How Do A-Site Cations Regulate Trap States at Defective Surfaces of Lead Iodide Perovskites?

The defect properties at surfaces or grain boundaries of metal halide perovskites are largely unexplored due to the complexity of surface structures stirred by the rotational A-site cations with varied dipole moments. Using a combination of density functional theory (DFT) and time-dependent DFT methods, we study the nature of iodine vacancies at the surfaces of lead iodide perovskites (APbI3) with A-site cations including methylammonium (MA = CH3NH3+), formamidinium, and cesium. It is found that the light-induced charge distributions are sensitively dependent on MA orientation at the MAI-terminated surfaces with vacancies at the apical position while the electronic excitation is marginally affected by A-site species at both the AI- and PbI-terminated surfaces with vacancies at the equatorial site. Such variations of electronic excitation are rationalized by analyzing the electrostatic interactions between the A-site cations and charged defects as well as the projected p orbitals of Pb atoms at the bottom of the conduction band.