Electrochemically active, crystalline, mesoporous covalent organic frameworks on carbon nanotubes for synergistic lithium-ion battery energy storage

被引:337
作者
Xu, Fei [1 ,2 ]
Jin, Shangbin [1 ]
Zhong, Hui [2 ]
Wu, Dingcai [2 ]
Yang, Xiaoqing [2 ]
Chen, Xiong [1 ]
Wei, Hao
Fu, Ruowen [2 ]
Jiang, Donglin [1 ]
机构
[1] Natl Inst Nat Sci, Inst Mol Sci, Dept Mat Mol Sci, Okazaki, Aichi 4448787, Japan
[2] Sun Yat Sen Univ, Inst Mat Sci, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
基金
美国国家科学基金会;
关键词
PERFORMANCE; CATHODE; ANODES;
D O I
10.1038/srep08225
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Organic batteries free of toxic metal species could lead to a new generation of consumer energy storage devices that are safe and environmentally benign. However, the conventional organic electrodes remain problematic because of their structural instability, slow ion-diffusion dynamics, and poor electrical conductivity. Here, we report on the development of a redox-active, crystalline, mesoporous covalent organic framework (COF) on carbon nanotubes for use as electrodes; the electrode stability is enhanced by the covalent network, the ion transport is facilitated by the open meso-channels, and the electron conductivity is boosted by the carbon nanotube wires. These effects work synergistically for the storage of energy and provide lithium-ion batteries with high efficiency, robust cycle stability, and high rate capability. Our results suggest that redox-active COFs on conducting carbons could serve as a unique platform for energy storage and may facilitate the design of new organic electrodes for high-performance and environmentally benign battery devices.
引用
收藏
页数:6
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