No-ITO or FTO
No-ITO or FTO
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Bipin Saha,1 Bipanko Kumar Mondal,2 Shaikh Khaled Mostaque,1 Mainul Hossain,3
and Jaker Hossain1,a)
AFFILIATIONS
1
Solar Energy Laboratory, Department of Electrical and Electronic Engineering, University of Rajshahi,
Rajshahi 6205, Bangladesh
2
Department of Electrical and Electronic Engineering, Pundra University of Science and Technology, Bogura 5800, Bangladesh
3
Department of Electrical and Electronic Engineering, University of Dhaka, Dhaka 1000, Bangladesh
a)
Author to whom correspondence should be addressed: jak_apee@ru.ac.bd
ity issues, which limit their long-term applicability.13 Highly stable, terms of the orthorhombic structure of CuSbSe2 in which the lone
inorganic, dual-heterojunction solar cells promise to deliver high pair electron configuration of Sb distorts the tetragonal bonds,
PCE at low cost. Our previous simulations have achieved a PCE resulting in a layered structure with zero dangling bonds that are
over 40% with application of back surface field layer in CdTe-based primarily responsible for grain boundary carrier recombination.
double-heterojunction structures.14 Hence, CuSbSe2 structure is more defect tolerant.15,19 ZnSe is
Here, we propose a dual-heterojunction n-ZnSe/p- chosen as window material owing to the suitable properties, such
CuSbSe2 /p+ -copper gallium selenide (CGS) solar cell, having as wide bandgap (2.7 eV), earth-abundance, and high optical
ZnSe as the window and CGS (CuGaSe2 ) as the back surface field transmission in the visible range.20–23 The thin layer of ZnSe
(BSF) layers. The p-doped CuSbSe2 serves as the main absorber allows more than 80% of the incoming light to reach the under-
layer with a carrier density of 5.6 × 1015 cm−3 , suitable bandgap lying CuSbSe2 absorber layer without being absorbed.20,24,25 In
between 1.0 and 1.6 eV, and higher absorption coefficient in the addition, as compared to other more commonly used window
order of 104 cm−1 . The excellent electrical and optical properties, layers, ZnSe is less sensitive to moisture and oxidation.21 CGS
low cost, earth abundance, and non-toxic nature have further (CuGaSe2 ) possesses an energy bandgap of 1.68 eV and a high
exemplified CuSbSe2 as a propitious absorber.15 Unlike Si, which absorption coefficient in longer wavelengths,26,27 which make CGS
requires a very high processing temperature, the growth of CuSbSe2 an excellent BSF layer for enhancing the PCE of the proposed solar
is favored at low temperatures ranging between 380 and 410 ○ C.16,17 PV cell.
The existence of the lone pair of 5s2 electrons in CuSbSe2 plays role In the present work, we employ numerical calculations in Solar
behind significant absorption of light. CuSbSe2 reduces the surface Cell Capacitance Simulator-1 dimensional (SACPS-1D) software
roughness and back surface recombination in the absorption layer, that solves Poisson’s equation and the continuity equations for free
facilitating the collection of carriers.18 This can be explained in electrons and holes to assess how well the absorber, window, and
TABLE I. Input parameters used for simulating ZnSe/CuSbSe2 /CGS heterojunction solar cells at a temperature of 300 K.
BSF layers functions in relation to their thickness, doping levels, and On the contrary, CGS has an electron affinity and bandgap of 3.61
defect levels.28 and 1.66 eV, respectively. As a result, it can also construct a proper
pp+ interface with the CuSbSe2 layer. In Fig. 1(b), EFn and EFp
represent the developed quasi-Fermi levels of electron and hole,
II. DEVICE STRUCTURE AND SIMULATION MODEL respectively, in each of the layers. The electrons generated in the
In the modeled structure shown in Fig. 1(a), the incident CuSbSe2 and CGS layers can be easily transported to the cathode
sunlight passes through the ZnSe layer and is absorbed in the and holes generated in the CuSbSe2 , and CGS can also move toward
CuSbSe2 and CGS layers. ZnSe has the electron affinity and ion- the anode favored by the suitable energy barriers.
ization potential of 4.09 and 6.79 eV, respectively,24 whereas those The numerical simulations were performed considering one-
of CuSbSe2 are 4.11 and 5.19 eV, respectively.29 Therefore, ZnSe sun illumination with a power density of 100 mW/cm2 of the global
comprises a compatible pn heterojunction with CuSbSe2 compound. air mass (AM) 1.5G spectrum and the cell temperature of 300 K.
Note that the values of series and shunt resistances of the device were As the recombination increases with the absorber thickness, V OC
considered as ideal and the coefficient of radiative recombination gets slightly decreased from 0.94 to 0.92 V after expanding the
was not taken into account. Acceptor and donor doping profiles in absorber layer thickness from 0.6 to 1 μm. The FF and PCE remain
the bulk layers were considered to be Gaussian, and the interface fairly constant, ranging between 79.72% and 79.25% for the FF and
defects were also taken into account. 43.76% and 43.64% for the PCE. The maximum PCE is 43.79% and
The experimental values of absorption coefficients for ZnSe, is obtained with a 0.7 μm thick CuSbSe2 absorber layer. Figure 2(b)
CuSbSe2 , and CGS layers were obtained from previous studies.15,33 shows the change in device characteristics when the doping con-
SCAPS-1D automatically takes into consideration the influence centration in CuSbSe2 is varied. J SC remains almost unchanged,
of low energy (sub-bandgap) absorption from the optical data. varying only slightly between 58.94 and 58.93 mA/cm2 for dop-
The simulation parameters used for different layers are pro- ing concentrations of 1014 to 1018 cm−3 , respectively. Voc follows
vided in Table I, and the interfaces parameters are provided a similar trend, maintaining a steady value of around 0.93 V. The
in Table II. FF, however, drops from 78.88% to 71.86% below a doping level
of 1017 cm−3 , affecting the overall PCE. The PCE varies between
III. RESULTS AND DISCUSSION 43.8% and 39.39% with doping concentrations of 1014 to 1018 cm−3 ,
respectively.
A. CuSbSe2 absorber layer The change of PV performance parameters with CuSbSe2 bulk
The short circuit current density (J SC ), open circuit voltage defect density is exhibited in Fig. 2(c). The bulk defects ranges
(V OC ), fill factor (FF), and overall PCE of the modeled photovoltaic from 1012 to 1018 cm−3 . A high defect level impedes the creation
cell were calculated for CuSbSe2 thickness ranging between 0.6 and of electron–hole pairs, leading to decreasing J SC with defect density.
1.0 μm, as shown in Fig. 2(a). A thick absorber layer absorbs addi- Furthermore, the Shockley–Read–Hall (SRH) carrier recombination
tional photons and generates large number of electron–hole pairs. mechanism leads to the increase in the dark current and the decrease
Hence, J SC increases from 57.94 mA/cm2 when CuSbSe2 is 0.6 μm in V OC . Thus, V OC gets abruptly down from 1.03 to 0.44 V and the
thick to 59.58 mA/cm2 when the layer thickness becomes 1 μm. corresponding FF drops from 81.26% to 72.55% due to the high
defects of CuSbSe2 layer, causing the corresponding PCEs to vary the same trend with the PCE ranging from 43.63% to 43.79% for a
from 49.32% to 13.45%. specified ZnSe doping range.
Figure 2(d) shows how the QE of the modeled PV cell changes The defect density of ZnSe also affects the PV parameters as
with CuSbSe2 thickness. As expected, the thicker absorber layer depicted in Fig. 3(c). Bulk defects of the ZnSe window layer have
results in higher QE due to higher number of absorbed photons. At negligible effects on the J SC and V OC , but the FF and PCE decreases
shorter wavelengths, QE is almost independent of CuSbSe2 thick- at defect levels greater than 1017 cm−3 .
ness. However, at a longer wavelength regime, QE decreases as
photon energy, hν of the incident light less than the bandgap Eg of C. CGS BSF layer
CuSbSe2 .
The CGS layer on the back surface serves as the bottom
absorber layer and contributes significantly to the improvement of
the output PV parameters on the proposed solar cell. In Fig. 4(a),
B. ZnSe window layer the CGS layer thickness is varied from 0.1 to 0.5 μm. J SC is found
The changes in J SC , V OC , FF, and PCE for varying thickness of to be 44.07 mA/cm2 without the BSF layer. However, when only
the ZnSe window are shown in Fig. 3(a). It is noticed in the figure 0.1 μm thick CGS layer is employed in the structure, the current
that a modest increment in J SC , occurs when the thickness of the is significantly enhanced to 54.43 mA/cm2 . Furthermore, J SC con-
window ZnSe layer is increased. Over the thickness range, the rest of tinuously increases with increasing thickness of CGS layer reaching
the parameters remains constant. 65.04 mA/cm2 when the CGS becomes 0.5 μm thick. This occurs
Figure 3(b) illustrates the fluctuation in J SC , V OC , FF, and PCE because the CGS BSF layer absorbs longer wavelength incident pho-
with change in doping concentrations in the ZnSe layer. The dop- tons through a two-step upconversion technique by Urbach energy
ing level in ZnSe was altered from 1016 to 1020 cm−3 . Both J SC and states, namely, tail-state-assisted (TSA) upconversion.34,35 In the
V OC remain fairly unchanged, with J SC and V OC showing a slightly process of TSA upconversion, low energy light transmitted to the
decreasing and increasing trends, respectively, as the doping con- bottom BSF is absorbed in two steps by the Urbach states, creating
centration is raised from 1016 to 1020 cm−3 . The FF and PCE follows an extra electron–hole pair.32,36 This in turn leads to significantly
highest J SC with increasing CGS BSF layer thickness. Correspond- the CuSbSe2 /ZnSe interface cause the V OC to drop from ∼0.94 to
ingly, the open circuit voltage V OC enhances from 0.73 to 0.93 V ∼0.80 V, as depicted in Fig. 5(a). J SC remains fairly constant while
with the CGS thickness. The insertion of the CGS layer generates the FF increases from 79.2% to 83.6%, causing the PCE to drop from
a high built-in potential in the CuSbSe2 /CGS interface that is the 43.5% to 39% as the defect density increases. A similar trend, as
responsible for high V OC . The FF decreases when the CGS layer is shown in Fig. 5(b), is noticed for the CGS/CuSbSe2 interface.
introduced. However, it remains constant with the change in thick-
ness of the CGS layer. Since both J SC and V OC are enhanced, the E. Temperature dependence
overall PCE increases from 40.21% to 48.61%, over the range of CGS Carrier mobilities in semiconductors decrease with increasing
thickness.
D. Interface defects
Defect densities at the CuSbSe2 /ZnSe and CGS/CuSbSe2 inter-
faces influence the PV performance of the proposed model as
FIG. 6. PV parameters with respect to operating temperature.
depicted in Figs. 5(a) and 5(b), respectively. High defect levels at
slightly increases from 58.85 to 59.31 mA/cm2 when the tempera- ACKNOWLEDGMENTS
ture is raised from 273 to 500 K. On the contrary, the V OC drops
The authors would like to thank Professor Dr. Marc Burgel-
from 0.96 to 0.75 V for the same temperature range, which can be
man, University of Gent, Belgium, for providing SCAPS simulation
explained in terms of the increment of the recombination current.
software.
The FF also decreases at higher temperatures, causing the PCE to
DATA AVAILABILITY
IV. CONCLUSION
Herein, we used numerical computations to demonstrate the The data that support the findings of this study are available
high-performance n-ZnSe/p-CuSbSe2 /p+ -CGS solar device. Results from the corresponding author upon reasonable request.
confirm that the inclusion of the CGS back surface layer in the
photovoltaic cell remarkably improves the PCE through the TSA
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