钙钛矿(结构)
钝化
材料科学
位阻效应
掺杂剂
单层
分子间力
能量转换效率
氧化物
化学工程
分子
氧化铟锡
无机化学
催化作用
氧化锡
胶束
咔唑
电子迁移率
钙钛矿太阳能电池
离子
金红石
纳米技术
碘化物
菁
光化学
铟
化学
佩多:嘘
太阳能电池
光伏系统
卤化物
图层(电子)
载流子
有机太阳能电池
反应性(心理学)
多元醇
氧化还原
烷基
作者
Jiawei Zhan,Qinyi Zhang,Huazhong Wang,Shuyu Zhang,Minglin Zhang,Ying Zhang,Tingna Fan,Pengyun Zhang,Huizhen Ke
出处
期刊:Chemsuschem
[Wiley]
日期:2025-12-09
卷期号:19 (1): e202501970-e202501970
被引量:2
标识
DOI:10.1002/cssc.202501970
摘要
The interfacial properties of the hole transport layer (HTL) are absolutely critical for perovskite solar cells (PSCs) nowadays. [4‐(3,6‐Dimethyl‐9H‐carbazol‐9‐yl)butyl]phosphonic acid (Me‐4PACz) is widely used HTL within the class of self‐assembled materials. However, during its self‐assembly process, Me‐4PACz tends to form molecular clusters and micelles on indium tin oxide (ITO), leading to insufficient coverage. Therefore, we propose a co‐assembled monolayer (Co‐SAM) strategy via co‐depositing phenylphosphonic acid (PPA) or its derivatives as co‐dopants with Me‐4PACz, the intermolecular steric hindrance between phenyl and carbazole groups effectively suppresses Me‐4PACz aggregation. Simultaneously, the phosphonic acid groups of both molecules form a synergistic dual‐anchoring effect, significantly enhancing HTL uniformity and coverage. Furthermore, active substituents (‐OH, ‐NH 2 , ‐Br) in the dopants can passivate uncoordinated Pb 2+ ions and iodine vacancies at the perovskite interface, thereby optimizing the HTL/perovskite contact and improving carrier extraction ability. Results show that inverted devices based on Me‐4PACz+BrPPA Co‐SAM achieve a power conversion efficiency (PCE) of 23.73%, representing a substantial increase from 21.39% while maintaining excellent stability. This strategy provides a new direction for developing high‐performance Co‐SAM and advancing the industrialization of PSCs.
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