Abstract
Over the past few years, metal halide perovskite solar cells have made significant advances. Currently, the single-junction perovskite solar cells reach a conversion efficiency of 25.7%. Perovskite solar cells with a wide band gap can also be used as top absorber layers in multi-junction tandem solar cells. We examined the dynamical and thermal stability, electronic structure, and optical features of In2PtX6 (X = Cl, Br, and I) perovskites, utilizing first-principle calculations. The stability is predicted using phonon dispersion spectrum and ab initio molecular dynamics simulation and also through the convex hull approach. The lattice constants and the optimized volume show an increasing trend with changing halide ions. The band structures computed for In2PtCl6, In2PtBr6, and In2PtI6 indicate their semiconducting nature with band gap values of 2.06, 2.01, and 1.35 eV, respectively. Halogens p and Pt d orbitals, respectively, play a prominent role in the formation of states around valence band maximum and conduction band minimum. The compounds, namely, In2PtBr6 and In2PtI6, exhibit high dielectric constants and small carrier effective masses. Furthermore, we found that In2PtI6 reveals a maximum theoretical efficiency owing to its optimum band gap and high optical absorption and is comparable to MAPbI(3) in the studied range. Our results suggest that In2PtX6 (X = Cl, Br, and I) are suitable materials for single-junction and top absorber layers in tandem solar cells.