钙钛矿(结构)
非阻塞I/O
化学
串联
能量转换效率
钝化
带隙
甲脒
光电子学
纳米技术
热稳定性
碱金属
化学工程
图层(电子)
材料科学
结晶学
有机化学
催化作用
复合材料
工程类
生物化学
作者
Hui Zhang,Yuan Zhou,Tonghui Guo,Xiang Zhang,Zhenkun Zhu,Junjun Jin,Xiaxia Cui,Dan Zhang,Zhen Wang,Lin Li,Nai Wang,Guanqi Tang,Qidong Tai
标识
DOI:10.1002/cjoc.202300245
摘要
Comprehensive Summary Formamidinium (FA)‐based Sn‐Pb perovskite solar cells (FAPb0.5Sn0.5I3 PSCs) with ideal bandgap and impressive thermal stability have caught enormous attention recently. However, it still suffers from the challenge of realizing high efficiency due to the surface imperfections of the transport materials and the energy‐level mismatch between functional contacts. Herein, it is demonstrated that the modification on buried interface with alkali metal salts is a viable strategy to alleviate these issues. We systematically investigate the role of three alkali metal bromide salts (NaBr, KBr, CsBr) by burying them between the NiOx hole transport layer (HTL) and the perovskite light‐absorbing layer, which can effectively passivate interface defects, improve energy‐level matching and release the internal residual strain in perovskite layers. The device with CsBr buffer layer exhibits the best power conversion efficiency (PCE) approaching 20%, which is one of the highest efficiencies for FA‐based Sn‐Pb PSCs employing NiOx HTLs. Impressively, the long‐term storage stability of the unencapsulated device is also greatly boosted. Our work provides an efficient strategy to prepare desired FA‐based ideal‐bandgap Sn‐Pb PSCs which could be applied in tandem solar cells.
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