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      Designing Modules to Prevent Reverse Bias Degradation in Perovskite Solar Cells when Partial Shading Occurs

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          Intrinsic Thermal Instability of Methylammonium Lead Trihalide Perovskite

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            Not All That Glitters Is Gold: Metal-Migration-Induced Degradation in Perovskite Solar Cells

            Perovskite solar cells (PSCs) have now achieved efficiencies in excess of 22%, but very little is known about their long-term stability under thermal stress. So far, stability reports have hinted at the importance of substituting the organic components, but little attention has been given to the metal contact. We investigated the stability of state-of-the-art PSCs with efficiencies exceeding 20%. Remarkably, we found that exposing PSCs to a temperature of 70 °C is enough to induce gold migration through the hole-transporting layer (HTL), spiro-MeOTAD, and into the perovskite material, which in turn severely affects the device performance metrics under working conditions. Importantly, we found that the main cause of irreversible degradation is not due to decomposition of the organic and hybrid perovskite layers. By introducing a Cr metal interlayer between the HTL and gold electrode, high-temperature-induced irreversible long-term losses are avoided. This key finding is essential in the quest for achieving high efficiency, long-term stable PSCs which, in order to be commercially viable, need to withstand hard thermal stress tests.
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              Fast oxygen diffusion and iodide defects mediate oxygen-induced degradation of perovskite solar cells

              Methylammonium lead halide perovskites are attracting intense interest as promising materials for next-generation solar cells, but serious issues related to long-term stability need to be addressed. Perovskite films based on CH3NH3PbI3 undergo rapid degradation when exposed to oxygen and light. Here, we report mechanistic insights into this oxygen-induced photodegradation from a range of experimental and computational techniques. We find fast oxygen diffusion into CH3NH3PbI3 films is accompanied by photo-induced formation of highly reactive superoxide species. Perovskite films composed of small crystallites show higher yields of superoxide and lower stability. Ab initio simulations indicate that iodide vacancies are the preferred sites in mediating the photo-induced formation of superoxide species from oxygen. Thin-film passivation with iodide salts is shown to enhance film and device stability. The understanding of degradation phenomena gained from this study is important for the future design and optimization of stable perovskite solar cells.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Solar RRL
                Sol. RRL
                Wiley
                2367-198X
                2367-198X
                May 13 2021
                : 2100239
                Affiliations
                [1 ]Department of Applied Physics Stanford University Stanford CA 94305 USA
                [2 ]National Renewable Energy Laboratory Golden CO 80401 USA
                [3 ]Materials Science and Engineering University of Colorado Boulder CO 80309 USA
                [4 ]Department of Chemical and Biological Engineering University of Colorado Boulder CO 80309 USA
                Article
                10.1002/solr.202100239
                f70014bb-ef9f-4688-96db-de971c0aefe3
                © 2021

                http://onlinelibrary.wiley.com/termsAndConditions#am

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                http://doi.wiley.com/10.1002/tdm_license_1.1

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