Evaluating the performance of Cs(2)PtI(6)(−)(x)Br(x) for photovoltaic and photocatalytic applications using first-principles study and SCAPS-1D simulation

All inorganic free-lead halide double perovskites are attractive materials in solar energy harvesting applications. In this study, density functional theory calculations have been used to predict the structures, band structures, and density of states of Cs(2)PtI(6)(−)(x)Br(x) with (x = 0, 2, 4, and 6). The optical properties (reflectivity, refractive index, absorption, dielectric function, conductivity, and loss function) of these materials have been predicted and discussed. The band edges calculations showed that the Cs(2)PtI(6)(−)(x)Br(x) may be an efficient visible-light photocatalyst for water splitting and CO(2) reduction. The calculated bandgap value of Cs(2)PtI(6) exhibited a great match with the reported experimental values. It has been seen that increasing the doping content of Br(−) in Cs(2)PtI(6)(−)(x)Br(x) (x = 0, 2, 4, and 6) increases the bandgaps from 1.4 eV to 2.6 eV and can be applied in single junction and tandem solar cells. Using Solar Cell Capacitance Simulator (SCAPS), a 1D device modelling has been performed on Cs(2)PtI(6) inorganic lead-free solar cells. For the fully inorganic device, the effect of replacing organic hole transport materials (HTL) and electron transport materials (ETL) with inorganic ones is investigated while keeping high efficiencies and stabilities of solar cell devices. From the obtained results, it was found that WS(2) as ETL and Cu(2)O as HTL were the most suitable materials compared to the others. Further investigation studies are performed on the effect of changing metal back contact work function, absorber layer thickness, doping density, and defect density on the power conversion efficiency (PCE) of the solar cell. The optimized suggested structure (FTO/WS(2)/Cs(2)PtI(6)/Cu(2)O/Carbon) obtained a PCE of 17.2% under AM1.5 solar illumination.