4.8 Article

Fullerene-like WS2 supported Pd catalyst for hydrogen evolution reaction

期刊

JOURNAL OF CATALYSIS
卷 380, 期 -, 页码 215-223

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2019.10.007

关键词

Electrocatalytic hydrogen evolution; Tungsten disulfide; Palladium catalyst; Tungsten trioxide; Reaction mechanism

资金

  1. National Natural Science Foundation of China [21976141, 21601128, 21761162016]
  2. Key Research and Development Program of MOST [2017YFE0131200]
  3. Central Committee Guides Local Science and Technology Development Special Project of Hubei Province [2019ZYYD073]

向作者/读者索取更多资源

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 similar to 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 H-ads intermediate and the Pd NPs are active sites of H-2 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. (C) 2019 Elsevier Inc. All rights reserved.

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