钙钛矿(结构)
串联
钝化
材料科学
光电子学
重组
带隙
纳米技术
结晶学
化学
图层(电子)
复合材料
生物化学
基因
作者
Ruitian Sun,Pengshuai Wang,Tao Wang,Lin Zhang,Zhizhong Ge,Liang Qiao,Tianshi Ye,Fan Li,Weijun Liu,Yanjie Wen,Xudong Yang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-12-23
卷期号:25 (1): 138-146
被引量:9
标识
DOI:10.1021/acs.nanolett.4c04652
摘要
The performance of narrow-bandgap (NBG) perovskite solar cells (PSCs) is limited by the severe nonradiative recombination and carrier transport barrier at the electron selective interface. Here, we reveal the importance of the molecular orientation for effective defect passivation and protection for Sn2+ at the perovskite/C60 interface. We constructed an internally self-anchored dual-passivation (ISADP) layer, where the orientation of PCBM can be significantly enhanced by the interaction between ammonium and carbonyl groups. It can facilitate the contact with C60 and minimize the nonradiative energy loss at the electron transport interface. This strategy remarkably enhances the FF of NBG PSCs, from 77.45% to 82.88%, and the power conversion efficiency (PCE) from 20.67% to 24.02%. Moreover, monolithic all-perovskite TSCs exhibit a high certified PCE (under reverse scan) of 28.12% and a record FF of 84.25%. This work opens up a new pathway for enhancing the performance of monolithic all-perovskite TSCs.
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