钙钛矿(结构)
带隙
材料科学
结晶
能量转换效率
串联
开路电压
溴
卤化物
太阳能电池
伏特
化学工程
光电子学
电压
化学
无机化学
电气工程
复合材料
冶金
工程类
作者
Qi Jiang,Jinhui Tong,Rebecca A. Scheidt,Xiaoming Wang,Amy E. Louks,Yeming Xian,Robert Tirawat,Axel F. Palmstrom,Matthew P. Hautzinger,Steven P. Harvey,Steve Johnston,Laura T. Schelhas,Bryon W. Larson,Emily L. Warren,Matthew C. Beard,Joseph J. Berry,Yanfa Yan,Kai Zhu
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-12-22
卷期号:378 (6626): 1295-1300
被引量:157
标识
DOI:10.1126/science.adf0194
摘要
The development of highly stable and efficient wide-bandgap (WBG) perovskite solar cells (PSCs) based on bromine-iodine (Br-I) mixed-halide perovskite (with Br greater than 20%) is critical to create tandem solar cells. However, issues with Br-I phase segregation under solar cell operational conditions (such as light and heat) limit the device voltage and operational stability. This challenge is often exacerbated by the ready defect formation associated with the rapid crystallization of Br-rich perovskite chemistry with antisolvent processes. We combined the rapid Br crystallization with a gentle gas-quench method to prepare highly textured columnar 1.75-electron volt Br-I mixed WBG perovskite films with reduced defect density. With this approach, we obtained 1.75-electron volt WBG PSCs with greater than 20% power conversion efficiency, approximately 1.33-volt open-circuit voltage (Voc), and excellent operational stability (less than 5% degradation over 1100 hours of operation under 1.2 sun at 65°C). When further integrated with 1.25-electron volt narrow-bandgap PSC, we obtained a 27.1% efficient, all-perovskite, two-terminal tandem device with a high Voc of 2.2 volts.
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