Coupling electrode-redox electrolyte within carbon nanotube arrays for supercapacitors with suppressed self-discharge

被引:12
作者
Cao, Runyuan [1 ]
Zhang, Yu [1 ]
Du, Yinan [1 ]
Zeng, Yueying [1 ]
Yu, Minghao [2 ,3 ]
Zhai, Teng [1 ]
Xia, Hui [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Mat Sci & Engn, Herbert Gleiter Inst Nanosci, Nanjing 210094, Peoples R China
[2] Tech Univ Dresden, Fac Chem & Food Chem, D-01062 Dresden, Germany
[3] Tech Univ Dresden, Ctr Adv Elect Dresden Cfaed, D-01062 Dresden, Germany
基金
中国国家自然科学基金;
关键词
CNT; Redox electrolytes; Coupling; Oxygen functional groups; Confinement; Self discharge; ENERGY-DENSITY; PERFORMANCE; WASTE;
D O I
10.1016/j.susmat.2021.e00284
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Carbon materials together with various redox electrolytes have been developed intensively in recent years to assemble large-capacitance and high-rate supercapacitors. However, the weak interactions between carbon elec-trodes and redox electrolytes result in the severe shuttle of redox ions in electrolytes, causing critical self-discharge performance. Here we report a functional interface to establish strong adhesion of redox ions on the liquid side towards carbon nanotube arrays, leading to efficient confinement of redox ions around carbon electrode and enhanced electronic transfer between the electrode and redox electrolyte. Benefiting from the interface, the coupling carbon nanotube arrays-K3Fe(CN)(6) system exhibits a substantially boosted self-discharge rate with no decay after 32 h under the open-circuit stage, as well as a large areal capacitance up to 3.048 F cm(-2). The introduction of functionalized interface suggests a general and versatile concept for carbon-based electrodes to achieve battery-like charge storage with reliable features. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页数:6
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