Nanoscale Studies at the Early Stage of Water-Induced Degradation of CH3NH3PbI3 Perovskite Films Used for Photovoltaic Applications

Understanding the surface properties of hybrid perovskite materials is a key aspect to improve not only the interface properties in photovoltaic cells but also the stability against moisture degradation. In this work, we study the local electronic properties of two series of CH3NH3PbI3 perovskite films by atomic force microscopy-based methods. We correlate nanoscale features such as the local surface potential (as measured by Kelvin probe force microscopy) to the current response (as measured by conductive atomic force microscopy). CH3NH3PbI3 perovskites made using lead acetate as a precursor result in films with high purity and crystallinity and also result in heterogeneous local electrical properties, attributed to variations in the density of surface states. In contrast, when using lead iodide as a precursor, the perovskite surface exhibits a uniform distribution of surface states. This work also aims to understand the early stages of water-induced degradation at the surface of those films. Through high-precision exposure to small amounts of water vapor, we observe a higher stability for surfaces prepared with lead iodide precursors. More importantly, each precursor-based fabrication route is associated with either n- or p-type behavior of the films. These characteristics are determined by the type of surface states, which also and eventually preside over stability. This work should help discriminate between perovskite synthesis routes and improve their stability in photovoltaic cell applications.