钙钛矿(结构)
光伏系统
材料科学
电子
分子
极性效应
工程物理
纳米技术
化学物理
化学
光化学
物理
结晶学
工程类
电气工程
有机化学
量子力学
作者
Xiaoqing Jiang,Kaiwen Dong,P. Li,Likai Zheng,Bingqian Zhang,Yanfeng Yin,Guangyue Yang,Linqin Wang,Minhuan Wang,Suying Li,Lina Zhu,Shiyuan Niu,Shitao Yu,Shiwei Liu,Wenming Tian,Xin Guo,Mingyang Wei,Shaik M. Zakeeruddin,Licheng Sun,Shuping Pang
标识
DOI:10.1002/anie.202414128
摘要
Electron-withdrawing molecules (EWMs) have exhibited remarkable efficacy in boosting the performance of perovskite solar cells (PSCs). However, the underneath mechanisms governing their positive attributes remain inadequately understood. Herein, we conducted a comprehensive study on EWMs by comparing 2,2'-(2,5-cyclohexadiene-1,4-diylidene) bismalononitrile (TCNQ) and (2,3,5,6-tetrafluoro-2,5-cyclohexadiene-1,4-diylidene) dimalononitrile (F4TCNQ) employed at the perovskite/hole transport layer (HTL) interfaces. Our findings reveal that EWMs simultaneously enhance chemical passivation, interface dipole effect, and chemically binding of the perovskite to the HTL. Notably, F4TCNQ, with its superior electron-withdrawing properties, demonstrates a more pronounced impact. Consequently, PCSs modified with F4TCNQ achieved an impressive power conversion efficiency (PCE) of 25.21 %, while demonstrating excellent long-term stability. Moreover, the PCE of a larger-area perovskite module (14.0 cm
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