Electrocatalytic glucose oxidation at bimetallic gold–copper nanoparticle-modified carbon electrodes in alkaline solution

Abstract

To achieve both oxidation reactions at a more negative potential and better reactions in electrocatalytic glucose oxidation, AuCu alloy nanoparticles were synthesized and their activities for glucose oxidation in alkaline solution were investigated by voltammetric and controlled-potential electrolysis studies. Decanethiol-encapsulated (DT-) Au nano, DT-Au 97Cu 3 (m: atomic%), and DT-Cu nano nanoparticles were synthesized, and their core sizes were determined to be 2 (±1), 2 (±1), and 4 (±2) nm, respectively. To remove the DT monolayer from the DT-Au nano, DT-Au 97Cu 3 and DT-Cu nano nanoparticles, nanoparticle-modified plastic-formed carbon plate (PFC) electrodes were heated at 300 °C for 2 h. Elimination of the DT was confirmed by FT-IR and XPS measurements. The surface metal atomic content ratios of DT-Au 97Cu 3 eventually changed to Au 77Cu 23, after the heat-treatment. The voltammetric behavior of electrocatalytic glucose oxidation at the Au 77 Cu 23 nanoparticle-modified electrodes in alkaline solution was similar to the Au nano nanoparticle-modified electrodes, in which the potential was more negative than a Cu nano nanoparticle-modified electrode and bulk-like Cu electrodes. Upon controlled-potential electrolysis, Au 77 Cu 23 nanoparticle-modified electrodes gave gluconolactone and formate as main products, which indicated that electrocatalytic oxidation, was promoted in comparison with the Au nano nanoparticle-modified electrodes. It is concluded that Au 77Cu 23 nanoparticles have both advanced properties of Au nano and Cu nano nanoparticles for glucose oxidation.