This study explores the influence of central metals and halide anions on the structural, electronic, and optical properties of LiBX3 perovskites (B = Ge, Sn, Pb, X = F, Cl, Br, I) in both unit cell and supercell configurations, aiming for potential applications in photovoltaic devices. Density functional theory calculations reveal that increasing the atomic radius of halogens and central metals directly affects the lattice parameters. Our research indicates that Ge and Sn-based perovskites (except for unit cell LiSnF3) exhibit semiconductor properties with direct band gap energies, while Pb-based perovskites in the unit cell configuration display an indirect band gap. Key factors contributing to the reduction of the band gap energy in most materials include the expansion of the atomic radius of halogens and the examination of perovskites in their supercell state, such that perovskites like LiGeI3, LiSnI3, and LiPbI3 represent a band gap value of 0.001 eV in their supercell configuration. Furthermore, the light absorption characteristics of these perovskites demonstrate a high absorption coefficient ranging from 105 to 106. Among the studied compounds, I-based perovskites exhibit the highest static dielectric constant, surpassing other perovskite variants, with for example, unit cell and supercell of LiSnI3 having static dielectric constant values of 38 and 70, respectively. Additionally, the investigation of perovskites in their supercell form suggests that the number of atoms in the network does not significantly impact their optical properties. In conclusion, based on various analyses, I-based perovskites are proposed as ideal candidates for application in Photovoltaic Solar Cells (PSCs).

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