Nanoscale Res Lett (2009) 4:14391446

DOI 10.1007/s11671-009-9417-4

NANO EXPRESS

Preparation of Fe3O4 Spherical Nanoporous Particles

Facilitated by Polyethylene Glycol 4000
Li-Li Wang Ji-Sen Jiang

Received: 20 April 2009 / Accepted: 12 August 2009 / Published online: 2 September 2009
to the authors 2009

Abstract Much interest has been attracted to the magnetic

materials with porous structure because of their unique
properties and potential applications. In this report, Fe3O4
nanoporous particles assembled from small Fe3O4 nanoparticles have been prepared by thermal decomposition of
iron acetylacetonate in the presence of polyethylene glycol
4000. The size of the spherical nanoporous particles is
100200 nm. Surface area measurement shows that these
Fe3O4 nanoporous particles have a high surface area of
87.5 m2/g. Magnetization measurement and Mossbauer
spectrum indicate that these particles are nearly superparamagnetic at room temperature. It is found that the morphology of the products is greatly influenced by polyethylene
glycol concentration and the polymerization degree of
polyethylene glycol. Polyethylene glycol molecules are
believed to facilitate the formation of the spherical assembly.
Keywords Nanoporous
Magnetite
Polyethylene
glycol
Transmission electron microscopy
Magnetic
measurement

Introduction
In the past decade, a variety of methods have been developed
to form highly structure-controlled materials of functionalized metal, semiconductor, and copolymer nanoparticles on
the nano- or microscale. As a versatile kind of material,
magnetite has attracted much attention in recent years.

L.-L. Wang
J.-S. Jiang (&)

Department of Physics, Center of Functional Nanomaterials
and Devices, East China Normal University, North Zhongshan
Rd. 3663, 200062 Shanghai, Peoples Republic of China
e-mail: [email protected]

Magnetite is a common ferrite that has a cubic inverse spinel

structure [1]. The compound has exhibited unique electric
and magnetic properties based on the transfer of electrons
between Fe2? and Fe3? in the octahedral sites. Besides
having practical applications in industry such as in ferrofluids [2, 3], catalysis [4], ceramics [5], and energy storage
[6], properly coated or surface-modified magnetite nanoparticles can be applied in clinical diagnosis and used as a
medicine transporter [710].
Magnetite nanoparticles are usually synthesized in
aqueous solutions [11, 12] via coprecipitation of Fe2? and
Fe3? ions by a base. During these reactions, several
parameters have to be controlled carefully, including pH
value, mixing way of raw materials, temperature, nature,
and concentration of anions. Other synthesis methods such
as polyol-mediated solgel [13] and sonochemical [14] are
also proposed. To overcome the limitations introduced by
aqueous precipitation reactions, several groups have
developed nonaqueous approaches for the production of
magnetite [1518]. Monodispersed magnetite nanoparticles
with tunable size can be produced by these nonaqueous
approaches.
Mesoporous Fe3O4 nanostructures with strong enough
magnetization strength are especially interesting for high
capacity drug loading and targeted drug delivery as well as
other biomedical and catalytic applications. To our
knowledge, several researches reported the successful
preparations of mesoporous Fe3O4. Zhu et al. [19] successfully prepared nanoporous and monodispersed Fe3O4
aggregated spheres by hydrothermal method. Hou et al. [20]
reported a route to assemble magnetic particles into sizecontrolled 3D spheres with cyclodextrins as surfactants by
solvothermal method. Here, we report a new-route preparation of Fe3O4 nanoporous particles assembled from the
small Fe3O4 nanoparticles by thermal decomposition of iron

123

1440

acetylacetonate [Fe(acac)3]. Polyethylene glycol 4000

(PEG 4000), an easily available chemical, was introduced in
the reactions. The effect of PEG on the morphology of
products is investigated.

Experimental
Chemicals
[Fe(acac)3] and octadecyl amine were purchased from Alfa
Aesar Company. PEG 4000, oleic acid, and diphenyl ether
were purchased from Sinopharm Chemical Reagent Co.,
Ltd. All chemicals were used without further treatment.
Synthesis of Fe3O4 Spherical Nanoporous Particles
The synthesis was carried out using airless procedures. The
synthesis of magnetic Fe3O4 spherical nanoporous particles
was developed from previous method [16]. In a typical
synthesis, Fe(acac)3 (2 mmol), PEG 4000 (6 mmol), oleic
acid (6 mmol), and octadecyl amine (6 mmol) were mixed
into 40 mL of diphenyl ether in a N2 atmosphere under
vigorous stirring. The mixture was stirred at 70 C until
PEG 4000 melted, then heated to 265 C, and refluxed for
30 min. The product was black. The black powder was
collected with a permanent magnet, then redispersed in
ethanol by supersonic for 15 min. The washing process
was repeated three times. At last, the powder was dried at
40 C in vacuum.
Characterization
X-ray diffraction (XRD) patterns of the samples were
recorded on a Rigaku D/max 2550V diffractometer equip ) X-ray source. The morpholped with a Cu KR (1.5418 A
ogy and chemical composition of the products were
examined by transmission electron microscopy (TEM, JEM2100F). Samples were dispersed in ethanol by supersonic for
15 min and then dropped onto carbon film-coated grids.
Magnetization measurements were taken with a vibrating
sample magnetometer (VSM) at room temperature. The
surface area of the products was measured by nitrogen
adsorptiondesorption isotherms using the Brunauer
EmmettTeller (BET) method (Micromeritics Tristar3000).
The samples were degassed under vacuum at room temperature before measurements were taken. Mossbauer
spectrum of the product at room temperature was recorded
on a Wissel spectrometer with the 57Co in Pd matrix as the
source moving in constant-acceleration regime. Hyperfine
interaction parameters were derived from the Mossbauer
spectrum using a least-squares method. The spectrometer
was calibrated using a standard 25-lm a-Fe foil.

123

Nanoscale Res Lett (2009) 4:14391446

Results and Discussion

The crystalline structure of the black product was characterized by the powder XRD technique. As shown in Fig. 1,
the product displays several relatively strong diffraction
peaks in the 2h region of 2070. These strong peaks are
), 35.4
at the 2h angles of 30.1 (d = 2.967 A

),
(d = 2.532 A), 43.0 (d = 2.101 A), 53.4 (d = 1.714 A

56.9 (d = 1.616 A), and 62.5 (d = 1.484 A). The pattern

can be easily indexed to Fe3O4 (JCPDS 19-629) according
to the diffraction peak positions and relative intensities,
which confirms the magnetite structure of this material.
The average size of the Fe3O4 nanoparticles deduced from
Sherrers formula is about 9.6 nm, which is consistent with
the result obtained from the TEM observation of the same
sample.
The morphology and structures of the black Fe3O4
products were investigated by TEM. Figure 2a shows a
representative TEM image of the products. It can be found
that the Fe3O4 product is nearly spherical, and the sizes of
the spherical particles are 100200 nm. The structural
details are shown in Fig. 2b, d. It can be observed clearly
from Fig. 2b that large Fe3O4 spherical particles have
rough surfaces and are composed of many small Fe3O4
nanoparticles. It demonstrates that the small Fe3O4 nanoparticles have self-assembled into Fe3O4 spherical aggregated particles. The size of these small Fe3O4 nanoparticles
is less than 10 nm. The size values of the small Fe3O4
nanoparticles got from XRD and TEM are very close. It
also can be seen that the disordered pores exist among the
primary nanoparticles within the spherical assembly.
Therefore, these assembled particles have a nanoporous
structure. Energy-dispersive X-ray spectroscopy (EDS)

Fig. 1 XRD patterns of nanoporous sample

Nanoscale Res Lett (2009) 4:14391446

1441

Fig. 2 Morphology and

component of nanoporous
sample: a, b TEM images;
c EDS analysis; d HRTEM
image; and e TEM image of
nanoporous sample after one
more hour supersonic treatment

spectrum (Fig. 2c) shows the expected presence of Fe and O.

Element analysis (inset table in Fig. 2c) shows the ratio of
Fe to O is very close to the standard value of Fe3O4. Highresolution transmission electron microscopy (HRTEM)
analysis provides more detailed structural information. A
representative HRTEM image took from the edge of an
assembled particle is shown in Fig. 2d. The parallel lattice
fringes across almost all the primary nanoparticles are
clearly visible. The lattice planes of (2 2 0) (0.297 nm),
(3 1 1) (0.254 nm), and (4 0 0) (0.210 nm) for Fe3O4 are

easily distinguished. It should be accentuated that these

samples were kept at least 2 weeks and underwent supersonic for about 1 h discontinuously in the washing process
before TEM measurement. To further investigate the stability of the assemblies, the porous sample was dispersed
by supersonic for one more hour. Figure 2e shows the
morphology of the sample after the supersonic treatment. It
is clear that the morphology maintained without breakdown into constituent Fe3O4 nanoparticles. So the morphology is considered to be stable.

123

1442

Nanoscale Res Lett (2009) 4:14391446

Nitrogen adsorptiondesorption measurements were

carried out for Fe3O4 spherical assemblies (Fig. 3). The
particles display a characteristic hysteresis in the desorption isotherm at relative pressure (P/P0) in the range
0.41.0. This behavior is indicative of mesoporous structure of the tested sample [2123]. The pore size distribution (Fig. 3 inset) indicates that most of the nanopores is
less than 4 nm in the sample. The surface area of the Fe3O4
assemblies is 87.5 m2/g calculated from the linear part of
the BET plot. The single-point adsorption total volume at
P/P0 = 0.978 is 0.324 cm3/g. The high BET surface area
and large pore volume support the fact that the Fe3O4
assembled particles have a nanoporous structure.
Figure 4 shows the magnetization of Fe3O4 spherical
nanoporous particles at room temperature (300 K). The
curves obtained at 300 K are nearly superimposable as the

field is cycled between -5 and 5 kOe. The magnetic

remanence and coercivity of Fe3O4 spherical nanoporous
particles are 1.0 emu/g and 1.2 Oe. The curves may imply
the superparamagnetic behavior and the nanoscale dimensions of the particles [24, 25]. The magnetization saturation
of product is 56.4 emu/g. It has been reported that the
magnetic Fe3O4 particles exhibit superparamagnetic
behavior when the particle size decreases to below a critical value, generally around 10 nm, and the magnetization
saturation values of Fe3O4 of several nanometers are usually low due to the small size.
The room-temperature Mossbauer spectrum of Fe3O4
spherical nanoporous particles is shown in Fig. 5 in the
absence of an external magnetic field. The bulk phase
Mossbauer spectrum of Fe3O4 is composed of two sets of
magnetic sextets at room temperature [26]. The spectrum
of our sample is composed of one doublet and two broad
sextets. The values of hyperfine parameters are shown in
Table 1. The two broad sextets correspond to two sets of Fe
ions located in octahedron and tetrahedron sites of spinelstructured Fe3O4 according to the isomer shift and quadrupole splitting [26]. The values of hyperfine field are much
smaller than the values of bulk material due to the small
nanoparticle size of the sample. When the size of Fe3O4
reduces to less than 10 nm, the particles exhibit the
superparamagnetic behavior for the quantum size effect. In
Mossbauer spectrum, two sets of magnetic sextets change
into superparamagnetic relaxation doublet [2729]. The
large doublet of the sample possesses 73.1% area of the
spectrum, which indicates the superparamagnetic behavior
of most particles at room temperature. This result is consistent with magnetization measurement of low remanence
and coercivity. Superparamagnetic behavior is a character
of small magnetic nanoparticles (usually \10 nm). So, the

Fig. 4 Room-temperature magnetization curve of Fe3O4 spherical

nanoporous particles

Fig. 5 Room-temperature Mossbauer spectrum of Fe3O4 spherical

nanoporous particles

Fig. 3 N2 adsorptiondesorption isotherm and pore size distribution

of Fe3O4 spherical nanoporous particles

123

Nanoscale Res Lett (2009) 4:14391446

1443

Table 1 Hyperfine parameters of room-temperature Mossbauer spectrum for Fe3O4 spherical nanoporous particles
Fitted spectra

Hyperfine field (KOe)

Doublet

Isomer shift (mm s-1)

Quadrupole splitting (mm s-1)

Line width (mm s-1)

Area (%)

0.35

0.74

0.82

73.1

Sextet1

424.35

0.38

0.02

1.47

15.7

Sextet2

218.24

0.61

0.01

1.13

11.2

Fig. 6 TEM images of Fe3O4

samples of different heating
time: a 10 min; b 20 min;
c 30 min; and d 1 h

nearly superparamagnetic behaviors of Fe3O4 spherical

nanoporous particles in Mossbauer spectrum and magnetization measurements at room temperature further confirm
that these spherical particles are assemblies of small primary Fe3O4 nanoparticles.
In order to investigate the formation process of such
Fe3O4 spherical assemblies, the products were collected
when the reaction solutions were heated for different time
periods at 265 C. Their structures were investigated by
TEM. As shown in Fig. 6, when a sample was heated for
10 min at 265 C, Fe3O4 nanoparticles were formed, but
they did not self-assemble (Fig. 6a). When heating for
20 min, the small spherical assemblies were partly formed.
They were structurally loose, and some dispersed particles

remained (Fig. 6b). When the sample was heated at 265 C

for 30 min, all Fe3O4 nanoparticles were self-assembled
into the spherical particles (Fig. 6c). When the heating time
prolonged to 1 h, spherical assemblies still appeared in the
sample without obvious change in shape and dimension
(Fig. 6d).
Samples of different PEG 4000 amount were also prepared for comparison. The amount of PEG 4000 was found
to be effective to the morphology of samples. When PEG
4000 amount reduced to 2 mmol, particles in the sample
heated at 265 C for 30 min were nearly monodisperse
with the size of about 8 nm (Fig. 7a). When the heating
time prolonged to 1 h, the dispersion of particle was not so
good as the sample heated for 30 min, but no obvious

123

1444

Nanoscale Res Lett (2009) 4:14391446

Fig. 7 TEM images of Fe3O4 samples of different PEG 4000 amount: a 2 mmol PEG 4000, 30 min at 265 C; b 2 mmol PEG 4000, 1 h at
265 C; and c 4 mmol PEG 4000, 30 min at 265 C

Fig. 8 TEM images of samples prepared using PEG 2000 (a) and PEG 6000 (b, c)

tendency to form assembled sphere was detected (Fig. 7b).

When PEG 4000 amount increased to 4 mmol, particles
began to assemble (Fig. 7c). However, the assemblies
morphology was rough, and disperse particles still existed.
The morphology of products prepared using different
polymerization degree of PEG was also studied. PEG 2000
and 6000 were chosen. The preparing conditions of two
samples were the same as the samples in Fig. 2a. The
morphologies of the two samples were shown in Fig. 8.
Figure 8a is the sample prepared using PEG 2000. We can
see from the figure that most of the small particles were
dispersed. Only a few particles assembled, and the morphology of them were not so regular. Big spheres emerged
in the sample prepared using PEG 6000 (Fig. 8b). These
spheres were about 600 nm, much bigger than the particles
prepared using PEG 4000. They turned out to be solid
investigated from the higher resolution TEM image
(Fig. 8c). The morphology of samples prepared using PEG
of different polymerization was so various. It is an interesting result that porous structure can be obtained only
using PEG 4000 under the same condition.
From these results, the use of PEG 4000 is the key in
preparing a sphere-like assembly. When the PEG 4000

123

amount decreases to 2 mmol, spherical assembly is hard to

form even if the heating is prolonged. When the PEG 4000
amount increases to 6 mmol, the particles were from dispersed to assembled as the heating prolonged. Therefore,
on the one hand, PEG 4000 prevents the single particle
from growing larger by coating on the particle surface. On
the other hand, intermolecular cross-link among long
chains of PEG 4000 is beneficial to the fabrication of
assemblies. So, PEG 4000 may act as a bridge among
original particles. The effect of PEG 4000 concentration
(represented by [PEG]) on the morphology of products is
shown in Scheme 1. When [PEG] is low, the TEM image
shows that the uniform Fe3O4 nanoparticles about 8 nm are
obtained. These nanoparticles are well-separated due to the
PEG 4000 coating on their surfaces, as well as amine and
acid, reducing their tendency to agglomerate. This result is
consistent with recent reports [30] suggesting that Fe3O4
nanoparticles do not assemble in the presence of a low
concentration of polymer. The increase in [PEG] leads to
more surface coating. The PEG 4000 molecules on surfaces
entangle each other in high [PEG] forming network
structure [31, 32]. Further, the spherical particles form
together with Fe3O4 nanoparticles due to the self-assembly

Nanoscale Res Lett (2009) 4:14391446

1445

Scheme 1 The effect of PEG

4000 concentration on the
morphology of products

ability of PEG 4000. The assembly results in the nanoporous structure of product. The high enough surface area
of Fe3O4 sphere nanoporous particles promises potential
applications in chemical industry. The possible reasons are
considered why PEG 2000 and PEG 6000 do not lead to the
porous structure. The final temperature (265 C) nearly
reaches the boiled temperature of PEG 2000. The reduction
of PEG 2000 concentration caused by quick evaporation
may be a reason for the failure of porous structures fabrication. Decreasing the reaction temperature can be a
method to reduce the evaporation. However, once the
reaction temperature is below 250 C, the yield of products
sharply decreases. Higher polymerization degree means
that PEG 6000 has longer flexural chain than PEG 4000,
which can lead to the more intermolecular cross-link,
facilitating the bigger assemblies. Whereas, the product
prepared using PEG 6000 is solid instead of porous. Further research is needed to find out the exact reasons for the
interesting result of PEG 6000.

Conclusions
In summary, the Fe3O4 nanoporous particles are synthesized in the presence of polymer PEG 4000 by thermal
decomposition of iron acetylacetonate. The morphology of
product can be tuned by the amount of PEG 4000. When the
concentration of PEG 4000 is decreased, monodispersed
Fe3O4 nanoparticles around 8 nm are produced. Particles
tend to assemble as the PEG 4000 amount increase, and last
form spherical nanoporous particles. The size of the
spherical nanoporous particles is 100200 nm. BET measurement shows these Fe3O4 nanoporous particles have a
high surface area of 87.5 m2/g and a number of porous less

than 4 nm. The saturation magnetization of nanoporous

particles is 56.4 emu/g. Magnetization measurement and
Mossbauer spectrum indicate that these particles are nearly
superparamagnetic at room temperature, which confirms
that these spherical particles are assembly of small monodispersed Fe3O4 nanoparticles. Moreover, polymerization
degree of PEG also has great influence on the morphology
of the product. We believe that these Fe3O4 spherical
nanoporous particles will be promising materials for
applications in advanced magnetic materials.
Acknowledgments This research project was supported by Shanghai Nanotechnology Promotion Center (0852nm03200) and Equipment Sharing Platform of East China Normal University.

References
1. R.M. Cornell, U. Schwertmann, The Iron Oxides: Structure,
Properties, Reactions, Occurrence and Uses (VCH, England,
1996)
2. K. Raj, R. Moskowitz, J. Magn. Magn. Mater. 85, 233 (1990)
3. A. Jordan, R. Scholz, P. Wust, H. Fahling, R. Felix, J. Magn.
Magn. Mater. 201, 413 (1999)
4. Z.F. Wang, B. Shen, A.H. Zou, N.Y. He, Chem. Eng. J. 113, 27
(2005)
5. O. Bretcanu, S. Spriano, E. Verne, M. Coisson, P. Tiberto,
P. Allia, Acta Biomater. 1, 421 (2005)
6. Z.G. Huang, Z.P. Guo, A. Calka, D. Wexler, C. Lukey, H.K. Liu,
J. Alloys Compd. 422, 299 (2006)
7. I. Brigger, C. Dubernet, P. Couvreur, Adv. Drug Deliv. Rev. 54,
631 (2002)
8. J.S. Jiang, Z.F. Gan, Y. Yang, B. Du, M. Qian, P. Zhang,
J. Nanopart. Res. 11, 1321 (2009)
9. Z.F. Gan, J.S. Jiang, Y. Yang, B. Du, M. Qian, P.J. Zhang,
J. Biomed. Mater. Res. A 84A, 10 (2008)
10. Y. Yang, J.S. Jiang, B. Du, Z.F. Gan, M. Qian, P. Zhang,
J. Mater. Sci. Mater. Med. 20, 301 (2009)
11. T. Sugimoto, E. Matijevic, J. Colloid Interface Sci. 74, 227
(1980)

123

1446
12. Y.S. Kang, S. Risbud, J.F. Rabolt, P. Stroeve, Chem. Mater. 8,
2209 (1996)
13. C. Feldmann, H.O. Jungk, Angew. Chem. Int. Ed. Engl. 40, 359
(2001)
14. R.V. Kumar, Y. Koltypin, Y.S. Cohen, Y. Cohen, D. Aurbach,
O. Palchik, I. Felner, A. Gedanken, J. Mater. Chem. 10, 1125
(2000)
15. J. Rockenberger, E.C. Scher, A.P. Alivisatos, J. Am. Chem. Soc.
121, 11595 (1999)
16. S. Sun, H. Zeng, J. Am. Chem. Soc. 124, 8204 (2002)
17. T. Hyeon, S.S. Lee, J. Park, Y. Chung, H.B. Na, J. Am. Chem.
Soc. 123, 12798 (2001)
18. Z. Li, H. Chen, H. Bao, M. Gao, Chem. Mater. 16, 1391 (2004)
19. Y.F. Zhu, W.R. Zhao, H.R. Chen, J.L. Shi, J. Phys. Chem. C 111,
5281 (2007)
20. Y.L. Hou, H.S. Kondoh, M. Shimojo, E. Sako, N. Ozaki,
T. Kogure, T. Ohta, J. Phys. Chem. B 109, 4845 (2005)
21. C. Song, J.P. Du, J.H. Zhao, S.A. Feng, G.X. Du, Z.P. Zhu,
Chem. Mater. 21, 1524 (2009)
22. W. Cho, H.J. Lee, M. Oh, J. Am. Chem. Soc. 130, 16943 (2008)

123

Nanoscale Res Lett (2009) 4:14391446

23. J. Kobler, T. Bein, ACS Nano 2, 2324 (2008)
24. G. Bidan, O. Jarjayes, J.M. Fruchart, E. Hannecart, Adv. Mater.
6, 152 (1994)
25. B.Z. Tang, Y. Geng, J.W.Y. Lam, B. Li, X. Jing, X. Wang,
F. Wang, A.B. Pakhomov, X.X. Zhang, Chem. Mater. 11, 1581
(1999)
26. N.N. Greenwood, T.C. Gibb (eds.), Mossbauer Spectroscopy
(Chapman and Hall, London, 1971)
27. A.A. Novakovaa, V.Y. Lanchinskayaa, A.V. Volkov, T.S. Gendler, T.Y. Kiseleva, M.A. Moskvina, S.B. Zezin, J. Magn. Magn.
Mater. 354, 258 (2003)
28. S. Si, A. Kotal, T.K. Mandal, S. Giri, H. Nakamura, T. Kohara,
Chem. Mater. 16, 3489 (2004)
29. K. Woo, J.W. Hong, S.M. Choi, H.W. Lee, J.P. Ahn, C.S. Kim,
S.W. Lee, Chem. Mater. 16, 2814 (2004)
30. A. Ditsch, P.E. Laibinis, D.I.C. Wang, T.A. Hatton, Langmuir 21,
6006 (2005)
31. L.M. Yang, Y.J. Wang, Y.W. Sun, G.S. Luo, Y.Y. Dai, J. Colloid
Interface Sci. 299, 823 (2006)
32. S.R. Zhai, C.S. Ha, Micropor. Mesopor. Mat. 102, 212 (2007)