单层
材料科学
钙钛矿(结构)
光伏
能量转换效率
制作
热稳定性
纳米技术
光电子学
响应度
光伏系统
热的
共轭体系
钙钛矿太阳能电池
聚合物
连接器
芯(光纤)
薄膜
混合太阳能电池
解吸
热导率
紫外线
双功能
化学工程
页眉
作者
Xingzheng Yan,Xinyu Tong,Weifu Zhang,Songyu Du,Yanyang Zhou,Jiahan Xie,Hengyu Zhou,Luan Yuan,Yang Zhang,Ruixiang Peng,Mengjin Yang,Lisha Xie,Ziyi Ge
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-08-14
卷期号:12 (33): eaec3096-eaec3096
标识
DOI:10.1126/sciadv.aec3096
摘要
Perovskite solar cells (PSCs) using self-assembled monolayers (SAMs) as hole transporting materials have achieved impressive efficiencies. However, the vulnerability of SAMs causes desorption under light and thermal stress. While various modifications to the conjugated core and anchoring group of SAMs have been explored, challenges in balancing efficiency and stability remain. Here, we introduce a new class of cross-linkable SAMs, uniquely functionalized at the molecular linker. Upon in situ cross-linking, these hybrid monolayers exhibit impressive conductivity and optimal energy level alignment, enabling a power conversion efficiency (PCE) of 26.76% (certified 26.45%) in PSCs. The perovskite solar cells with cross-linkable SAMs also demonstrate superior durability in ageing tests, retaining 99% of its initial PCE under more than 2000 hours thermal stress and 95% of that under 500 hours ultraviolet irradiation. Furthermore, the strategy has been applied in the fabrication of high-efficiency rigid and flexible mini-modules. This molecular design strategy offers a promising and versatile modification site for advancing SAMs-based interfaces in optoelectronic devices.
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