Effect of electrolytes on the electrochemical performance of nickel cobaltite-titania nanotubes composites as supercapacitive materials

被引:4
作者
Chua, Chi Wing [1 ]
Zainal, Zulkarnain [1 ,2 ]
Lim, Hong Ngee [1 ,2 ]
Chang, Sook-Keng [1 ,2 ]
机构
[1] Univ Putra Malaysia, Dept Chem, Fac Sci, Upm Serdang 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Inst Adv Technol, Mat Synth & Characterizat Lab, Upm Serdang 43400, Selangor, Malaysia
关键词
TIO2; NANOTUBES; ARRAYS; FABRICATION; CAPACITANCE; ELECTRODES; OXIDE; EFFICIENT; HYBRID; GROWTH; MEDIA;
D O I
10.1007/s10854-018-9577-z
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
The effects of electrolytes on the electrochemical performance of nickel cobaltite-titania nanotubes composites as electrochemical capacitors were evaluated. Four types of electrolytes were selected to assess their effects on the prepared composites, namely aqueous electrolytes of 1.0 M KCl, 1.0 M HCl, 1.0 M KOH; and an organic electrolyte, 0.27 M tetra-n-butylammonium tetrafluoroborate (TBATFB) ionic liquid salt in acetonitrile. The composites performed better in 1.0 M HCl and 1.0 M KOH, than in 1.0 M KCl and 0.27 M TBATFB, which suggested that aqueous electrolytes with non-neutral pH would improve the specific areal capacitance values of the composites. Results have shown optimal performance in 1.0 KOH, which endowed the composite with excellent rate capability up to 200 mV s(-1). Cyclic voltammogram of the composite analysed in 1.0 M KOH produced a leaf-shaped like profile, with higher current densities towards more positive potentials. Charge-discharge analyses in 1.0 M KOH has shown that the composite possessed specific areal capacitance of up to 214.76 A mu F cm(-2) when it was evaluated at the current density of 350 A mu A cm(-2). The composite also retained up to 97.79% of its specific areal capacitance when current density was increased to 400 A mu A cm(-2). This material has demonstrated potential application for electrochemical capacitors through its facile fabrication technique.
引用
收藏
页码:14445 / 14454
页数:10
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