富勒烯
有机太阳能电池
聚合物
光活性层
轨道能级差
接受者
材料科学
光化学
降级(电信)
电子受体
聚合物太阳能电池
化学工程
化学
纳米技术
分子
有机化学
计算机科学
物理
复合材料
工程类
凝聚态物理
电信
作者
Emily M. Speller,Andrew J. Clarke,Nicholas Aristidou,Mark F. Wyatt,Laia Francàs,George C. Fish,Hyojung Cha,Harrison Ka Hin Lee,Joel Luke,Andrew Wadsworth,Alex Evans,Iain McCulloch,Ji‐Seon Kim,Saif A. Haque,James R. Durrant,Stoichko Dimitrov,Wing Chung Tsoi,Zhe Li
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2019-03-12
卷期号:4 (4): 846-852
被引量:115
标识
DOI:10.1021/acsenergylett.9b00109
摘要
With the emergence of nonfullerene electron acceptors resulting in further breakthroughs in the performance of organic solar cells, there is now an urgent need to understand their degradation mechanisms in order to improve their intrinsic stability through better material design. In this study, we present quantitative evidence for a common root cause of light-induced degradation of polymer:nonfullerene and polymer:fullerene organic solar cells in air, namely, a fast photo-oxidation process of the photoactive materials mediated by the formation of superoxide radical ions, whose yield is found to be strongly controlled by the lowest unoccupied molecular orbital (LUMO) levels of the electron acceptors used. Our results elucidate the general relevance of this degradation mechanism to both polymer:fullerene and polymer:nonfullerene blends and highlight the necessity of designing electron acceptor materials with sufficient electron affinities to overcome this challenge, thereby paving the way toward achieving long-term solar cell stability with minimal device encapsulation.
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