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Updated: Jul 5, 2025

Synthesis of Platinum-nickel Nanowires and Optimization for Oxygen Reduction Performance
Published on: April 27, 2018
Oxygen-deficient tungsten oxide inducing electron and proton transfer: Activating ruthenium sites for hydrogen
Bowen Zhou1, Hao Ding1, Wei Jin2
1Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Xueyuan Road, Haidian District, Beijing 100083, PR China.
Abstract:
The design of electrocatalysts for the hydrogen evolution reaction (HER) that perform effectively across a broad pH spectrum is paramount. The efficiency of hydrogen evolution at ruthenium (Ru) active sites, often hindered by the kinetics of water dissociation in alkaline or neutral conditions, requires further enhancement. Metal oxides, due to superior electron dynamics facilitated by oxygen vacancies (OVS) and shifts in the Fermi level, surpass carbon-based materials. In particular, tungsten oxide (WO3) promotes the directed migration of electrons and protons which significantly activates the Ru sites. Ru/WO3-OV is prepared through a simple hydrothermal and low-temperature annealing process. The prepared catalyst achieves 10 mA cm-2 at overpotentials of 23 mV (1 M KOH), 36 mV (0.5 M H2SO4), 62 mV (1 M PBS), and 38 mV (1 M KOH + seawater). At an overpotential corresponding to 10 mA cm-2 in 1 M KOH and 1 M KOH + seawater, the mass activity of Ru/WO3-OV is about 7.7 and 7.86 times that of 20 wt% Pt/C. The improvement in activity and stability arises from electronic modifications attributed to metal-support interaction. This work offers novel insights for modulating the HER activity of Ru sites across a wide pH range.
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