• 文献标题:   Novel fabrication of PdCu nanostructures decorated on graphene as excellent electrocatalyst toward ethanol oxidation
  • 文献类型:   Article
  • 作  者:   DOUK AS, SARAVANI H, NOROOZIFAR M
  • 作者关键词:   electrochemical reduction reaction, pdcu nanostructure, fast synthesize method, ethanol oxidation
  • 出版物名称:   INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
  • ISSN:   0360-3199 EI 1879-3487
  • 通讯作者地址:   Univ Sistan Baluchestan
  • 被引频次:   30
  • DOI:   10.1016/j.ijhydene.2017.04.280
  • 出版年:   2017

▎ 摘  要

In this study, the electrochemical reduction reaction of copper(II) formate on the graphene/glassy carbon electrode (G/GCE) surface in the HCl (5 wt.%) was employed for fabrication of the Pd-Cu nanostructures by galvanic displacement reaction. This method has a number of advantages including being environmentally-friendly, simplicity, inexpensiveness and fast. The Pd-Cu nanostructures decorated on the G/GCE were fabricated in two steps: (1) electrochemical reduction reaction of copper(II) formate to Cu on the G/GCE and (2) the galvanic replacement reaction between Cu and Pd2+ ions. The physical and electrochemical properties of as-prepared Pd-Cu/G were investigated via Field Emission Scanning Electron Microscopy, Energy Dispersive X-ray Spectroscopy, Cyclic Voltammetry, Chronoamperometry, and Electrochemical Impedance Spectroscopy. The Pd-Cu/G compositional effect on ethanol oxidation in alkaline media is investigated. The results were shown that the catalytic activity and durability of Pd-Cu/G catalyst are superior to those of Pd/C electrocatalyst for ethanol oxidation. The Pd-Cu/G increased the current density 6.2 times more than Pd/C with a 50 my negative shift in onset potential for electrooxidation of ethanol. Besides, the novel Pd-Cu/G catalyst exhibits large electrochemically active surface area, lower apparent activation energy, higher levels of stability, poisoning tolerance, and lower charge transfer resistance compared to the Pd/C for the oxidation of ethanol. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier. Ltd. All rights reserved.