噻吩
卟啉
共轭体系
锂(药物)
电解质
化学工程
聚合
聚合物
材料科学
有机自由基电池
法拉第效率
化学
电化学
有机化学
电极
复合材料
物理化学
医学
内分泌学
工程类
作者
Xing‐Long Wu,Wang Zhou,Chao Ye,Jiahao Zhang,Zheyuan Liu,Chengkai Yang,Jinfeng Peng,Jilei Liu,Ping Gao
标识
DOI:10.1002/anie.202317135
摘要
Abstract Organic electrode materials are promising for next‐generation energy storage materials due to their environmental friendliness and sustainable renewability. However, problems such as their high solubility in electrolytes and low intrinsic conductivity have always plagued their further application. Polymerization to form conjugated organic polymers can not only inhibit the dissolution of organic electrodes in the electrolyte, but also enhance the intrinsic conductivity of organic molecules. Herein, we synthesized a new conjugated organic polymer (COPs) COP500‐CuT 2 TP (poly [5,10,15,20‐tetra(2,2′‐bithiophen‐5‐yl) porphyrinato] copper (II)) by electrochemical polymerization method. Due to the self‐exfoliation behavior, the porphyrin cathode exhibited a reversible discharge capacity of 420 mAh g −1 , and a high specific energy of 900 Wh Kg −1 with a first coulombic efficiency of 96 % at 100 mA g −1 . Excellent cycling stability up to 8000 cycles without capacity loss was achieved even at a high current density of 5 A g −1 . This highly conjugated structure promotes COP500‐CuT 2 TP combined high energy density, high power density, and good cycling stability, which would open new opportunity for the designable and versatile organic electrodes for electrochemical energy storage.
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