Functionalization of FeCoNiCu medium entropy alloy via nitridation and anodic oxidation for enhanced oxygen evolution and glycerol oxidation

Medium entropy alloys (MEAs) have emerged as a promising class of materials for electro¬catalysis due to their tunable properties and exceptional catalytic performance. This study successfully functionalized a bulk FeCoNiCu alloy using a combined anodic oxidation (AO) and nitridation (NT) approach to produce a highly porous, thin-film catalyst. The hierarchical structure formed during the surface treatments enhances the material's specific surface area and alters the oxidation states of the constituent metals, creating abundant active sites. The electrocatalytic performance of the modified bulk FeCoNiCu electrode was evalu¬ated for both the oxygen evolution reaction (OER) and glycerol oxidation reaction (GOR) in an alkaline electrolyte. Remarkably, the AO-NT-treated catalyst exhibited superior activity for OER, surpassing commercial IrOx benchmarks with lower overpotential requirements. For GOR, the FeCoNiCu electrode demonstrated excellent performance by significantly reducing energy input compared to OER, highlighting its potential as a dual-purpose catalyst for alkaline water splitting. Post-reaction product analysis via NMR confirmed the formation of value-added chemicals, with formic acid identified as the main product. These results underline the feasibility of surface-modified MEAs for sustainable energy and chemical production applications, offering a cost-effective alternative to noble metal-based catalysts.