卤化物
钝化
钙钛矿(结构)
材料科学
成核
能量转换效率
结晶
离子
化学工程
光电子学
冠醚
离子键合
无机化学
热稳定性
纳米技术
化学
有机化学
图层(电子)
工程类
作者
Jianxin Yu,Gang Xie,Sisi Zheng,Jintao Chen,Chuizheng Feng,Huiyu Li,Rihui Zhou,Zhiping Wang,Liqian Liu,Jianwei Zhao,Aihui Liang,Yiwang Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-08-08
标识
DOI:10.1021/acsnano.4c08168
摘要
Organic–inorganic hybrid metal halide perovskite solar cells have been considered as one of the most promising next-generation photovoltaic technologies. Nevertheless, perovskite defects and Li+ ionic migration will seriously affect the power conversion efficiency and stability of the formal device. Herein, we designed two crown ether derivatives (PC12 and PC15) with different cavity diameters, which selectively bind to different metal cations. It is found that PC15 in perovskite precursor solution can actively regulate the nucleation and crystallization processes and passivate the uncoordinated Pb2+ ions, while PC12 at the interface between the perovskite layer and hole-transporting layer can effectively inhibit the migration of Li+ ions and reduce nonradiative recombination losses. Therefore, PC12 and PC15 can act as "lubricant" and defect passivators, as well as inhibitors of ion migration, when they are synergistically applied at the surface and bulk of perovskite layer. Consequently, the optimized device achieved a champion efficiency of 24.8% with significantly improved humidity, thermal, and light stability.
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