铋
钙钛矿(结构)
光伏系统
相(物质)
材料科学
无机化学
化学工程
化学
光电子学
纳米技术
冶金
有机化学
工程类
生态学
生物
作者
Yanqiang Hu,Fan Bai,Xinbang Liu,Qingmin Ji,Xiaoliang Miao,Ting Qiu,Shufang Zhang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2017-08-31
卷期号:2 (10): 2219-2227
被引量:522
标识
DOI:10.1021/acsenergylett.7b00508
摘要
All-inorganic CsPbI3 perovskite is emerging to be an alternative light-harvesting material in solar cells owing to the enhanced stability and comparable photovoltaic performance compared to organic–inorganic hybrid perovskites. However, the desirable black phase α-CsPbI3 is not stable at room temperature and degrades rapidly to a nonperovskite yellow phase δ-CsPbI3. Herein, we introduce a compositional engineering approach via incorporating Bi3+ in CsPbI3 to stabilize the α-phase at room temperature. Fully inorganic solar cells based on the Bi-incorporated α-CsPb1–xBixI3 compounds demonstrate a high PCE of 13.21% at an optimal condition (incorporation of 4 mol % Bi3+) and maintain 68% of the initial PCE for 168 h under ambient conditions without encapsulation. This is the first attempt of partial substitution of the "B"-site of the perovskite to stabilize the α-CsPbI3, which paves the way for further developments of such perovskites and other optoelectronic devices.
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