光伏
钙钛矿(结构)
噻吩
富勒烯
材料科学
光伏系统
光电子学
纳米技术
光化学
化学
结晶学
有机化学
电气工程
工程类
作者
Xiangyang Li,Yuyang Wang,Hui Wang,Chen Chen,Shuai Zeng,Hailin Guo,Lingfeng Dong,Wei Li,Dan Liu,Fa‐Bao Li,Tao Wang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-06-26
卷期号:10 (7): 3451-3458
被引量:3
标识
DOI:10.1021/acsenergylett.5c01599
摘要
Defects at the bulk and grain boundaries of perovskites, along with weak n-type surface characteristics, remain critical obstacles to enhance the power conversion efficiency (PCE) of the perovskite solar cells (PSCs). Herein, an acceptor–donor–acceptor (A-D-A) type organic passivator structured with two C60 cages sandwiching a nonfullerene acceptor fragment indacenodithieno[3,2-b]thiophene (IT), namely C60-IT-C60, is designed. Morphological and spectroscopic measurements demonstrate that the S element in the IT unit and the fullerene cages of C60-IT-C60 act as a Lewis base and acid to passivate the uncoordinated Pb2+ cation and anion defects. This interaction not only aligns the energy diagram and work functions of perovskite, but also encourages the crystallization of perovskite and suppresses the deep- and shallow-level defects, leading to a maximum PCE of 24.16% (fill factor of 84.75%) with improved storage and thermal stability in the corresponding PSCs. This work provides a new design paradigm of fullerene derivatives in PSCs.
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