Enhanced electrocatalytic glycerol oxidation on CuCoN0.6/CP at significantly reduced potentials

Electrocatalytic alcohol oxidation coupled with the hydrogen evolution reaction, wherein a thermodynamically favorable oxidation reaction replaces the sluggish kinetics of the oxygen evolution reaction, has recently attracted considerable attention. However, the development of nonprecious-metal electrocatalysts capable of delivering much lower oxidation potentials holds great significance. In this study, we proposed and developed CuCoN0.6 nanowires loaded on conductive carbon paper (denoted as CuCoN0.6/CP) as an efficient catalyst for selective glycerol oxidation to formate. Our catalyst achieved a remarkably high faradic efficiency of 90.0% towards formate production. More notably, it required an anode potential as low as 1.07 V to achieve a current density of 10 mA cm−2, a significantly lower potential than that reported in the literature. Experimental characterizations reveal that the oxidations of Cu+ and Co2+ ions promoted the formation of reactive hydroxyl species, which are responsible for the substantially reduced oxidation potential and enhanced glycerol oxidation performance. Furthermore, we investigated the reaction pathway of glycerol oxidation and structural changes in the catalysts. The catalyst reconstruction led to the formation of CoOOH, which is considered as the active site for glycerol oxidation. Finally, we successfully separated high-purity and value-added potassium diformate product. This work not only advances the electrocatalytic conversion of biomass-derived alcohols but also provides insights into the design of electrocatalysts with broad applications.