Water-based asymmetric supercapacitors with 2.5 V wide potential and high energy density based on Na0.6CoO2 nanoarray formed via electrochemical oxidation

被引:21
作者
Liu, Zhiqiang [1 ,2 ]
Qiu, Yanling [2 ]
Cui, Liang [1 ]
Zheng, Rongkun [1 ]
Yang, Wenrong [3 ]
Barrow, Colin J. [3 ]
Razal, Joselito M. [4 ]
Liu, Jingquan [1 ,2 ]
机构
[1] Linyi Univ, Coll Mat Sci & Engn, Linyi 276000, Shandong, Peoples R China
[2] Qingdao Univ, Inst Graphene Appl, Coll Mat Sci & Engn, Technol Innovat, Qingdao 266071, Peoples R China
[3] Deakin Univ, Inst Frontier Mat, Sch Life & Environm Sci, Geelong, Vic 3216, Australia
[4] Deakin Univ, Inst Frontier Mat, Geelong, Vic 3216, Australia
基金
中国国家自然科学基金;
关键词
Water-based asymmetric supercapacitors; Carbon cloth; Electrochemical oxidation; Na0.6CoO2; nanoarray; HIGH-PERFORMANCE; COBALT OXIDE; NANOSHEET ARRAYS; NANOPARTICLES; NANOWIRES; ELECTRODE; STORAGE;
D O I
10.1016/j.carbon.2021.12.058
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
The voltage limit of water-based asymmetric supercapacitors is usually 2 V, which prevents further improvement of energy density. Na0.6CoO2 nanoarrays with high Na content are formed on carbon cloth (CC) by cyclic electrochemical oxidation (EO) and can work stably in 0-1.2 V wide potential, and the specific capacitance is up to 575.98C g(-1) at 1 A g(-1). Using carbon coated Fe2O3 nanoarrays on CC as the negative electrode and Na0.6CoO2/CC as the positive electrode, a water-based asymmetric supercapacitor (ASC) which can operate stably in 0-2.5 V wide voltage window is assembled. The Na0.6CoO2/CC// Fe2O3@C/CC ASC exhibits an energy density of 133.92 Wh kg(-1) at a power density of 1250Wkg(-1), which is better than previously reported Co-based supercapacitors. This study provides a scheme for the working voltage of water-based ASCs to be further expanded to more than 2 V. Utilizing cationic pre-inserted Co3O4 nanoarray to construct high operating voltage composite electrode should have broad application prospect. (C) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页码:81 / 92
页数:12
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