Formamidinium and Cesium Hybridization for Photo- and Moisture-Stable Perovskite Solar Cell

被引:1386
作者
Lee, Jin-Wook
Kim, Deok-Hwan
Kim, Hui-Seon
Seo, Seung-Woo
Cho, Sung Min
Park, Nam-Gyu [1 ]
机构
[1] Sungkyunkwan Univ SKKU, Sch Chem Engn, Suwon 440746, South Korea
基金
新加坡国家研究基金会;
关键词
cesium; formamidinium; mixed cations; perovskite solar cells; stabilities; HIGH-PERFORMANCE; NANOCRYSTALLINE TIO2; EFFICIENCY; PHASE; STABILITY; TRIHALIDE; LENGTHS; LAYER; SIZE;
D O I
10.1002/aenm.201501310
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Although power conversion efficiency (PCE) of state-of-the-art perovskite solar cells has already exceeded 20%, photo- and/or moisture instability of organolead halide perovskite have prevented further commercialization. In particular, the underlying weak interaction of organic cations with surrounding iodides due to eight equivalent orientations of the organic cation along the body diagonals in unit cell and chemically non-inertness of organic cation result in photo- and moisture instability of organometal halide perovskite. Here, a perovskite light absorber incorporating organic-inorganic hybrid cation in the A-site of 3D APbI(3) structure with enhanced photo- and moisture stability is reported. A partial substitution of Cs+ for HC(NH2)(2)(+) in HC(NH2)(2)PbI3 perovskite is found to substantially improve photo- and moisture stability along with photovoltaic performance. When 10% of HC(NH2)(2)(+) is replaced by Cs+, photo- and moisture stability of perovskite film are significantly improved, which is attributed to the enhanced interaction between HC(NH2)(2)(+) and iodide due to contraction of cubo-octahedral volume. Moreover, trap density is reduced by one order of magnitude upon incorporation of Cs+, which is responsible for the increased open-circuit voltage and fill factor, eventually leading to enhancement of average PCE from 14.9% to 16.5%.
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页数:9
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