两性离子
材料科学
弹性体
钙钛矿(结构)
钝化
固化(化学)
能量转换效率
成核
复合材料
结晶
光电子学
化学工程
图层(电子)
化学
工程类
有机化学
分子
作者
Yaohua Wang,Yuanyuan Meng,Chang Liu,Ruikun Cao,Bin Han,Lisha Xie,Ruijia Tian,Xiaoyi Lü,Zhenhua Song,Jun Li,Shuncheng Yang,Congda Lu,Ziyi Ge
出处
期刊:Joule
[Elsevier]
日期:2024-02-01
被引量:9
标识
DOI:10.1016/j.joule.2024.01.021
摘要
Summary
Organometallic halide perovskites are promising candidates for high-performance flexible perovskite solar cells (f-PSCs). However, f-PSCs still face significant challenges in the formation of uniform and highly crystalline films with mechanical robustness. Here, a zwitterion elastomer (SBMA) was introduced into a perovskite film. SBMA cross-linked in situ to regulate the nucleation and crystallization of the perovskite by forming an intermediate SBMA-PbI2 adduct. In addition, the polar sulfo-end group on SBMA offered chemical passivation to perovskite vacancies and created a large dielectric environment, screening the carrier capture process and suppressing nonradiative recombination. The zwitterionic fusion within the cross-linked elastomers, residing on grain boundaries, endowed the flexible perovskite films with instantaneous self-curing ability under mild treating conditions (40°C for 15 min). The resultant device achieved a record-breaking power conversion efficiency (PCE) of 24.51% (certified 24.04%) and demonstrated excellent mechanical sustainability and durability, retaining over 90% of the initial PCE after 10,000 bending cycles.
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