Bimetallic superalkali substitution in the CsPbBr₃ perovskite: Pseudocubic phases and tunable bandgap

Perovskites attract attention as efficient light absorbers for solar cells due to their high-power conversion efficiency (up to 24%). The high photoelectric conversion efficiency is greatly affected by a suitable band structure. Cation substitution can be an effective approach to tune the electronic band structure of lead halide perovskites. In this work, superalkali cations were introduced to replace the Cs⁺ cation in the CsPbBr₃ material. The bimetallic superalkalis (LiMg, NaMg, LiCa, and NaCa) were inserted since they are structurally simple systems and have a strong tendency to lose one electron to achieve a closed-shell cation. The cation substitution in the lead halide perovskite leads to changes in the shape of both valence and conduction bands compared to CsPbBr₃. Introducing superalkali cations produces extra electronic states close to the Fermi level, which arise from the formation of alkali earth metal states at the top of the valence band. Our first-principles computations reveal that bimetallic superalkali substitution decreases the bandgap of the perovskite. The bandgaps of MgLi-PbBr₃ (1.35 eV) and MgNa-PbBr₃ (1.06 eV) are lower than the bandgap of CsPbBr₃ (2.48 eV) and within the optimal bandgap (i.e., 1.1-1.4 eV) for single-junction solar cells. Thus, the MgLi-PbBr₃ and MgNa-PbBr₃ inorganic perovskites are promising candidates for high-efficiency solar cells.