Visible Light–Induced Degradation of Inverted Polymer:Nonfullerene Acceptor Solar Cells: Initiated by the Light Absorption of ZnO Layer

光化学 聚合物太阳能电池 材料科学 电子顺磁共振 太阳能电池 解吸 有机太阳能电池 光电子学 聚合物 吸收(声学) 化学 降级(电信) 吸附 有机化学 复合材料 计算机科学 物理 电信 核磁共振
作者
Bowen Liu,Yunfei Han,Zerui Li,Huimin Gu,Lingpeng Yan,Yi Lin,Qun Luo,Shangfeng Yang,Chang‐Qi Ma
出处
期刊:Solar RRL [Wiley]
卷期号:5 (1) 被引量:63
标识
DOI:10.1002/solr.202000638
摘要

Power conversion efficiencies (PCEs) of polymer solar cells (PSCs) have exceeded 18% in the last few years. Stability has therefore become the next most important issue before commercialization. Herein, the degradation behaviors of the inverted PM6:IT‐4F (PBDB‐T‐2F:3,9‐bis(2‐methylene‐((3‐(1,1‐dicyanomethylene)‐6,7‐difluoro)‐indanone))‐5,5,11,11‐tetrakis(4‐hexylphenyl)‐dithieno[2,3‐ d :2′,3′‐ d ′]‐ s ‐indaceno[1,2‐ b :5,6‐ b ′]dithiophene) solar cells with different ZnO layers are systematically investigated. The PCE decay rates of the cells and the photobleaching process of the IT‐4F containing organic films on ZnO surface are directly correlated with the light‐absorption ability of the ZnO layer in the visible light range, indicating that photochemical decomposition of IT‐4F is initiated by the light absorption of ZnO layer. By analyzing the products of the aged ZnO/IT‐4F films with matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry (MALDI‐TOF‐MS), it is confirmed that photochemical reactions at the IT‐4F/ZnO interface include de‐electron‐withdrawing units and dealkylation on the side‐phenyl ring. Hydroxyl radicals generated by the photo‐oxidation of dangling hydroxide by ZnO are confirmed by electron spin resonance (ESR) spectroscopy measurements, which is attributed as the main reason causing the decomposition of IT‐4F. Surface treatment of ZnO with hydroxide and/or hydroxyl radical scavenger is found to be able to improve the stability of the PSCs, which further supports the proposed degradation mechanism.
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