堆积
单层
材料科学
钙钛矿(结构)
同质性(统计学)
纳米技术
能量转换效率
二进制数
光电子学
化学物理
化学工程
钙钛矿太阳能电池
光伏系统
表面能
分子
太阳能
自组装单层膜
氢
太阳能转换
科技与社会
结晶学
作者
Haojiang Shen,Yeming Jin,Fuqiang Li,Kangning Zhao,N. Shen,Jie Yang,Ya Li,Zhengyuan Long,Yuxuan Sheng,H. Li,Fei Guo,Zong-Xiang Xu,Yong Ding,Xingzhu Wang,Geping Qu,Shi Chen,Mohammad Khaja Nazeeruddin
标识
DOI:10.1038/s41467-026-71301-6
摘要
Abstract Self-assembled monolayers (SAMs) have emerged as efficient hole-transport layers for inverted perovskite solar cells (PSCs), yet molecular self-aggregation during assembly limits interfacial homogeneity and device performance. Here we report an indole-carbazole co-adsorption strategy by incorporating N-indoleacetic acid (Nd) into (4-(3,6-diphenyl-9H-carbazol-9-yl)butyl)phosphonic acid (Ph-4PACz) to construct phase-homogeneous monolayers. Nd interacts with Ph-4PACz via synergistic π–π stacking and hydrogen bonding, resulting in a uniform alternating Ph-4PACz/Nd molecular arrangement. This co-adsorbed structure enables optimized interfacial energy alignment, enhances perovskite film uniformity, and suppresses trap-assisted non-radiative recombination. As a result, devices achieve an efficiency of 26.95% (certified 26.57%) on 0.0717 cm 2 and 25.61% on 1 cm 2 , retaining 93.36% of their initial efficiency after 1500 h of maximum power point tracking under continuous illumination and 91.10% after 1200 h at 85 °C. The strategy is broadly applicable to carbazole-based SAMs and wide-bandgap PSCs, offering a general co-adsorption route toward efficient and stable devices.
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