有机太阳能电池
材料科学
共轭体系
富勒烯
光伏
商业化
接受者
纳米技术
分子
小分子
混合太阳能电池
聚合物
化学工程
光伏系统
降级(电信)
有机化学
化学
复合材料
计算机科学
工程类
法学
政治学
物理
生物
电信
生物化学
凝聚态物理
生态学
作者
Olga R. Yamilova,Ilya V. Martynov,Allison S. Brandvold,Irina V. Klimovich,Alex H. Balzer,Alexander V. Akkuratov,Ilya E. Kusnetsov,Natalie Stingelin,Pavel A. Troshin
标识
DOI:10.1002/aenm.201903163
摘要
Abstract In view of a rapid development and increase in efficiency of organic solar cells, reaching their long‐term operational stability represents now one of the main challenges to be addressed on the way toward commercialization of this photovoltaic technology. However, intrinsic degradation pathways occurring in organic solar cells under realistic operational conditions remain poorly understood. The light‐induced dimerization of the fullerene‐based acceptor materials discovered recently is considered to be one of the main causes for burn‐in degradation of organic solar cells. In this work, it is shown that not only the fullerene derivatives but also different types of conjugated polymers and small molecules undergo similar light‐induced crosslinking regardless of their chemical composition and structure. In the case of conjugated polymers, crosslinking of macromolecules leads to a rapid increase in their molecular weight and consequent loss of solubility, which can be revealed in a straightforward way by gel permeation chromatography analysis via a reduction/loss of signal and/or smaller retention times. Results of this work, thus, shift the paradigm of research in the field toward designing a new generation of organic absorbers with enhanced intrinsic photochemical stability in order to reach practically useful operation lifetimes required for successful commercialization of organic photovoltaics.
科研通智能强力驱动
Strongly Powered by AbleSci AI