Hydrothermally Grown SnO2 and SnO2/rGO Nanocomposite and Its Physio-Electrochemical Studies for Pseudocapacitor Electrode Applications

被引:3
|
作者
Osora, Helen [1 ]
Kolkoma, David [1 ]
Anduwan, Gabriel [1 ]
Waimbo, Mathew [1 ]
Velusamy, Senthilkumar [1 ]
机构
[1] Papua New Guinea Univ Technol, Dept Appl Phys, Private Mail Bag 411, Lae, Morobe, Papua N Guinea
关键词
Hydrothermal; SnO2/rGO Nanocomposite; Pseudocapacitor Electrode; Energy Storage; Cyclic Voltammetry; Impedance Analysis; HIGH-PERFORMANCE ANODE; CARBON; ENERGY; NANOSTRUCTURES; COMPOSITE; DEPOSITION; NANOSHEETS;
D O I
10.1007/s10876-023-02517-5
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In this present work, the transition metal oxides of SnO2 and SnO2/rGO nanocomposite were synthesized through a facile hydrothermal method for supercapacitor electrode material applications. The structural, morphological, and elemental analysis of the synthesised samples were characterised by X-ray diffractometer technique (XRD), Field emission scanning electron microscopy (FESEM), Energy dispersive X-ray analysis (EDX), and High-resolution transmission electron microscopy (HR-TEM). The morphology of SnO2 was an agglomeration of quasi-spherical-shaped particles with a diameter range of 12-19 nm, as observed using the HR-TEM technique. The optical properties were characterised by UV-vis and Raman spectroscopy. The electrochemical performance of SnO2 and SnO2/rGO nanocomposite electrode was studied in a 3 M KOH electrolyte. A specific capacitance of 346 F g(-1) at a current density of 0.95 A g(-1) for the SnO2/rGO nanocomposite electrode was recorded, which was significantly higher than that of the as-synthesised SnO2 electrode (267 F g(-1)). The higher capacitance obtained was due to the synergistic effect of excellent conductivity and a high surface area of rGO within the composite electrode. The exceptional electrochemical properties clearly indicate that the SnO2/rGO nanocomposites are the best for highly efficient pseudocapacitor electrodes in future energy storage device applications.
引用
收藏
页码:875 / 889
页数:15
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