材料科学
紫外线
钙钛矿(结构)
单层
光伏
光电子学
能量转换效率
太阳能电池
纳米技术
限制
抵抗
紫外线
降级(电信)
光伏系统
分子
解吸
化学工程
太阳能电池效率
图层(电子)
分子动力学
锚固
结构稳定性
极端紫外线
作者
Keli Wang,Wanli Li,Yuheng Li,Bo Li,Jiandong He,Peng Gao,Zhen Guan,Jing Wei,Zhuye Bi,Changling Zhan,Ma Yh,Yingzhuang Ma,Chengbo Tian,Zhanhua Wei,J F,Zaiwei Wang,Chao Luo,Qing Zhao
标识
DOI:10.1038/s41467-026-73426-0
摘要
Self-assembled monolayers (SAMs) have boosted perovskite solar cell (PSCs) efficiencies, but their ultrathin nature causes structural vulnerability under outdoor solar illumination, particularly in the ultraviolet (UV) regime, limiting long-term operation and practical deployment of PSCs. Extensive experiments with ab initio molecular dynamics reveal conventional SAMs undergo rapid structural degradation under UV irradiation, leading to molecular desorption and film collapse. Here, we introduced a SAM featuring dual-dimensional reinforcement. Vertically, multiple anchoring sites and flexible π-conjugated framework enable strong adhesion to bidirectional adjacent layers, providing exceptional interfacial UV durability. Horizontally, intrinsically structural stability and interlocked networks further prevent the film collapse caused by high-energy UV invasion. The champion device achieved a power conversion efficiency of 27.10% (certified 26.90%). After 2100 hours of maximum power point tracking (ISOS-L-2) at 65 °C, only 2% of the efficiency was lost. Moreover, the devices retained 86.7% of initial PCE after 2200 hours under high-intensity UV light (1.73-fold the intensity of natural sunlight), and 90.5% after 2035 hours of outdoor exposure, representing the highest UV stability of SAM-based PSCs. Self-assembled molecules improve perovskite solar cells but fail under ultraviolet light, limiting durability. Wang et al. designed a dual reinforced molecular layer with stronger interfacial anchoring and interlocked networks that resists ultraviolet damage and enables long-term stable devices.
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