Electroless Deposition of Silver Dendrite Nanostructure onto Glassy Carbon Electrode and Its Electrocatalytic Activity for Ascorbic Acid Oxidation

被引:19
|
作者
Hasan, Md Mahmudul [2 ]
Rakib, Riad Hussain [1 ]
Abul Hasnat, Mohammad [1 ]
Nagao, Yuki [2 ]
机构
[1] Shahjalal Univ Sci & Technol, Grad Sch Phys Sci, Dept Chem, Sylhet 3114, Bangladesh
[2] Japan Adv Inst Sci & Technol, Sch Mat Sci, Nomi, Ishikawa 9231292, Japan
来源
ACS APPLIED ENERGY MATERIALS | 2020年 / 3卷 / 03期
关键词
electroless deposition; electrocatalysis; ascorbic acid; electron transfer kinetics; dendrite structure; VOLTAMMETRIC DETERMINATION; SELECTIVE DETECTION; GREEN SYNTHESIS; AG DENDRITES; NANOPARTICLES; MECHANISM; DOPAMINE; REDUCTION; CRYSTALLINE; PERFORMANCE;
D O I
10.1021/acsaem.9b02513
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
Well-defined silver dendrite nanostructures with primary and secondary branches on a glassy carbon electrode (GCE) surface are first demonstrated using a simple wet chemical electroless deposition method without any aid of a surfactant. The properties of dendrite structures were characterized using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). Results of XPS and XRD indicated that most of the silver particles were not oxidized. The obtained silver dendrite GCE (Ag/GCE) showed high electrochemical activity toward catalytic oxidation for ascorbic acid (AA). The oxidation process followed a stepwise mechanism at slower scan rates (upsilon < 0.15 V s(-1)) and a concerted mechanism at faster scan rates (upsilon > 0.15 V s(-1)). The silver nanostructures are stable on the GCE surface and could be employed as an anode for an AA fuel cell.
引用
收藏
页码:2907 / 2915
页数:9
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