100 cycles at a current of 0.5 A g 1.197
electrochemical performance of urchin-like Fe3O4@C–N compo- Sun et al. also demonstrated that the Se2S6/NMC electrode
sites was attributed to the unique urchin-like structure and the exhibited an initial discharge capacity of 1195 mA h g 1, which
N-doped mesoporous carbon shell. was almost close to the theoretical capacity of 1226 mA h g 1
Shen et al. have used mesoporous Li4Ti5O12/C nanocomposites for Se2S6. They also registered excellent cycling stability
as an anode material in Li ion batteries. The cyclic voltammetry and a high initial Coulombic efficiency of 96.5% as well as a
curve of the mesoporous Li4Ti5O12/C electrode at a scan rate high reversible capacity of 883 mA h g 1 after 100 cycles and
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780 mA h g 1 after 200 cycles at 250 mA g 1, respectively importance of doping of dual heteroatoms in the carbon
(Fig. 20C and D).198 HNMC material prepared from honey showed framework structure of NOMCs.
a superior performance towards the Li ion battery with a reversible
capacity of 1359 mA h g 1 after 10 cycles at 100 mA g 1 and 6.6 Nanoporous carbon for carbon capture and storage
excellent rate capability and cycling stability of 722 mA h g 1 after Global warming leading to drastic climatic changes due to the
200 cycles at 1 A g 1 (Fig. 20A and B). The same material demon- increasing concentration of carbon dioxide in the atmosphere
strated the initial discharge and charge capacities of 977 and added through various anthropogenic sources is inevitably one
427 mA h g 1, respectively, for the Na ion battery.58 of the major environment crises of our times.272,273 There is an
Liang et al. have investigated the performance of the meso- urgent need for developing materials and technologies to
porous nanocomposite by using N-OMC/SiO2 as an anode combat the dangerous emissions of CO2 from industrial sectors
material for lithium-ion batteries. The initial discharge and such as power generation plants, cement production, petrochemical
charge capacities of the N-OMC/SiO2 nanocomposite electrode production, aluminium, steel and plastic manufacturing industries,
were measured to be as high as 3900 and 1996 mA h g 1, etc. Carbon based materials, especially ordered mesoporous
respectively, with a Coulombic efficiency of 51%. The discharge carbon-based adsorbents with highly developed textural para-
capacity retained a large value of 740 mA h g 1 after 50 cycles, meters, are regarded as a potential solution to tackle the problem
which was about two times higher than the theoretical value of of industrial CO2 emission. Two key parameters required for
graphite.93 TiO2 supported on nitrogen-doped carbon foams efficient CO2 capture by an adsorbent include high specific
(NCFs) were also used as a free-standing and flexible electrode surface area and the presence of nitrogen containing functional
for lithium-ion batteries (LIBs). When TiO2–NCF was directly groups on the surface of carbon.274 Several reports can be found
used as a flexible electrode in a LIB, a capacity of 188 mA h g 1 in the literature for increasing the surface area of different kinds
was achieved at a current density of 200 mA g 1 under a of carbons using chemical activation.275,276 However, this proce-
potential window of 1.0–3.0 V, and a specific capacity of dure might not be suitable for ordered carbons as it may result in
149 mA h g 1 after 100 cycles at a current density of 1000 mA g 1 deformation of the order and affect the properties of the carbon.
was maintained.269 The addition of sulphur into the NOMCs can A few ordered mesoporous carbons are discussed below to
help these nanostructures to be used in Li–S battery applications. ascertain the role they can play in capturing CO2.
Qu et al. reported on the preparation of the sulfur–HNMC composite Wang et al. synthesized ordered mesoporous carbon CMK-3
with 53.3 wt% sulphur by a melt-diffusion method for high rate through the hard templating procedure using SBA-15 as a
capability and long cycling stability cathode materials in Li–S template for CO2 capture.277 They reported a surface area of
batteries.270 The S–HNMC composite cathode exhibited a high 1115 m2 g 1 and a pore volume of 1.11 cm3 g 1 and the
initial discharge capacity of 1209 mA h g 1 and retained as high material adsorbed 42 mmol g 1 of CO2 under high-pressure
as 600 mA h g 1 after 200 cycles at 1C. Chen et al. reported on conditions (36 bar). It is to be noted this much high CO2 uptake
the usage of the NM–CMK-3/S composite with 50 wt% sulfur in was observed using CMK-3 preabsorbed with water that decreased
the Li–S battery, which showed a high initial capacity of ca. to 18.5 mmol g 1 with dry CMK-3. The heat of adsorption was
950 mA h g 1, 100% Coulombic efficiency, and excellent cycling observed to be 55 kJ mol 1, which indicates strong physisorption
stability with a capacity retention ratio of 80% (750 mA h g 1) between CMK-3 and CO2.
after 100 cycles with a decay of only 0.2% per cycle.139 The high As previously discussed, the textural properties of the OMCs
performance was attributed to the presence of microporosity were significantly improved after the activation with KOH.
and nitrogen contents which provided synergetic effects. These Especially, the quantity of the micropores can be significantly
results explained the importance of having nitrogen on the enhanced after the activation. Bao et al. reported that the
surface of the carbon walls for energy storage applications. presence of ultra micropores of size o0.5 nm is a critical factor
Balach et al. described a high initial discharge capacity of for enhancing the CO2 adsorption and CO2/N2 selectivity of the
1364 mA h g 1 at 0.2C for the NOMC/S composite with 50 wt% nitrogen doped hierarchical carbon derived from polypyrrole.278
sulfur. The composite material also showed extremely high cycling They compared the CO2 adsorption statistics for N-doped
stability with a high reversible capacity of 566 mA h g 1 and a carbons made at 500 1C and 800 1C and even though the latter
negligible degradation rate of 0.037% after 1200 cycles at had a significantly high surface area, it still showed a relatively
0.5C.145 Liu et al. demonstrated that the S/CPAN-800 composite smaller amount of CO2 adsorption, which defies the common
was an excellent material for Li–S cells, which delivered a high theory that high surface area leads to high CO2 adsorption.
initial discharge capacity of 1585 mA h g 1 and an enhanced Eventually, a low temperature carbonization to protect the widening
capacity retention of 862 mA h g 1 at 0.1C after 100 cycles and a of ultra micropores and retention of nitrogen containing functional
high Coulombic efficiency of around 100%. These results groups was concluded as one of the most critical parameters for
greatly outperformed the S/CMK-3 composite cell without a high CO2 adsorption.
nitrogen doping, which maintained only 400 mA h g 1 capacity
at 0.1C after 100 cycles.271 The enhanced performance 6.7 Electrocatalysis
was attributed to nitrogen doping combined with sulphur, Heteroatom and non-precious foreign element doped carbon
which significantly improved the wettability of the electrolyte nanomaterials are considered as the low cost and highly efficient
and the conductivity of the electrode. These results reveal the electrocatalytic alternatives to the commercial platinum (Pt)
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based electrocatalysts. Among the doped carbon nanomater- NOMC prepared from honey and glucose/ammonia precur-
ials, nanoporous carbon materials modified with B, N, S, P and sors exhibited a significantly lower potential at 0.23 V as well
non-precious elements are more attractive electrocatalysts for as a sharply increased peak current towards the ORR. The
the oxygen reduction reaction (ORR), hydrogen evolution reac- apparent number of electrons involved in ORR for NOMC-800
tion (HER) and oxygen evolution reaction (OER). In this section, prepared at 800 1C is close to 4-electrons, according to the
we will summarize the role of structure, morphology and the Koutecky–Levich equation. This indicates that the oxygen reduction
single or dual heteroatom doping in the OMCs in affecting the follows mainly the four-electron pathway either by reducing oxygen
final electrocatalytic performance of these materials. directly to OH ions or by reducing it to hydrogen peroxide which
6.7.1 Oxygen reduction reaction (ORR). ORR is a key process is subsequently further reduced to OH ions.57,98,161
in the fuel cells (FCs) for generating electricity by electrochemical NOMCs synthesized via a facile dual soft-templating proce-
reduction of oxygen and oxidation of hydrogen by production of dure showed the most positive onset potential ( 0.11 V) and
water as the by-product. The most suitable electrocatalyst for the highest reaction current density at a certain overpotential,
ORR is the platinum (Pt) based electrodes. However, the scarcity suggesting the fastest reaction kinetics via close to four electron
and the high cost of Pt are the primary barriers to commercialize reaction pathway with higher limiting current density.90,99,101
the Pt based electrocatalyst for fuel cells. Apart from the high NOMC materials prepared from pyrrole or aminopyridine and
cost, the Pt-based electrode also suffers from susceptibility to Fe catalyst outperformed the Pt counterpart and the perfor-
fuel crossover and CO poisoning under electrochemical condi- mance was significantly improved by increasing the pyrolysis
tions. Therefore, numerous efforts have been devoted to seeking temperature from 800 to 1000 1C.67,281 Nitrogen-doped meso-
alternative non-platinum ORR electrocatalysts for FCs with a low porous carbon nanosheets (NMCNs) fabricated from the thermal
cost and a high ORR activity. In this part, we review the latest treatment of polyaniline enwrapped cobalt hydroxide (Co(OH)2)
advances in the fabrication of electrocatalysts based on the nanosheets followed by the subsequent acid etching manifested
doped and functionalized nanoporous carbon materials. Choi an excellent ORR performance with an onset potential of
et al. demonstrated that the additional doping of B and/or P in 0.119 V, a half-wave potential of 0.182 V and a limiting
the nitrogen doped nanoporous carbon can enhance the asym- current density of 5.06 mA cm 2. These values were comparable
metry of atomic spin density and improve the ORR catalytic to the commercial Pt/C ( 0.164 V and 5 mA cm 2).282
activity.279 The ORR activity of the B,N-doped and P,N-doped A nitrogen-doped mesoporous carbon containing a network
nanoporous carbon was 1.2 and 2.1 times higher than that of of carbon nanotubes (CNTs) also showed an excellent ORR
N-doped nanoporous carbons at 0.6 V (vs. RHE) in acidic media. activity, with 59 mV more positive onset potential and 30 mV
The nanoporous nitrogen doped carbon catalyst incorporated more positive half-wave potential than a Pt/C catalyst, and also
with both B and P (BPNDC) showed the best ORR activity of much longer durability and stronger tolerance to methanol
2.3 times higher than NDC at 0.6 V (vs. RHE), which records crossover than a Pt/C catalyst.283 Highly ordered N-doped
6.0 mA mg 1 of mass activity (Fig. 21A and B).279,280 mesoporous carbon/graphene frameworks (N-MCF/N-MGF)
prepared by using the super lattice of self-assembled Fe3O4
nanoparticles as template showed a 47 mV positive shift in the
half-wave potential and higher current densities compared with
the Pt/C (2.24 and 0.74 mA cm 2), demonstrating their superior
ORR activity compared with the commercial Pt/C catalyst.284
Park et al. showed the ORR catalytic activity of NOMC
materials, which demonstrated high selectivity toward H2O2
over 90%. At 0.1 V, NOMC exhibited a ring current of 0.148 mA,
which corresponds to H2O2 formation at a rate of 3.06 pmol s 1.62
Chen et al. also observed a well-defined oxygen reduction peak at
0.68 V (vs. RHE) in the CV curve under O2 saturated 0.1 M KOH
solution for NHPCM prepared by using a N-doped hierarchically
porous silica monolith template and furfuryl alcohol as the
carbon source. The number of electrons involved in ORR for
NHPCM is in the range of 3.7 to 3.9 indicating that an intrinsic
four-electron pathway is the dominant mechanism. No signifi-
cant change was observed in the ORR current density of
the NHPCM electrode after MeOH was added into the electro-
Fig. 21 (A) ORR results in 1 M HClO4 for the prepared catalysts, (1) NDC, chemical cell, suggesting that it has remarkably improved
(2) BNDC, (3) PNDC, (4) BPNDC, and (5) Pt/C (40 wt%). (B) Calculated mass ability to avoid the crossover effects.65
activities at 0.6 V (vs. RHE) for the prepared catalysts and other N-doped
Sulfur doped OMCs such as OMC-S-1, OMC-S-2 and OMC-S-3
carbon catalysts. (C) RDE polarization curves of Fe–N-GC materials prepared
at different carbonization temperatures and Pt/C. (D) RDE voltammograms
having sulphur contents in the range of 1.4 to 1.5 wt% exhibited
of FeNCSs and Pt/C at 1600 rpm. Reproduced with permission from ref. 279 higher currents of 238.0, 282.3 and 376.4 mA, during the ORR,
and 182. Copyright 2012 and 2014, American Chemical Society. which are higher than that of the unmodified OMC electrode.
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The number of electrons calculated for ORR on OMC-S-3 were Pt nanoparticles supported on nitrogen-doped porous carbon
3.3, 3.4, 3.5, 3.6 and 3.8 at different potentials, which indicates microspheres (Pt/CN) demonstrated ultrahigh ORR activity
that OMC-S-3 typically provides a four-electron transfer path- at a pH of 8.4 with a mass activity and specific activity of
way for ORR.113 Yang et al. observed an ORR peak at 0.19 V 564 mA mg 1 Pt and 834 mA cm 2 Pt, respectively, which may
for P doped well-ordered mesoporous carbon (POMC), which have been due to the presence of an appropriate amount of N
confirmed the excellent electrocatalytic activity of POMC for atoms doped into the nanoporous carbon matrix.177 Pt nano-
oxygen reduction. particles on N-doped ordered mesoporous carbon–Co compo-
POMC also exhibited high catalytic activity for ORR with an sites (Pt/Co–N-OMC) displayed the mixed kinetic diffusion
extraordinary selectivity for oxygen to evade the crossover current between 0.48 and 0.75 V with the highest onset
effects of methanol and thereby outperformed the commercial potential at B0.72 V in an oxygen saturated 0.5 mol l 1
Pt/VC electrode. For the Pt/VC catalyst, a very strong peak at H2SO4 electrolyte at a rotation rate of 1600 rpm and a scan rate
0.18 and 0.21 V was observed for methanol oxidation in the of 5 mV s 1 and they also exhibited the highest limiting current
CV curve, whereas the cathodic ORR peak vanished. In contrast, and onset potential.287
no noticeable change was observed in the oxygen-reduction Hollow graphitic carbon spheres with Fe–N-doped meso-
current on the POMC electrode.107,285 Boron doped ordered porous shells (FeNCSs) prepared via in situ polymerization
mesoporous carbons (BOMCs) were also employed for ORR. exhibited very superior ORR activity with a half-wave potential
These catalysts exhibited a substantial ORR cathodic peak at (E1/2) of 0.886 V in 0.1 M KOH, 15 mV more positive than that of
around 0.27 V. The maximum peak current density on BOMCs commercial Pt/C catalysts.288 Liang et al. elucidated the four-
was 1.46 mA cm 2, whereas unmodified OMCs and Pt/C electron reduction performance of oxygen in 0.5 M H2SO4 at
registered maximum peak current densities of 0.84 and room temperature by using cobalt–nitrogen-doped (C–N–Co)
0.97 mA cm 2, respectively.103 The BOMC electrode showed and iron–nitrogen-doped nanoporous carbon (C–N–Fe),
a significant onset potential shift towards the positive side to prepared from vitamin B12 (VB12) and the polyaniline–Fe
0.16 V with the limiting diffusion current density at 0.80 V, (PANI–Fe) complex. Among all of the catalysts, C–N–Co fabri-
which is about 1.7 times stronger than that of undoped OMC cated from VB12 and silica nanoparticles exhibited a remarkable
catalysts. The number of electrons that participated in the ORR ORR activity with a half-wave potential of 0.79 V, which is only
for the BOMC electrode at 0.50 V was found to be 3.86 and B58 mV deviation from Pt/C, and further demonstrated the high
this increased to 4 at more negative potentials, indicating that selectivity of the four electron pathway, and excellent electro-
oxygen reduction follows mainly the four-electron pathway chemical stability up to 10 000 cycles.180
either by reducing oxygen directly to OH ions or by reducing Mesoporous Fe10@NOMC catalyst prepared from a ferrocene-
it to peroxide which is subsequently further reduced to OH based ionic liquid was also utilized for ORR. The results showed
ions. S and N dual doped ordered mesoporous carbon (SN-OMC) that the catalyst exhibited a comparable onset potential and
materials were also successfully employed for ORR applications. half-wave potential (0 V vs. MMO) for the Pt/C and close values
It was found that the dual doping helped to enhance the ORR to the Fe/Fe3C–melamine/N-KB composite but superior long-
electrocatalytic activity ( 0.186 V) in alkaline media with desir- term stability compared to 20 wt% Pt/C in identical test condi-
able current density, methanol tolerance and long-term stability. tions for ORR with the four-electron transfer pathway under
The number of electrons involved for SN-OMC during the ORR alkaline conditions. The Fe10@NOMC catalyst showed perfect
ranges from 3.93 to 3.95, very close to 4.0, indicating that it ORR selectivity in a methanol containing electrolyte, whereas a
favoured a four-electron ORR process.111,112 significantly high methanol oxidation current was detected for
The ORR onset-potential (1.01 V), E1/2 value (0.86 V), and the Pt/C catalyst under the same conditions.183 Fe3O4 embedded
current density (9.6 mA cm 2) of the Fe–N-GC electrode pre- into nitrogen-doped mesoporous carbon spheres (Fe3O4/NMCS)
pared by heating 2,2-bipyridine and Fe chelates at 900 1C with with an iron content of 3.35 wt% was used as a robust catalyst for
0.2 mg cm 2 loading were higher and larger than the values the ORR in alkaline media. It showed excellent electrochemical
obtained on the commercial Pt/C-JM electrode with 20 mgPt cm2 performance in terms of a more positive onset potential of
loading and the previously reported NPMCs with 0.3–0.4 mg cm 2 1.036 V vs. RHE, a half-wave potential of 0.861 V and much
loading in 0.1 M KOH solution. These results indicated its superior better methanol tolerance and long-term durability, in compar-
catalytic activity in alkaline medium (Fig. 21C and D).181,182 ison with that of 20% Pt/C.289
Ultra fine Fe2N nanocrystals incorporated in mesoporous nitro- Three-dimensionally (3D) ordered mesoporous Fe–N/C fabri-
gen doped graphitic carbon spheres (Fe2N/MNGCS) were also cated from the soft templating approach manifested high onset
utilized for ORR applications. The catalysts demonstrated a potential (1.018 V), half-wave potential (0.812 V) and limited-
half-wave potential of 0.881 V vs. RHE, high selectivity towards diffusion current density (5.98 mA cm 2) in both acidic and
the 4e oxygen reduction process, excellent long-term stability alkaline electrolytes. The number of transferred electrons (n) was
with 95.2% of the initial current retention after 60 000 s of calculated to be 4.08–4.20 between 0.40 and 0.60 V for meso-
continuous operation and good tolerance against the methanol porous Fe–N/C, confirming the dominant 4e oxygen reduction
crossover effect (94.9% of the current remained prior to 4.0 M mechanism.290 Cobalt–nitrogen-doped three-dimensionally (3D)
methanol injection in alkaline media). This performance ordered macro-/mesoporous carbons (Co–N-OMMCs) prepared
was much superior to that of the commercial Pt/C catalyst.286 from the dual-templating synthesis approach exhibited a highly
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positive ORR half-wave potential of B0.83 V vs. RHE, which is

only B0.01 V deviation from the Pt/C catalyst (B0.84 V vs.
RHE). The catalysts also provided a higher diffusion-limited
current density than commercial Pt/C, indicating a large quantity
of exposed active sites on the Co–N-OMMC. The number of
electrons involved in the ORR for Co–N-OMMC was calculated to
be 3.9 at 0.5 V vs. RHE, revealing that the Co–N-OMMC favoured
a 4e oxygen reduction process and O2 was reduced to OH ,
which is the same with Pt/C catalyst. The chronoamperogram of

Co–N-OMMC showed negligible performance attenuation even
after 25 h of continuous operation at 0.5 V vs. RHE, in contrast to
a sharp activity loss of commercial Pt/C, demonstrating the high
stability of Co–N-OMMC for ORR.187
6.8 Nanoporous carbon for supercapacitance

Supercapacitors, which are also known as electrochemical
capacitors, provide a high power density (410 kW kg 1), a fast
charge/discharge process (within seconds) and long cycling life
(4105 cycles).291,292 Nanoporous carbon based materials are
considered as attractive electrode materials for supercapacitors
owing to their extremely high specific surface areas, large pore
volumes and pore diameters, in combination with the simple
synthesis processing, non-toxicity and high chemical stability.
There have been quite a number of review articles reported on
this topic.291–293 Therefore, in this review, recent developments
in the utilization of these nanostructures for supercapacitor
applications for the past five years are reviewed. In 2015, Lin
Fig. 22 (A) OMFLC-N devices retain 492% after 100 hours of sustained
et al. successfully used N-doped mesoporous few-layer carbon loading and retain 480% of their initial response after 50 000 cycles.
with a large surface area of 1900 m2 g 1 for supercapacitor (B) Ragone plot of specific energy versus specific power for OMFLC-N SM
applications. It was reported that the materials showed the symmetric devices using 0.5 M H2SO4 and 2 M Li2SO4 electrolytes, along
highest ever specific capacitance of 810 F g 1 and 710 F g 1 and with other standard devices. Reproduced with permission from ref. 56.
volumetric capacity of 560 F cm 3 at 1 A g 1 in a 0.5 M H2SO4 Copyright 2015, American Association for the Advancement of Science.
and 2 M Li2SO4 electrolyte using an Ag/AgCl reference electrode

and a Pt counter electrode.56 The electrochemical cell withstood
the capacity for 50 000 cycles between 0 and 1.2 V. The device at 5 A g 1.164 NOMC prepared from phenol–urea–formaldehyde
also demonstrated the highest specific energy of 23.0 W h kg 1 exhibited a specific capacitance of 225 F g 1 at a current density
and a specific power density of 18.5 kW kg 1 based on the device of 0.5 A g 1 and it showed good electrochemical stability even
weight in a 2 M Li2SO4 electrolyte. Electrochemical impedance after 1000 cycles at a current density of 5.0 A g 1.92
spectroscopy showed that OMFLC-N has the lowest equivalent Microporosity has been introduced in the NOMCs via activa-
series resistance of B0.8 ohms, better than that of OMFLC tion and other techniques to enhance the specific capacitance
without N doping and CMK-3 (Fig. 22). Wei et al. reported on of the materials. Liu et al. reported on the enhanced super-
the supercapacitor device fabrication by using rich nitrogen- capacitor performance of activated NOMC electrode materials
doped ordered mesoporous carbon, which showed the specific with a mass loading of B3 mg cm 2 which yielded a high specific
capacitances of 262 F g 1 (in H2SO4) and 227 F g 1 (in KOH) capacitance of 186 F g 1 at a current density of 0.25 A g 1 and a
at a current density of 0.2 A g 1 and 244 F g 1 (in H2SO4) and good capacitance retention of 75% at a high discharge current
213 F g 1 (in KOH) at a current density of 0.5 A g 1, which density of 20 A g 1 in an ionic liquid electrolyte. Increasing the
are much better than that for the mesoporous carbon FDU-15 mass loading to B12 mg cm 2 gave rise to only a 10% capacitance
without any nitrogen content (110–130 F g 1).87 These results decay at 20 A g 1.159 Almeida et al. demonstrated that the NMC-T
revealed that the coating of nitrogen doped carbon on the material showed a specific capacitance of 190.2 F g 1 and retained
surface of the support was much more effective than the bulk 73% of its capacitance when the current density was increased
NOMSs in the supercapacitor applications. from 0.5 to 8.0 A g 1. In addition, the specific capacitance of
The nitrogen doped hierarchically porous carbon nets exhibited NMC-T materials was retained up to 98% of their stored charges
a high specific capacitance of 537.3 F g 1 and 306.3 F cm 3 at or initial capacitance after 1000 charge–discharge cycles at a
0.5 A g 1 current density in a 0.5 M H2SO4 electrolyte. The current density of 2.0 A g 1.66 NOMCs prepared via the aqueous
material also presented an outstanding cycling stability with cooperative assembly route demonstrated a high specific capa-
98.8% retention of their initial capacitance after 10 000 cycles citance of 186 F g 1 at a current density of 0.25 A g 1 and a good
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capacitance retention of 75% at a high discharge current best value for electrodes in microcapacitors. The functional
density of 20 A g 1 in an ionic liquid electrolyte.159 groups on these microporous carbons play a huge role in
Nitrogen-doped micro-mesoporous carbon material exhibited enhancing the electrochemical performance of the ZTCs. For
a reversible specific capacitance of 226.3 F g 1 at a current example, Kyotani et al. also reported on the large pseudocapa-
density of 1.0 A g 1 in a 6 M KOH electrolyte and 75.5% of its citance (330 F g 1) of electrochemically oxygen functionalized
initial capacity could be retained after 2000 cyclic tests.137 A zeolite template carbon (ZTC) in an organic electrolyte.296 The
maximum capacitance of 237 F g 1 was reached for the NOMC formation of anion and cation radicals of oxygen functionalities
prepared by using an ionic liquid precursor at a current density offers pseudocapacitance which is responsible for the enhance-
of 0.1 A g 1. The specific energy of a cell made from two identical ment of the total specific capacitance of the functionalized
NOMC electrodes was more than 83 W h kg 1 (unpackaged) for ZTC. These results provide clear evidence that the functionali-
1100 cycles at a current density of 1 A g 1, which corresponds to zation of the ZTC is one of the key elements and can be used for
a specific energy of 25 W h kg 1 in a commercial-style, packaged tuning the electrochemical performance of ZTC.
device, which typically contains 30 wt% active material.81 Linnemann et al. demonstrated simplifying the supercapacitor
Hierarchically mesoporous carbons with different boron electrode fabrication process through the electrodeposition of the
contents (from 0.42 to 2.37 wt%) showed a specific capacitance carbonized metal organic framework (MOF) based films on the
of 180 F g 1 in H2SO4 aqueous solution at a current density of current collector.297 The MOF films are well attached to the metal
1 A g 1.106 Sun et al. described an advanced supercapacitor substrate during the carbonization process under an argon atmo-
material based on nitrogen doped porous graphitic carbon sphere forming highly electrochemically active Co3O4/C and
(NPGC), which showed an excellent capacitive behaviour with a Mn3O4/C hybrid materials. At the 50th cycle, the integral capaci-
specific capacitance of 293 F g 1 at a current density of 1 A g 1, tance of the Mn3O4/C bilayered system was 160 F g 1 referring
long-term cycling stability at about 5000 cycles, and high coulombic to Mn, 116 F g 1 referring to Mn3O4 and 102 F g 1 referring to
efficiency in a KOH electrolyte.96 Tang et al. implemented a super- MnO2 at a scan rate of 20 mV s 1. This value is superior to the
capacitor device by using NHPC-3D having 8.2 wt% nitrogen Mn3O4/graphene material reported by Lee et al.298
functionalities as the active electrode material, which exhibited Fransaer et al. reported on the preparation of mesoporous
a specific capacitance as high as 252 F g 1 at a current density layered Ni–Co mixed metal oxide–carbon composite electrodes
of 2 A g 1. The device also showed a high capacitance retention on the Ni foam by using Ni–Co mixed metal–organic frame-
of 75.7% with a specific capacitance of 190 F g 1 at a higher works (MOFs) with the above mentioned method.299 This
current density of 20 A g 1.73 A NOMC material demonstrated a electrode exhibited a high capacitance of 2098 mF cm 2 and
reversible specific capacitance of 308 F g 1 at a current density a superior rate performance of 93% from 1 to 20 mA cm 2 at a
of 0.2 A g 1 in an aqueous H2SO4 electrolyte with 58% capacity current density of 1 mA cm 2. These are the best methods
retention of 131 F g 1 at a current density of 20 A g 1.97 Song for the fabrication of efficient supercapacitor electrodes using
et al. depicted that the NMMC electrode has a high specific MOF derived carbons which do not require any additional
capacitance of 325 F g 1 at a current density of 0.2 A g 1 in an processing steps or templates.
aqueous H2SO4 electrolyte.76 Xu et al. demonstrated that a N- and O functional groups containing nanoporous carbon
microsphere-like nitrogen-doped mesoporous carbon/nickel– derived from the zeolite template showed a large pseudo-
cobalt layered double hydroxide (NMC/NiCo-LDHs-M) composite capacitance of 312.4 F g 1 in a H2SO4 electrolyte and it can operate
displayed a high specific capacitance of 272.6 F g 1 at 1 A g 1 at 1.2 V in H2SO4 with a good durability beyond 4000 cycles.300
and an outstanding electrochemical capacitance retention of Wang et al. demonstrated that the NOMC materials can have the
87.2% of initial capacitance even after 10 000 cycles.101 specific capacitances of 76 F g 1 and 21 F g 1, respectively, at a
OMCs derived from zeolite based templates have been employed current density of 0.1 A g 1, which was measured by the galvanic
as electrodes for supercapacitor applications owing to their charge and discharge process.86 The diffusive resistances (RD) of
better specific surface area and small pores. Kyotani et al. NOMC electrodes are 0.7 and 1.3 ohm, respectively. The specific
studied the supercapacitance performance of zeolite templated capacitance of nitrogen and sulphur doped ordered mesoporous
B and N doped ordered microporous carbon (N-ZTC) materials carbon (NSOMC) reached 180 F g 1 in KOH aqueous solution at
by using zeolite Y as a template. Among the materials prepared, a current density of 1 A g 1, with approximately 39.5% enhance-
N-ZTC demonstrated a high capacitance of 180 F g 1 in a 1 M ment over CMK-3, despite the fact that the specific surface area
TEABF4/PC electrolyte.294 Amoros et al. reported on the fabrica- of NSOMC is only about 70% of the CMK-3.110 NOMC material
tion of thin films of zeolite-templated carbon (ZTC) on a carbon with a nitrogen content of 6.7 wt% showed a high capacitance
current collector by the combination of chemical and electro- of 264 F g 1 in a 1.0 M H2SO4 electrolyte at a current density of
chemical synthesis protocols.295 FAU nanozeolites were deposited 0.5 A g 1 and a good rate capability with a capacitance retention
by an electrophoretic deposition (EPD) technique from colloidal of 226 F g 1 at 10 A g 1. The NOMC electrode also delivered
suspensions on porous carbon discs. Binderless continuous thin an excellent cycling stability without capacitance fading over
films of ZTC were materialized by subjecting the resulting 10 000 cycles.59 Ling et al. demonstrated that NOMC prepared by
composites to chemical vapour deposition (CVD) of acetylene using the PDA precursor exhibited a high specific capacitance of
gas followed by HF washing. The prepared thin ZTC layers show 538 F g 1 at a sweep rate of 5 mV s 1. NOMC material delivered
area capacitance values over 12 mF cm 2, which is one of the a large capacitance of 186 F g 1 at a high current density of
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3 A g 1. The NONC supercapacitor electrode retained more than very fast and sensitive fluorescent detection of Salmonella
93% of the initial capacitance even after 5000 cycles, exhibiting typhimurium. The limit of bacterial detection was 50 CFU ml 1
excellent cycling stability.60 A graphitic ordered mesoporous while a linear relation was found between the concentration
carbon (G-OMC) prepared from DA and NiO template showed of bacteria and fluorescence intensity in the range of 103 to
a specific capacitance of 183 F g 1 and 68 mF cm 2 at a current 105 CFU ml 1. This conjugated probe was also tested for real
density of 0.1 A g 1.61 Although the N and NiO functionalities samples of eggshell and tap water and the results were very
were there in the samples, they registered poor specific capaci- similar to the conventional plate count method which suggests
tance which might be attributed to the low specific surface area the potential application of these systems for detection of
of the prepared samples. Salmonella typhimurium in real situations.302

Nitrogen- and sulfur-codoped 3D cubic ordered mesoporous Simultaneous detection of Vibrio parahaemolyticus and
carbon (KNOMC) with controlled dopant content (10.0–4.6% for Salmonella typhimurium was also possible using a combination
nitrogen and 0.94–0.75% for sulfur) demonstrated a specific capa- of green (gQD) and red quantum (rQD) dots with carbon
citance of 320 F g 1 at a current density of 1 A g 1 in a 2 M aqueous nanoparticles. With the attachment of a specific aptamer, the
KOH electrolyte. However, the specific capacitance decreased quickly respective QDs-CNP assembly was able to measure the FRET
during the first 10 cycles, but the specific capacitance remained at fluorescence changes from the interaction of target bacteria
almost 100.0% during the 20–1000th cycles. After 1000 cycles, the within a linear range of 50 to 106 CFU ml 1 and the detection
specific capacitance reached 247 F g 1.301 NOMCs with a high limit was 25 and 35 CFU ml 1 for each bacterium respectively.
surface area of 1741 m2 g 1 and nitrogen content up to 15 wt% The detection capability of the sensor platform using the plate
exhibited a specific capacitance of 230 F g 1 at a current density of count method showed consistency when compared to shrimp
0.5 A g 1 and a good rate capability of 175 F g 1 at 20 A g 1 with a and chicken as real solid samples for analysis.303
capacitance retention of 77.4% in a 6 M KOH aqueous electrolyte.78 A GQDs–AuNPs FRET biosensor was developed for S. aureus
These results revealed that the optimum amount of N and S specific gene sequence detection by immobilising the capture
together with the excellent surface area and structural order is probe on GQDs and conjugation of reporter probes on AuNPs.
the key to obtain high specific capacitance for the samples. Then, the hybridization of target S. aureus oligos within a conc.
Nitrogen and phosphorus dual doped ordered mesoporous range of 100 nM to 400 nM packed between the GQD and AuNP
carbon (NPOMC) demonstrated a high specific capacitance of layers formed a sandwich structure which triggered the fluorescence
220 F g 1 at a current density of 1 A g 1, a good rate capability resonance energy transfer (FRET) effect. One of the interesting
of 178 F g 1 at 16 A g 1 with a capacitance retention of 81% and features of this work was that the detection limit of this biosensor
an excellent cycling stability of 91% in a 6 M KOH aqueous was 1 nM for S. aureus specific gene detection, which clearly
electrolyte.171 This value was lower than the N and S doped or N demonstrated the good selectivity. In a single and double
and O doped NOMCs. Hierarchically nitrogen doped ordered mismatched oligos system at 200 nM, the sensor recorded a
mesoporous carbons (HNMC) synthesized from polyhedral oligo- quencher efficiency of 93% for target oligos and 22–37%
silsesquioxanes (POSS) demonstrated a nearly ideal rectangular for mismatched oligos which indicated the specificity of the
shaped CV in a wide voltage window from 2 to 2 V. These sensor. This simple technology could be used for the whole
HNMC materials showed a gravimetric and volumetric specific genome detection of S. aureus which would open the platform
capacitance of 163 F g 1 and 106 F cm 3 at a current density of for the detection of foodborne pathogens. This would signifi-
0.25 A g 1 in an ionic liquid electrolyte and also showed a slow cantly support the food safety and environmental screening.304
capacitance decay with the increase of discharge rates, in parti-
cular, at 20 A g 1. They also showed a high capacity of 141 F g 1
with 89% capacitance retention.162 Binder free supercapacitor 7. Conclusion and future prospects
electrodes based on nitrogen-doped mesoporous carbon micro-
fibers (NMCMFs) exhibited a specific capacity of 189 F g 1 at a Despite the fact that a tremendous amount of progress has
scan rate of 5 mV s 1, an excellent rate capability of 107 F g 1 at been made in the fabrication of nanoporous carbons with
100 mV s 1 and durability (maintained over 96% of the initial contemporary structures and unique morphologies, exciting
capacitance after 10 000 cycles) in a 6 M KOH aqueous opportunities have still persisted for their functionalization in
electrolyte.163 All these results revealed that optimized doping developing multifunctional properties for divergent specific
and the structural control of OMCs are the key to fabricate the applications. The integration of different heteroatoms into
best electrode system for energy storage applications. Ultimately, the nanoporous carbon framework together provided us a
this information could be used for the design of the best energy new class of materials exhibiting many unmatched properties.
storage system with a considerable cost reduction by adopting By controlling both chemistry and geometry of these function-
necessary low-cost modification of OMCs. alized hybrid nanoporous carbon based materials using
different templates or micelles, these functional materials
6.9 Carbon nanomaterial based pathogen sensors have already had applications in a wide variety of different
Carboxyl modified carbon dots prepared by hydrothermal technological and scientific fields. Various strategies have been
carbonization of citric acid combined with amine based aptamer applied for the fabrication of nanoporous carbon materials
formed a very effective CD–aptamer complex which provided a with exemplary textural parameters starting from the basic
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synthesis methods, such as templating techniques, to the mesoporous carbons overcoming the intrinsic limitations
advanced surfactant mediating approaches. imposed by the hard template method.
In this review, we have reviewed and discussed the recent In this review, we have thoroughly conferred the recent
significant breakthroughs in the synthesis and control of research developments and trends in both hard templating
the structure, morphology and functionalities of ordered nano- and soft templating techniques for the synthesis of highly
porous carbon materials. We have also shown how the struc- ordered nanoporous carbons without any dopants and also
tures and morphological control affect the final textural functionalized nanoporous carbons with mono, binary and
properties of the materials, and their roles in the final perfor- ternary heteroatom doping and foreign elements. Heteroatom
mance of the materials in various applications including doping, functionalization and morphological control of nano-
adsorption, carbon capture, energy storage batteries and super- porous carbon materials are highly dependent on the processing
capacitors, electrocatalysis and heterogeneous catalysis have conditions. These modification processes also play a key role in
been discussed in detail. We have also imparted the exhaustive controlling the textural parameters such as specific surface area,
analysis of the structure–function correlation of functionalized pore volume and pore diameter of the functionalized nano-
nanoporous carbon materials and considered their diverse pre- porous carbon materials. Precise control of these parameters is
paration methods including mono or binary and even ternary important as they dictate the efficiency of the nanoporous
doping methods by using different heteroatoms (B, N, O, S, carbon materials in many applications.
and P) and foreign elements (Fe, Co, Ni and Cu) containing In the last few decades, there has been a tremendous amount
natural and synthetic carbonaceous precursors, surface modifi- of research and development activities devoted to the discovery
cations and functionalization with organic and inorganic mole- of new materials and technology for energy generation, storage
cules and nanostructures. and conversion, owing to the development of alternative,
With these developed robust and reliable doping, function- economical and sustainable energy resources to meet the ever
alization and templating strategies, a broad range of nano- growing global energy demand and environmental impact on
porous functionalized carbon materials with pore cavity sizes in the heavy dependence of traditional fossil fuel based energy
the range of 2–50 nm and with various dimensions (1D, 2D and resources, which poses serious challenges to human health,
3D) can be readily and selectively fabricated for promising energy security, and environmental protection. As presented in
advanced technological applications. The prepared function- this review, the fuel cell technology offers a viable approach to
alized nanoporous carbon materials have been effectively used generate electricity from the electrochemical reaction of hydro-
mainly in electrochemical energy conversion and storage device gen and oxygen by production of water as the by-product, and
fabrication technologies. Their involvement in electrochemical virtually no pollution. The slow ORR kinetics on the cathode side
energy storage applications, including Li-ion batteries, post is a key step limiting the energy conversion efficiency of a
Li-ion batteries including Li–S, Li–air and Na-ion batteries, fuel cell and requires a substantial amount of the catalyst.
and supercapacitors, was presented in detail. Recent discov- Traditionally, platinum (Pt) has been regarded as the best ORR
eries in energy conversion applications such as electrochemical catalyst. However, the Pt-based electrode suffers from multiple
oxygen reduction reaction (ORR), hydrogen evolution reaction drawbacks such as high cost, scarcity, and susceptibility to fuel
(HER) and oxygen evolution reaction (OER) on functionalized crossover, time-dependent drift and CO poisoning under elec-
nanoporous carbon materials were also introduced in detail. By trochemical conditions. Along with the intensive research efforts
finely tuning the textural parameters, morphology and doping in reducing or replacing the Pt-based electrode in fuel cells,
concentrations of the nanoporous carbon materials at different heteroatom and non-precious metal doped nanoporous carbon
length scales, their performance in adsorption, carbon capture, materials have been discovered as a new class of electrocatalysts
sensing, and electrochemical energy storage and conversion for ORR, which could dramatically reduce the cost and increase
can be significantly enhanced. the efficiency of fuel cells. The functionalized nanoporous
Before inception of the block copolymer assisted soft carbon materials successfully catalyze the O2 molecule via 4
template synthesis method for the preparation of highly electron reduction pathways at the same or lower potentials than
ordered mesoporous carbon materials, the pre-prepared golden standard Pt based catalysts under both acidic and basic
inorganic porous material mediated hard template nanocasting conditions. The nanoporous carbon materials also possessed
approach was considered as the only method that can be used excellent long-term stability with almost 100% retention of the
for the successful fabrication of mesoporous carbon with well- initial current even after several hours of continuous operation.
defined pores. The soft-template method relies on supramole- They also showed a good tolerance against the methanol cross-
cular micelle assemblies, which enhances the polymerization over effect. The enhanced catalytic performance of the function-
processes of carbon molecular precursors. The soft templating alized nanoporous carbon materials has been attributed to the
method is thermodynamically driven, and therefore depends on electron-accepting/donating abilities of the heteroatoms or func-
the chemical interactions between supramolecular templates and tional elements present in the nanoporous carbon framework,
carbon molecular precursors. Because of their facile synthesis which create a net charge on adjacent carbon atoms to facilitate
and processing characteristics, soft templating synthesis the O2 adsorption and net charge transfer for ORR.
processes governed by the block copolymer templates have Another great opportunity for functionalized nanoporous
dominated and created new possibilities for the synthesis of carbon materials lies in the efficient storage of energy generated
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by fuel cell technology, which is a win–win situation for these Moreover, the low yield of ordered nanoporous carbon materials
fascinating materials. The use of functionalized nanoporous provided by the current synthesis methods also remains an issue
carbon materials has generated much excitement in the field from the perspective of their potential use in industrial pro-
of energy storage systems, including supercapacitors, Li-ion cesses. By irreversible acidic and basic moiety functionalization
batteries and post Li-ion batteries. As it was clearly explained in of nanoporous carbons with known and desired functional
this review, the functionalized nanoporous carbon architec- groups, it is possible to control the anchoring of heteroatoms
tures can be introduced with heteroatoms, redox functional on their surface in a desirable way. Surface functionalization of
groups, functional elements, metals, metal oxides, conducting nanoporous carbons also improves their solubility and stability
polymers and alloy based materials to enhance both electron and reduces the agglomeration, which can help them with
and ion transport in the active materials for improvement of energy improved performance towards selective sensing of hazardous
storage capability and stability of the batteries and supercapacitor heavy metals, pathogens and toxins. It is quite surprising that in
devices. Apart from the energy conversion and storage devices recent days the interest towards the application of functionalised
including fuel cells, batteries and supercapacitors, the future nanoporous carbon for drug delivery has been increasing,
challenge is to design and develop functionalized nanoporous mainly due to the functionalisation methods that have the ability
carbon materials having a suitable band structure, with inbuilt to enhance the compatibility of nanoporous carbon materials.
functional moieties including organic or inorganic nanostructures These methodologies allow immobilisation of DNA, proteins,
in the mesochannels of electrodes. These electrodes should be able enzymes and drugs that can be finally involved in the in vivo
to split the water molecules under electrochemical conditions for drug delivery. However, the practical applications of these mate-
the facile production of hydrogen and oxygen which can be rials are still under investigation and very few studies have
connected to fuel cell technology that offers a viable approach to offered a proof of concept. Therefore, a wide spectrum of
electricity generation directly from water without any pollution. research is deliberately needed for the biomedical applications.
Although the functionalised nanoporous carbons offer excellent The research articles reviewed in this review article illustrate
performances in the energy oriented applications, it is still required the fabrication of nanoporous carbons and the great interest
to achieve a cost-effective way for the large-scale production of towards their properties and applications. Carbons have already
cheap electrode materials and electrocatalysts which are both made a revolution in the world and the nanoporous carbon
highly stable and reliable. These are the major limitations for these materials are their fascinating parts and the present trend in
exciting materials. Therefore, the future challenge is to synthesize the ocean of carbon is the functionalisation of nanoporous carbon
highly pure functionalized nanoporous carbon materials without which is now making history through small modifications and an
any contamination in a more economical way without using harsh outstanding improvement in the world. There is no doubt that a
conditions and expensive reagents but with low-cost biodegradable lot of opportunities are hidden and the researchers should explore
carbon or nitrogen precursors. As discussed above in this review, more on utilizing the amazing potential of these functionalized
the functionalized nanoporous carbon materials having high spe- ordered nanoporous carbons in the above suggested applications
cific areas were found to be the best materials for CO2 adsorption. covering the energy, environment and health sectors. We are
The future mega challenge for materials scientists is to utilize both confident that the information presented in this review would
the in-built electronic and absorption properties of the function- definitely support advances in the research and development of
alized nanoporous carbons to convert the adsorbed CO2 into fuels ordered nanoporous carbon materials.
and chemicals by using water as the hydrogen source through
electrocatalysis. The proof-of-concept studies will certainly stimu-
late more research in the electrochemical reduction of CO2. Conflicts of interest
Nowadays, functionalized nanoporous carbon materials are
fascinating even in the biomedical fields. Their biocompatibility There are no conflicts to declare.
for tissue engineering and theragnostic applications such as bio
sensing, drug delivery, gene therapy, bio imaging, phototherapy
and hybrid theragnostic is highly challenging by which one can Acknowledgements
understand that numerous research efforts are needed in these One of the authors A. Vinu is grateful to ARC for the award of
areas to develop and invent novel functionalised nanoporous future fellowship (FT100100970) and for grants DP1501048248
materials in the future. and DP170104478, and the University of Newcastle for the start-up
Irreversible agglomeration of nanoporous carbon layers and grants and Alexander von Humboldt foundation for the Friedrich
uncontrollable doping of heteroatoms at the molecular level Wilhelm Bessel Research Award.
during their preparation through the high temperature pyrolysis
methods are important challenges and are yet to be addressed.
Although the heteroatom doping has made remarkable progress, References
its facile synthetic routes are still being developed with the
multiple heteroatom doping in nanoporous carbon frameworks. 1 R. Ryoo, S. H. Joo and S. Jun, J. Phys. Chem. B, 1999, 103,
Further, process simplification is needed to lower the consumption 7743–7746.
of consumables and energy as well as decrease waste generation. 2 M. E. Davis, Nature, 2002, 417, 813.
View Article Online
3 C. Vix-Guterl, E. Frackowiak, K. Jurewicz, M. Friebe, 32 A. Almasoudi and R. Mokaya, Microporous Mesoporous

J. Parmentier and F. Béguin, Carbon, 2005, 43, 1293–1302. Mater., 2014, 195, 258–265.
4 C. Liang, Z. Li and S. Dai, Angew. Chem., Int. Ed., 2008, 47, 33 A. Almasoudi and R. Mokaya, J. Mater. Chem. A, 2014, 2,
3696–3717. 10960–10968.
5 M. Notarianni, J. Liu, K. Vernon and N. Motta, Beilstein 34 E. Masika and R. Mokaya, Energy Environ. Sci., 2014, 7,
J. Nanotechnol., 2016, 7, 149–196. 427–434.
6 L. Wen, F. Li and H.-M. Cheng, Adv. Mater., 2016, 28, 35 K. Kim, T. Lee, Y. Kwon, Y. Seo, J. Song, J. K. Park, H. Lee,
4306–4337. J. Y. Park, H. Ihee, S. J. Cho and R. Ryoo, Nature, 2016,
7 R. Ryoo, S. H. Joo, M. Kruk and M. Jaroniec, Adv. Mater., 535, 131.

2001, 13, 677–681. 36 H. Lee, K. Kim, S.-H. Kang, Y. Kwon, J. H. Kim, Y.-K. Kwon,
8 S. Jun, S. H. Joo, R. Ryoo, M. Kruk, M. Jaroniec, Z. Liu, R. Ryoo and J. Y. Park, Sci. Rep., 2017, 7, 11460.
T. Ohsuna and O. Terasaki, J. Am. Chem. Soc., 2000, 122, 37 K. Kim, Y. Kwon, T. Lee, S. J. Cho and R. Ryoo, Carbon,
10712–10713. 2017, 118, 517–523.
9 S. H. Joo, S. J. Choi, I. Oh, J. Kwak, Z. Liu, O. Terasaki and 38 X. Meng and F.-S. Xiao, Chem. Rev., 2014, 114, 1521–1543.
R. Ryoo, Nature, 2001, 412, 169–172. 39 Y. Ren, Z. Ma and P. G. Bruce, Chem. Soc. Rev., 2012, 41,
10 S. Che, K. Lund, T. Tatsumi, S. Iijima, S. H. Joo, R. Ryoo and 4909–4927.
O. Terasaki, Angew. Chem., Int. Ed., 2003, 42, 2182–2185. 40 W. Li and D. Zhao, Chem. Commun., 2013, 49, 943–946.
11 A.-H. Lu, W.-C. Li, W. Schmidt, W. Kiefer and F. Schüth, 41 M. Enterrı́a and J. L. Figueiredo, Carbon, 2016, 108, 79–102.
Carbon, 2004, 42, 2939–2948. 42 K. Na, C. Jo, J. Kim, K. Cho, J. Jung, Y. Seo, R. J. Messinger,
12 A. Sayari and Y. Yang, Chem. Mater., 2005, 17, 6108–6113. B. F. Chmelka and R. Ryoo, Science, 2011, 333, 328–332.
13 J. Lee, S. Yoon, S. M. Oh, C. H. Shin and T. Hyeon, Adv. 43 J. Grand, S. N. Talapaneni, A. Vicente, C. Fernandez,
Mater., 2000, 12, 359–362. E. Dib, H. A. Aleksandrov, G. N. Vayssilov, R. Retoux,
14 J. Lee, S. Yoon, T. Hyeon, S. M. Oh and K. Bum Kim, Chem. P. Boullay, J.-P. Gilson, V. Valtchev and S. Mintova, Nat.
Commun., 1999, 2177–2178, DOI: 10.1039/a906872d. Mater., 2017, 16, 1010.
15 T.-Y. Ma, L. Liu and Z.-Y. Yuan, Chem. Soc. Rev., 2013, 42, 44 Y. Wan and D. Zhao, Chem. Rev., 2007, 107, 2821–2860.
3977–4003. 45 Y. Shi, Y. Wan and D. Zhao, Chem. Soc. Rev., 2011, 40,
16 J. C. Ndamanisha and L.-p. Guo, Anal. Chim. Acta, 2012, 3854–3878.
747, 19–28. 46 F. Schüth, Chem. Mater., 2001, 13, 3184–3195.
17 W. Li, J. Liu and D. Zhao, Nat. Rev. Mater., 2016, 1, 16023. 47 L. Chuenchom, R. Kraehnert and B. M. Smarsly, Soft
18 T. Kyotani, Bull. Chem. Soc. Jpn., 2006, 79, 1322–1337. Matter, 2012, 8, 10801–10812.
19 M. Inagaki, M. Toyoda and T. Tsumura, RSC Adv., 2014, 4, 48 J. Parmentier, F. O. M. Gaslain, O. Ersen, T. A. Centeno and
41411–41424. L. A. Solovyov, Langmuir, 2014, 30, 297–307.
20 M. Inagaki, Y. A. Kim and M. Endo, J. Mater. Chem., 2011, 49 F. O. M. Gaslain, J. Parmentier, V. P. Valtchev and J. Patarin,
21, 3280–3294. Chem. Commun., 2006, 991–993, DOI: 10.1039/B512002K.
21 V. Malgras, Q. Ji, Y. Kamachi, T. Mori, F.-K. Shieh, 50 J. Li, E. Fiset, J. Yang, P. Yuan, X. Ling, D. Hulicova-
K. C. W. Wu, K. Ariga and Y. Yamauchi, Bull. Chem. Soc. Jurcakova, C. Yu and L. Wang, J. Mater. Chem., 2012, 22,
Jpn., 2015, 88, 1171–1200. 21472–21480.
22 W. Xia, A. Mahmood, R. Zou and Q. Xu, Energy Environ. 51 L. Sterk, J. Górka, A. Vinu and M. Jaroniec, Microporous
Sci., 2015, 8, 1837–1866. Mesoporous Mater., 2012, 156, 121–126.
23 H. B. Wu and X. W. Lou, Sci. Adv., 2017, 3, eaap9252. 52 L. Liu, Q.-F. Deng, B. Agula, T.-Z. Ren, Y.-P. Liu, B. Zhaorigetu
24 J. Schuster, G. He, B. Mandlmeier, T. Yim, K. T. Lee, T. Bein and Z.-Y. Yuan, Catal. Today, 2012, 186, 35–41.
and L. F. Nazar, Angew. Chem., Int. Ed., 2012, 51, 3591–3595. 53 T. Kimura, A. M. Emre, K. Kato and Y. Hayashi, J. Mater.
25 Y. Seo, K. Kim, Y. Jung and R. Ryoo, Microporous Mesoporous Chem. A, 2013, 1, 15135–15141.
Mater., 2015, 207, 156–162. 54 G. P. Mane, S. N. Talapaneni, C. Anand, S. Varghese,
26 G. Tao, L. Zhang, Z. Hua, Y. Chen, L. Guo, J. Zhang, Z. Shu, H. Iwai, Q. Ji, K. Ariga, T. Mori and A. Vinu, Adv. Funct.
J. Gao, H. Chen, W. Wu, Z. Liu and J. Shi, Carbon, 2014, 66, Mater., 2012, 22, 3596–3604.
547–559. 55 S. N. Talapaneni, K. Fugane, A. Vinu and T. Mori, Adv.
27 L. Wang and R. T. Yang, J. Phys. Chem. C, 2012, 116, 1099–1106. Porous Mater., 2017, 5, 26–35.
28 A. Castro-Muñiz, Y. Hoshikawa, T. Kasukabe, H. Komiyama 56 T. Lin, I.-W. Chen, F. Liu, C. Yang, H. Bi, F. Xu and
and T. Kyotani, Langmuir, 2016, 32, 2127–2135. F. Huang, Science, 2015, 350, 1508–1513.
29 K. Kim, M. Choi and R. Ryoo, Carbon, 2013, 60, 175–185. 57 J. Lu, X. Bo, H. Wang and L. Guo, Electrochim. Acta, 2013,
30 K. Nueangnoraj, H. Nishihara, K. Imai, H. Itoi, T. Ishii, 108, 10–16.
M. Kiguchi, Y. Sato, M. Terauchi and T. Kyotani, Carbon, 58 Y. Zhang, L. Chen, Y. Meng, J. Xie, Y. Guo and D. Xiao,
2013, 62, 455–464. J. Power Sources, 2016, 335, 20–30.
31 E. Masika and R. Mokaya, Prog. Nat. Sci.: Mater. Int., 2013, 59 D.-D. Zhou, W.-Y. Li, X.-L. Dong, Y.-G. Wang, C.-X. Wang
23, 308–316. and Y.-Y. Xia, J. Mater. Chem. A, 2013, 1, 8488–8496.
View Article Online
60 Y. Liang, H. Liu, Z. Li, R. Fu and D. Wu, J. Mater. Chem. A, 87 J. Wei, D. Zhou, Z. Sun, Y. Deng, Y. Xia and D. Zhao, Adv.
2013, 1, 15207–15211. Funct. Mater., 2013, 23, 2322–2328.
61 D. Yuan, F. Zeng, J. Yan, X. Yuan, X. Huang and W. Zou, 88 J. Xu, X. Zhao, A. Wang and T. Zhang, Carbon, 2014, 80,
RSC Adv., 2013, 3, 5570–5576. 610–616.
62 J. Park, Y. Nabae, T. Hayakawa and M.-a. Kakimoto, ACS 89 D. Saha, A. Spurri, J. Chen and D. K. Hensley, Microporous
Catal., 2014, 4, 3749–3754. Mesoporous Mater., 2016, 229, 8–13.
63 A. Chen, K. Xia, Y. Yu, H. Sun, L. Liu, S. Ren and Y. Li, 90 J. Li, Z. Li, J. Tong, C. Xia and F. Li, RSC Adv., 2015, 5,
J. Electrochem. Soc., 2016, 163, A3063–A3068. 70010–70016.
64 A. Chen, K. Xia, L. Zhang, Y. Yu, Y. Li, H. Sun, Y. Wang, 91 A. Chen, Y. Yu, Y. Zhang, W. Zang, Y. Yu, Y. Zhang, S. Shen
Y. Li and S. Li, Langmuir, 2016, 32, 8934–8941. and J. Zhang, Carbon, 2014, 80, 19–27.
65 Y. Chen, R. Ma, Z. Zhou, G. Liu, Y. Zhou, Q. Liu, S. Kaskel 92 M. Xie, Y. Xia, J. Liang, L. Chen and X. Guo, Microporous
and J. Wang, Adv. Mater. Interfaces, 2015, 2, 1500199. Mesoporous Mater., 2014, 197, 237–243.
66 V. C. Almeida, R. Silva, M. Acerce, O. P. Junior, A. L. Cazetta, 93 Y. Liang, L. Cai, L. Chen, X. Lin, R. Fu, M. Zhang and
A. C. Martins, X. Huang, M. Chhowalla and T. Asefa, D. Wu, Nanoscale, 2015, 7, 3971–3975.
J. Mater. Chem. A, 2014, 2, 15181–15190. 94 J. H. Lee, H. J. Lee, S. Y. Lim, B. G. Kim and J. W. Choi,
67 K. Wan, G.-F. Long, M.-Y. Liu, L. Du, Z.-X. Liang and J. Am. Chem. Soc., 2015, 137, 7210–7216.
P. Tsiakaras, Appl. Catal., B, 2015, 165, 566–571. 95 M. Li and J. Xue, J. Phys. Chem. C, 2014, 118, 2507–2517.
68 S. Shrestha, N. Morse and W. E. Mustain, RSC Adv., 2014, 4, 96 L. Sun, C. Tian, Y. Fu, Y. Yang, J. Yin, L. Wang and H. Fu,
47039–47046. Chem. – Eur. J., 2014, 20, 564–574.
69 K. Wan, M.-y. Liu, Z.-p. Yu, Z.-x. Liang, Q.-b. Liu, J.-h. Piao and 97 Y. Song, L. Li, Y. Wang, C. Wang, Z. Guo and Y. Xia,
Y.-y. Zheng, Int. J. Hydrogen Energy, 2016, 41, 18027–18032. ChemPhysChem, 2014, 15, 2084–2093.
70 K. Wu and Q. Liu, Appl. Surf. Sci., 2016, 379, 132–139. 98 C. Guo, X. Tong and X.-Y. Guo, Int. J. Hydrogen Energy,
71 Á. Sánchez-Sánchez, F. Suárez-Garcı́a, A. Martı́nez-Alonso 2016, 41, 22941–22951.
and J. M. D. Tascón, Carbon, 2015, 94, 152–159. 99 B. Bayatsarmadi, Y. Zheng, M. Jaroniec and S. Z. Qiao,
72 G. Tao, L. Zhang, L. Chen, X. Cui, Z. Hua, M. Wang, Chem. – Asian J., 2015, 10, 1546–1553.
J. Wang, Y. Chen and J. Shi, Carbon, 2015, 86, 108–117. 100 G. Shen, X. Sun, H. Zhang, Y. Liu, J. Zhang,
73 J. Tang, T. Wang, R. R. Salunkhe, S. M. Alshehri, V. Malgras A. Meka, L. Zhou and C. Yu, J. Mater. Chem. A, 2015, 3,
and Y. Yamauchi, Chem. – Eur. J., 2015, 21, 17293–17298. 24041–24048.
74 D.-S. Yang, D. Bhattacharjya, M. Y. Song, F. Razmjooei, 101 C.-T. Hung, N. Yu, C.-T. Chen, P.-H. Wu, X. Han, Y.-S. Kao,
J. Ko, Q.-H. Yang and J.-S. Yu, ChemCatChem, 2015, 7, T.-C. Liu, Y. Chu, F. Deng, A. Zheng and S.-B. Liu, J. Mater.
2882–2890. Chem. A, 2014, 2, 20030–20037.
75 K. Huo, W. An, J. Fu, B. Gao, L. Wang, X. Peng, G. J. Cheng 102 T. Zhou, Y. Zhou, R. Ma, Z. Zhou, G. Liu, Q. Liu, Y. Zhu and
and P. K. Chu, J. Power Sources, 2016, 324, 233–238. J. Wang, Carbon, 2017, 114, 177–186.
76 Y. Song, S. Hu, X. Dong, Y. Wang, C. Wang and Y. Xia, 103 X. Bo and L. Guo, Phys. Chem. Chem. Phys., 2013, 15,
Electrochim. Acta, 2014, 146, 485–494. 2459–2465.
77 X. Gao, Z. Chen, Y. Yao, M. Zhou, Y. Liu, J. Wang, 104 A. Nsabimana, X. Bo, Y. Zhang, M. Li, C. Han and L. Guo,
W. D. Wu, X. D. Chen, Z. Wu and D. Zhao, Adv. Funct. J. Colloid Interface Sci., 2014, 428, 133–140.
Mater., 2016, 26, 6649–6661. 105 T. Wang, C. Zhang, X. Sun, Y. Guo, H. Guo, J. Tang, H. Xue,
78 Q. Shi, R. Zhang, Y. Lv, Y. Deng, A. A. Elzatahrya and M. Liu, X. Zhang, L. Zhu, Q. Xie and J. He, J. Power Sources,
D. Zhao, Carbon, 2015, 84, 335–346. 2012, 212, 1–12.
79 X. Yang, H. Ma and G. Zhang, Langmuir, 2017, 33, 3975–3981. 106 M. Enterrı́a, M. F. R. Pereira, J. I. Martins and J. L. Figueiredo,
80 F. Hasché, M. Oezaslan, P. Strasser and T.-P. Fellinger, Carbon, 2015, 95, 72–83.
J. Energy Chem., 2016, 25, 251–257. 107 D.-S. Yang, D. Bhattacharjya, S. Inamdar, J. Park and
81 B. E. Wilson, S. He, K. Buffington, S. Rudisill, W. H. Smyrl J.-S. Yu, J. Am. Chem. Soc., 2012, 134, 16127–16130.
and A. Stein, J. Power Sources, 2015, 298, 193–202. 108 P. Song, L. Zhu, X. Bo, A. Wang, G. Wang and L. Guo,
82 A. Chen, Y. Yu, Y. Zhang, T. Xing, Y. Wang, Y. Zhang and Electrochim. Acta, 2014, 127, 307–314.
J. Zhang, J. Hazard. Mater., 2014, 279, 280–288. 109 J. Xu, Y. Zhao, C. Shen and L. Guan, ACS Appl. Mater.
83 D. Liu, J.-H. Lei, L.-P. Guo, D. Qu, Y. Li and B.-L. Su, Interfaces, 2013, 5, 12594–12601.
Carbon, 2012, 50, 476–487. 110 D. Zhang, Y. Hao, L. Zheng, Y. Ma, H. Feng and H. Luo,
84 L. Liu, Q.-F. Deng, X.-X. Hou and Z.-Y. Yuan, J. Mater. J. Mater. Chem. A, 2013, 1, 7584–7591.
Chem., 2012, 22, 15540–15548. 111 T. Jiang, Y. Wang, K. Wang, Y. Liang, D. Wu, P. Tsiakaras
85 J. Yu, M. Guo, F. Muhammad, A. Wang, G. Yu, H. Ma and and S. Song, Appl. Catal., B, 2016, 189, 1–11.
G. Zhu, Microporous Mesoporous Mater., 2014, 190, 117–127. 112 X. Song, H. Ren, J. Ding, C. Wang, X. Yin and H. Wang,
86 X. Wang, C.-G. Liu, D. Neff, P. F. Fulvio, R. T. Mayes, Mater. Lett., 2015, 159, 280–283.
A. Zhamu, Q. Fang, G. Chen, H. M. Meyer, B. Z. Jang and 113 H. Wang, X. Bo, Y. Zhang and L. Guo, Electrochim. Acta,
S. Dai, J. Mater. Chem. A, 2013, 1, 7920–7926. 2013, 108, 404–411.
View Article Online
114 X. Zhao, Q. Zhang, B. Zhang, C.-M. Chen, A. Wang, T. Zhang 138 Y. Kwon, K. Kim and R. Ryoo, RSC Adv., 2016, 6,
and D. S. Su, J. Mater. Chem., 2012, 22, 4963–4969. 43091–43097.
115 S. R. Stoyanov, A. V. Titov and P. Král, Coord. Chem. Rev., 139 H. Chen, Q. Li, N. Teng, D. Long, C. Ma, Y. Wei, J. Wang
2009, 253, 2852–2871. and L. Ling, Electrochim. Acta, 2016, 214, 231–240.
116 Y. Deng, Y. Xie, K. Zou and X. Ji, J. Mater. Chem. A, 2016, 4, 140 Y. Liu, X. Zhao, G. S. Chauhan and J.-H. Ahn, Appl. Surf.
1144–1173. Sci., 2016, 380, 151–158.
117 K. N. Wood, R. O’Hayre and S. Pylypenko, Energy Environ. 141 B. Han, E. J. Lee, W. H. Choi, W. C. Yoo and J. H. Bang,
Sci., 2014, 7, 1212–1249. New J. Chem., 2015, 39, 6178–6185.
118 L. Dai, Y. Xue, L. Qu, H.-J. Choi and J.-B. Baek, Chem. Rev., 142 H. Tang, Y. Zeng, D. Liu, D. Qu, J. Luo, K. Binnemans,
2015, 115, 4823–4892. D. E. De Vos, J. Fransaer, D. Qu and S.-G. Sun, Nano Energy,
119 S. Joseph, D. M. Kempaiah, M. Benzigar, A. V. Baskar, 2016, 26, 131–138.
S. N. Talapaneni, S. H. Jhung, D.-H. Park and A. Vinu, 143 L. Cheng, C. Hou, B. Zhang and G. Liu, RSC Adv., 2016, 6,
J. Mater. Chem. A, 2017, 5, 21542–21549. 114361–114373.
120 S. N. Talapaneni, S. Anandan, G. P. Mane, C. Anand, 144 S. Jiao, J. Du, Z. Du, D. Long, W. Jiang, Z. Pan, Y. Li and
D. S. Dhawale, S. Varghese, A. Mano, T. Mori and X. Zhong, J. Phys. Chem. Lett., 2017, 8, 559–564.
A. Vinu, J. Mater. Chem., 2012, 22, 9831–9840. 145 J. Balach, T. Jaumann, M. Klose, S. Oswald, J. Eckert and
121 S. N. Talapaneni, G. P. Mane, A. Mano, C. Anand, D. S. L. Giebeler, J. Power Sources, 2016, 303, 317–324.
Dhawale, T. Mori and A. Vinu, ChemSusChem, 2012, 5, 146 C. Goel, H. Bhunia and P. K. Bajpai, RSC Adv., 2015, 5,
700–708. 46568–46582.
122 S. N. Talapaneni, J. H. Lee, S. H. Je, O. Buyukcakir, T.-W. 147 H. Chen, F. Sun, J. Wang, W. Li, W. Qiao, L. Ling and
Kwon, K. Polychronopoulou, J. W. Choi and A. Coskun, D. Long, J. Phys. Chem. C, 2013, 117, 8318–8328.
Adv. Funct. Mater., 2017, 27, 1604658. 148 J. Hu, K. T. Ho, X. U. Zou, W. H. Smyrl, A. Stein and
123 G. P. Mane, S. N. Talapaneni, K. S. Lakhi, H. Ilbeygi, P. Bühlmann, Anal. Chem., 2015, 87, 2981–2987.
U. Ravon, K. Al-Bahily, T. Mori, D.-H. Park and A. Vinu, 149 J. Hu, X. U. Zou, A. Stein and P. Bühlmann, Anal. Chem.,
Angew. Chem., Int. Ed., 2017, 56, 8481–8485. 2014, 86, 7111–7118.
124 S. N. Talapaneni, J. Kim, S. H. Je, O. Buyukcakir, J. Oh and 150 K. Sakaushi and M. Antonietti, Bull. Chem. Soc. Jpn., 2014,
A. Coskun, J. Mater. Chem. A, 2017, 5, 12080–12085. 88, 386–398.
125 K. S. Lakhi, D.-H. Park, K. Al-Bahily, W. Cha, B. Viswanathan, 151 J. Gong, M. Antonietti and J. Yuan, Angew. Chem., Int. Ed.,
J.-H. Choy and A. Vinu, Chem. Soc. Rev., 2017, 46, 72–101. 2017, 56, 7557–7563.
126 O. Buyukcakir, S. H. Je, S. N. Talapaneni, D. Kim and 152 H. Wang, S. Min, C. Ma, Z. Liu, W. Zhang, Q. Wang, D. Li,
A. Coskun, ACS Appl. Mater. Interfaces, 2017, 9, 7209–7216. Y. Li, S. Turner, Y. Han, H. Zhu, E. Abou-hamad,
127 K. S. Lakhi, D.-H. Park, S. Joseph, S. N. Talapaneni, U. Ravon, M. N. Hedhili, J. Pan, W. Yu, K.-W. Huang, L.-J. Li, J. Yuan,
K. Al-Bahily and A. Vinu, Chem. – Asian J., 2017, 12, 595–604. M. Antonietti and T. Wu, Nat. Commun., 2017, 8, 13592.
128 A. Vinu, K. Ariga, T. Mori, T. Nakanishi, S. Hishita, 153 S. Mascotto, D. Kuzmicz, D. Wallacher, M. Siebenbürger,
D. Golberg and Y. Bando, Adv. Mater., 2005, 17, 1648–1652. D. Clemens, S. Risse, J. Yuan, M. Antonietti and
129 A. Vinu, Adv. Funct. Mater., 2008, 18, 816–827. M. Ballauff, Carbon, 2015, 82, 425–435.
130 X. Jin, V. V. Balasubramanian, S. T. Selvan, D. P. Sawant, 154 N. Fechler, T.-P. Fellinger and M. Antonietti, Adv. Mater.,
M. A. Chari, G. Q. Lu and A. Vinu, Angew. Chem., Int. Ed., 2013, 25, 75–79.
2009, 48, 7884–7887. 155 T.-P. Fellinger, A. Thomas, J. Yuan and M. Antonietti, Adv.
131 D.-H. Park, K. S. Lakhi, K. Ramadass, M.-K. Kim, Mater., 2013, 25, 5838–5855.
S. N. Talapaneni, S. Joseph, U. Ravon, K. Al-Bahily and 156 P. Hu, D. Meng, G. Ren, R. Yan and X. Peng, Appl. Mater.
A. Vinu, Chem. – Eur. J., 2017, 23, 10753–10757. Today, 2016, 5, 1–8.
132 Y. J. Lee, S. N. Talapaneni and A. Coskun, ACS Appl. Mater. 157 D. Liu, D. Zheng, L. Wang, D. Qu, Z. Xie, J. Lei, L. Guo,
Interfaces, 2017, 9, 30679–30685. B. Deng, L. Xiao and D. Qu, J. Phys. Chem. C, 2014, 118,
133 S. N. Talapaneni, G. P. Mane, D.-H. Park, K. S. Lakhi, 2370–2374.
K. Ramadass, S. Joseph, W. M. Skinner, U. Ravon, K. Al- 158 M. Chen, L.-L. Shao, Y.-P. Liu, T.-Z. Ren and Z.-Y. Yuan,
Bahily and A. Vinu, J. Mater. Chem. A, 2017, 5, 18183–18192. J. Power Sources, 2015, 283, 305–313.
134 K. S. Lakhi, D.-H. Park, G. Singh, S. N. Talapaneni, 159 D. Liu, C. Zeng, D. Qu, H. Tang, Y. Li, B.-L. Su and D. Qu,
U. Ravon, K. Al-Bahily and A. Vinu, J. Mater. Chem. A, J. Power Sources, 2016, 321, 143–154.
2017, 5, 16220–16230. 160 Y. Yang, B. Zhao, P. Tang, Z. Cao, M. Huang and S. Tan,
135 X.-h. Li, K. Wan, Q.-b. Liu, J.-h. Piao, Y.-y. Zheng and Carbon, 2014, 77, 113–121.
Z.-x. Liang, Chin. J. Catal., 2016, 37, 1562–1567. 161 B. Nagy, S. Villar-Rodil, J. M. D. Tascón, I. Bakos and
136 Y. Yang, G. Lan, X. Wang and Y. Li, Chin. J. Catal., 2016, 37, K. László, Microporous Mesoporous Mater., 2016, 230,
1242–1248. 135–144.
137 A. Chen, Y. Wang, Q. Li, Y. Yu, Y. Li, Y. Zhang, Y. Li, K. Xia 162 D. Liu, G. Cheng, H. Zhao, C. Zeng, D. Qu, L. Xiao, H. Tang,
and S. Li, J. Electrochem. Soc., 2016, 163, A1959–A1964. Z. Deng, Y. Li and B.-L. Su, Nano Energy, 2016, 22, 255–268.
View Article Online
163 R. Liu, L. Pan, L. Wan and D. Wu, Phys. Chem. Chem. Phys., 191 W. Wang, W. Jing, L. Sheng, D. Chai, Y. Kang and Z. Lei,
2015, 17, 4724–4729. Appl. Catal., A, 2017, 538, 123–130.
164 L.-N. Han, X. Wei, Q.-C. Zhu, S.-M. Xu, K.-X. Wang and 192 L. Shen, X. Zhang, E. Uchaker, C. Yuan and G. Cao, Adv.
J.-S. Chen, J. Mater. Chem. A, 2016, 4, 16698–16705. Energy Mater., 2012, 2, 691–698.
165 Y. Chang, F. Hong, J. Liu, M. Xie, Q. Zhang, C. He, H. Niu 193 W. Wei, C. Yu, Q. Zhao, X. Qian, G. Li and Y. Wan, Appl.
and J. Liu, Carbon, 2015, 87, 424–433. Catal., B, 2014, 146, 151–161.
166 A. Sánchez-Sánchez, F. Suárez-Garcı́a, A. Martı́nez-Alonso 194 M. Chen, X. Shen, K. Chen, Q. Wu, P. Zhang, X. Zhang and
and J. M. D. Tascón, Carbon, 2014, 70, 119–129. G. Diao, Electrochim. Acta, 2016, 195, 94–105.
167 A. Sánchez-Sánchez, F. Suárez-Garcı́a, A. Martı́nez-Alonso 195 W. Hu, Q. Wang, S. Wu and Y. Huang, J. Mater.
and J. M. D. Tascón, Appl. Surf. Sci., 2014, 299, 19–28. Chem. A, 2016, 4, 16920–16927.
168 C. Weinberger, S. Haffer, T. Wagner and M. Tiemann, Eur. 196 J. Xiao, Y. Xia, C. Hu, J. Xi and S. Wang, J. Mater.
J. Inorg. Chem., 2014, 2787–2792. Chem. A, 2017, 5, 11114–11123.
169 U. Byambasuren, Y. Jeon, D. Altansukh and Y.-G. Shul, 197 X. Tan, C. Cui, S. Wu, B. Qiu, L. Wang and J. Zhang, Chem.
J. Solid State Electrochem., 2016, 20, 645–655. – Asian J., 2017, 12, 36–40.
170 T. Panja, D. Bhattacharjya and J.-S. Yu, J. Mater. Chem. A, 198 F. Sun, H. Cheng, J. Chen, N. Zheng, Y. Li and J. Shi, ACS
2015, 3, 18001–18009. Nano, 2016, 10, 8289–8298.
171 J. Feng, W. Song, L. Sun and L. Xu, RSC Adv., 2016, 6, 199 K. Fu, Y. Wang, L. C. Mao, J. H. Jin, S. L. Yang and G. Li,
110337–110343. Electrochim. Acta, 2016, 215, 427–434.
172 Z. Li, J. Liu, C. Xia and F. Li, ACS Catal., 2013, 3, 2440–2448. 200 G. P. Hao, Z. Y. Jin, Q. Sun, X. Q. Zhang, J. T. Zhang and
173 H. Huang, X. Wang, M. Tan, C. Chen, X. Zou, W. Ding and A. H. Lu, Energy Environ. Sci., 2013, 6, 3740–3747.
X. Lu, ChemCatChem, 2016, 8, 1485–1489. 201 G. Sun, J. Lu, S. Ge, X. Song, J. Yu, M. Yan and J. Huang,
174 F. Wang, J. Xu, X. Shao, X. Su, Y. Huang and T. Zhang, Anal. Chim. Acta, 2013, 775, 85–92.
ChemSusChem, 2016, 9, 246–251. 202 H. B. Ren, J. Y. Zhu, Y. T. Bi, Y. W. Xu and L. Zhang, RSC
175 D. Ye, R. Zhang, Y. Fu, J. Bu, Y. Wang, B. Liu and J. Kong, Adv., 2016, 6, 89140–89147.
Electrochim. Acta, 2015, 160, 306–312. 203 L. R. Nan, W. B. Yue and Y. Jiang, J. Mater. Chem. A, 2015,
176 C. Ray, S. Dutta, R. Sahoo, A. Roy, Y. Negishi and T. Pal, 3, 22170–22175.
Chem. – Asian J., 2016, 11, 1588–1596. 204 L. R. Nan, Z. T. Fan, W. B. Yue, Q. Dong, L. S. Zhu, L. Yang
177 R. Balgis, G. M. Anilkumar, S. Sago, T. Ogi and and L. Z. Fan, J. Mater. Chem. A, 2016, 4, 8898–8904.
K. Okuyama, J. Power Sources, 2013, 229, 58–64. 205 S. W. Zhou, Q. X. Xie, S. H. Wu, X. L. Huang and P. Zhao,
178 B. Duan, W. Wang, H. Zhao, B. Xu, K. Yuan and Y. Yang, Ionics, 2017, 23, 1499–1507.
J. Electrochem. Soc., 2012, 159, A2092–A2095. 206 X. S. Zhang, J. L. Jin, P. T. Yan, J. Xu, R. J. Zhang and C. Wu,
179 X.-H. Yan and B.-Q. Xu, J. Mater. Chem. A, 2014, 2, 8617–8622. Mater. Lett., 2015, 160, 190–193.
180 H.-W. Liang, W. Wei, Z.-S. Wu, X. Feng and K. Müllen, 207 X. Jia, C. Zhang, J. Liu, W. Lv, D. W. Wang, Y. Tao, Z. Li,
J. Am. Chem. Soc., 2013, 135, 16002–16005. X. Zheng, J. S. Yu and Q. H. Yang, Nanoscale, 2016, 8,
181 C. You, D. Dang, X. Qiao, G. Wang, W. Fan, R. Chen, Y. Li, 4447–4451.
X. Li and S. Liao, J. Mater. Chem. A, 2015, 3, 23512–23519. 208 X. Yang, F. Y. Qu, H. Niu, Q. Wang, J. Yan and Z. J. Fan,
182 A. Kong, X. Zhu, Z. Han, Y. Yu, Y. Zhang, B. Dong and Electrochim. Acta, 2015, 180, 287–294.
Y. Shan, ACS Catal., 2014, 4, 1793–1800. 209 K. Ding, Q. Liu, Y. K. Bu, Y. Y. Huang, J. Q. Lv, J. Wu,
183 Z. Li, G. Li, L. Jiang, J. Li, G. Sun, C. Xia and F. Li, Angew. S. C. Abbas and Y. B. Wang, RSC Adv., 2016, 6, 93318–93324.
Chem., Int. Ed., 2015, 54, 1494–1498. 210 D. den Boer, G. D. Han and T. M. Swager, Langmuir, 2014,
184 C. Deng, H. Zhong, L. Yao, S. Liu, Z. Xu and H. Zhang, 30, 762–767.
ChemSusChem, 2014, 7, 3435–3441. 211 L. K. Shrestha, R. G. Shrestha, Y. Yamauchi, J. P. Hill,
185 G.-H. An, E.-H. Lee and H.-J. Ahn, J. Alloys Compd., 2016, T. Nishimura, K. Miyazawa, T. Kawai, S. Okada,
682, 746–752. K. Wakabayashi and K. Ariga, Angew. Chem., Int. Ed.,
186 Y. Yang, L. Jia, B. Hou, D. Li, J. Wang and Y. Sun, 2015, 54, 951–955.
ChemCatChem, 2014, 6, 319–327. 212 V. I. Berezkin, V. V. Popov and M. V. Tomkovich, Phys. Solid
187 T. Sun, L. Xu, S. Li, W. Chai, Y. Huang, Y. Yan and J. Chen, State, 2017, 59, 620–628.
Appl. Catal., B, 2016, 193, 1–8. 213 Z. Tan, K. Ni, G. Chen, W. Zeng, Z. Tao, M. Ikram,
188 T. Maiyalagan, T. O. Alaje and K. Scott, J. Phys. Chem. C, Q. Zhang, H. Wang, L. Sun, X. Zhu, X. Wu, H. Ji,
2012, 116, 2630–2638. R. S. Ruoff and Y. Zhu, Adv. Mater., 2017, 29, 1603414.
189 G.-H. Wang, Z. Cao, D. Gu, N. Pfänder, A.-C. Swertz, 214 M. Benzigar, S. Joseph, H. Ilbeygi, D. H. Park, S. Sarkar,
B. Spliethoff, H.-J. Bongard, C. Weidenthaler, W. Schmidt, G. Chandra, S. Umapathy, S. Srinivasan, S. Talapaneni and
R. Rinaldi and F. Schüth, Angew. Chem., Int. Ed., 2016, 55, A. Vinu, Angew. Chem., Int. Ed., 2018, 57, 569–573.
8850–8855. 215 R. Chakravarti, M. L. Kantam, H. Iwai, S. S. Al-deyab,
190 M.-S. Wu, Z.-Z. Ceng, C.-Y. Chen and C. Wang, J. Alloys K. Ariga, D.-H. Park, J.-H. Choy, K. S. Lakhi and A. Vinu,
Compd., 2016, 688, 342–349. ChemCatChem, 2014, 6, 2872–2880.
View Article Online
216 V. Švorčı́k, Z. Makajová, N. Slepičková Kasálková, Z. Kolská, 240 L. Zou, Z. S. Lu, Y. H. Huang, Z. E. Long and Y. Qiao,
P. Žáková, J. Karpı́šková, I. Stibor and P. Slepička, Carbon, J. Power Sources, 2017, 359, 549–555.
2014, 69, 361–371. 241 G. B. Xu, L. W. Yang, Z. Y. Li, X. L. Wei and P. K. Chu,
217 P. Zakova, N. Slepickova Kasalkova, Z. Kolska, J. Leitner, J. Mater. Chem. A, 2017, 5, 2749–2758.
J. Karpiskova, I. Stibor, P. Slepicka and V. Svorcik, Mater. 242 D. S. T. Martinez, J. P. V. Damasceno, L. S. Franqui,
Sci. Eng., C, 2016, 60, 394–401. J. Bettini, I. O. Mazali and M. Strauss, Mater. Sci. Eng., C,
218 W. Lu, J. P. Sculley, D. Yuan, R. Krishna, Z. Wei and 2017, 78, 141–150.
H.-C. Zhou, Angew. Chem., Int. Ed., 2012, 51, 7480–7484. 243 H. Ma, C. Li, M. Zhang, J.-D. Hong and G. Shi, J. Mater.
219 S.-H. Chai, Z.-M. Liu, K. Huang, S. Tan and S. Dai, Ind. Eng. Chem. A, 2017, 5, 17040–17047.
Chem. Res., 2016, 55, 7355–7361. 244 J. L. Figueiredo, J. Mater. Chem. A, 2013, 1, 9351–9364.
220 L. Yu, N. Brun, K. Sakaushi, J. Eckert and M. M. Titirici, 245 J. Lai, A. Nsabimana, R. Luque and G. Xu, Joule, 2018, 2,
Carbon, 2013, 61, 245–253. 76–93.
221 M. Gholami, M. R. Talaie and S. F. Aghamiri, J. Taiwan Inst. 246 N. A. Travlou, E. Rodriguez-Castellon and T. J. Bandosz,
Chem. Eng., 2016, 59, 205–209. Carbon, 2016, 100, 64–73.
222 D. Lee, C. Zhang and H. Gao, Macromol. Chem. Phys., 2015, 247 N. A. Travlou and T. J. Bandosz, Carbon, 2017, 121, 114–126.
216, 489–494. 248 N. A. Travlou and T. J. Bandosz, Adsorption, 2017, 23,
223 V. Guillerm, L. J. Weselinski, M. Alkordi, M. I. Mohideen, 271–280.
Y. Belmabkhout, A. J. Cairns and M. Eddaoudi, Chem. 249 L. Cui, J. Wu and H. Ju, ACS Appl. Mater. Interfaces, 2014, 6,
Commun., 2014, 50, 1937–1940. 16210–16216.
224 M. Hu, J. Reboul, S. Furukawa, N. L. Torad, Q. Ji, 250 Y. Li, M. F. Zhang, X. P. Zhang, G. C. Xie, Z. Q. Su and
P. Srinivasu, K. Ariga, S. Kitagawa and Y. Yamauchi, G. Wei, Nanomaterials, 2015, 5, 1891–1905.
J. Am. Chem. Soc., 2012, 134, 2864–2867. 251 L. Jia, G. Lawrence, V. V. Balasubramanian, G. Choi,
225 M. R. Andalibi and H. C. Foley, Int. J. Hydrogen Energy, J.-H. Choy, A. M. Abdullah, A. Elzatahry, K. Ariga and
2016, 41, 8506–8513. A. Vinu, Chem. – Eur. J., 2015, 21, 697–703.
226 M. R. Andalibi, A. Qajar and H. C. Foley, J. Phys. Chem. C, 252 P. Salazar, V. Rico and A. R. González-Elipe, J. Electrochem.
2015, 119, 21314–21322. Soc., 2016, 163, B704–B709.
227 X. Y. Chen, C. Chen, Z. J. Zhang, D. H. Xie and J. W. Liu, 253 L. Donero, N. Bouts, A. A. El Mel, B. Le Borgne, E. Gautron,
J. Mater. Chem. A, 2013, 1, 4017–4025. L. Le Brizoual, F. Le Bihan and P. Y. Tessier, Thin Solid
228 X. Y. Chen, Y. Y. He, H. Song and Z. J. Zhang, Carbon, 2014, Films, 2017, 630, 59–65.
72, 410–420. 254 H. L. Poh and M. Pumera, Chem. – Asian J., 2012, 7, 412–416.
229 M. T. Stone and M. Kozlov, Langmuir, 2014, 30, 8046–8055. 255 H. L. Poh, A. Bonanni and M. Pumera, RSC Adv., 2012, 2,
230 C. N. Nanev, E. Saridakis and N. E. Chayen, Sci. Rep., 2017, 1021–1024.
7, 35821. 256 E. Moazzen, H. Ebrahimzadeh, M. M. Amini and
231 S. Khurshid, E. Saridakis, L. Govada and N. E. Chayen, Nat. O. Sadeghi, J. Sol-Gel Sci. Technol., 2013, 66, 345–351.
Protoc., 2014, 9, 1621–1633. 257 N. L. Torad, Y. Li, S. Ishihara, K. Ariga, Y. Kamachi, H.-Y.
232 M. Mahesh, K. V. Arivizhivendhan, P. Maharaja, R. Boopathy, Lian, H. Hamoudi, Y. Sakka, W. Chaikittisilp, K. C. W. Wu
V. Hamsavathani and G. Sekaran, J. Mol. Catal. B: Enzym., and Y. Yamauchi, Chem. Lett., 2014, 43, 717–719.
2016, 133, 43–54. 258 Y. Zhang, E. Che, M. Zhang, B. Sun, J. Gao, J. Han and
233 F. Hippauf, D. Lunow, L. Borchardt, T. Henle and Y. Song, Int. J. Pharm., 2014, 473, 375–383.
S. Kaskel, Carbon, 2014, 77, 191–198. 259 Q.-L. Zhu, N. Tsumori and Q. Xu, Chem. Sci., 2014, 5,
234 F. Hippauf, D. Lunow, C. Huettner, W. Nickel, 195–199.
L. Borchardt, T. Henle and S. Kaskel, Carbon, 2015, 87, 260 C. Feng, Y. Hao, L. Zhang, N. Shang, S. Gao, Z. Wang and
309–316. C. Wang, RSC Adv., 2015, 5, 39878–39883.
235 B. Nagy, A. Toth, I. Savina, S. Mikhalovsky, L. Mikhalovska, 261 L. F. Velasco, A. Gomis-Berenguer, J. C. Lima and
I. Grillo, E. Geissler and K. Laszlo, Carbon, 2016, 106, C. O. Ania, ChemCatChem, 2015, 7, 3012–3019.
142–151. 262 L. Hao, C. Wang, Q. Wu, Z. Li, X. Zang and Z. Wang, Anal.
236 B. Nagy, A. Toth, I. Savina, S. Mikhalovsky, L. Mikhalovska, Chem., 2014, 86, 12199–12205.
E. Geissler and K. Laszlo, Carbon, 2017, 112, 103–110. 263 W. Wang and D. Yuan, Sci. Rep., 2014, 4, 5711.
237 C. Z. Guo, R. Hu, W. L. Liao, Z. B. Li, L. T. Sun, D. P. Shi, 264 N. Farzin Nejad, E. Shams, M. K. Amini and J. C. Bennett,
Y. R. Li and C. G. Chen, Electrochim. Acta, 2017, 236, Fuel Process. Technol., 2013, 106, 376–384.
228–238. 265 A. Koolivand, A. Badiei, P. Arab and G. M. Ziarani, J. Iran.
238 S. M. Alatalo, K. P. Qiu, K. Preuss, A. Marinovic, M. Sevilla, Chem. Soc., 2016, 13, 1315–1324.
M. Sillanpaa, X. Guo and M. M. Titirici, Carbon, 2016, 96, 266 X. Ma, M. Cao and C. Hu, RSC Adv., 2013, 3, 10396–10402.
622–630. 267 L. L. Perreault, S. Giret, M. Gagnon, J. Florek, D. Lariviere
239 Y. M. Lin, Y. S. Zhu, B. S. Zhang, Y. A. Kim, M. Endo and and F. Kleitz, ACS Appl. Mater. Interfaces, 2017, 9,
D. S. Su, J. Mater. Chem. A, 2015, 3, 21805–21814. 12003–12012.
View Article Online
268 K. Vasanth Kumar and F. Rodrı́guez-Reinoso, RSC Adv., 288 T. Zhou, Y. Zhou, R. Ma, Q. Liu, Y. Zhu and J. Wang,
2012, 2, 9671–9678. J. Mater. Chem. A, 2017, 5, 12243–12251.
269 S. Chu, Y. Zhong, R. Cai, Z. Zhang, S. Wei and Z. Shao, 289 H. Wang, W. Wang, M. Gui, M. Asif, Z. Wang, Y. Yu, J. Xiao
Small, 2016, 12, 6724–6734. and H. Liu, ACS Appl. Mater. Interfaces, 2017, 9, 335–344.
270 Y. Qu, Z. Zhang, X. Zhang, G. Ren, Y. Lai, Y. Liu and J. Li, 290 H. Tan, Y. Li, X. Jiang, J. Tang, Z. Wang, H. Qian, P. Mei,
Carbon, 2015, 84, 399–408. V. Malgras, Y. Bando and Y. Yamauchi, Nano Energy, 2017,
271 Y. Liu, X. Zhao, G. S. Chauhan and J.-H. Ahn, Appl. Surf. 36, 286–294.
Sci., 2016, 380, 151–158. 291 L. Liu, Z. Niu and J. Chen, Chem. Soc. Rev., 2016, 45,
272 S. F. Wang, Y. Z. Wu, N. Zhang, G. W. He, Q. P. Xin, 4340–4363.

X. Y. Wu, H. Wu, X. Z. Cao, M. D. Guiver and Z. Y. Jiang, 292 A. Borenstein, O. Hanna, R. Attias, S. Luski, T. Brousse and
Energy Environ. Sci., 2016, 9, 3107–3112. D. Aurbach, J. Mater. Chem. A, 2017, 5, 12653–12672.
273 S. Chu, Y. Cui and N. Liu, Nat. Mater., 2016, 16, 16–22. 293 T. Chen and L. Dai, Mater. Today, 2013, 16, 272–280.
274 K. S. Lakhi, D. H. Park, G. Singh, S. N. Talapaneni, 294 H. Itoi, H. Nishihara and T. Kyotani, Langmuir, 2016, 32,
U. Ravon, K. Al-Bahily and A. Vinu, J. Mater. Chem. A, 11997–12004.
2017, 5, 16220–16230. 295 A. Berenguer-Murcia, R. R. Ruiz-Rosas, J. Garcia-Aguilar,
275 G. Singh, I. Y. Kim, K. S. Lakhi, P. Srivastava, R. Naidu and K. Nueangnoraj, H. Nishihara, E. Morallon, T. Kyotani and
A. Vinu, Carbon, 2017, 116, 448–455. D. Cazorla-Amoros, Phys. Chem. Chem. Phys., 2013, 15,
276 G. Singh, K. S. Lakhi, I. Y. Kim, S. Kim, P. Srivastava, 10331–10334.
R. Naidu and A. Vinu, ACS Appl. Mater. Interfaces, 2017, 9, 296 K. Nueangnoraj, H. Nishihara, T. Ishii, N. Yamamoto,
29782–29793. H. Itoi, R. Berenguer, R. Ruiz-Rosas, D. Cazorla-Amorós,
277 J. Zhou, W. Su, Y. Sun, S. G. Deng and X. J. Wang, E. Morallón, M. Ito and T. Kyotani, Energy Storage Mater.,
J. Chem. Eng. Data, 2016, 61, 1348–1352. 2015, 1, 35–41.
278 J. W. To, J. He, J. Mei, R. Haghpanah, Z. Chen, T. Kurosawa, 297 J. Linnemann, L. Taudien, M. Klose and L. Giebeler,
S. Chen, W. G. Bae, L. Pan, J. B. Tok, J. Wilcox and Z. Bao, J. Mater. Chem. A, 2017, 5, 18420–18428.
J. Am. Chem. Soc., 2016, 138, 1001–1009. 298 J. W. Lee, A. S. Hall, J.-D. Kim and T. E. Mallouk, Chem.
279 C. H. Choi, S. H. Park and S. I. Woo, ACS Nano, 2012, 6, Mater., 2012, 24, 1158–1164.
7084–7091. 299 X. Zhang, J. Luo, P. Tang, X. Ye, X. Peng, H. Tang, S.-G. Sun
280 Y.-N. Yu, M.-Q. Wang and S.-J. Bao, J. Solid State Electrochem., and J. Fransaer, Nano Energy, 2017, 31, 311–321.
2017, 21, 103–110. 300 J. Zhou, W. Li, Z. Zhang, X. Wu, W. Xing and S. Zhuo,
281 E. Zhang, M. Wu, Q. Tang, Q. Gong, S. Sun, J. Qiao and Electrochim. Acta, 2013, 89, 763–770.
L. Zhang, RSC Adv., 2017, 7, 669–677. 301 D. Zhang, L. Zheng, Y. Ma, L. Lei, Q. Li, Y. Li, H. Luo,
282 F. Jing, M. Chen, Y. Tang, Z. Xu, T. Huang, Y. Su and H. Feng and Y. Hao, ACS Appl. Mater. Interfaces, 2014, 6,
D. Wu, J. Colloid Interface Sci., 2017, 492, 8–14. 2657–2665.
283 J.-C. Li, S.-Y. Zhao, P.-X. Hou, R.-P. Fang, C. Liu, J. Liang, 302 R. J. Wang, Y. Xu, T. Zhang and Y. Jiang, Anal. Methods,
J. Luan, X.-Y. Shan and H.-M. Cheng, Nanoscale, 2015, 7, 2015, 7, 1701–1706.
19201–19206. 303 N. Duan, S. J. Wu, S. L. Dai, T. T. Miao, J. Chen and
284 C. Zhang, B. Wang, X. Shen, J. Liu, X. Kong, S. S. C. Chuang, Z. P. Wang, Microchim. Acta, 2015, 182, 917–923.
D. Yang, A. Dong and Z. Peng, Nano Energy, 2016, 30, 503–510. 304 J. Shi, C. Chan, Y. Pang, W. Ye, F. Tian, J. Lyu, Y. Zhang and
285 D.-S. Yang, D. Bhattacharjya, M. Y. Song and J.-S. Yu, M. Yang, Biosens. Bioelectron., 2015, 67, 595–600.
Carbon, 2014, 67, 736–743. 305 H.-F. Ju, W.-L. Song and L.-Z. Fan, J. Mater. Chem. A, 2014,
286 J. Xiao, Y. Xu, Y. Xia, J. Xi and S. Wang, Nano Energy, 2016, 2, 10895–10903.
24, 121–129. 306 X. Li, X. Zang, Z. Li, X. Li, P. Li, P. Sun, X. Lee, R. Zhang,
287 J. Tang, T. Wang, X. Pan, X. Sun, X. Fan, Y. Guo, H. Xue and Z. Huang, K. Wang, D. Wu, F. Kang and H. Zhu, Adv. Funct.
J. He, J. Phys. Chem. C, 2013, 117, 16896–16906. Mater., 2013, 23, 4862–4869.

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Featuring work from the research group of Professor As featured in:

Ajayan Vinu, The University of Newcastle, Australia.

Recent advances in functionalized micro and mesoporous

The team is actively working in the field of ordered micro and

See Ajayan Vinu et al.,

Recent advances in functionalized micro and

mesoporous carbon materials: synthesis

Review Article Chem Soc Rev

Mrs Mercy R. Benzigar is a final Dr Siddulu Naidu Talapaneni is a

Dr Stalin Joseph is a Research Dr Kavitha Ramadass is a

Chem Soc Rev Review Article

Dr Khalid Al-Bahily has been the Prof. Ajayan Vinu is a Global

Template and Heteroatom dpore SABET VTotal

This journal is © The Royal Society of Chemistry 2018

Chem. Soc. Rev., 2018, 47, 2680--2721 | 2683

Template and Heteroatom dpore SABET VTotal

2684 | Chem. Soc. Rev., 2018, 47, 2680--2721

This journal is © The Royal Society of Chemistry 2018

Template and Heteroatom dpore SABET VTotal

This journal is © The Royal Society of Chemistry 2018

Chem. Soc. Rev., 2018, 47, 2680--2721 | 2685

Template and Heteroatom dpore SABET VTotal

2686 | Chem. Soc. Rev., 2018, 47, 2680--2721

This journal is © The Royal Society of Chemistry 2018

Review Article Chem Soc Rev

but the scale of production is of a nanoscale order. In the nano

recently reported synthesis methods and templating strategies

2.1 Hard templating method for OMCs

The hard templating approach is considered as one of the most

straightforward ways for synthesizing OMCs.7 Ordered meso-

porosity in carbon materials can be easily introduced by the

Various mesoporous carbons with diﬀerent textural properties

have been prepared by using diﬀerent porous templates through

materials have been prepared, the control of structure and

nano templating approach by using the phenol and formalde-

hyde mixture precursor and spherical silica as a hard template.24

using 400 nm PMMA spheres with a close packed opal structure.

demonstrated the preparation of OMCs by using furfuryl alcohol

impregnated acidified mesoporous silica as a precursor.25 This

nanoporous carbon in the form of monoliths. Hierarchically

mesoporosity and three-dimensionally connected macroporosity,

and trimethyl benzene (TMB) mixture as a carbon source. These

Chem Soc Rev Review Article

Review Article Chem Soc Rev

commercialization is the removal of the mesoporous silica

2.2 Soft templating method for OMCs

synthesis of various mesoporous materials including zeolites,

Chem Soc Rev Review Article

Thus, nitrogen doping into the OMCs could change their

ing N atoms including polymeric compounds, acetonitrile,

Review Article Chem Soc Rev

Chem Soc Rev Review Article

Review Article Chem Soc Rev

Chem Soc Rev Review Article

which supports the formation of highly ordered structures. The

Review Article Chem Soc Rev

assembly of a triblock copolymer F127, resols and prehydro-

Instead of POSS, TiO2 nanostructures were also used as inorganic

Chem Soc Rev Review Article

of carbon precursors with inorganic metal or metal oxides will