H 2 Evolution with Silicotungstic Acid Electron Mediator over V-Doped MoS 2 Electrocatalysts

作者：Haibing Zheng, Qing‐Nan Wang, Zijin Wang, Weiguang Ma, Guifa Long, Ben Chang, Shijun Liao, Can Li · 发表于：ACS Energy Letters · 年份：2025 · DOI：10.1021/acsenergylett.4c03305 · 被引用次数：33 · 研究领域：Electrocatalysts for Energy Conversion、Advanced battery technologies research、CO2 Reduction Techniques and Catalysts

Metal-doped molybdenum sulfide (MoS 2 ) shows promise for achieving platinum-like catalytic activity in the hydrogen evolution reaction (HER) of electrocatalysis, though the proton and electron transfer kinetics remain poorly understood. In this study, we investigated the HER kinetics and mechanism on both pristine and vanadium(V)-doped MoS 2 catalysts using silicotungstic acids as electron mediators. V-doped MoS 2 exhibits an HER rate approximately 5 times that of MoS 2 (696.4 vs 140.7 mmol H2 g –1 min –1 ). This enhancement is attributed to accelerated proton adsorption and transfer kinetics, driven by an increased number of active sites and favorable proton transfer in the Volmer step. Moreover, silicotungstic acids mediate electron transfer through an inner-sphere mechanism, showing identical reaction orders on both pristine and V-doped MoS 2 . Electrochemical Tafel slopes reveal that H 2 evolution follows a Volmer–Heyrovsky mechanism, regardless of V doping. This work highlights the significance of proton adsorption and transfer kinetics in enhancing HER rates.