Direct observation of cation-exchange in liquid-to-solid phase transformation in FA1−xMAxPbI3 based perovskite solar cells

Abstract

Mixed-organic-cation FA_1−xMA_xPbI₃ perovskites are currently attracting intensive attention for their high photovoltaic performance. However, FA_1−xMA_xPbI₃ usually has an undesired non-perovskite phase leading to a compromised efficiency, and a facile strategy to achieve pure-phase FA_1−xMA_xPbI₃ has been rarely reported. Here, we demonstrate a facile approach to form δ-phase free FA_1−xMA_xPbI₃ using a non-stoichiometric precursor solution. It is found that a small amount of excess methylammonium iodide (MAI) added to the precursor solution has a profound effect on perovskite crystallization during the liquid-to-solid phase transformation. Using an in situ photoluminescence spectroscopy measurement, it is found that the excess MAI can promote the formation of FA_1−xMA_xPbI₃ and facilitate the cation-exchange between organic FA⁺ and MA⁺ during the film formation. Based on the optimized pure-phase FA_1−xMA_xPbI₃, the perovskite solar cells exhibit an encouraging power conversion efficiency (PCE) of 17.40%. This study demonstrates a facile method to achieve high performance FA dominating mixed-organic-cation perovskite devices while providing insight into the ion-exchange process during perovskite crystallization.