钝化
材料科学
卤化物
光电子学
载流子寿命
能量转换效率
无机化学
图层(电子)
钙钛矿(结构)
纳米技术
化学工程
化学
硅
工程类
作者
Dingjian Zhou,Jincheng Huang,Jun Liu,Huibo Yan,Jianfeng Zhang,Meng Zhang,Guangxing Liang,Lei Lü,Xiuwen Zhang,Ping Xu,Hoi Sing Kwok,Guijun Li
出处
期刊:Solar RRL
[Wiley]
日期:2021-03-25
卷期号:5 (5)
被引量:23
标识
DOI:10.1002/solr.202100112
摘要
Inorganic metal halide perovskite solar cells have achieved incredible progress in recent years. However, the power conversion efficiency of the inorganic perovskite solar cells is still low compared with their hybrid counterparts due to the inescapable nonradiative losses from the charge recombination. Herein, a strategy is demonstrated to minimize the nonradiative recombination loss in CsPbI 2 Br solar cells by establishing a synergetic passivation from the mutual effect of alkali‐ and alkylammonium‐salt. Accordingly, a sequential passivation process employing KBr and phenethylammonium chloride overcomes their limited passivation effect in one single step. This dual passivation is beneficial to an improved CsPbI 2 Br film with reduced trap defects, enlarged grain size, as well as to form an ultrathin low‐dimensional perovskite surface layer. As a result, a very high power conversion efficiency of 16.9% is obtained for inorganic CsPbI 2 Br solar cells. The proposed dual passivation scheme provides a feasible route not only for the design of high‐efficiency perovskite solar cells but also for other perovskite‐related optoelectronic devices.
科研通智能强力驱动
Strongly Powered by AbleSci AI