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‐Huan Hou,Sumit S. Bhosale,He‐Shiang Chuang,Sudhakar Narra,Eric Wei‐Guang Diau
出处
期刊:Chemsuschem
[Wiley]
日期:2021-09-12
卷期号:14 (20): 4415-4421
被引量:35
标识
DOI:10.1002/cssc.202101475
摘要
Abstract 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 AZxFA1‐xSnI3. As AZ has a similar size to FA but a larger dipole moment, hybrid AZxFA1‐xSnI3 films exhibit variation in optical and electronic properties on increasing the proportion of AZ. Trifluoromethylbenzene (CF3C6H5) 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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