钙钛矿(结构)
带隙
能量转换效率
材料科学
化学工程
光电子学
溶剂
成核
钙钛矿太阳能电池
粒度
萃取(化学)
蒸发
薄膜
发光二极管
真空蒸发
卤化物
无机化学
动力学
光伏
硒化铜铟镓太阳电池
催化作用
载流子寿命
相(物质)
作者
Tao Dong,Chenxu Shen,Boyang Yu,Shengyang Zhao,Haoyu Wu,Chenyuan Ding,Binkai Shi,Ziyu Cai,Wenzheng Hu,Biyun Shi,Feng Ye,Qiufeng Ye,Zebo Fang
出处
期刊:
[Wiley]
日期:2025-10-06
卷期号:4 (6)
被引量:2
摘要
ABSTRACT As an intermediate composition between CsPbI 2 Br and CsPbIBr 2 , the inorganic perovskite material CsPbI 1.5 Br 1.5 is expected to exhibit both high efficiency and enhanced stability, attracting significant attention. However, as a Br‐rich perovskite, CsPbI 1.5 Br 1.5 suffers from poor film quality, primarily due to the substantial disparity in solvent evaporation rates and nucleation growth kinetics of the precursor films. This leads to severe non‐radiative recombination, closely related to the larger open‐circuit voltage loss ( V OC loss) and lower efficiencies compared to mainstream inorganic perovskites (e.g., CsPbI 3 and CsPbI 2 Br). To address these issues, we employed a Sequential Extraction Vacuum Method (SEVM), which integrates antisolvent extraction with vacuum treatment, to minimize solvent residues in perovskite films. This approach promotes grain densification, mitigates pinhole formation, and enhances film coverage, thereby significantly inhibiting non‐radiative recombination. Following SEVM treatment, the champion device achieved a power conversion efficiency (PCE) of 14.29% and a V OC of 1.336 V, representing the highest PCE and smallest V OC loss for ultra‐wide bandgap (> 1.95 eV) inorganic perovskite solar cells (PSCs). Furthermore, the SEVM‐based PSCs retained 90% of their initial PCE after 500 h of unencapsulated storage.
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