One-dimensional covalent organic framework-Carbon nanotube heterostructures for efficient capacitive energy storage

被引:10
|
作者
Liu, Fei [1 ,2 ]
Wang, Chaojun [2 ,3 ]
Liu, Chang [2 ]
Yu, Zixun [2 ]
Xu, Meiying [1 ]
Chen, Yuan [2 ]
Wei, Li [2 ]
机构
[1] Guangdong Acad Sci, Guangdong Inst Microbiol, State Key Lab Appl Microbiol Southern China, Guangzhou 510070, Peoples R China
[2] Univ Sydney, Sch Chem & Biomol Engn, Darlington, NSW 2006, Australia
[3] Beijing Inst Aerial Mat, 8 Hangcai Ave, Beijing 100095, Peoples R China
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
POWER-DENSITY; SUPERCAPACITORS; METAL; EXFOLIATION;
D O I
10.1063/5.0073426
中图分类号
O59 [应用物理学];
学科分类号
摘要
Covalent organic frameworks (COFs) with redox-active moieties are potential capacitive energy storage materials. However, their performance is limited by their poor electrical conductivity and sluggish ion diffusion in their nanopores. Herein, we report coaxial one-dimensional van der Waals heterostructures (vdWHs) comprised of a carbon nanotube (CNT) core and a pyrene-pyridine COF shell synthesized by an in situ wrapping method. The coaxial structure allows efficient electronic interaction between the CNT core and COF shell and improves the electrical conductivity significantly. It also improves electrolyte ion accesses to redox-active pyridine groups in the COF, resulting in excellent capacitive energy storage performance with a high specific capacitance of & SIM;360 F g(-1), an excellent rate capability of & SIM;80%, and a good stability of 92% capacitance retention after 20 000 charge/discharge cycles. Our strategy opens the door to create other multi-dimensional vdWHs for various potential applications.
引用
收藏
页数:7
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