Fullerene-like WS2 supported Pd catalyst for hydrogen evolution reaction
Ping Xiao (Heilongjiang University, Wuhan Textile University)
Josephus G. Buijnsters (TU Delft - Mechanical Engineering)
Yanxi Zhao (South-Central University for Nationalities)
Huan Yu (Shenyang Normal University)
Xuelian Xu (Shenyang Normal University, Wuhan Textile University)
Yujun Zhu (Heilongjiang University)
Duihai Tang (Shenyang Normal University)
Junjiang Zhu (Wuhan Textile University, Shenyang Normal University)
Zhen Zhao (Shenyang Normal University)
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Abstract
Hydrogen is the most desirable green energy carrier and electrocatalytic hydrogen evolution reaction (HER) from water is a promising route for hydrogen production. The search for efficient, low-cost HER catalysts is a challenging and attracting topic. In this work, we report that inorganic fullerene-like WS2 supported Pd nanoparticles (Pd/WS2), with Pd loading of 0.76 wt%, are active for electrocatalytic HER conducted in 0.5 M H2SO4 solution, with overpotential at 10 mA cm−2 current density of ~130 mV and Tafel slope of 82.4 mV dec−1, which is comparable to that of Pt/WS2 (0.88 wt% Pt loading) with higher costs. Characteristic results indicate that WO3 impurities were in-situ produced on the WS2 surface and the Pd NPs are primarily located inside the WS2 nanocages. Contrasting experiments suggest that the WO3 impurities play a crucial role in generating Hads intermediate and the Pd NPs are active sites of H2 production, and a reaction mechanism is proposed. The Pd/WS2 catalyst also shows good long-term stability owing to the location of Pd NPs inside the WS2 cages. The high HER activity, low costs and good stability make the Pd catalyst a potential alternative to Pt catalyst for HER.