Codeposition of Platinum and Gold on Nickel Wire Electrodes via Galvanic Replacement Reactions for Electrocatalytic Oxidation of Alcohols

Codeposition of Pt and Au on Ni wire was performed using a simple treatment of immersing Ni wire in aqueous solutions containing both K2PtCl4 and HAuCl4. For evaluating the electrochemical properties of the thus-prepared electrodes, cyclic voltammograms (CVs) of 1.0 M ethanol in 1.0 M NaOH aqueous solutions were recorded. Compared with Pt- or Au-deposited Ni wire electrodes prepared by treating Ni wire in aqueous solutions of a single component, e.g., 1.0 mM K2PtCl4 or 1.0 mM HAuCl4, a noteworthy increase in the electrocatalytic current was observed for the oxidation of ethanol with a PtAu-codeposited Ni (PtAu/Ni) wire electrode even when it was prepared in an aqueous solution containing both 0.10 mM K2PtCl4 and 0.10 mM HAuCl4. In addition, the shape and the peak potentials of CVs recorded using PtAu/Ni wire electrodes were found to be different from those recorded with the Pt- or Au-deposited Ni wire electrodes. Because the CV responses typical of the PtAu/Ni wire electrodes were observed even when a PtAu/Ni wire electrode was prepared in an aqueous solution containing both 0.010 mM K2PtCl4 and 1.0 mM HAuCl4, it is considered that a small amount of Pt was effectively modified or incorporated and affected the electrochemical properties significantly. The CV results for ethanol oxidation were compared with those for the electrocatalytic oxidations of methanol, 1-propanol, and 2-propanol. Besides, the CV results recorded with the present PtAu/Ni wire electrodes are discussed in comparison with some previous results obtained using other PtAu nanoelectrocatalysts.

Automated summary

Pt and Au were successfully codeposited on Ni wire using a simple treatment in aqueous solutions, resulting in PtAu/Ni electrodes with enhanced electrocatalytic current and distinct CV responses. A small amount of Pt was considered to be effectively modified or incorporated into the Ni wire, significantly affecting the electrochemical properties.