Molecular-Level Insight Into Correlation Between Surface Defects And Stability Of Methylammonium Lead Halide Perovskite Under Controlled Humidity

Perovskite-based photovoltaics (PVs) have garnered tremendous interest, enabling power conversion efficiencies exceeding 25%. Although much of this success is credited to the exploration of new compositions, defects passivation and process optimization, environmental stability remains an important bottleneck to be solved. The underlying mechanisms of thermal and humidity-induced degradation are still far from a clear understanding, which poses a severe limitation to overcome the stability issues. Herein, in situ X-ray diffraction (XRD), in operando liquid-cell transmission electron microscopy (TEM) and ex situ solid-state (ss)NMR spectroscopy are combined with time-resolved spectroscopies to reveal new insights about the degradation mechanisms of methylammonium lead halide (MAPbI(3)) under 85% relative humidity (RH) at different length scales. Liquid-cell TEM enables the live visualizations from meso-to-nanoscale transformation between the perovskite particles and water molecules, which are corroborated by the changes in local structures at sub-nanometer distances by ssNMR and longer range by XRD. This work clarifies the role of surface defects and the significance of their passivation to prevent hydration and decomposition reactions.