钙钛矿(结构)
能量转换效率
材料科学
制作
化学工程
碘化物
沉积(地质)
Crystal(编程语言)
相(物质)
载流子寿命
纳米技术
无机化学
硅
光电子学
化学
有机化学
沉积物
工程类
计算机科学
替代医学
程序设计语言
医学
古生物学
病理
生物
作者
Xinning Jiao,Wei‐Min Gu,Yanting Xu,Ke‐Jian Jiang,Guanghui Yu,Qing-Wu Zhang,Caiyan Gao,Cai‐Ming Liu,Xin‐Heng Fan,Lian‐Ming Yang,Yanlin Song
标识
DOI:10.1016/j.cej.2022.139326
摘要
PbI2 as precursor has been extensively employed for the fabrication of organic–inorganic hybrid perovskite films for high-efficiency perovskite solar cells (PSCs) by using two-step solution deposition method. However, the resultant perovskite film suffers from the incomplete reaction of PbI2 and the volumetric expansion of the film, affecting both the performance and stability of the PSCs. Here, a single-crystal complex FA4Pb3I6Ac4 (Ac−: CH3COO−) is synthesized, and utilized to replace PbI2 for the fabrication of FAPbI3-based perovskite film in ambient conditions. The solution-processed crystal complex has good film-forming ability, and can be directly converted into stable black-phase FAPbI3 perovskite at room temperature through anion exchange reaction between Ac− and I− upon coating with iodide salt solution. By the strategy, a dense and uniform perovskite film is obtained with reduced trap-state density and prolonged charge lifetime. The champion device delivers a power conversion efficiency (PCE) of 23.65% with high reproductivity. Importantly, the unencapsulated device exhibits a dramatically improved operational stability under temperature and humidity conditions.
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