电子顺磁共振
共轭微孔聚合物
聚合物
阴极
电化学
微型多孔材料
聚合
共轭体系
化学工程
锂(药物)
材料科学
蒽醌
激进的
化学
电极
光化学
高分子化学
无机化学
有机化学
物理化学
工程类
内分泌学
物理
医学
核磁共振
作者
Juan Zhou,Yunfei Bai,Qun Qiu,Shuo Liu,Haotian Qiu,Xinlei Zhang,Hao Zhao
标识
DOI:10.1016/j.cej.2022.139576
摘要
Electron paramagnetic resonance (EPR) spectroscopy is an important technique to probe the evolution of organic radicals during battery charging and discharging. Herein, we co-polymerize arylboron units and anthraquinone groups into a new organic electrode material, B-AQ, which has both the material characteristics of a conjugated microporous polymer and the special electronic properties of arylboron units and exhibits excellent thermodynamic stability and electrochemical properties. The experimental results show that the B-AQ cathode has fast charging/discharging capability at high current density and remarkable long cycle performance with very low capacity decay of 0.004 % per cycle over 2000 cycles. Adequate EPR method reveals the charging and discharging mechanism of the B-AQ electrode, i.e., the anthraquinone units gradually undergo anthraquinone radical species and enol lithium salt intermediates. In addition, comparative test studies show that inert gas protection of the discharge products in ex-situ EPR tests is necessary. This work will expand the research and application direction of boron-containing polymers and also provides an effective way to explore the reaction processes in organic lithium-ion batteries.
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