甲脒
三碘化物
钙钛矿(结构)
能量转换效率
材料科学
锡
异质结
钙钛矿太阳能电池
纳米技术
太阳能电池
化学工程
光电子学
氧化锡
光伏
碘化物
化学
物理化学
色素敏化染料
电极
冶金
工程类
电解质
作者
Efat Jokar,Ping Hou,Sumit S. Bhosale,He Shiang Chuang,Sudhakar Narra,Eric Wei−Guang Diau
出处
期刊:Chemsuschem
[Wiley]
日期:2021-09-22
卷期号:14 (20): 4415-4421
被引量:17
标识
DOI:10.1002/cssc.202101475
摘要
Overcoming the issue of the stability of tin-based perovskites is a major challenge for the commercial development of lead-free perovskite solar cells. To attack this problem, a new organic cation, azetidinium (AZ), is incorporated into the crystal structure of formamidinium tin triiodide (FASnI3 ) to form the mixed-cation perovskite AZx FA1-x SnI3 . As AZ has a similar size to FA but a larger dipole moment, hybrid AZx FA1-x SnI3 films exhibit variation in optical and electronic properties on increasing the proportion of AZ. Trifluoromethylbenzene (CF3 C6 H5 ) serves as antisolvent to fabricate smooth and uniform perovskite films for the devices with an inverted planar heterojunction structure. The device performance is optimized to produce the greatest efficiency at x=0.15 (AZ15), for which a power conversion efficiency of 9.6 % is obtained when the unencapsulated AZ15 device is stored in air for 100 h. Moreover, the device retains 90 % of its initial efficiency for over 15 days. The significant performance and stability of this device reveal that the concept of mixed cations is a promising approach to stabilize tin-based perovskite solar cells for future commercialization.
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