材料科学
能量转换效率
钙钛矿(结构)
卤化物
碳纤维
光伏系统
相(物质)
光电子学
化学工程
无机化学
复合材料
化学
有机化学
复合数
工程类
生态学
生物
作者
Ziting Qi,Jiabao Li,Xinyu Zhang,Jie Dou,Qiyao Guo,Yuanyuan Zhao,Peizhi Yang,Qunwei Tang,Jialong Duan
标识
DOI:10.1021/acsami.4c01876
摘要
Perovskite solar cells (PSCs) have attracted extensive attention in photovoltaic applications owing to their superior efficiency, and the buried interface plays a significant role in determining the efficiency and stability of PSCs. Herein, a plant-derived small molecule, ergothioneine (ET), is adopted to heal the defective buried interface of CsPbIBr2-based PSC to improve power conversion efficiency (PCE). Because of the strong interaction between Lewis base groups (–C═O and –C═S) in ET and uncoordinated Pb2+ in the perovskite film from the theoretical simulations and experimental results, the defect density of the CsPbIBr2 perovskite film is significantly reduced, and therefore, the nonradiative recombination in the corresponding device is simultaneously suppressed. Consequently, the target device achieves a high PCE of 11.13% with an open-circuit voltage (VOC) of 1.325 V for hole-free, carbon-based CsPbIBr2 PSCs and 14.56% with a VOC of 1.308 V for CsPbI2Br PSCs. Furthermore, because of the increased ion migration energy, the detrimental phase segregation in this mixed-halide perovskite is weakened, delivering excellent long-term stability for the unencapsulated device in ambient conditions over 70 days with a 96% retention rate of initial efficiency.
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