Synthesis of Co3O4 nanosheets via electrodeposition followed by ozone treatment and their application to high-performance supercapacitors

被引:118
作者
Kung, Chung-Wei [1 ]
Chen, Hsin-Wei [1 ]
Lin, Chia-Yu [1 ]
Vittal, R. [1 ]
Ho, Kuo-Chuan [1 ,2 ]
机构
[1] Natl Taiwan Univ, Dept Chem Engn, Taipei 10617, Taiwan
[2] Natl Taiwan Univ, Inst Polymer Sci & Engn, Taipei 10617, Taiwan
关键词
Capacitor performance; Charge-discharge current density; Cobalt oxide; Electrodeposition; Flexible supercapacitor; UV-ozone treatment; OXIDE THIN-FILMS; COBALT HYDROXIDE; STAINLESS-STEEL; CAPACITANCE; NANOTUBES;
D O I
10.1016/j.jpowsour.2012.04.076
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
A thin film of Co3O4 nanosheets is electrodeposited on a flexible Ti substrate by a one-step potentiostatic method, followed by an UV-ozone treatment for 30 min. The films before and after the UV-ozone treatment are characterized with X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The film is composed of Co(OH)(2) before UV-ozone treatment, and of Co3O4 after the treatment. The morphologies of both films are examined by scanning electron microscopy (SEM) and transmission electron microscope (TEM). The obtained films are composed of nanosheets, and there is no change in their sheet-like morphology before and after the UV-ozone treatment. When applied for a supercapacitor, the Co3O4 modified Ti electrode (Co3O4/Ti) shows a far higher capacitance than that of the Co(OH)2 modified Ti electrode. The electrodeposition time and NaOH concentration in the electrolyte are optimized. A remarkably high specific capacitance of 1033.3 F g(-1) is obtained for the Co3O4 thin film at a charge-discharge current density of 2.5 A g(-1). The long-term stability data shows that there is still 77% of specific capacitance remaining after 3000 repeated charge-discharge cycles. The high specific capacitance and long-term stability suggest the potential use of CO3O4/Ti for making a flexible supercapacitor. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 99
页数:9
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