Abstract
Hybrid organic-inorganic perovskites such as MAPbI3 hold great promise for photovoltaic applications with power conversion efficiencies already exceeding 26 %. Despite the unprecedented advantages of these materials in photovoltaics and optoelectronics they exhibit a range of complex phenomena under light illumination that remain poorly understood. Here we use a combination of photoluminescence (PL) spectroscopy, cathodoluminescence imaging and theoretical calculations to correlate PL fluctuations in MAPbI3 thin films with changes in the spatial distribution and concentration of native defects. We demonstrate that short-term illumination results in a more homogeneous distribution of emitting and quenching sites, whereas prolonged illumination causes PL quenching. Our findings support the conclusion that the photo-induced transformation of MAPbI3 can be explained within a bistable amphoteric native defect model, wherein a neutral native defect can undergo a transition between a donor-like and acceptor-like configuration.
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