双层
钙钛矿(结构)
材料科学
能量转换效率
图层(电子)
萃取(化学)
化学工程
纳米技术
光电子学
化学
有机化学
膜
生物化学
工程类
作者
Geping Qu,Letian Zhang,Ying Qiao,Shaokuan Gong,Yuanjia Ding,Yuli Tao,Siyuan Cai,Xiaoyong Chang,Qian Chen,Pengfei Xie,Junyuan Feng,Changqin Gao,Guopeng Li,Hui Xiao,Fei Wang,Hanlin Hu,Jie Yang,Chen Shi,Alex K.‐Y. Jen,Xihan Chen,Zong‐Xiang Xu
标识
DOI:10.1038/s41467-024-55523-0
摘要
While self-assembled material based inverted perovskite solar cells have surpassed power conversion efficiencies of 26%, enhancing their performance in large-area configurations remains a significant challenge. In this work, we report a self-assembled material based hole-selective layer 4-(7H-dibenzo[c,g]carbazol-7-yl)phenyl)phosphonic acid, with a π-expanded conjugation. The enhanced intermolecular π–π interactions facilitate the self-assembly of 4-(7H-dibenzo[c,g]carbazol-7-yl)phenyl)phosphonic acid molecules to form an ordered bilayer with a hydrophilic surface, which passivates the buried perovskite interface defect and enables high-quality and large-area perovskite preparation, while simultaneously enhancing interfacial charge extraction and transport. The certified efficiency of 4-(7H-dibenzo[c,g]carbazol-7-yl)phenyl)phosphonic acid based small-area (0.0715 cm2) device is 26.39% with high stability. Furthermore, a certified efficiency of 25.21% is achieved for a 99.12 mm2 large area device. Qu et al. report a self-assembled material with π-expanded conjugation to form hydrophilic ordered bilayer as hole selective layer for inverted perovskite solar cells. The enhanced interfacial charge extraction and transport enable certified efficiency of 26.39% and 25.21% for 7.15 mm2 - and 99.12 mm2 -devices, respectively.
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