储能
氧化还原
共价键
电容感应
激进的
电容
纳米技术
化学
超级电容器
化学工程
材料科学
电极
计算机科学
有机化学
物理
物理化学
功率(物理)
工程类
操作系统
量子力学
作者
Fei Xu,Hong Xu,Xiong Chen,Dehai Wu,Wei Yang,Hao Líu,Cheng Gu,Ruowen Fu,Donglin Jiang
标识
DOI:10.1002/anie.201501706
摘要
Ordered π-columns and open nanochannels found in covalent organic frameworks (COFs) could render them able to store electric energy. However, the synthetic difficulty in achieving redox-active skeletons has thus far restricted their potential for energy storage. A general strategy is presented for converting a conventional COF into an outstanding platform for energy storage through post-synthetic functionalization with organic radicals. The radical frameworks with openly accessible polyradicals immobilized on the pore walls undergo rapid and reversible redox reactions, leading to capacitive energy storage with high capacitance, high-rate kinetics, and robust cycle stability. The results suggest that channel-wall functional engineering with redox-active species will be a facile and versatile strategy to explore COFs for energy storage.
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