Unraveling the Influence of Solvent on Side Reactions between Formamidinium Lead Triiodide and Methylammonium Cations

Abstract

Formamidinium lead triiodide (FAPbI₃) perovskite thin films are commonly deposited through a solution process, often incorporating a specific amount of methylammonium halide to stabilize the α-phase or enhance their crystallinity. The precursor solution for such coatings significantly influences the fabrication of perovskite solar cells (PSCs), involving time-dependent aging and byproduct formation. The chemical principle underlying this behavior is believed to be related to the deprotonation of methylamine cations (MA⁺) and subsequent chemical reactions with FA⁺ to generate <i>N</i>-methylformamidinium. Nevertheless, the role of the solvent in the side reactions between these organic cations remains unclear. This work systematically investigates the reaction reactivity in three protic solvents and three aprotic solvents. We uncover the hidden role of dimethylamine from the hydrolysis products of <i>N</i>,<i>N</i>-dimethylformamide, promoting the reaction between FA⁺ and MA⁺. Additionally, we elucidate the impact of environmental factors, such as water and oxygen, in stabilizing precursor solutions. This work establishes a basic concept and scientific direction for rationalizing high-efficiency, reproducible, and long-term-stable PSCs.