Implication of surface oxidation of nanoscale molybdenum carbide on electrocatalytic activity

• Published in: Journal of materials chemistry. A, Materials for energy and sustainability Vol. 12; no. 25; pp. 15163 - 15176
• Main Authors: Yu, Siying, Gautam, Ankit Kumar, Gao, Di, Kuhn, Andrew N, He, Haozhen, Mironenko, Alexander V, Yang, Hong
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 25.06.2024
• Subjects: Acidic oxides; Adsorption; Anodizing; Capacitance; Catalysts; Charge transfer; Chemical synthesis; Density functional theory; Electrocatalysts; Electrochemical oxidation; Electrochemistry; Heavy metals; Hydrogen evolution reactions; Metal carbides; Molybdenum; Molybdenum carbide; Noble metals; Oxidation; Oxidation process; Oxycarbides; Oxygen atoms; Photoelectron spectroscopy; Photoelectrons; Transition metals; X ray photoelectron spectroscopy
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/d4ta01746c

Transition metal carbides, such as molybdenum carbides, are promising substitutes for noble metals as low-cost, durable electrocatalysts. Under ambient conditions, however, these carbides are subject to oxidation due to their oxophilic nature. The partially oxidized surface may possess both oxygen-modulated metallic-like hydrogen adsorption sites and Brønsted-acidic hydroxyl sites. However, the impact of surface oxidation on electrochemical processes such as the hydrogen evolution reaction (HER) has rarely been studied. Here, we synthesized β-Mo 2 C catalysts and oxidized their surfaces electrochemically to varying extents to study the effects of surface oxidation on HER activity. The degree of surface oxidation was controlled by applying different potential windows to metal carbide catalysts. The samples with varying degrees of surface oxidation were tested for their HER activity. Experimental data indicate that the Tafel slope for the HER and double-layer capacitance were negatively affected by surface oxidation, particularly due to the loss of carbon and the formation of electrochemically less active surface oxides. The surface oxidation was studied experimentally by X-ray photoelectron spectroscopy and simulated using density functional theory (DFT), ab initio thermodynamics, and charge transfer estimates. Our DFT calculation results suggest that the model β-Mo 2 C (011) surface favors the adsorption of O* from water during the electrochemical oxidation, giving rise to the anodic current. Oxygen atoms preferentially interact with surface C sites, forming stable -C&z.dbd;O species and oxycarbide-like surfaces. Highly oxidized surfaces become kinetically unstable and undergo a deeper, substitutional oxidation through -C&z.dbd;O replacement by O*, forming a thermodynamically stable Mo( iv ) surface oxide, where each Mo atom coordinates with up to six O atoms. The rate-limiting step switches from CO desorption, occuring within the potential window from 0.28 to 0.51 V, to water dissociation above 0.51 V. The computational results agree well with experimental observations, such as the onset potential (0.6 V) for rapid surface oxidation. This work helps to unravel the details of evolution of surface sites during an oxidation process of molybdenum carbides along with their effects on catalytic properties and lays the foundation for their practical use in various applications. The surface oxidation of molybdenum carbide nanoparticles was controlled by the electrochemical method. The impact of surface oxidation on catalytic properties was studied by both spectroscopic and computational methods.