材料科学
光电流
串联
能量转换效率
兴奋剂
开路电压
钙钛矿(结构)
离子
带隙
分析化学(期刊)
光电子学
钙钛矿太阳能电池
载流子
电压
结晶学
有机化学
化学
电气工程
复合材料
工程类
作者
Huan Zhao,Yu Han,Zhuo Xu,Chenyang Duan,Shaomin Yang,Shihao Yuan,Zhou Yang,Zhike Liu,Shengzhong Liu
标识
DOI:10.1002/aenm.201902279
摘要
Abstract The Cs‐based inorganic perovskite solar cells (PSCs), such as CsPbI 2 Br, have made a striking breakthrough with power conversion efficiency (PCE) over 16% and potential to be used as top cells for tandem devices. Herein, I − is partially replaced with the acetate anion (Ac − ) in the CsPbI 2 Br framework, producing multiple benefits. The Ac − doping can change the morphology, electronic properties, and band structure of the host CsPbI 2 Br film. The obtained CsPbI 2− x Br(Ac) x perovskite films present lower trap densities, longer carrier lifetimes, and fast charge transportation compared to the host CsPbI 2 Br films. Interestingly, the CsPbI 2− x Br(Ac) x PSCs exhibit a maximum PCE of 15.56% and an ultrahigh open circuit voltage ( V oc ) of 1.30 V without sacrificing photocurrent. Notably, such a remarkable V oc is among the highest values of the previously reported CsPbI 2 Br PSCs, while the PCE far exceeds all of them. In addition, the obtained CsPbI 2− x Br(Ac) x PSCs exhibit high reproducibility and good stability. The stable CsPbI 2− x Br(Ac) x PSCs with high V oc and PCE are desirable for tandem solar cell applications.
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