Glucose electrooxidation reaction on Ni-based nanocatalysts for replacing OER in alkaline electrolyser

Abstract

In a backdrop of energy transition and geopolitical tensions, efficient biomass-assisted hydrogen production with non-platinum group metals is sought out. Understanding of the related reaction mechanisms is crucial for the rational development of effective electrocatalytic materials but said mechanisms can sometimes be uncritically trusted and cited extensively in contexts deviating from the original working hypotheses. This is the case of Fleischmann’s mechanism for the glucose oxidation reaction (GOR) on nickel, where the initial information was progressively modified and extrapolated carelessly. In line with recent research, this work attempts to tackle some preconceptions on the glucose oxidation reaction on nickel and nickel-based electrodes. The electrooxidation of xylose, other major product of lignocellulosic biomass, but very scarcely discussed in the literature, is also studied, alone and in a biomass-like mixture with glucose. Based on electrochemical (cyclic voltammetry, chronoamperometry and impedance spectroscopy) and analytical (product distribution obtained during 5 hours aldose electrolysis experiments) results on different anode materials (Ni foam, Ni@(NiOxH)y/C and Ni5Mn5Ox/C), the aldose electrooxidation mechanisms of are revisited. Additionally, this study addresses some previously unexplored questions concerning this system such as material poisoning, the viability of using a membrane in GOR electrolysis cells, or the impact of aldose chemical degradation by the alkaline electrolyte on selectivity interpretation.

Supplementary files

Article information

Article type
Paper
Submitted
28 Apr 2026
Accepted
28 May 2026
First published
05 Jun 2026

Faraday Discuss., 2026, Accepted Manuscript

Glucose electrooxidation reaction on Ni-based nanocatalysts for replacing OER in alkaline electrolyser

A. Rigoulet, T. Rafaïdeen, T. W. Napporn and C. Coutanceau, Faraday Discuss., 2026, Accepted Manuscript , DOI: 10.1039/D6FD00078A

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