钙钛矿(结构)
材料科学
钝化
能量转换效率
光电子学
基质(水族馆)
光热治疗
电荷(物理)
太阳能转换
能量转换
纳米技术
表面能
图层(电子)
太阳能
极限(数学)
光伏系统
化学工程
钙钛矿太阳能电池
异质结
功率(物理)
作者
Yi Pan,Lei Liu,Haoxuan Guo,Changqing Lin,Pengfei Wu,Zeping Ou,Can Wang,Peidong Chen,Qin Gao,Mingyang Gao,Xiaoxue Lin,Dingqin Hu,Tingming Jiang,Yujie Zheng,Zeyun Xiao,Ke Yang,Zeyu Zhang,Rui Wang,Nabonswendé Aïda Nadège Ouedraogo,Zedong Lin
标识
DOI:10.1038/s41467-026-76497-1
摘要
Abstract The use of self-assembled multilayer (SAM) layers as hole transport layers (HTLs) represents a major advance for high-efficiency perovskite solar cells (PSCs). However, many SAMs materials suffer from aggregation, poor wettability, and weak interactions with the perovskite, which hinder charge transfer and cause energy losses that limit both power conversion efficiency (PCE) and long-term stability. In this study, we synthesized two SAMs, namely 2-(10-(3,5-dimethoxyphenyl)−7H-benzo[c]carbazol-7-yl)ethyl)phosphonic acid (denoted as DMPA) and 2-(7H-benzo[c]carbazol-7-yl)ethyl)phosphonic acid (denoted as BCPA). DMPA SAM effectively suppresses self‑aggregation and enhances substrate coverage. The methoxy groups in DMPA interact with the perovskite, thereby enabling DMPA to passivate defects at the buried interface and optimize perovskite crystallization. These interfacial improvements facilitate more efficient charge extraction and enhance interfacial stability. As a result, DMPA-based PSCs achieve a PCE of 27.59% (certified PCE of 27.2%) and show remarkable photothermal stability, retaining 94.5% of their initial efficiency after 1600 hours of continuous illumination under 1 Sun at 65 °C.
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