吩恶嗪
阴极
吩噻嗪
有机自由基电池
化学工程
材料科学
化学
电化学
纳米技术
聚合物
电极
有机化学
物理化学
医学
药理学
工程类
作者
Fabian Otteny,Verena Perner,Daniel Wassy,Martin Kolek,Peter Bieker,Martin Winter,Birgit Esser
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2019-11-24
卷期号:8 (1): 238-247
被引量:72
标识
DOI:10.1021/acssuschemeng.9b05253
摘要
Organic cathode materials are attractive for a new generation of more sustainable batteries due to their comparably low environmental footprint and toxicity. There is a continued quest for new compounds that meet the requirements of a competitive potential and a good cycling performance. We herein present phenoxazine-based polymers as cathode materials with good cycling stability, excellent rate performance, and a high discharge potential of 3.52 V vs Li|Li+ in composite electrodes. At the ultra-fast rate of 100C, a cross-linked phenoxazine poly(vinylene) showed only slow capacity decay over 10 000 cycles with a capacity retention of 74% in cycle 10 000. Mechanistic investigations using UV/vis/near-infrared (NIR) spectroscopy and density functional theory (DFT) calculations unveiled that unlike in the homologous phenothiazine polymers, π-interactions played a minor role in phenoxazine-based polymers. Our study is the first to present phenoxazine as a redox-active unit for cathode materials and shows that an elemental change of one atom (S vs O compared to known phenothiazine-based polymers) can have a profound effect on electrochemical performance.
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