材料科学
谷胱甘肽
钙钛矿(结构)
单层
偶极子
结晶
劈理(地质)
紫外线
能量转换效率
光伏系统
钙钛矿太阳能电池
太阳能电池
光电子学
辐照
氧化还原
工作(物理)
光化学
化学工程
纳米技术
降级(电信)
太阳能电池效率
有机太阳能电池
电极
作者
Mengqi Jin,Dong Yang,Hu Shen,Shiying Tang,Lili Liu,Yang Wang,Chaofan Zheng,Jiajin Kuang,Chaoyang Wang,Faisal Naveed,Chong Chen
摘要
ABSTRACT Self‐assembled monolayer (SAM)‐based inverted perovskite solar cells (PSCs) suffer from a persistent efficiency‐stability trade‐off issue, which limits their commercialization. Herein, we propose a synergistic stabilizing strategy using reduced glutathione (GSH) as a multifunctional additive, integrating dipole modulation and redox‐driven self‐healing. GSH enables cross‐scale regulation: inducing interfacial dipole via a concentration gradient, passivating bulk defects through Pb 2+ coordination, optimizing crystallization kinetics, providing chemical protection against O 2 • − and moisture, and establishing a GSH/oxidized glutathione (GSSG)‐Ni 2+ /Ni 3+ redox cycle for self‐healing at the NiO x /SAM interface. Moreover, the interaction between GSSG and NiO x opens an additional hole transport channel, effectively suppressing device performance degradation induced by ultraviolet (UV) irradiation and thermally‐triggered cleavage of hydroxy groups in the SAM. Benefiting from the aforementioned advantages endowed by GSH, the small‐area cell (4 mm 2 ) achieved a high efficiency of 26.17%, while the 12.50 cm 2 minimodule reached 23.14%—among the highest values reported for modules with comparable active areas. Target devices also exhibit exceptional ISOS (International Summit on Organic Photovoltaic Stability) protocols stability: retaining 69.8% (ISOS‐T‐1, 200 h), 91.0% (ISOS‐D‐1, 1056 h), and 78.44% (ISOS‐L‐2, 336 h) of their initial efficiency. This work breaks the efficiency‐stability trade‐off and offers a “dynamic regulation‐static protection” design principle for PSCs.
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