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TRANSCRIPT
Abstract--This paper analyzes the Copper-Indium-Selenium (CIS)
and Copper-Indium-Gallium-Selenium (CIGS) based solar cell
performance by AMPS-1D numerical modeling. Various factors
which affect the solar cell’s performance are investigated,
carefully referring to practical cells, to obtain the optimum
parameters for the CIS and CIGS solar cells. Among the factors
studied are thickness and bandgap energy of absorber layer,
thickness of buffer layer of the cells. In this study, an efficiency of
19.4% has been achieved with CdS based buffer layer with
performance parameters of 0.68 V for open circutit voltage (Voc),
35 mA/cm2 for short circuit current (Jsc) and 0.82 for fill factor
(FF). This solar cell has been used as a base case for simulation. It
is found that the optimum solar cell, regardless whether it is CIS
or CIGS type, has the absorber thickness between 2000 nm and
3000 nm. Moreover, the optimum bandgap of the CIS and CIGS
absorber layer are found to be 1.04 eV and 1.15 eV, respectively.
The thickness of buffer layer has been found in the range of 40
nm to 50 nm as the optimum value.
Index Terms – Numerical Analysis, AMPS-1D, Solar Cells,
CIS, CIGS.
I. INTRODUCTION
HIN film CuInSe2 (CIS) and Cu(In, Ga)Se2 (CIGS) solar
cells possess major potentials as the source of low-cost,
high-efficiency solar electricity [1]. In a CIS/CIGS model, the
absorber acts as a p-type doped region with typical thickness
of 2 to 3 µm [2]. The band gap, Eg for CIS absorber layer is
around 1 eV (0.98 eV-1.04 eV) [3]. By adding the gallium
content into the CIS model, the resulting bandgap of CIGS is
ranged from 1.0-1.7eV [5]. However, the optimum CIGS
bandgap is ranged from 1.16 eV [6] to 1.38 eV. In this study,
CIGS bandgap is simulated from 1eV to 1.6eV to show the
effect of bandgap in the properties of the solar cell. Apart from
that, it is also found that the thickness of CdS buffer layer is
used within the range of 40 nm to 50 nm.
Besides, Nakada and Mizutani [7] have shown that the use
of chemical bath deposition (CBD) ZnS (Eg>3 eV) as buffer
N. Amin is with the Department of Electrical, Electronic & System
Engineering, Faculty of Engineering, National University of Malaysia,
Malaysia (e-mail: [email protected]).
K. Sopian is the director of Solar Energy Research Institute (SERI),
National University of Malaysia, Malaysia (email: [email protected]).
layer has reached higher efficiency. ZnS is a very promising
material as a replacement for CdS as it has recorded the
second highest efficiency after CdS in the thin film industry.
Although the CBD technique is very efficient in forming a
heterojunction in the cell with good rectifying properties, but it
does not perform well for technique which is based on vacuum
technology [3].
Another replacement for CdS buffer layer is the Zn1−xMgxO.
The best Zn1−xMgxO cell efficiency of 16.2% (active area) was
achieved by Matsushita Electric Industrial [8]. Zn1−xMgxO is
used as a barrier layer for the modulation of bandgap to
enhance light transmission. It also helps to increase the current
generation of the solar cell [9].
Another buffer layer material which is used in this paper is
zinc oxide (ZnO). ZnO has a wider bandgap of 3.3eV than
CdS. ZnO which is grown by chemical bath deposition (CBD)
method has recorded an efficiency of 14.3%. Furthermore, the
solar cells with this new buffer layer didn't show the light-
soaking effect [10]. On the other hand, if the ZnO based buffer
layer is grown by atomic layer deposition (ALD) technique,
the light-soaking effect exist and it is mainly associate with the
CIGS surface properties. This phenomenon can be overcome
by surface etching or doping CIGS surface with Zinc [11]. The
solar cell which is grown by ALD technique has achieved an
efficiency of 13.9% without the light soaking effect.
II. EXPERIMENTAL
In this study, a one dimensional numerical analysis tools
that stands for Analysis of Microelectronic and Photonic
Structures (AMPS-1D) is used to construct various solar cell
models as well as to obtain performance results once the
design parameters are adopted from various practical
references. Four different layers of CIS/CIGS solar cell are
required for the modeling. More layers can be added as long as
the width does not exceed the limitation of 400 grid points or 6
µm. However, it is not necessary to increase the layer
thickness as this project is about thin film CIS/CIGS solar cell
and the aim is to find the optimum efficiency with a narrow
width solar cell. The four layers that are emphasized in this
modeling is the n-type ZnO, i-ZnO, CdS and CIS/CIGS. Table
I and Table II show the description for the parameters used in
the simulation and the base parameter that is used throughout
the study [12].
Numerical Modeling of the Copper-Indium-Selenium (CIS) based Solar Cell Performance
by AMPS-1D Nowshad Amin, Member, IEEE, Michael Tang and Kamaruzzaman Sopian
T
The 5th
Student Conference on Research and Development –SCOReD 2007
11-12 December 2007, Malaysia
1-4244-1470-9/07/$25.00 ©2007 IEEE.
Table I: Overall electronic properties.
Table II: Base parameters for CIS/CIGS solar cells.
III. RESULTS AND DISCUSSION
A. Modeling with Variable CIS Absorber Thicknesses
The efficiency the of the solar cell, as can be seen in Figure
1, is increasing with the thickness of the CIS absorber layer,
but almost saturates while exceeds 5000 nm. At 1000 nm,
3000 nm and 5000 nm of the absorber layer, the efficiency
obtained are 14.64%, 16.92% and 17.83%, respectively. A
2000 nm decrease of absorber layer thickness from the
optimum layer thickness would result in 2.28% decrease in
efficiency. Open circuit voltage (Voc) and short circuit current
density (Jsc) of the solar cell are also shown in Figure 1. Both
values are increasing with the thickness of the absorber layer.
This was mainly due to the increasing of the absorber layer,
which was the p-type region in solar cell. This allows the
longer wavelengths of the illumination to be collected which in
turn contribute to electron-hole pair generation. If the absorber
layer thickness is reduced, the back contact will be very near
to the depletion region. Thus electrons will be captured easily
by the back contact for the recombination process. Therefore,
fewer electrons will contribute to the quantum efficiency of the
solar cell and the values for Voc and Jsc will be low. The J-V
characteristics of the solar cell is shown in Figure 2. It shows
an increase in Voc and Jsc when the absorber layer was
increased.
Spectral response of the solar cells with different
thicknesses of absorber layers is shown in Figure 3. It has been
found that the quantum efficiency of the solar cell is increasing
with the increasing absorber layer thickness. For thicker
absorbers, a greater percentage of electron-hole pairs would be
generated from the absorbed photons. Therefore, the quantum
efficiency would be increasing with the increment of the
absorber layer thickness.
Figure 1: Cell performance with variable CIS absorber layer
thickness.
Figure 2: J-V characteristic of solar cell with variable CIS
absorber layer thickness.
V (v)
J (m
A/c m
2)
Figure 3: Spectral response of solar cells with variable CIS
absorber layer thickness.
B. Modeling with Variable CIGS Absorber Thicknesses
In this part, the numerical modeling for variable CIGS
absorber thickness is presented. The parameters used in this
part of simulation are the same as those used in Section A.
The only difference would be the bandgap energy as bandgap
energy for CIS used in previous simulation was 1.04 eV [4]
while the bandgap energy for CIGS used for current
simulation was 1.15 eV. At the recommended thickness of the
absorber layer (3000 nm) [4], an efficiency of 19.39%,
almost equal to the 19.5% of the highest recorded efficiency
[13] has been obtained. From the simulated result at 1000 nm
and 5000 nm, conversion efficiencies of 16.98% and 20.2%
are achieved, respectively. Comparing the results with the
19.39% efficiency at 3000 nm, it was found that a decrease in
2000 nm of the absorber thickness resulted in 2.42% decrease
of efficiency.
For the CIGS absorber layer, a much higher efficiency was
achieved as compared to CIS absorber layers as shown in
Figure 4. This is mainly due to the introduction of gallium in
CIGS. Gallium is introduced to increase the bandgap energy
of the material. CIS without gallium concentration has
bandgap value in the range of 0.98 eV to 1.04 eV [3]. But
with the introduction of gallium into CIS, the range of the
CIGS bandgap value is 1.0 eV to 1.7 eV [5]. Thus an increase
in bandgap value would result in increase of solar cell’s
efficiency, as it approaches to the optimum value of 1.5 eV.
The simulated results showed that the optimum thickness
of absorber layer should be within the range of 2000 nm to
3000 nm, which was consistent with Pudov’s finding [14]. It
would not be cost effective if a solar cell with the absorber
width greater than 3000 nm were fabricated. Furthermore it
would lead to material wastage and would not comply with
conservation of solar cell material.
Voc and Jsc values were increasing with CIGS absorber
layer. Besides, the spectral response of the solar cell is also
illustrated in Figure 5, where the absorber thickness shows a
major role in the increase of photocurrent.
Figure 4: Cell performance with variable thickness of CIGS
absorber layer.
Figure 5: Spectral response of solar cell with variable
thickness of CIGS absorber layer.
C. Effect of CIS Bandgap on Solar Cell Performance
CIS which stands for Copper-Indium-Selenium has
bandgap value in the range of 0.98 eV to 1.04 eV [3]. Studies
have shown that the optimum bandgap energy for CIS
absorber layer is 1.04eV [4]. Besides, it is also known that
higher bandgap energy will result in high efficiency solar cell.
Thus in order to increase the bandgap energy for CIS solar
cell, indium is needed to be added. Although the introduction
of indium may increase the CIS bandgap energy, it is not cost
effective to do so. This is because indium is a rare material.
Thus, most of the studies conducted have introduced gallium
into the solar cell to form CIGS, Copper-Indium-Gallium-
λ (µm)
QE
λ (µm)
QE
Selenium. Gallium is added to replace as much indium as
possible due to gallium's relative availability to indium.
In this section, CIS bandgap energy ranged from 0.95eV to
1.05eV is chosen for simulation. Performance for the CIS
solar cell is observed. It is found that Voc of the solar cell is
increasing if the bandgap energy is increased. On the other
hand, Jsc is found decreasing as shown in Figure 7. This may
be due to the higher bandgap energy of the solar cell which
prevents the absorbed photons to excite the electrons of the
valence band into conduction band. Efficiency which is
shown in Figure 6 also indicates that higher bandgap energy
will result in higher efficiency.
Figure 6: Cell performance with variable CIS bandgap.
Figure 7: Energy band diagram of solar cell with variable
CIGS bandgap.
D. Effect of CIGS Bandgap on Solar Cell Performance
In order to achieve high efficiency CIGS solar cell, two
different criterions need to be considered; the bandgap
grading in a CIGS absorber layer and also the conduction
band offset at hetero-junction [15]. Studies have shown that
the optimum bandgap energy for CIGS absorber layer is
1.40eV [16], but the range for the bandgap energy is 1.0eV to
1.7eV [5]. The bandgap can be varied by varying the gallium
concentration in CuIn1-xGaxSe2 (x is ranged from 0 to 1)
[18]. If x is 0, then the bandgap energy would be 1.0eV which
means that CIGS has no concentration of gallium. On the
other hand, the bandgap energy would be 1.7eV if x is equal
to 1. This means that CIGS has the highest concentration of
gallium as forming CGS.
Figure 7 shows the energy band diagram for the simulation.
The bandgap energy of 1.0eV and 1.6eV is shown. It was
found out that the conduction band for the 1.6eV is much
higher than the conduction band for the 1.0eV. This means
that for higher bandgap energy, more photons energy is
required to free the electrons into the conduction band. On
the other hand, high bandgap energy creates fast
recombination of electrons and holes at the p-type region in
solar cell. The free carriers are being recombined before they
are diffused to depletion region to contribute to the
generation of electricity. Thus a decrease in Jsc was recorded
with an increasing value of bandgap energy. Besides, high
bandgap energy have a small positive value of conduction
band offset between the absorber layer and buffer layer where
it eventually became negative when the bandgap energy is
further increased.
Figure 8: Cell performance with variable CIGS bandgap.
The CIGS bandgap ranges from 1.0eV to 1.6eV has been
chosen for simulation. From Figure 8, it has been found out
that the Voc is increasing with bandgap. However the Voc
becomes constant at around 0.895 V over the bandgap value
of 1.48 eV. Jsc is decreasing with the bandgap value. Due to
the high bandgap value of the CIGS, the photons that are
position (µm)
eV
being absorbed at the p-type region of the solar cell do not
have enough energy to surpass the bandgap of CIGS solar
cell. If the bandgap energy is 1.5eV, this means that only the
photons which carried energy greater than 1.5eV contributes
to electron hole pair generation. All the other photons which
are carrying lesser energy would be wasted. As a whole,
efficiency is increasing with the increment of bandgap value,
but it decreases afterwards. The highest efficiency that was
obtained from this simulation is 21.297% at 1.36eV, which is
quite near to the optimum bandgap energy of CIGS absorber
layer of 1.4eV. The bandgap energy of 1.36eV is the
optimum bandgap energy for our simulation as both the Jsc
and efficiency are decreasing after this optimum value.
However, currently the laboratory scale best CIGS solar cells
are having bandgap values of 1.15eV to 1.20eV [17].
Figure 9 shows the J-V characteristics of the solar cell
where an increase of CIGS bandgap value results in a
decrease of short circuit current density. Besides, it also
results in an increase of open circuit voltage until a saturation
point.
Figure 9: J-V characteristics of solar cells with variable CIGS
bandgap values.
E. Effect of CdS BufferLayer Thicknesses
Generally the thickness of the optimum CdS buffer layer
should be within 50 nm and 60 nm [19]. The buffer layer
thickness of 50 nm has been used as the base parameter for
all of the simulation in this study. In this section, the effect of
the thickness variation of the CdS buffer layer on the
parameters of solar cell is shown. Here, the thickness of the
CdS buffer layer was varied from 10 nm to 100 nm.
Voc of the solar cell is shown in Figure 10 where the values
are almost constant for all the varying thicknesses of the CdS
buffer layer. Beside, Jsc values of the solar cell are found
decreasing with the increase of CdS buffer layer thickness.
This is because a thicker buffer layer will result in higher
photon absorption as loss [14]. When the buffer layer is
increased, more photons which carry the energy are being
absorbed by this layer. Therefore it would lead to a decrease
in the photons which could reach the absorber layer. A
decrease in the numbers of photons at the absorber layer
would decrease the quantum efficiency of the solar cell as
shown in Figure 12.
Figures 10 and 11 also show the efficiency of the solar cell
and the J-V characteristics with increasing CdS buffer layer
thickness. As explained earlier, both the values were found
decreasing because most of the photons are being absorbed
by the buffer layer. From Figure 10, it was found that buffer
thickness of 10 nm gives the highest efficiency. But it is
impossible to be fabricated practically because of the
complexity in fabrication. It is found that the optimum buffer
thickness would be from 40 nm to 50 nm as Jsc is found
decreasing after 50 nm.
Figure 10: Cell performance with variable thickness of CdS
buffer layer.
Figure 11: J-V characteristics of solar cells with variable
thicknesses of CdS buffer layer.
V (v)
J (m
A/c m
2)
J (m
A/c m
2)
V (v)
Figure 12: Spectral response of solar cells with variable
thicknesses of CdS buffer layer.
IV. CONCLUSION
Optimum parameters for the CIS and CIGS based solar
cells are obtained from numerical modeling. From the
simulation results, it is found that the increasing thickness of
the absorber layer results in higher efficiency of solar cell,
where the optimum thickness is around 3000 nm. Moreover,
it is found that the energy bandgap of 1.48eV was the
optimum for the CIGS, as the bandgap value greater than this
affects the efficiency. Furthermore, thickness of the CdS
buffer layer is needed to be at an optimum value of 50 nm to
reduce the photon loss. All these optimization results give
helpful indication for practical usage in fabrication process.
V. REFERENCES
[1] James R. Sites, Tokio Nakada, Hans-Werner Schock, Sigeru Niki,
Akira Yamada, Miguel A. Contreras, “Research and Development of
High-Voltage CIS-Based Thin Film Solar Cells for Industrial
Technology (2005)”.
[2] A. O. Pudov, “Impact of Secondary Barriers on CuIn1−xGaxSe2
Solar-Cell Operation”, Department of Physics, Colorado State
University, 2005.
[3] K. Ramanathan, M. Contreras, C. Perkins, S. Asher, F. Hasoon, J.
Keane, D. Young, M. Romero, W. Metzger, R. Noufi, J. Ward and A.
Duda, “Properties of 19.2% Efficiency ZnO/CdS/CuInGaSe2 Thin-
film Solar Cells”, Prog. Photovolt: Res. Appl. 2003; 11:225-230.
[4] M. Gloeckler, J. R. Sites, “Bandgap grading in Cu (In. Ga) Se2 solar
cells”, Department of Physics, Colorado State University, pp 4,
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[5] Clas Persson, “Thin-film ZnO/CdS/CuIn1-xGaxSe2 solar cells:
anomalous physical properties of the CuIn1-xGaxSe2 absorber”,
Brazilian Journal of Physics. v.36 n.3b São Paulo sep. 2006.
[6] C. H. Huang, Sheng S. Li, T. J. Anderson, “Modeling and Parameter
Optimization of CuInSe2-based Solar Cells”, University of Florida,
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[7] T. Nakada and M. Mizutani. Jpn. J. Appl. Phys. 41 (2002), p. 165.
Source: http://jjap.ipap.jp/journal/html/JJAP-41-2B/L165/
[8] T. Negami, T. Aoyagi, T. Satoh, S. Shimakawa, S. Hayashi and Y.
Hashimoto, Proceedings 29th IEEE Photovoltaic Specialist
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[9] Jae Won Kim, Hong Seong Kang, Jong Hoon Kim, and Sang Yeol Lee,
Jung-Kun Lee and Michael Nastasi, “Variation of structural, electrical,
and optical properties of Zn1−xMgxO thin films”, Journal of Applied
Physics pp100, 033701 2006
[10] Rui Mikami, Hisashi Miyazaki, Tatunobu Abe, Akira Yamada and
Makoto Konagai, “Chemical Bath Dposited (CBD)-ZnO Buffer Layer
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Conversion May 11-18. 2003, Pages 519.
[11] Sutichai Chaisitsak, Akira Yamada, and Makoto Konagai,
“Comprehensive Study of Light-Soaking Effect in ZnO/Cu(InGa)Se2
Solar Cells With Zn-Based Buffer Layers”, MRS.
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Volume 1, Issue, 11-18 May 2003 Page(s): 491 - 494 Vol.1.
[13] K. Ramanathan, M. Contreras, C. Perkins, S. Asher, F. Hasoon, J.
Keane, D. Young, M. Romero, W. Metzger, R. Noufi, J. Ward and A.
Duda, “Properties of 19.2% Efficiency ZnO/CdS/CuInGaSe2 Thin-
film Solar Cells”, Prog. Photovolt: Res. Appl. 2003; 11:225-230.
[14] A. O. Pudov, “Impact of Secondary Barriers on CuIn1−xGaxSe2
Solar-Cell Operation”, Department of Physics, Colorado State
University, 2005.
[15] G. Cernivec, J. Krc, F. Smole and M. Topic, “Band-gap engineering in
CIGS solar cells using Nelder-Mead simplex optimization algorithm,
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[17] C. H. Huang, S. S. Li, T. J. Anderson, “Device Modeling And
Simulation of CIS-Based Solar Cells”, University of Florida, 2002.
[18] G. Hanna, A. Jasenek, U. Rau and H. W. Schock, “Influence of the
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Films, Volume 387, Issues 1-2, 29 May 2001, Pages 71-73.
[19] Y. Hashimoto, T. Satoh, S. Shimakawa and T. Negami, “High
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VI. BIOGRAPHIES
Nowshad Amin was born in Chittagong,
Bangladesh, on January 5, 1972. He graduated
from the Comilla Cadet College, Bangladesh,
and later studied at the Universities of Gunma
National College of Technology for diploma in
Electrical Engineering, Toyohashi University of
Technology for BS, Tokyo Institute of
Technology for MS and PhD in Electronics, in
Japan. His special fields of interest include
Semiconductor Physics and Devices,
Optoelectronics.
Michael Tang was born in Sarawak, Malaysia, on
February 23, 1984. He graduated from Multimedia
University, Malaysia in 2007. His field of interest
includes electronics, optoelectronics.
Kamaruzzaman Bin Sopian was born in the
historical town of Batu Gajah, Perak in 1962.
He obtained his BSc in Mechanical Engineering
from the University of Wisconsin-Madison in
1985, MSc in Energy Resources from the
University of Pittsburgh in 1989 and PhD. in
Mechanical Engineering from the Dorgan Solar
Laboratory, University of Miami in 1997.
Currently, he is the Director of the Solar
Energy Research Institute, a center of excellence
for the research and development in solar energy
technology.
QE
λ (µm)