Solar Cell Technology Research Articles

Generated power forecast of dye-sensitized solar plant with deep neural network

ABSTRACT The enormous amount of solar power and its state-of-the-art capturing technology that produces electricity, increases the grid interconnection rate of photovoltaic (PV) plants. Prior knowledge of the aperiodic characteristics of solar energy received by the Earth’s surface is essential for PV plants to ensure reliable operation and stable, secure grid connections. Power generation under diffused sunlight by PV plants with the most widely used first-generation solar cells has significant limitations. A dye-sensitized solar plant (DSSP), utilizes dye-sensitized solar cell (DSSC) technology, remains active in low light conditions. Though the activeness enables such plants to generate electricity throughout the year while receiving diffuse sunlight, unlike conventional solar technologies the plants have a requirement of knowledge of future power generation. This could be the first paper to report on the generated power forecast for such plants. The study has utilized a machine learning approach with a proposed DSSP model for the forecast. Spyder, an open-source integrated development environment, is the test workbench for the experimentation. The results show the robustness and reliability of the method, regardless of the weather conditions in the test area. The DSSP, along with the prediction model, will moderately overcome the shortcomings of power generation under diffuse daylight with intermittent solar radiation and grid connections.

From ideal to realistic compact hybrid PV-CSP systems: A technoeconomic evaluation

Compact PV/CSP hybrid systems, based on the integration of both PV and CSP technologies within a single power plant, have been attracting interest in recent years, because of their potential to lower the cost of solar electricity and minimize the land footprint required. However, the objective evaluation of these technologies is complicated by the fact that they involve two separate converters, each delivering a different form of energy (dispatchable for CSP, non-dispatchable for PV). We propose here an original evaluation and optimization approach based on 3 techno-economic indicators quantifying (1) the overall conversion efficiency of these systems compared to their standalone CSP counterparts, (2) the energy production balance between PV and CSP, and (3) the extra manufacturing cost compared to standalone CSP systems. These different indicators are evaluated for two families of hybrid systems (PV Topping and PV Mirror) and for 3 geometries of concentrating optics (Linear Fresnel Lenses, Parabolic Troughs and Solar Towers). One originality of our approach lies in its ability to determine the optoelectronic properties of PV cells likely to lead to the best hybrid performance, taking into account whether or not they are able to reach their own theoretical limits. Another original feature is that the hybrid systems considered in our analysis are compared with CSP equivalents which have been independently optimized. It is shown that the integration of realistic solar cell technologies whose performances deviate significantly from their theoretical limits notably restricts the range of operating conditions for which hybrid systems could outperform their standalone CSP counterparts. We conclude this work by discussing a number of key challenges that need to be overcome in order to develop more competitive and efficient hybrid systems.

The Sustainable Development Trend, Progress and Challenge of Solar Cells

The current development of solar cells indicates that this field is experiencing rapid technological progress and market expansion. Various types of solar cells, from traditional silicon-based ones to emerging thin-film, dye-sensitized, perovskite, and organic solar cells, are constantly being developed to improve efficiency, reduce costs, and meet different application needs. While silicon-based solar cells remain one of the most mainstream types on the market, researchers are exploring third-generation photovoltaic devices such as multi-junction series cells, intermediate band gap cells, multiple exciton-generating cells hot carrier cells thermal-light photovoltaic solar cells to further bolster efficiency and reduce costs. These new solar cell technologies theoretically offer higher conversion efficiency and are anticipated to replace traditional silicon-based ones in the future. Advancements in the technology of solar cells mainly involve continuous progress and innovation in materials' development structural design manufacturing processes-from early silicon-based designs to today's thin-film arrays. Each generation is developed with the goal improving efficiency lowering costs; subsequently leading to recent developments in organic and perovskite arrays currently under exploration creating a final product at a lower price. At present, current attention within development primarily lies towards material components advancement efficiency maximization. Cost reduction strategies large scale production Although faced with certain obstacles; through consistent research proving their overwhelming effectiveness; implications for widespread use suggest performance. Overall prospects within Solar energy appear limitless.

Enhanced charge separation at the interface of Cu2O/CuSCN composite thin films synthesized by electrodeposition technique

This study focuses on the synthesis and characterization of hole transport layers (HTLs) for solar cells, par- ticularly copper(I) thiocyanate (CuSCN) and cuprous oxide (Cu2O), synthesized via electrodeposition tech- niques. CuSCN and Cu2O offer promising properties for efficient charge transport in photovoltaic devices. The synthesis processes involve precise control of deposition parameters to achieve desired film morpholo- gies and properties. Characterization techniques including scanning electron microscopy (SEM), atomic force microscopy (AFM), and ultraviolet-visible (UV-Vis) spectroscopy provide insights into film morphology and optical properties. Optimization of synthesis parameters for Cu2O films is explored to enhance their electrical properties. Photoelectric response measurements indicate improved charge separation at the interface of Cu2O/CuSCN composite films. These findings can contribute to the advancement of solar cell technology. Furthermore, the study extends its exploration to the fabrication of Cu2O by electrodeposition at different pH levels. SEM and X-ray diffraction (XRD) analyses reveal the impact of deposition parameters on film mor- phology and crystal structure, providing valuable insights for tailored synthesis approaches. Overall, this comprehensive study not only advances the understanding of HTL materials synthesis and optimization but also provides valuable guidance for the development of high-efficiency and stable solar cell devices.

Stable RbCsFAPbI3 perovskite solar cell: numerical modelling and optimisation using SCAPS-1D

The studies concerning solar cell technology has consistently been captivating and inspiring, largely because of its environmentally friendly and sustainable characteristics. The outstanding electronic, optical, mechanical, and electrical characteristics of perovskite materials make them crucial for the development of the photovoltaic industry. In order to model the mixed cation Rb0.05Cs0.1FA0.85PbI3 perovskite solar cells, the SCAPS-1D tool was used. The main feature of RbCsFAPbI3 perovskite is its remarkable stability, and wide bandgap. Rubidium (Rb) and cesium (Cs) cations improve the optoelectronic characteristics of the material, resulting in less non-radiative recombination and improved charge transfer. In this work, the effects of different hole transport layers (CuSCN, CuSbS2,Cu2O) and back metal contacts (Ag, Fe, C-Cu, Au, Ni, Pt) on solar cell performance were investigated. The maximum efficiency of the solar cell has been achieved by studying various parameters like temperature, series resistance, shunt resistance, defect density, and absorber layer thickness. With FF = 84.12%, Jsc = 24.52 mA cm−2, Voc = 1.19 V, and the configuration of FTO/TiO2/RbCsFAPbI3/Cu2O/Au, the optimised device obtains a PCE of 24.64%. The impressive enhancements in performance parameters observed in the structure of the device make it highly suitable for applications in solar energy harvesting systems.

Effectiveness of 2-Terminal Perovskite/Perovskite/c-Si Triple-Junction Solar Cells: An Integrated Study with an Emphasis on Methylammonium Bismuth Iodide.

The growing interest in high-efficiency solar energy technologies has driven research on multijunction solar cells to flourish over the last several years. This study sheds light on the optical, structural, and morphological aspects of the (CH3NH3)3Bi2I9 ((MA)3Bi2I9) film by fabricating and analyzing it experimentally. This thorough investigation lays the groundwork for more research into the film's possible uses in solar cell technology. We performed simulations to enhance the efficiency of two-terminal (2T) perovskite/perovskite double junction and perovskite/perovskite/c-Si triple-junction solar cells (TJSC) by using the MA3Bi2I9 material. The power conversion efficiency was greatly increased by using 2T triple-junction solar cells; the increase was around 116.59% from single junction (13.80-29.89%) and 31.91% from double junction (22.66-29.89%). As far as we know, this is the first investigation of the efficacy of MA3Bi2I9 as a top layer in multijunction tandem configurations. This revolutionary approach allows both academics and industry experts to produce cost-effective and efficient tandem solar cells, thereby enhancing earth-based solar energy development.

Growth temperature-dependent properties of electrodeposited CdSe thin films for optoelectronic application

Cadmium selenide (CdSe) thin films were synthesized using a two-electrode electrodeposition technique in potentiostatic mode. The solution matrix contains 0.3 M Cd(NO3)2.4H2O and 0.03 M SeO2 on conductive glass substrates/fluorine-doped tin oxide (FTO). The electrodeposited CdSe thin films were examined at various growth temperatures of 55, 65, and 85 °C, both as-deposited (AD) and annealed (HT) samples. A polycrystalline cubic structure of the prepared CdSe thin films was identified using x-ray powder diffraction. The energy bandgap of films was found to vary with deposition temperature and was recorded as 1.85, 2.00, and 2.13 eV for AD and 1.86, 2.16 and 2.70 eV for HT samples deposited at 55, 65, and 85 °C, respectively. Surface morphology images show that the form and grain size varied with growth temperature. The average surface roughness varied with deposition temperature. The elemental analysis confirmed that the proportion of cadmium (Cd) increased while that of Se decreased as the deposition temperature increased for both AD and HT films. The film that was deposited at low temperature (55 °C) can be as a layer for absorption. Conversely, however the film deposited at a high growth temperature (85 °C) is capable of serving as a buffer layer in thin-film solar cell technology.

Fabrication of cost-effective lead-free silver bismuth iodide based mesoscopic Rudorffite solar cells

Lead-free Ag–Bi–I Rudorffite materials, specifically AgBiI4, Ag2BiI5, Ag3BiI6 and AgBi2I7, have garnered substantial attention as prospective alternatives to lead halide perovskites in solar cell technology. Rudorffite-based solar cells have conventionally employed a mesoporous structure, integrating unstable and costly hole-transport layers (HTLs) in conjunction with noble metal electrodes. This study presents carbon-based, all-inorganic AgBiI4, Ag2BiI5, Ag3BiI6 and AgBi2I7 Rudorffite solar cells that circumvent the need for HTLs and noble metal electrodes. The absorber layers composed of AgBiI4, Ag2BiI5, Ag3BiI6 and AgBi2I7 materials were synthesized via melt-solidification. Notably, Ag2BiI5 based solar cell achieved PCE of 0.93 % among all the Silver Bismuth Iodide (SBI) devices which is the highest efficiency reported for Ag2BiI5 solar cell to date. The corresponding solar cell parameters include an open-circuit voltage (Voc) of 0.634 V and a short-circuit current (Jsc) of 3.63 mA/cm2. Consequently, our work presents a pathway toward developing Rudorffite solar cells with simplified fabrication methods and reduced cost.

Investigation of thermally induced surface composition and morphology variation of magnetron sputtered Sb2Se3 absorber layer for thin film solar cells

One of the most promising semiconductor materials for the development of sustainable thin-film solar cell technology is antimony selenide (Sb2Se3). Its excellent optical and electrical properties have drawn attention lately for potential application in thin-film solar cells. In this study, Sb2Se3 films deposited using the direct current (DC) magnetron sputtering technique have been subjected to a post-annealing process without an extra selenium supply at temperatures between 150 and 450 °C. Without an extra selenium supply, the impact of post-annealing temperature on the surface composition as well as the physical properties of the fabricated films was investigated. The overall evaluations revealed that the post-annealing temperature is highly efficient in altering the physical properties of the Sb2Se3 absorber thin films. We further observed that the post-annealing process improved the crystallization and the heat treatment temperature quite affected preferential orientation. The surface morphology of films exhibited structural deformation at high post-annealing temperatures (> 350 °C). According to optical and electrical characterizations, respectively, the optical energy gap and the resistivity of Sb2Se3 films reduced with an increment in the post-annealing temperature. Based on the XPS result, the variation in temperature of post-annealing led to a change in the surface composition of the films. The findings on the growth of Sb2Se3 thin films indicate the existence of an intermediate growth temperature that permits the growth of Sb2Se3 films to be optimized. The study’s conclusions can serve as a guide to the growth of Sb2Se3 thin films with the desired crystallinity, surface morphology, and composition for thin film solar cell applications.

Enhancing Multi-Junction Solar Cell Performance: Advanced Predictive Modeling and Cutting-Edge CIGS Integration Techniques

Historically, multi-junction solar cells have evolved to capture a broader spectrum of sunlight, significantly enhancing efficiency beyond conventional solar technologies. In this study, we utilized Silvaco TCAD tools to optimize a five-junction solar cell composed of AlInP, AlGaInP, AlGaInAs, GaInP, GaAs, InGaAs, and Ge, drawing on advancements documented in the literature. Our research focused on optimizing these cells through sophisticated statistical modeling and material innovation, particularly examining the relationship between layer thickness and electrical yield under one sun illumination. Employing III-V tandem solar cells, renowned for their superior efficiency in converting sunlight to electricity, we applied advanced statistical models to a reference solar cell configured with predefined layer thicknesses. Our analysis revealed significant positive correlations between layer thickness and electrical performance, with correlation coefficients (R2 values) impressively ranging from 0.86 to 0.96 across different regions. This detailed statistical insight led to an improvement in overall cell efficiency to 44.2. A key innovation in our approach was replacing the traditional germanium (Ge) substrate with Copper Indium Gallium Selenide (CIGS), known for its adjustable bandgap and superior absorption of long-wavelength photons. This strategic modification not only broadened the absorption spectrum but also elevated the overall cell efficiency to 47%. Additionally, the optimization process involved simulations using predictive profilers and Silvaco Atlas tools, which systematically assessed various configurations for their spectral absorption and current–voltage characteristics, further enhancing the cell’s performance. These findings underscore the critical role of precise material engineering and sophisticated statistical analyses in advancing solar cell technology, setting new efficiency benchmarks, and driving further developments in the field.

Numerical simulation and structural optimization of the diffusion furnace for crystal silicon solar cells

The diffusion furnace is an important device for crystalline silicon solar cell production. Given the rapid evolution of solar cell technology, large-scale, high-efficiency and mass-produced diffusion furnaces are required by the market. This puts forward higher requirements for the diffusion furnaces. In this study, a large-scale 3D model is established and validated by measured data in practical diffusion furnace. Its internal temperature, velocity and gas concentration fields are analyzed. The silicon wafer temperatures are found to be high at the top but low at the bottom. The temperature uniformity at both ends of silicon wafer groups is poor. To solve these problems, three structural optimization methods, namely the inlet pipe optimization, adding uniform-flow plates and the quartz boat optimization, are proposed and analyzed. The average mass fraction in the diffusion furnace is improved by 6.311% using the two-tube forked intake pipe. The uniform flow plates with evenly distributed pores on the lower half effectively improve the gas concentration uniformity on silicon wafer surfaces. The optimized quartz boat can improve the temperature uniformity of silicon wafers, though its deformation slightly increases by 0.338%. The silicon wafer temperature differences after quartz boat optimization are 13.77–50.27% smaller than those before optimization, which are conducive to reducing the thermal stress, the risk of thermal damage and the failure during manufacture and utilization of silicon wafers. Results in this study give guidelines for design and utilization of crystal silicon solar cell diffusion furnaces, some of which have been successfully used in Trina Solar Energy Co., China.

Tailoring Diversified Peripheral Anchor Groups in Spirofluorene‐Dithiolane‐Based Hole Transporting Materials for Efficient Organic and Perovskite Solar Cells from First‐Principle

AbstractThis quantum mechanical approach recommends push–pull molecular engineering to fabricate hole‐transporting materials (HTMs) for photovoltaic cells. It integrates acceptor moieties via thiophene to fluorene core, resulting in five novel HTMs (SFD‐1 to SFD‐5). The results exhibit that derivative HTMs show excellent coherence in excitation, dispersion, and transportation of charge carriers, ensuring robust hole mobility. The anchor moieties functionalized HTMs unveil excellent band alignment with perovskite with fitting HOMO energy levels (−4.93–−5.35 eV), less optical absorption in visible portion ( < 520). This acceptor integration has improved the hole mobility in derivatives, accredited to the smaller hole reorganization energy (0.14–0.68 eV), and greater hole transfer integral (0.22–0.33 eV). The transition density matrix analysis exhibited robust electronic coupling, subtler charge carrier overlapping and greater charge transfer length (7.48–13.73 Å). This resulted in an excellent upsurge in intrinsic charge transference (70.75–92.70%) and smaller exciton binding energy, leading to easier exciton dissociation, and fewer recombination fatalities. However, an adequate variation in dipole moment (4.04 D to 16.34 D) and Gibbs solvation‐free energy (−18.06 to −21.89 kcal mol−1) ensures facile film formation and processability. In conclusion, this approach recommends these flourene‐based HTMs are highly desireable for forthcoming solar cell technology.

Bifacial perovskite/silicon heterojunction tandem solar cells based on FAPbI3-based perovskite via hybrid evaporation-spin coating

Combining the two technologies of tandem solar cells and bifacial solar cells has a great potential to maximize energy harvesting while minimizing material and surface usage. Mid-bandgap perovskites (1.50–1.60 eV) are important for fulfilling current matching in bifacial perovskite/silicon heterojunction tandem solar cells. Herein, efficient (>20 %) and stable planar FAPbI3-based perovskite (1.54 eV) solar cells have been fabricated via a hybrid evaporation-spin coating process. X-ray diffraction and electron microscopy data reveal the formation of highly crystalline (001) perovskite domains. The fabricated high-quality perovskite films lead to a more homogenized contact potential difference at the film surface and a reduction in non-radiative losses, resulting in a quasi-Fermi-level splitting (half-cell) of 1.16 eV, rendering 120 mV non-radiative losses. Transferring these films into tandem devices atop single-side textured silicon heterojunction bottom cells, we obtain an efficiency of >24 % under AM1.5 G illumination for monofacial devices with an active area of 1.21 cm2. Furthermore, the bifacial devices generate >27 mW cm−2 power output with 15 % rear illumination fraction.

Improving Perovskite Solar Cell Performance and Stability via Thermal Imprinting-Assisted Ion Exchange Passivation.

The latest development in perovskite solar cell (PSC) technology has been significantly influenced by advanced techniques aimed at passivating surface defects. This work presents a new approach called thermal imprinting-assisted ion exchange passivation (TIAIEP), which delivers a different approach to conventional solution-based methods. TIAIEP focuses on addressing surface imperfections in solid-state films by using a passivator that promotes ion exchange specifically at the defect sites within the perovskite layer. By adjusting the time and temperature of the TIAIEP process, we achieve substantial enhancement in the creation of a compositional gradient within the films. This optimization slows the cooling rate of hot carriers, leading to minimizing charge recombination and improving the device performance. Remarkably, devices treated with TIAIEP achieve a 22.29% power conversion efficiency and show outstanding stability, with unencapsulated PSCs maintaining 91% of their original efficiency after over 2000 h of storage and 90% efficiency after 1200 h of constant illumination. These results highlight TIAIEP's effectiveness in mitigating surface defects, improving both the photoelectric and stability performance of PSCs, and indicating significant potential for large-scale application in perovskite film passivation, promoting the widespread adoption of this technology.

Water-Based Recycling Process of FTO/SnO2 Substrate for Sustainable Perovskite Solar Cell Technology.

Fluorine-doped tin oxide (FTO) substrate is an important and expensive component in perovskite solar cells (PSCs), which accounts for up to 40% of a typical PSC raw material cost. In this study, we investigated the recyclability of SnO2/FTO in PSCs by washing the spent PSCs using different solvent such as dimethylformamide (DMF), dimethylsulfoxide (DMSO), acetone, water, and acetone/water mixture. Characterisation of properties of the SnO2/FTO substrates recovered from the PSCshow the surface wettability of SnO2/FTO is largely unchanged with water washing while a higher hydrophobicity is obtained with organic solvent washing. Comparison of electronic properties of the SnO2/FTO substrate shows a downward shift of the conduction band by 180 meV with water washing, creating favourable energy alignment with adjacent perovskite for efficient interfacial charge injection. Consequently, PSCs using the water-based recycled SnO2/FTO substrates produced a high power conversion efficiency (PCE) of 19.33% which is comparable to the device using fresh SnO2/FTO substrate (PCE = 19.85%). Furthermore, we demonstrated that the water washing process could retain property of SnO2/FTO substrate for decent PSC performance up to four recycling cycles. This study opens new avenues towards recycling of valuable FTO substrates in PSCs for increased sustainability and cost-effectiveness.

Zinc Oxide–Based Grätzel Cells Employing Anthocyanin Dye Sensitizers Emphasizing Environmental Sustainability

ABSTRACTThis research is centered on the investigation of a dye‐sensitized solar cell (DSSC) with a particular focus on the utilization of anthocyanin as a sensitizing agent, in conjunction with zinc oxide (ZnO) and lithium‐doped ZnO aggregates. A notable feature of this study is its emphasis on employing cost‐effective materials in the fabrication process, aligning with the quest for sustainable and economically viable solar cell technologies. This study explores a DSSC, specifically employing anthocyanin as a sensitizer, along with ZnO and lithium‐doped ZnO aggregates. The fabrication utilizes cost‐effective materials. The research delves into morphological studies of both ZnO and its doped counterpart. Fourier transform infrared spectra were recorded for both crude and purified dyes extracted from purple cabbage. The current density–voltage profile highlights superior power conversion efficiency in the DSSC using purified dye from purple cabbage sensitized with lithium‐doped ZnO semiconductor. Overall, these experimental findings underscore the potential of anthocyanin pigments for efficient energy conversion within the realm of renewable energy technologies. By employing low‐cost materials and thoroughly investigating the morphological and spectroscopic properties of the involved components, this research contributes to the ongoing efforts in advancing clean and sustainable solar cell technologies, thereby paving the achievement of environmental sustainability.

Photon shifting and trapping in perovskite solar cells for improved efficiency and stability

Advanced light management techniques can enhance the sunlight absorption of perovskite solar cells (PSCs). When located at the front, they may act as a UV barrier, which is paramount for protecting the perovskite layer against UV-enabled degradation. Although it was recently shown that photonic structures such as Escher-like patterns could approach the theoretical Lambertian-limit of light trapping, it remains challenging to also implement UV protection properties for these diffractive structures while maintaining broadband absorption gains. Here, we propose a checkerboard (CB) tile pattern with designated UV photon conversion capability. Through a combined optical and electrical modeling approach, this photonic structure can increase photocurrent and power conversion efficiency in ultrathin PSCs by 25.9% and 28.2%, respectively. We further introduce a luminescent down-shifting encapsulant that converts the UV irradiation into Visible photons matching the solar cell absorption spectrum. To this end, experimentally obtained absorption and emission profiles of state-of-the-art down-shifting materials (i.e., lanthanide-based organic-inorganic hybrids) are used to predict potential gains from harnessing the UV energy. We demonstrate that at least 94% of the impinging UV radiation can be effectively converted into the Visible spectral range. Photonic protection from high-energy photons contributes to the market deployment of perovskite solar cell technology, and may become crucial for Space applications under AM0 illumination. By combining light trapping with luminescent downshifting layers, this work unravels a potential photonic solution to overcome UV degradation in PSCs while circumventing optical losses in ultrathin cells, thus improving both performance and stability.

Combine Improvement for Dye-Sensitized Solar Cells

Dye Sensitized-Solar Cells (DSSC) represent a third-generation solar cell technology based on photoelectrochemical principles. This study explores the use of Clitoria ternatea (butterfly pea) extract as an organic dye for DSSCs, focusing on its ability to absorb sunlight effectively. Excitation of electrons triggered by light in photocatalysis is strongly influenced by the position of the band gap. To be effective as a photocatalyst, the material must have a conduction band with a high positive potential compared to the electron accepting potential. Doping metal oxides such as CuO, MgO, Fe2O3, and ZnO into TiO2 can change the band edge properties or surface states which can increase light absorption. This research presents the synthesis of TiO2 nanoparticles as photoanodes doped using metal oxides to evaluate characteristic that can influence DSSC performance. TiO2 nanoparticles doped with metal oxide were synthesized using the solvothermal method and characterized by XRD, SEM-EDX, FTIR, and UV-Vis. Comprehensive analysis of samples doped with metal oxides significantly affects the crystal structure, morphology, elemental composition, and optical properties of the material. The results showed that Cu-doped TiO2 samples allowed for the most significant performance improvement in DSSC, followed by Fe-doped TiO2, Mg-doped TiO2, and Zn-doped TiO2, with pure TiO2 having the lowest performance potential. These results provide important insights into material optimization to improve DSSC efficiency.

Exploring eco-friendly novel charge transport materials for enhanced performance of tin based perovskite solar cell

This pioneering simulation study explores the potential of perovskite materials, particularly the non-toxic methyl ammonium tin iodide (MASnI3), in solar cell technology. The investigation focuses on eco-friendly, solution-processed compounds—specifically, WO3 and In2S3 as Electron Transport Layers (ETL) and MoO3 and WSe2 as Hole Transport Layer (HTL)—to develop planar n-i-p MASnI3 perovskite solar cell (PSC) devices. WO3 is chosen for its solution processing and high electron mobility, while In2S3 offers n-type properties, superior carrier mobility, non-toxicity, and thermal durability. MoO3 and WSe2 are selected as HTLs for their efficient charge transport capabilities. Utilizing the solar cell capacitance simulator (SCAPS-1D) software, the study systematically evaluates alternative charge-selective materials, considering various parameters such as thickness (0.1 µm to 1.5 µm for absorber and 0.1 µm to 0.35 µm for CTLs), doping concentration (3.2E10 to 3.2E16 for absorber and E16 to E20 for CTLs), defect density, and energy band offset for MASnI3 PSCs. Four distinct n-i-p device structures are optimized, yielding impressive PCE improvements ranging from 14.63 % to 25.34 %, a significant 3 % enhancement compared to initial results. Notably, the WO3/MASnI3/WSe2 configuration exhibits limitations in electrical performance, while the other optimized structures demonstrate substantial efficiency gains. Further analysis investigates the impact of reflecting coatings (10 % to 90 %), varying contact work functions (5.2–5.8 eV), and temperature (300–400 K) on photovoltaic parameters. Critical factors including energy band offset, recombination current profile, and built-in potential, are meticulously examined, laying the groundwork for advanced PSC implementation. The study culminates in the In2S3/MASnI3/MoO3 device configuration, which achieves a peak efficiency of 25.34 %, showcasing superior thermal stability and an enhanced fill factor, thus propelling all-inorganic PSCs towards practical implementation.

Optimization of a novel lead-free MASiI3 based perovskite solar cell: A comprehensive study on device performance enhancement

Methylammonium Silicon Iodide (MASiI3), a novel perovskite material, has recently garnered significant attention for its potential to enhance the stability of solar cells. However, MASiI3-based perovskite solar cells (PSCs) have yet to achieve high performance. In this study, we utilized SCAPS-1D device modeling to investigate and optimize the performance of MASiI3-based PSCs, focusing on several key parameters. Our optimization efforts included the electron and hole transport layers (ETL and HTL), their respective thicknesses, doping densities (ND and NA), the TiO2/MASiI3 and MASiI3/Cu2O interface layers, series and shunt resistances, the metal back contact, and the influence of temperature. Through comparative analysis of various prospective materials, we identified TiO2 as the optimal ETL and Cu2O as the optimal HTL due to their superior band alignment. Our findings also highlighted the critical role of ambient temperature in maximizing power conversion efficiency (PCE). The proposed ETL and HTL materials demonstrated effective charge transport properties, contribute to enhanced device performance. Our optimized device achieved a Voc of 0.896 V, a Jsc of 42.47 mA/cm2, an FF of 76.94 %, and a remarkable PCE of 29.29 %. These results underscore the potential of MASiI3-based PSCs when utilizing TiO2 and Cu2O as charge-carrying materials and pave the way for further advancements in perovskite solar cell technology.