材料科学
堆积
钙钛矿(结构)
单层
非阻塞I/O
光电子学
电压
能量转换效率
极化(电化学)
重组
纳米技术
化学工程
光伏系统
化学物理
钝化
异质结
分子间力
科技与社会
八面体
作者
Wenjun Song,Qin Zhou,Zilong Zhang,Yibo Tu,Yao Wang,Chunming Liu,Gaoyuan Yang,Yong Chen,Huichao Chen,Zaifang Li,Min Xu,Peng Gao,Wensheng Yan
标识
DOI:10.1002/adfm.202531060
摘要
ABSTRACT Self‐assembled monolayers (SAMs) such as the carbazole‐based [4‐(3,6‐dimethyl‐9H‐carbazol‐9‐yl)butyl]phosphonic acid (Me‐4PACz) are widely used as hole‐selective layers in inverted perovskite solar cells (PSCs). However, their performance is fundamentally constrained by (i) inadequate coverage of NiO x surfaces caused by molecular self‐aggregation and (ii) severe non‐radiative recombination at the buried perovskite interface due to insufficient defect passivation. Here, we introduce 4‐(trifluoromethyl) benzamide (4‐TB) into Me‐4PACz to form a synergistic SAM (Syn‐SAM) that simultaneously addresses both issues. The strong intermolecular π–π stacking between 4‐TB and Me‐4PACz suppresses aggregation, enhances surface uniformity, and increases the interfacial dipole, thereby improving hole extraction. Meanwhile, the carbonyl functionality of 4‐TB effectively passivates undercoordinated Pb 2+ defects at the buried interface, reducing interfacial energy losses. Consequently, the champion device delivers an efficiency of 25.27% with an ultralow voltage loss of 0.356 V and retains 80% of its initial efficiency after over 1300 h of continuous 1‐sun operation. A 1.82 eV wide‐bandgap PSC also achieves an efficiency of 19.44% with a high V OC of 1.33 V, demonstrating the broad applicability of this synergistic molecular‐engineering strategy.
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