Hidalgo, J.; Kaiser, W.; An, Y.; Li, R.; Oh, Z.; Castro-Méndez, A.-F.; LaFollette, D.K.; Kim, S.; Lai, B.; Breternitz, J.; Schorr, S.; Perini, C.A.R.; Mosconi, E.; De Angelis, F.; Correa-Baena, J.-P.: Synergistic Role of Water and Oxygen Leads to Degradation in Formamidinium-Based Halide Perovskites. Journal of the American Chemical Society 145 (2023), p. 24549–24557
10.1021/jacs.3c05657
Open Access Version
Abstract:
Mixed-cation metal halide perovskites have shown remarkable progress in photovoltaic applications with high power conversion efficiencies. However, to achieve large-scale deployment of this technology, efficiencies must be complemented by long-term durability. The latter is limited by external factors, such as exposure to humidity and air, which lead to the rapid degradation of the perovskite materials and devices. In this work, we study the mechanisms causing Cs and formamidinium (FA)-based halide perovskite phase transformations and stabilization during moisture and air exposure. We use in situ X-ray scattering, X-ray photoelectron spectroscopy, and first-principles calculations to study these chemical interactions and their effects on structure. We unravel a surface reaction pathway involving the dissolution of FAI by water and iodide oxidation by oxygen, driving the Cs/FA ratio into thermodynamically unstable regions, leading to undesirable phase transformations. This work demonstrates the interplay of bulk phase transformations with surface chemical reactions, providing a detailed understanding of the degradation mechanism and strategies for designing durable and efficient perovskite materials.