结晶度
钙钛矿(结构)
配体(生物化学)
能量转换效率
热稳定性
化学工程
锑
化学
光电子学
材料科学
结晶学
生物化学
复合材料
受体
工程类
冶金
作者
Riming Nie,Peikun Zhang,Jiaxing Gao,Yucheng Wang,Weicun Chu,Luyao Li,Kaiyu Wang,Dongmin Qian,Fanrong Lin,Xuefeng Xia,Yong Wu,Lingfeng Chao,Chunyang Miao,Xiaoming Zhao,Wanlin Guo,Zhuhua Zhang
标识
DOI:10.1038/s41467-025-61563-x
摘要
Abstract Conventional passivating ligands bind to perovskite surfaces through only a single active site, which not only creates a resistive barrier due to dense ligand packing but also restricts the enhancement of device stability. Here, we identify an antimony chloride-N,N-dimethyl selenourea complex, Sb(SU) 2 Cl 3 , as a multi-anchoring ligand to significantly enhance perovskite crystallinity, suppress defect formation, and dramatically improve moisture resistance and overall stability. As a result, we achieve a power conversion efficiency of 25.03% in fully air-processed perovskite solar cells fabricated using a two-step method—among the highest efficiencies reported for devices prepared under ambient conditions. Remarkably, unencapsulated cells exhibited linear extrapolated T 80 lifetimes of 23,325 h during dark shelf storage. Furthermore, these unencapsulated devices demonstrate exceptional thermal and operational stability, with T 80 lifetimes of 5,004 (at 85 °C) and 5,209 hours (under 1-sun illumination), respectively, ranking them among the most stable perovskite solar cells to date.
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