电极
阳离子聚合
材料科学
离子
阴极
扩散
储能
化学工程
电流密度
体积热力学
纳米技术
无机化学
化学
有机化学
高分子化学
物理化学
热力学
功率(物理)
工程类
物理
量子力学
作者
Zhangyuan Cheng,Jia‐Bo Le,Jun Wang,Wenlu Sun,Lei Zheng,Lifeng Cai,Derong Lu,Yanbin Shen,Jihuai Wu,Fang Fu,Hongwei Chen
标识
DOI:10.1002/aenm.202101930
摘要
Abstract The low capacity of current anion‐hosting electrodes makes it challenging to meet future energy requirements. Maintaining the high capacity of ions per unit volume and/or weight is always the ultimate goal for an optimal electrode design. Here, an organic framework is reported that can efficiently co‐store anions and cations in a single discharge/charge process, accompanied with a special cation‐assisted electrode activation process. The inserted cations not only facilitate anion diffusion kinetics, but also make a considerable contribution to the total capacity of the electrodes. This anion–cation co‐storage cathode thus can deliver a high capacity of 530 mAh g −1 at 3.4–1.0 V and a high energy density of 901 Wh kg −1 after 800 cycles (at 0.15 A g −1 ). The understanding of the self‐activation process is expected to inspire electrode design that utilizes anionic–cationic hybrid electrode chemistries beyond current Li‐ion batteries.
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