Impact of A‐Site Cation Modification on Charge Transport Properties of Lead Halide Perovskite for Photovoltaics Applications

Perovskite solar cells (PSCs) have reached a formidable power conversion efficiency of 25.7% over the years of development. One of the strategies that has been responsible for the development of stable and highly efficient PSCs is modifications of the monovalent A‐site cations (methylammonium, MA; formamidinium, FA; cesium, Cs, etc.) in lead halide perovskites. Herein, the impact of modifying the monovalent cation (MA, FAMA, CsFAMA, potassium‐passivated CsFAMA, rubidium‐passivated CsFAMA) in lead halide perovskite on their optoelectronic, charge transport, and photovoltaic behavior is systematically studied. Reduced trap density and improved charge carrier mobility after introduction of FA and Cs in the MAPb(I 0.85 Br 0.15 ) 3 system are confirmed. Further passivation of the triple‐cation perovskite with K and Rb enhances the optoelectronic characteristics, charge transport, and charge extraction efficiency in halide perovskite solar cells.