Direct observation of cation-exchange in liquid-to-solid phase transformation in FA(1-x)MA(x)PbI(3) based perovskite solar cells

Mixed-organic-cation FA(1-x)MA(x)PbI(3) perovskites are currently attracting intensive attention for their high photovoltaic performance. However, FA(1-x)MA(x)PbI(3) usually has an undesired non-perovskite phase leading to a compromised efficiency, and a facile strategy to achieve pure-phase FA(1-x)MA(x)PbI(3) has been rarely reported. Here, we demonstrate a facile approach to form delta-phase free FA(1-x)MA(x)PbI(3) 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-x)MA(x)PbI(3) and facilitate the cation-exchange between organic FA(+) and MA(+) during the film formation. Based on the optimized pure-phase FA(1-x)MA(x)PbI(3), 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.