钙钛矿(结构)
材料科学
单层
偶极子
咔唑
能量转换效率
光伏系统
钙钛矿太阳能电池
异构化
工作(物理)
力矩(物理)
光电子学
自组装单层膜
共价键
化学物理
光异构化
重组
纳米技术
电荷(物理)
磁滞
光化学
化学工程
作者
Chao Lv,Yawei Miao,Jing Wang,Jiayu Li,Zeyuan Hu,Yuexing Zhang,Ping Wu,Longlong Geng,Minghao Yin,Xiangchuan Meng,Fariba Tajabadi,Nima Taghavinia,Ke Gao,Qifan Xue
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-09-25
卷期号:64 (46): e202513338-e202513338
被引量:4
标识
DOI:10.1002/anie.202513338
摘要
Abstract Carbazole‐based SAMs show great promise as interfacial modifiers in inverted perovskite solar cells (PSCs). Their large dipole moments and covalent binding capabilities suppress charge recombination and enhance device stability. We designed two isomeric carbazole SAMs (EPACz and PPACz) by adjusting the phenyl ring position. PPACz exhibits a higher dipole moment (2.60 D versus 1.77 D for EPACz) and a narrower HOMO‐LUMO gap (2.39 eV), enabling superior hole extraction. PPACz‐based devices achieved an excellent PCE of 26.1% (versus 22.0% for EPACz), with 23.5% efficiency for 1 cm 2 devices. The stronger tridentate anchoring of PPACz to ITO (compared with EPACz) improves interfacial stability. Unencapsulated devices retained over 90% of their initial efficiency after 540 h, demonstrating exceptional durability. This work provides key insights for designing high‐performance SAMs in perovskite photovoltaics.
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