The ambient stability of ambient-processed lead-free perovskite absorbers remains a critical challenge toward scalable, eco-friendly photovoltaics. Herein, we systematically investigate the time-dependent structural and morphological evolution of drop-cast ambient-processed Cs3Sb2I9 thin films, being a potential non-toxic and stable solar absorber candidate (energy bandgap ~2 eV) for solar cells, stored under uncontrolled ambient condition (~60% Relative humidity) for 28 days. Sequential X-ray diffraction (XRD) and surface morphology analyses using scanning electron microscope (SEM) reveal that the films preserve their trigonal P3̅m1 phase throughout aging, confirming phase stability. Moderate moisture exposure may induce partial recrystallization and subtle structural reorganization, possibly including minor c-axis realignment, leading to reduced lattice strain and improved crystallite coherence. Even after prolonged aging, no secondary phases or micro-cracks are detected, underscoring the slow degradation kinetics and robust Sb–I bonding that stabilize the layered Sb2I93− dimers. The late-stage increase in diffraction intensity and partial recovery of crystallographic parameters could indicate transient structural reorganization, potentially associated with moisture-mediated reordering within an overall degradation pathway. These observations suggest some degree of morphological persistence and structural tolerance of Cs3Sb2I9 under ambient conditions, rather than complete stability. This behavior offers useful insights into ambient processing and the long-term reliability of lead-free perovskite photovoltaics.
Barua et al. (Fri,) studied this question.