Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV22)
DOI: https://doi.org/10.29363/nanoge.hopv.2022.192
Publication date: 20th April 2022
The long-term stability of perovskite solar cells is jeopardized by its sensitiveness to humidity even though technological encapsulation offers a first barrier to shield moisture-induced degradation. Different degradation pathways are activated depending on the perovskite composition for which ex situ characterization techniques provide a comparative view of the degradation before and after a certain ageing time.1 Herein, we exploit the latest advances in in situ X-ray diffraction, real-time electron imaging and liquid-cell transmission electron microscopy to reveal, in live, from early stage to the degradation propagation of triple cation Cs0.05(MA0.17FA0.83)0.95Pb(Br0.17I0.83)3 (CsMAFA) perovskite leading to phase segregation and decomposition.2-3 We reveal two competitive degradation paths leading on one hand to the decomposition of CsMAFA into PbI2 through a dissolution/recrystallization mechanism and on the other hand, to a non-equilibrium phase segregation leading to CsPb2Br5 and a cesium-poor/iodide-rich Cs0.05-x(MA0.17FA0.83)0.95Pb(Br0.17-2yI0.83+2y)3 perovskite. As a consequence of the dissolution/recrystallization mechanism under 85% R.H., such exposure leads to a film containing important heterogeneities in terms of morphology, photoluminescence (PL) intensities and lifetimes. The structural, morphological and chemical changes will be discussed in this communication based on operando liquid-cell TEM combined to SAED analysis and 4D-STEM-ASTAR investigations.