钝化
成核
钙钛矿(结构)
结晶
材料科学
载流子寿命
微晶
甲脒
化学工程
能量转换效率
钙钛矿太阳能电池
光电子学
纳米技术
化学
硅
冶金
有机化学
工程类
图层(电子)
作者
Jun Jiang,Xiang Fang,Yibo Xu,Xuguang Jia,Yu Chen,Yiqi Chen,Hongwei Hu,Ningyi Yuan,Jianning Ding
出处
期刊:Chemsuschem
[Wiley]
日期:2019-11-03
卷期号:13 (2): 412-418
被引量:6
标识
DOI:10.1002/cssc.201902488
摘要
Abstract Perovskite solar cells are sensitive to subtle changes in atmospheric conditions, resulting in problems such as the collapse of the perovskite structure and sharp drops in efficiency. Internal defects are also a big obstacle for high‐quality polycrystalline perovskites. At present, it is difficult to control the density of the trapping sites. By using the bidentate chelating agent thenoyltrifluoroacetone (ttfa), the crystallization kinetics, grain sizes, and crystal defect of Cs‐, methylammonium‐, and formamidinium‐based perovskite materials can be to effectively controlled through a nucleation and growth process for the preparation of perovskite crystals. Crystalline‐state tuning during the crystallization process to obtain better quality perovskite thin films can be achieved with no additional operation, which is suitable for the needs of modern industrial production and management. The chelating agent can effectively passivate the defects in perovskite films, leading to a low defect density and a long charge carrier lifetime. As a result, the ttfa‐passivated perovskite solar cell demonstrated a high power conversion efficiency of 19.70 % with superior stability retention of 64 % of the initial power conversion efficiency after two weeks unencapsulated storage in an adverse atmosphere with approximately 50 % relative humidity.
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