Enhanced Charge Transport in A-site Ordered Perovskite Derivatives A2A'Bi2I9 (A = Cs; A'= Ag, Cu): A First-Principles Study

Recent experiments have synthesized Cs2AgBi2I9 by partially substituting Cs+ with Ag+ at the A-site of Cs3Bi2I9, resulting in enhanced charge transport properties compared to Cs3Bi2I9. However, the atomic-scale mechanisms behind this enhancement remain unclear. In this work, we investigate the carrier transport mechanisms in Cs2A'Bi2I9 (A' = Ag, Cu) using first-principles calculations and Boltzmann transport calculations. Our results reveal that A-site ordered Cs2A'Bi2I9 exhibits carrier mobilities that are 3-4 times higher than those of Cs3Bi2I9 within the 100-500 K temperature range. We identify polar phonon scattering as the dominant mechanism limiting mobility. Furthermore, the enhanced out-of-plane carrier mobility in Cs2A'Bi2I9, particularly between 100 and 200K, leads to reduced mobility anisotropy. These improvements are mainly due to the shorter A'-I bond lengths and increased Ag+/Cu+ s-I p orbital coupling. Notably, substitution with Cu+ results in a further reduction in the band gap and enhanced hole mobility compared to Ag+ substitution in Cs3Bi2I9. Further analysis reveals that the significant increase in carrier mobility in Cs2A'Bi2I9 can be largely explained by the smaller carrier effective masses (m*) and weaker Fr"ohlich coupling strengths ({\alpha}), resulting in a lower polar mass {\alpha}(m*/me), compared to Cs3Bi2I9. Our study provides valuable insights into the transport properties of Bi-based perovskite derivatives, paving the way for their future applications in optoelectronic devices.