One-step fabrication of NiOx-decorated carbon nanotubes-NiCo2O4 as an advanced electroactive composite for supercapacitors

被引:20
作者
Geuli, Ori [1 ]
Hao, Qingli [2 ]
Mandler, Daniel [1 ]
机构
[1] Hebrew Univ Jerusalem, Inst Chem, IL-9190401 Jerusalem, Israel
[2] Nanjing Univ Sci & Technol, Minist Educ, Key Lab Soft Chem & Funct Mat, Nanjing 210094, Jiangsu, Peoples R China
关键词
Carbon nanotubes; NiCo2O4; Electrophoretic deposition; Supercapacitors; ELECTROPHORETIC DEPOSITION; ELECTRODE MATERIALS; FLEXIBLE ELECTRODE; NICO2O4; NANOWIRES; NANOSHEET ARRAY; GRAPHENE OXIDE; THIN-FILM; PERFORMANCE; NANOSTRUCTURES; FOAM;
D O I
10.1016/j.electacta.2019.06.044
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Tailoring of battery-type NiCo2O4 with carbon-based materials for supercapacitors usually involves several steps, which require prolonged syntheses at high temperatures. Here, a facile one-step strategy is presented for the fabrication of a binder-free composite, made of NiOx decorated multi-walled carbon nanotubes (CNTs) and NiCo2O4 nanoparticles on nickel foam to form a stable supercapacitor with high specific capacity. The process is based on the electrophoretic co-deposition of carboxylated-CNTs and NiCo2O4 NPs, which were positively charged using Ni2+. The latter played a double role by stabilizing the nanomaterials and improving the electrochemical performance by decorating the nanomaterials with NiOx species. The well-dispersed NiCo2O4 NPs in the highly conductive porous matrix of CNTs provide efficient electron transfer, high surface area and superior electrochemical performance, such as high charge storage, high rate delivery and good cycling stability. The nanocomposite film exhibited high specific capacitance of 1363 F gr(-1) at 2 A gr(-1), while retaining 82% of the capacitance at higher current density (20 A gr(-1)). The straightforward fabrication process and the excellent electrochemical activity are of generic nature and can be applied for assembling other well-structured carbon-based composites. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:51 / 60
页数:10
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