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1st generation
The first generation PVs are the silicon wafers
Performance of 15-20%
They dominate the market due to their
High Performance and stability
However, a lot of energy is necessary to produce them
2nd Generation
Second generation PVs use amorphous Si, CIGS and
CdTe
Performance is 10-15%
Although they have lower production cost,
Still require much energy for fabrication thru vacuum
processing and high T treatment
Moreover they use scarce elements
3rd Generation
Third generation PVs, which would be our focus today
Since there are too many types of 3rd generation solar cells
Our group will be using three of the more popular ones for illustration of the
concepts
Namely: polymer-fullerene hybrids, polymer-perovskite hybrids and polymerquantum dot solar cells
Third generation
Use small molecules, polymers and perovskites
This is the example of the polymer-perovskite hybrid fabricated by UCLA
They were able to use get 17% efficiency using low quality silicon
These hybrids can reach 20%, on par with the silicon wafers
Currently a lot of research is being channelled to this particular type of hybrid
Flexibility
Compared to their precursors, silicon wafers which are
rigid
Thin-film polymer hybrids are flexible
Which opens up a much wider scope for application
Material Cost
The layers processed from solution can be
Easily up-scaled at a very low cost per unit area
Processability
printing & coating techniques of R2R technology
Makes fabrication
Simple
Fast
Low cost
Scarce Materials
Option to do away with scarce materials such as indium
In this particular configuration, ZnO is used instead
Efficiency
Efficiency wise where a lot of effect has been going
into there has been tremendous progress when
perovskite came into the picture
Next important graph to show the significance of
perovskite is the maximum photon energy utilization
(Vopencircuit/bandgap)
Not all the absorbed energy is converted to electricity
During a process called thermal relaxation, some of the
energy is loss as heat
With perovskite, this energy lost is reduced
This results in an efficiency increase
Process
As mentioned earlier
Solution processing &
Being able to use R2R
Has low fabrication cost
Stability
Left degraded right is a new one
Polymer based struggling to last even a year
Because they
Water
Decompose
Now that we have the general background
Lets take a look at the mechanism behind the polymer
hybrids
Mechanism
This diagram shows a general arrangement of materials
in a polymer hybrid
Called the layer stack
Consists of
Electricity Generation
First process is charge separation
The bulk heterojunction (you can take it as the active layer)
Consist of donor and acceptor materials
Donor energy levels are shown in green, acceptor in pink
Light absorbed in bhj forms excitons number 1
When the excitons reach the DA interface, they separate due to
the difference in energy levels of the donor and acceptor materials
The charge carriers are channelled to their respective electrodes
The energy difference helps to achieve directional flows of charge
carriers to their respective electrodes
Geometry
There are two type of geometries for polymer hybrids
Normal and inverted
The ITO you see in the diagram is the positive electrode in the normal
configuration
When the active and transport layers are reversed
It becomes the negative electrode
The corresponding positive electrode has to be changed as well to have a
lower work function
Inverted geometries are often preferred as they allow selection of
materials with smaller domains i.e. they can be made thinner which
improves efficiency
Selection of surface materials which are more resistant to corrosion
Perovskites
ABX3 structure
Borrow the name from calcium titanium oxide Ca Ti O3
Which is the perovskite
Inverted geometry
It allows materials of smaller domain to be chosen
This makes the film thinner and more efficiency
As we have learnt before, diffusion lengths for charge carriers are very
small
They have to quickly reach the D/A interface and be separated
Moreover, inverted geometry allows selection of more corrosion resistant
Al electrode can be changed to Ag.
Perovskite Tuning
As you conductivity of ceramics are altered by the
number schottsky and frenkel defects
By adding increasing the halide concentration into the
perovskite, the band gap can be lower.