Vacuum-deposited lead halide perovskite thin films enable solvent-free fabrication, eliminating residual processing solvents that might compromise the long-term stability. Here, we investigate the stability of thermally evaporated mixed-cation compositions FA0.8Cs0.2PbI3 and FA0.8MA0.2PbI3 (FA+ = formamidinium and MA+ = methylammonium) under thermal and light stress. Although from a thermodynamic perspective the phase stability hierarchy is typically described as MA+ < FA+ < Cs+, with Cs-based perovskites expected to be the most stable, both compositions exhibit thermal robustness, retaining their structural, optical, and morphological properties after continuous heating at 85 °C for over 500 h. Under continuous illumination, however, distinct degradation pathways emerge: FA0.8Cs0.2PbI3 shows the largest morphological and optical changes. This is attributed to chemical inhomogeneities caused by CsI-rich segregations during crystallization, which make point defects effective triggers for photodegradation. Film homogeneity improves by partially replacing iodide with bromide. Based on these results, we selected FA0.8MA0.2PbI3 and FA0.8Cs0.2Pb(I0.8Br0.2)3 for device fabrication and evaluated their operational stability. The resulting perovskite solar cells maintain their performance after four months of outdoor operation and withstand 900 h under continuous sun-equivalent indoor illumination at room temperature. These results demonstrate how a high-quality crystallization process can reveal the potential of MA-containing perovskite formulations for long-lived perovskite photovoltaics.
Poli et al. (Tue,) studied this question.
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