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y High specific power, high stowed packing efficiency, low processing cost, and high tolerance against environmental threats (high energy and charged particle radiation) make perovskite solar cell (PSC) a promising candidate for power generation in space. However, vacuum, as encountered in space, causes perovskite outgassing, raising concern for its long-term stability. In this work, we find that PSCs (ITO/SnO2/perovskite/Spiro-MeOTAD/Au) degrade ten times faster upon reducing the pressure from 9 x 10(4) to 5 x 10(3) Pa during operation, due to acceleration of the perovskite transformation and ion migration. Gas permeability of the layers atop perovskite and mobile ion-induced chemical reactions at charge transporting layers and related interfaces are two critical factors. We develop a PSC structure (ITO/PTAA/perovskite/PCBM/ZnO/AZO/[Ni/Al grid]) that effectively mitigates vacuum and illumination-induced degradation pathways, enabling PSCs to realize a low PCE loss rate of 0.007%/h over 1,037 h at the maximum power point under 100 mW cm(-2) illumination at 5 x 10(3) Pa.
Mohammad Khaja Nazeeruddin, Jianxing Xia, Muhammad Sohail
Michael Graetzel, Shaik Mohammed Zakeeruddin, Felix Thomas Eickemeyer, Yuhang Liu, Ulf Anders Hagfeldt, Mohammad Ibrahim Dar, Hong Zhang, Jiahuan Zhang, Jiyoun Seo, Seckin Akin, Hongwei Zhu