Nano-Micro Letters

Computational Study of Ternary Devices: Stable, Low-Cost, and Efficient Planar Perovskite Solar Cells

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Sajid Sajid 1, Ahmed Mourtada Elseman 2, Jun Ji1, Shangyi Dou1, Dong Wei1, Hao Huang1, Peng Cui1, Wenkang Xi1, Lihua Chu1, Yingfeng Li1, Bing Jiang1, Meicheng Li1,*

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Nano-Micro Lett. (2018) 10: 51

First Online: 09 April 2018 (Article)

DOI:10.1007/s40820-018-0205-5

*Corresponding author. E-mail: mcli@ncepu.edu.cn

 

Abstract

 


Toc

Although perovskite solar cells with power conversion efficiencies (PCEs) more than 22% have been realized with expensive organic charge transporting materials, their stability and high cost remain to be addressed. In this work, the perovskite configuration of MAPbX (MA = CH3NH3, X = I3, Br3, or I2Br) integrated with stable and low-cost Cu:NiOx hole-transporting material (HTM), ZnO electron-transporting material (ETM) and Al counter electrode was modeled as a planar PSC and studied theoretically. A solar cell simulation program (wxAMPS), which served as an update of the popular solar cell simulation tool (AMPS: Analysis of Microelectronic and Photonic Structures), was used. The study yielded a detailed understanding of the role of each component in the solar cell and its effect on the photovoltaic parameters as a whole. The bandgap of active materials and operating temperature of the modeled solar cell were shown to influence the solar cell performance in a significant way. Further, the simulation results reveal a strong dependence of photovoltaic parameters on the thickness and defect density of the light-absorbing layers. Under moderate simulation conditions, the MAPbBr3 and MAPbI2Br cells recorded the highest PCEs of 20.58% and 19.08%, respectively, while MAPbI3 cell gave a value of 16.14%.


 

Keywords

Perovskite solar cells; Copper-doped nickel oxide; Zinc oxide; Simulation

 

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1 Introduction

    Since the emergence of organic-inorganic halide perovskite materials as efficient light harvesters, perovskite solar cells (PSCs) have been widely investigated in terms of their power conversion efficiencies (PCEs). Fundamental studies on perovskite materials [1, 2], device architectures [3-5], fabrication processes [6, 7], and material engineering [8, 9] have assisted the rapid development of PSCs. Consequently, PCEs greater than 22% have been achieved, as certified by National Renewable Energy Laboratory (NREL) [10]. Presently, the PSC is considered as one of the most promising alternative energy conversion devices in terms of high efficiency and low cost. However, despite the major achievements in scaling efficiency levels in the laboratory ambient, the concern of long-term stability and performance of these solar cells under severe humidity and light illumination conditions as well as the requirement of expensive organic charge transporting materials (OCTMs) remain critical. In order to achieve high performance and improved stability, several material refinements have been attempted by substituting a mixture of suitable materials in the organic and halide sites (organic site: MA, HC(NH2)2; halide site: I, Br, Cl) [8, 9, 11-15]. Despite their application in most efficient devices, the expensive OCTMs are limited in use by a tendency to absorb water, difficulty in synthesizing, and inability to manage charge carriers effectively. Use of p-type and n-type inorganic materials would be a long-term solution for constructing stable PSCs more economically [16-19]. In this context, metal oxide semiconductors are considered chemically stable and highly transparent with tunable energy band levels [20-24]. They are nontoxic and abundantly available in the earth’s crust for universal use as photovoltaic materials. More attractively, thin layers of these materials have been deposited using low-cost techniques such as spin-coating, doctor-blading and spray-pyrolysis in ambient atmosphere. However, low charge carrier mobility and fill factor (FF) associated with inorganic-HTMs, particularly by the use of NiOx and Cu2O, are deterrents compared to organic HTMs. Highly efficient planar PSCs incorporated with solution-processed copper-doped NiOx as HTMs have been demonstrated by many researchers [25-27]. These studies revealed that the high conductivities (of HTM/ETM) obtained by doping or managing the charge carrier collection and valence/conduction band matching with perovskite absorber has a positive impact on PCE [6, 26, 28, 29]. In this work, we engaged a one-dimensional software program (wxAMPS), which is widely used for simulating carrier transport in solid state devices, to derive continuity and Poisson equations from first principles and to analyze the transport behavior of perovskite device structures. From the simulation output, solar cell parameters such as current–voltage characteristics in the dark and, if desired, under illumination can be obtained. For numerical simulation of PSCs such as the TiO2/MAPbI3/spiro-OMeTAD/Au, an effective method has been described by Liu et al., which helps in identifying the optimal operating conditions [30].

    In this context, we were inspired by Cu:NiOx as a hole-transporting layer (HTL) and ZnO as electron-transporting layer (ETL), which are highly conducting, environmental-friendly, and economically fabricable materials, together with Al back contact for integrating MAPbI3, MAPbI2Br, and MAPbBr3 thin layers to a p-i-n configuration. It was required to understand the role of each component and their combined effect so as to achieve incremental improvement in the photovoltaic characteristics of the PSC thus designed. In this endeavor, a theoretical study was performed to identify the optimal conditions of device operation using the simulation software wxAMPS and by employing intra-band and trap-assisted tunneling models for heterojunction analysis. This study represents the first (in our knowledge) numerical simulation of a PSC based on the perovskite series MAPbX (MA = CH3NH3, X = I3, Br3, or I2Br) in conjunction with Cu:NiOx (HTL), ZnO (ETL) and Al counter electrode and is aimed at improving the design of PSCs which are highly efficient, stable, and economical to fabricate. 

2 Modeling of Perovskite Solar Cell

    In the simulation process, device models were constructed with thin film stacks of glass/FTO/Cu:NiOx/MAPbX/ZnO/Al (MA = CH3NH3, X = I3, Br3 or I2Br) which are illustrated in Fig. 1a, and the corresponding energy band diagrams are shown in Fig. 1b. The paths of generation and recombination of charge carriers in PSCs are shown in Fig. 1c. The charge generation, separation, and extraction processes shown as steps (1), (2), and (3), respectively, are dynamic processes that are favorable for high-performance PSCs. In order to manage the charge collection efficiently, these processes should occur at a much faster rate than that of the recombination process (undesirable), which are shown in steps (4)–(6). For any further optimization and enhancement in photovoltaic parameters, one needs to address the time scale and charge carrier kinetics occurring at different interfaces in PSCs. In this context, three device layouts were created and labeled as device-A, B, and C using MAPbI3, MAPbI2Br and MAPbBr3 active layers, respectively. The AM1.5G solar spectrum was adopted as the illumination source for the simulation. The light reflectance at the top and bottom contacts were set to 0 and 1, respectively. The material parameters used for the simulation are summarized in Table 1; these were carefully chosen from earlier experimental reports [14, 23, 31]. Capture cross-sections of both electrons and holes were set to 1 × 10−16 cm2 which resulted in a carrier diffusion length of ~1 μm in light-absorbing materials. The thicknesses of the active layer were set to 0.4 μm for device A and 0.5 μm for devices B, and C, respectively, for efficient charge carrier collection. The possibility of Gaussian states that are either donor-like or acceptor-like and which are located anywhere in the bandgap can be predicted by wxAMPS. The donor-like tail states coming out of the valence band can be modeled in wxAMPS by Eq. 1,

10 3 51 gs1                 

where gd is donor-like tail Gaussian state, E1 is measured positively from the valence band edge (Ev) upward to the point located at x, Ed is the characteristic energy that determines the slope of the tail, and Gd0 represents the density of states. Similarly, the acceptor-like tail states coming out of the conduction band can be modeled by Eq. 2,

10 3 51 gs2

where ga is acceptor-like tail Gaussian state, E2 is measured negatively from the conduction band edge (Ec) downward to the same point x, Ea is the characteristic energy that determines the slope of the tail, and Ga0 represents the density of states.

Table 1 Basic material parameters used for the simulation, which were carefully chosen from experimental reports [14, 23, 31]

10 3 51 table1

    According to the Eqs. 1 and 2, the defect energy levels in the simulated thin film materials are located at the center of the bandgap with the Gaussian-type energy distribution (characteristic energy of 0.1 eV). The tail characteristic energy is 0.01 eV with density of band-tail states of 1 × 1014 cm−3 eV−1 [30, 32, 33].

Fig. 1 a Schematic cross-section of of p-i-n perovskite solar cells. b Energy band diagram of the corresponding heterojunctions. c Charge generation, separation, and extraction processes. d Simulated J–V characteristic curves under AM1.5G illumination at 100 mW cm−2 irradiance

Fig. 1 a Schematic cross-section of of p-i-n perovskite solar cells. b Energy band diagram of the corresponding heterojunctions. c Charge generation, separation, and extraction processes. d Simulated J–V characteristic curves under AM1.5G illumination at 100 mW cm−2 irradiance

    Since the performance of the solar cell is influenced by bimolecular electron-hole recombination rate, two assumptions have been made to understand the bimolecular recombination rate. In the first assumption, the conduction band electrons are directed to empty states in the valence band, a process known as band-to-band or direct recombination RD (also called intrinsic recombination). In the second assumption, electrons and holes recombine through intermediate gap states known as recombination centers or, by a process of extrinsic recombination. The latter is labeled as indirect recombination RI or Shockley–Read–Hall recombination. The total recombination term R(x) in the continuity equation takes into account both these processes as a sum of the two components (Eq. 3).

10 3 51 gs3

    Additionally, the bimolecular recombination rate simply relies on an overlap of electron and hole wavefunctions while Auger processes involve transfer of energy and momentum of the recombining electron-hole pair to a third charge carrier. On the other hand, experimental results of THz photoconductivity transients for perovskite materials have been documented [34] which lead to bimolecular and mono-molecular charge recombination rates according to Eq. 4,

10 3 51 gs4

where n denotes the photoinduced charge carrier density. The first term on the RHS of Eq. 4 represents bimolecular recombination rate of photogenerated carriers while the second term denotes mono-molecular recombination rate. In addition, the recombination dynamics associated with the free charge carrier density (n) could be described by the following differential equation (Eq. 5) [35],

10 3 51 gs5

where k3, k2, and k1 represent the decay constants describing Auger recombination, the bimolecular recombination constant, and the rate for monomolecular processes such as trap-assisted charge recombination, respectively. Applying the above equations, the value of the bimolecular recombination rate was approximated to 1 × 10−11 cm3 s−1 in the base-line simulation model as reported for the rates of recombination ranging from 10−11 to 10−9 cm3 s−1 [36, 37]. Further, the interface recombination velocity (S) was evaluated by a numerical approach using the expression given below (Eq. 6).

10 3 51 gs6

    Here, R, int, and m describe the recombination rate within the interface layer, the whole interface layer, and the concentration of holes and electrons, respectively. The values of R and m are estimable from the numerical solution, and the integral of R across the whole interface layer represents the total interface recombination as described in Eq. 3. The surface recombination velocities of electrons and holes at the top and bottom electrodes are estimated from Eq. 6 as 1 × 107 cm s−1. The interface recombination losses in each device configuration could be regulated by introducing two thin interfacial defect layers hypothetically at the HTL/perovskite and ETL/perovskite interfaces [38, 39] as outlined in Table S1. This approach facilitates performance evaluation of the device as also determines the compatibility between theoretical and experimental data by interface engineering [39-42].

3 Results and Discussions

    The motivation to optimize efficiency and durability of PSCs emerged from the need to design a thermally stable perovskite with all-inorganic charge transporting layers [43-46]. Using the codified AMPS-1D simulation tool, first-principle calculations were performed to find solutions for continuity and Poisson equations. The software was tweaked to simulate carrier transport in devices with single and multi-junction formats. This approach allows the researcher to implement optimized structures for microelectronic, photovoltaic, or optoelectronic applications [30, 39, 41, 47].

    The modeling process and results have led to a better understanding of the fabrication process and perovskite material stability. The simulated current–voltage (J–V) characteristic curves of the device-A, B, and C are given in Fig. 1d. Device-A (MAPbI3) showed the lowest PCE of 16.14%, open-circuit voltage (Voc) of 0.964 V, short-circuit current density (Jsc) of 20.87 mA cm−2, and fill factor (FF) of 79%. Devices B (MAPbI2Br) and C (MAPbBr3) yielded the highest PCE values of 19.08 and 20.58%, Voc of 1.098 and 1.107 V, Jsc of 22.53 and 22.99 mA cm−2, and FF of 79.45 and 81.67%, respectively. The simulated values of PCE of devices B and C are nearly consistent with the experimental value of 18.94% as reported by Kim et al. [46]. Notably, the realization of high Voc and FF in devices B and C were attributed to the use of absorber materials with large energy bandgap and low mismatch between the work functions of Cu:NiOx valence band, ZnO conduction band and the perovskite layer [27, 48, 49]. Hole extraction from the perovskite layer is considered a key process in enhancing photovoltaic performance. The incorporation of halide (Br) in perovskite materials results in rapid hole extraction and low carrier recombination rate by precisely tuning the bandgap [46, 50]. As an added advantage, the long carrier diffusion lengths in such mixed-halide devices yield higher values of FF and PCE. With this in mind, we further investigated the photoelectric behavior of the best devices, namely MAPbI2Br and MAPbBr3 (in lieu of MAPbI3). It can be clearly seen in Fig. 2a that the recombination rate is reduced and the efficiency of charge carrier collection improved by the application of Br-doped perovskites; the Cu:NiOx (HTM) and ZnO (ETM) layers remained the same in both cases. A relatively small trap-assisted recombination was evident in MAPbI2Br. The above findings are consistent with the experimental results obtained using transient THz spectroscopy [51]. It is also in agreement with the studies of Liu and Kelly and Snaith et al. who reported that the high degree of crystallinity in their perovskites helped to minimize the trap density within the material, thus lowering charge recombination and realizing high Voc values [6 , 28]. That a low recombination rate corresponds to high Voc is referenced to the results of transient open-circuit voltage decay (OCVD) and intensity-modulated photovoltage spectroscopy (IMVS) measurements [52]. The enhanced device performance is also credited to low series resistance, efficient carrier transport, and absence of Schottky barrier in the charge carrier materials (HTM and ETM) and electrode interfaces [53, 54, 25]. In the following sections, we will discuss specific factors that influence the device performance, namely film thickness, defect density, operating temperature, and bandgap energy of perovskite materials. There is also evidence that the crystal structure and morphology play an important role in the optimization process and in further improvements of device performance.

Fig. 2 a Simulated values of carrier recombination and generation rates in MAPbX (MA = CH3NH3, X = I3, I2Br or Br3) layers designed with Cu:NiOx (HTM) and ZnO (ETM). b–d Simulated J–V characteristic curves for different defect densities in the absorber film

Fig. 2 a Simulated values of carrier recombination and generation rates in MAPbX (MA = CH3NH3, X = I3, I2Br or Br3) layers designed with Cu:NiOx (HTM) and ZnO (ETM). b–d Simulated J–V characteristic curves for different defect densities in the absorber film

3.1 Effect of Defect Density

    The number of defects in the absorber material is crucial to the device performance. By effectively managing the generation-recombination rate of the photogenerated carriers within the absorber layer, the Voc of the device can be maximized. The simulated J–V curves in Figs. 2b–d illustrate that the defect states present in perovskite films cause a noticeable reduction in Voc while its effect on Jsc is much less discernible; this is in accordance with experimental results related to Br-doped perovskites [46]. A high degree of crystallinity in experimentally formed perovskite layers results in low trap density thus reducing charge recombination and realizing high Voc values [28 , 6]. It was earlier confirmed that the creation of a Br-rich layer within the tri-iodide perovskite structure enhanced moisture resistance, without sacrificing current density proving that the latter was less susceptible to defect density [55]. However, this resulted in a reduction in Voc. In our study, the Voc of device-B (MAPbI2Br) and device-C (MAPbBr3) are higher than that of device-A (MAPbI3) as shown in Figs. 2c–d. These results clearly establish that the relatively larger bandgap of the perovskite, especially in device-B and C (than in device-A), has been effective in lowering the charge recombination rate and is responsible for improving charge extraction as depicted in Fig. 2a [6, 14, 28, 46, 56, 57].

3.2 Effect of Active Layer Thickness

    The thickness of the photoactive perovskite layer also has a major role in improving the device performance. If the light-absorbing layer is too thin, the number of photons absorbed is small which will, in turn, give rise to low photocurrents; however, if a very thick perovskite layer is used, it results in low charge carrier extraction efficiency, and losses due to charge recombination becomes significant. Consequently, optimization of the absorber layer thickness assumes much importance in determining carrier generation and spectral response of the solar cells. Figure 3a shows the variation of PCE of the simulated devices as a function of the perovskite layer thickness. When the thickness was increased progressively in the range from 0.1 to 0.8 µm, the highest value of PCE was obtained for thicknesses of 0.4 for device A and 0.5 µm for devices B and C, respectively. The increase in efficiency is attributed to the increased number of electron-hole pairs generated in the photoactive layer. However, a decrease in efficiency at large thicknesses is due to increase in the recombination of charge carriers within the material before they reach the contact electrode. From the simulated results, which are summarized in Table 2, the thicknesses of 0.4 and 0.5 µm for perovskite layers were deduced as optimum values for achieving the highest PCE. Integrating the perovskite materials with suitable charge transporting layers such as Cu:NiOx (HTM) and ZnO (ETL), especially in the MAPbI2Br configuration, might serve as an effective method to collect charge carriers at low recombination rate using a specific absorber layer thickness(as illustrated in Fig. 2a). The process of accelerated hole extraction and improved carrier lifetime due to the Br concentration gradient in MAPb(I1−x­Brx)3 has been verified by Kim et al. by observing photoluminescence properties in this material [14, 46, 58]. Additionally, the large photocurrents generated in these materials were attributed to the high absorption coefficient of the perovskite layers. We noticed a discrepancy between the simulated and experimental results at large values of thickness beyond the optimized thickness values (0.4 and 0.5 µm) which, we believe, is due to large variations in structure and thickness of the absorber layer in actual devices, which was also reported by Sum and Mathews [59]. Additionally, we found supporting evidence in the reports on planar heterojunction devices that employed higher layer thicknesses in the range of 0.4–0.8 µm for fabricating highly efficient devices. Besides, large carrier diffusion lengths of up to 1 µm have been observed in mixed-halide perovskites which also lends support to the claim that thicker absorber layers can be used [60]. Benefiting from the long carrier diffusion length, perovskite semiconductors possess long carrier diffusion length  and a high charge collection efficiency [61]. Therefore, design of a thicker perovskite layer may serve as an effective solution to absorb more photons than that in solution-processed photovoltaic materials [62-65]. While our simulations have predicted the use of 0.4- and 0.5-μm-thick absorber layers for enhancing the device performance, available experimental data suggest that further increase in thickness may also help to achieve high values of PCE [61, 66, 67].

Table 2 Simulated photovoltaic characteristics of solar cells measured under standard AM1.5G illumination at 100 mW cm−2 irradiance

10 3 51 table2

Fig. 3 a Variation (simulated) of PCE obtained as a function of thickness of photoactive materials. b Variation (simulated) of PCE as a function of operating temperature. c–d Variation (simulated) of photovoltaic parameters as a function of bandgap energy in perovskite materials

Fig. 3 a Variation (simulated) of PCE obtained as a function of thickness of photoactive materials. b Variation (simulated) of PCE as a function of operating temperature. c–d Variation (simulated) of photovoltaic parameters as a function of bandgap energy in perovskite materials

3.3 Effect of Operating Temperature

    The performance of a PSC implicitly depends on its operating temperature. The standard test temperature (300 K) is generally used for performing simulations but the operating temperatures in actual conditions are much higher. In this study, the simulation models considered the working temperature of 300 K as listed in Tables 1, 2 and Table S1. It is worthwhile to note that high temperature often leads to increased stress and deformation in devices which is likely to create more interfacial defects and cause poor inter-connectivity between the layers. Consequently, a high recombination rate prevails which is accompanied by reduction in carrier diffusion length and increase in series resistance [68 , 69]. It has been previously reported that increase in temperature will significantly affect the electron and hole concentration, charge carrier mobility, material bandgap, and also device power conversion efficiency. This is illustrated by our simulation results in Fig. 3b. However, it was found that the decrease in PCE can be controlled to a certain extent by incorporating a homogeneous layer of mixed-halide perovskite (Br-substituted perovskite). Kim et al. fabricated a thermally stable Br-doped perovskite solar cell with PCE of 18.94% under high humid conditions (40−90%) and retained its efficiency without encapsulation for 28 days [27, 46]. The use of inorganic HTLs and ETLs have established that, by optimizing thermal and chemical stability, improved performance can be realized in PSCs at lower material and processing cost [16, 17, 23, 25, 31, 70, 71].

3.4 Effect of Energy Levels

    Incident photon harvesting in a solar cell plays a large role in achieving high photovoltaic performance [72, 73]. Photoactive materials are broadly defined as those capable of responding to light or electromagnetic radiation. The optical absorption can be varied by tuning the bandgap energy of perovskite materials to achieve high device performance [14, 74]. The bandgap of MAPbX3 is considered to be one of the major factors that influence the magnitude of electronegativity difference between the metal cation and the anion in perovskite materials. An increase in the anion electronegativity is likely to diminish the covalent character of the halogen bond with Pb2+ ion and, consequently, result in an increase of the bandgap energy [14, 75]. Changes in composition with respect to the halide ion such as in MAPbI3, MAPbI2Br, and MAPbBr3 are likely to influence the optical properties of the perovskite materials as shown in Fig. S1. The simulated variation in the photovoltaic parameters obtained by changing the bandgap energy of the absorber material from 1.5 to 2.2 eV under optimized conditions are illustrated in Figs. 3c–d. It is clearly seen that with increasing bandgap energy, Voc also increases in all cases. In a previous study related to the wide-bandgap perovskite (MAPb(I1−x­Brx)3) solar cell, the results showed an increase of Voc from 1.08 to 1.11 V and improvement of FF from 71 to 74% with thermally stable PCE of 18.94% [46]. The simulation results obtained in this study show an enhancement in FF and Jsc which are consistent with the energy band alignment of HTM and ETM with the absorber layer which can be seen in Figs. 1c and 2a, respectively [26]. These improvements have been attributed to increase in bandgap, reduced radiative recombination, and energy band matching [11, 23, 25, 27, 31, 46].

4 Conclusion

    In summary, the configurationally design of the perovskite solar cell MAPbX (MA = CH3NH3, X = I3, Br3 or I2Br) was systematically simulated using the simulation software wxAMPS which is an update of the popular solar cell simulation tool (AMPS; Analysis of Microelectronic and Photonic Structures). Various models were constructed with thin film stacks in the format, glass/FTO/Cu:NiOx/MAPbX/ZnO/Al. The shortcomings in each device configuration were overcome by introducing thin defect layers at the interfaces of HTL/absorber layer and ETL/absorber layer hypothetically. The simulated photovoltaic characteristics yielded the highest PCE value of 20.58% for the device-C (MAPbBr3), 19.08% for device-B (MAPbI2Br), and the lowest value of 16.14% for device-A (MAPbI3). The simulation results also indicated that thicker perovskite layers realized higher values of PCE in relation to thinner ones due to enhanced photon harvesting. The J–V characteristics provided evidence that the defect states present in perovskite films cause a noticeable reduction in Voc. However, this has very nominal effect on Jsc value, particularly for the MAPbI2Br perovskite cell. The increase in bandgap energy is responsible for the enhanced photovoltaic parameters such as PCE, FF, Jsc, and Voc. These findings are likely to serve as important inputs and guide to the design of new mixed-halide perovskite structures with Cu:NiOx-HTM, and ZnO-ETM for achieving high stability and low fabrication cost in perovskite solar cells.

Acknowledgements

    This work is supported partially by National Natural Science Foundation of China (Grant nos. 51772096, 51372082, 51402106 and 11504107), Beijing Natural Science Foundation (17L20075), Joint Funds of the Equipment Pre-Research and Ministry of Education(6141A020225), National High-tech R&D Program of China (863 Program, No. 2015AA034601), Par-Eu Scholars Program, Beijing Municipal Science and Technology Project (Z161100002616039) and the Fundamental Research Funds for the Central Universities (2016JQ01, 2017ZZD02).

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Citation Information

Sajid Sajid, Ahmed Mourtada Elseman, Jun Ji, Shangyi Dou, Dong Wei, Hao Huang, Peng Cui, Wenkang Xi, Lihua Chu, Yingfeng Li, Bing Jiang, Meicheng Li, Computational Study of Ternary Devices: Stable, Low-Cost, and Efficient Planar Perovskite Solar Cells. Nano-Micro Lett.(2018) 10: 51. https://doi.org/10.1007/s40820-018-0205-5

History

Received: 21 February 2018 / Accepted: 9 April 2018


Additional Info

  • Type of Publishing: JOUR - Journal
  • Title: Computational Study of Ternary Devices: Stable, Low-Cost, and Efficient Planar Perovskite Solar Cells
  • Author: Sajid Sajid, Ahmed Mourtada Elseman, Jun Ji, Shangyi Dou, Dong Wei, Hao Huang, Peng Cui, Wenkang Xi, Lihua Chu, Yingfeng Li, Bing Jiang, Meicheng Li
  • Year: 2018
  • Volume: 10
  • Issue: 3
  • Journal Name: Nano-Micro Letters
  • ISSN: 2150-5551
  • URL: http://dx.doi.org/10.1007/s40820-018-0205-5
  • Abstract: Although perovskite solar cells with power conversion efficiencies (PCEs) more than 22% have been realized with expensive organic charge transporting materials, their stability and high cost remain to be addressed. In this work, the perovskite configuration of MAPbX (MA = CH3NH3, X = I3, Br3, or I2Br) integrated with stable and low-cost Cu:NiOx hole-transporting material (HTM), ZnO electron-transporting material (ETM) and Al counter electrode was modeled as a planar PSC and studied theoretically. A solar cell simulation program (wxAMPS), which served as an update of the popular solar cell simulation tool (AMPS: Analysis of Microelectronic and Photonic Structures), was used. The study yielded a detailed understanding of the role of each component in the solar cell and its effect on the photovoltaic parameters as a whole. The bandgap of active materials and operating temperature of the modeled solar cell were shown to influence the solar cell performance in a significant way. Further, the simulation results reveal a strong dependence of photovoltaic parameters on the thickness and defect density of the light-absorbing layers. Under moderate simulation conditions, the MAPbBr3 and MAPbI2Br cells recorded the highest PCEs of 20.58% and 19.08%, respectively, while MAPbI3 cell gave a value of 16.14%.
  • Publish Date: Monday, 09 April 2018
  • Start Page: 51
  • DOI: 10.1007/s40820-018-0205-5