Facile Synthesis of Bio-Templated Tubular Co3O4 Microstructure and Its Electrochemical Performance in Aqueous Electrolytes

被引:12
作者
Guragain, D. [1 ]
Zequine, C. [2 ]
Poudel, T. [1 ]
Neupane, D. [3 ]
Gupta, R. K. [2 ]
Mishra, S. R. [1 ]
机构
[1] Univ Memphis, Dept Phys & Mat Sci, Memphis, TN 38152 USA
[2] Pittsburg State Univ, Dept Chem, Pittsburg, KS 66762 USA
[3] Univ Memphis, Dept Engn Technol, Memphis, TN 38152 USA
关键词
Biotemplated; Co3O4; Electrochemistry; Supercapacitance; Specific Capacitance; ENERGY-STORAGE; HYDROTHERMAL SYNTHESIS; PORE-SIZE; ACTIVATED CARBON; TIO2; ANATASE; SUPERCAPACITOR; COBALT; ELECTRODES; CAPACITANCE; COMPOSITES;
D O I
10.1166/jnn.2020.17414
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Template-assisted facile synthesis of tubular Co3O4 microstructures and its electrochemical performance was studied to understand its use as a potential electrode material for supercapacitors. Tubular porous Co3O4 microstructures were synthesized using cotton fibers as bio-template. The as-obtained templated Co3O4 structure inherits the morphology and microstructure of cotton fiber. The electrochemical performance of the electrode made up of tubular Co3O4 structure was evaluated in 3 M KOH, NaOH, and LiOH aqueous electrolytes. The large-surface-area of tubular Co3O4 microstructure has a noticeable pseudocapacitive performance with a capacitance of 401 F/g at 1 A/g and 828 F/g at 2 mV/s, a Coulombic efficiency averaging similar to 100%, and excellent cycling stability with capacitance retention of about 80% after 5,000 cycles. Overall, the tubular Co3O4 microstructure displayed superior electrochemical performance in 3 M KOH electrolyte with peak power density reaching 5,500 W/kg and energy density exceeding 22 Wh/kg. The superior performance of tubular Co3O4 microstructure electrode is attributed to its high surface area and adequate pore volume distribution, which allows effective redox reaction and diffusion of hydrated ions. The facile synthesis method can be adapted for preparing various metal oxide microstructures for possible applications in catalysis, electrochemical, sensors, and fuel cells applications.
引用
收藏
页码:3182 / 3194
页数:13
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