卤化物
材料科学
结晶
串联
钙钛矿(结构)
化学工程
太阳能电池
能量转换效率
光伏系统
钙钛矿太阳能电池
水分
光电子学
混合(物理)
光伏
图层(电子)
动力学
作者
Yi-Xiang Wang,Zonglong Song,Jiang He,Hu Shen,Shichu Peng,Jiasheng Zou,Liu Z,Yintai Xu,Wenbo Peng,Peide Zhu,Deng Wang,Jie Zeng,Zhiwei Lei,Ting Xue,Yulong Lv,Yuqi Bao,Yong Zhang,Lei Yan,Kazuma Nakajima,Kenjiro Fukuda
摘要
ABSTRACT Mixed‐halide wide‐bandgap (WBG) perovskites suffer from inhomogeneous crystallization and vertical halide segregation during film formation and device operation. Here, we report a gradient‐controlled crystallization strategy to regulate crystallization kinetics and halide distribution in mixed‐halide perovskite films. Enabled by selective interactions with halide species and surface‐directed accumulation, this approach establishes a surface‐to‐bulk additive concentration gradient that synchronizes halide incorporation and suppresses the formation of Br‐rich regions. The strategy alleviates compositional heterogeneity, and the resulting surface‐enriched layer further retards the penetration of moisture and oxygen. Importantly, this strategy is broadly effective for mixed‐halide compositions spanning diverse halide mixing ratios. Consequently, WBG perovskite devices deliver superior photovoltaic performance, achieving a high V OC of 1.385 V and a PCE of 17.78%. Integration of the WBG subcells into perovskite/organic tandem devices yields a champion efficiency of 25.91% with a V OC of 2.191 V, while retaining more than 80% of the initial PCE after 600 h of continuous operation.
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