4.7 Article

Low-temperature synthesis of molybdenum sulfides, tungsten sulfides, and composites thereof as efficient electrocatalysts for hydrogen evolution reaction

期刊

APPLIED SURFACE SCIENCE
卷 576, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apsusc.2021.151828

关键词

Molybdenum sulfides; Tungsten sulfides; Composites; Electrocatalysts; Hydrogen evolution reaction

资金

  1. National Research Foundation of Korea (NRF) [2021R1A4A3027878, 2021M3H4A1A02055684]
  2. National Research Foundation of Korea [2021M3H4A1A02055684, 2021R1A4A3027878] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In this work, a one-step approach for synthesizing molybdenum sulfides and tungsten sulfides was reported. The MoSx-100 degrees C exhibited the highest catalytic activity, while WS2 could produce hydrogen at 400 degrees C. A graphene oxide/MoSx-100 degrees C sample showed good stability and high performance in hydrogen production.
In this work, we report a one-step approach for synthesizing molybdenum sulfides and tungsten sulfides, using (N2H5)(2)MS4 (M = Mo, W) as highly energetic self-catalytic redox precursors and inducing a thermolysis process at various temperatures. These materials' thermodynamic advantages facilitate the formation of molybdenum/tungsten sulfides at low temperatures. As expected, MoSx-100 degrees C (which features the [Mo3S13](2-) active site model) exhibits the highest catalytic activity of the reported molybdenum sulfides. In addition, an optimized sample of crystalline WS2 was reported to produce hydrogen at 400 degrees C. Furthermore, the combination of carbon materials significantly enhanced the hydrogen production performance. The optimal sample of reduced graphite oxide (rGO)/MoSx-100 degrees C required an overpotential of only 125 mV to achieve a current density of 10 mA cm(-2) and a shallow Tafel slope of 48.8 mV dec(-1); this was attributed to the increased charge transfer from rGO. Furthermore, the catalyst exhibited good stability after 2000 cycles and 12 h of testing. This work may provide an alternative approach for the large-scale synthesis of transition metal dichalcogenides in high-performance catalyst applications.

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