卤化物
串联
钙钛矿(结构)
带隙
甲脒
材料科学
光电子学
相(物质)
铯
磁滞
化学
无机化学
结晶学
凝聚态物理
物理
复合材料
有机化学
作者
Kevin A. Bush,Kyle Frohna,Rohit Prasanna,Rachel E. Beal,Tomas Leijtens,Simon A. Swifter,Michael D. McGehee
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2018-01-19
卷期号:3 (2): 428-435
被引量:374
标识
DOI:10.1021/acsenergylett.7b01255
摘要
Metal halide perovskites are attractive candidates for the wide band gap absorber in tandem solar cells. While their band gap can be tuned by partial halide substitution, mixed halide perovskites often have lower open-circuit voltage than would be expected and experience photoinduced trap formation caused by halide segregation. We investigate solar cell performance and photostability across a compositional space of formamidinium (FA) and cesium (Cs) at the A-site at various halide compositions and show that using more Cs at the A-site rather than more Br at the X-site to raise band gap is more ideal as it improves both VOC and photostability. We develop band gap maps and design criteria for the selection of perovskite compositions within the CsxFA1–xPb(BryI1–y)3, space. With this, we identify perovskites with tandem-relevant band gaps of 1.68 and 1.75 eV that demonstrate high device efficiencies of 17.4 and 16.3%, respectively, and significantly improved photostability compared to that of the higher Br-containing compositions.
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