成核
光异构化
结晶度
偶氮苯
能量转换效率
材料科学
钙钛矿(结构)
化学工程
离子
化学
相(物质)
光化学
异构化
结晶学
光电子学
聚合物
催化作用
有机化学
复合材料
工程类
作者
Xuejiao Zuo,Yiyang He,Hongyu Ji,Yong Li,Xiuying Yang,Binxun Yu,Tao Wang,Zhike Liu,Wenliang Huang,Jing Gou,Ningyi Yuan,Jianning Ding,Shengzhong Liu
标识
DOI:10.1016/j.jechem.2022.06.013
摘要
Ion migration is a notorious problem in perovskite solar cells (PSCs) that severely mutilates device performance. Herein, a strategy to inhibit ion migration in situ is developed by using photoisomerization of azobenzene (AZO) to immobilize cations in the lattice. During the nucleation process, the photoisomerized cis-AZO reacts with FA+, MA+ and Pb2+ cations in the perovskite precursor by synergistic cation-π interaction and Lewis base coordination, leading to heterogeneous nucleation to produce uniform perovskite film. Meanwhile, it accelerates conversion of intermediate yellow δ-phase to desired black α-phase of FAPbI3 for improved crystallinity with well-passivated grain surface. Consequently, defect density is effectively reduced for the perovskite film to demonstrate suppressed carrier recombination and enhanced carrier extraction. Subsequently, the solar cell efficiency is elevated from 21.29% to 23.58% with negligible J-V hysteresis. Long-term stability is also improved, with the bare device without any encapsulation retaining 84% of its initial efficiency after aging 744 hours in ambient.
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