In situ growth of self-supported and defect-engineered carbon nanotube networks on 316L stainless steel as binder-free supercapacitors

被引:19
作者
Lei, Rui
Ni, Hongwei [1 ]
Chen, Rongsheng
Gu, Huazhi
Zhang, Hua
Dong, Shan
机构
[1] Wuhan Univ Sci & Technol, Hubei Prov Key Lab New Proc Ironmaking & Steelmak, Wuhan 430081, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Self-supported; Carbon nanotube networks; 316L stainless steel; Binder-free; Supercapacitors; N-DOPED CARBON; PERFORMANCE SUPERCAPACITORS; FUNCTIONALIZED CARBON; OXYGEN REDUCTION; ENERGY-STORAGE; FUEL-CELL; GRAPHENE; ELECTRODES; FIBERS; ELECTROCATALYSTS;
D O I
10.1016/j.jcis.2018.08.035
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Self-supported and defect-engineered carbon nanotube networks directly grown on 316L stainless steel are used for binder-free supercapacitors. In situ growth of the carbon nanotube networks on 316L stainless steel is obtained through the chemical vaporization deposition and thermal treatment to generate various defects. The relationship between the microstructures of carbon nanotube networks and electrochemical characteristics is investigated. The as-prepared carbon nanotube networks are characterized by scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and Raman analysis. Cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy tests are also carried out to evaluate their capacitive properties, suggesting that the electrochemical characteristics are significantly affected by annealing time, The carbon nanotube networks annealed at 500 degrees C for 2 h display high capacitance of 11 mF cm(-2) and excellent cycling lifetime with capacitance retention ration 97% at the scan rate of 0.5 mA cm(-2) for 5000 periods, which is attributed to the defect engineering increasing the defects of carbon nanotube networks, enhancing hydrophilic property and facilitating the transportation of electrolyte ions. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:622 / 629
页数:8
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