4.8 Article

A GO/CoMo3S13 chalcogel heterostructure with rich catalytic Mo-S-Co bridge sites for the hydrogen evolution reaction

Journal

NANOSCALE
Volume 14, Issue 26, Pages 9331-9340

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2nr01800d

Keywords

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Funding

  1. National Research Foundation of Korea (NRF) [2021R1A4A3027878, 2020R1A2C4001617, 2021M3H4A1A02055684]
  2. National Research Foundation of Korea [2021R1A4A3027878, 2021M3H4A1A02055684, 2020R1A2C4001617] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study develops an active sulfur site-controlled molybdenum sulfide catalyst for efficient hydrogen evolution reaction. The optimized graphene oxide/cobalt molybdenum sulfide heterostructure catalyst exhibits excellent HER performance and stability.
Molybdenum disulfide (MoS2)-based materials are extensively studied as promising hydrogen evolution reaction (HER) catalysts. In order to bring out the full potential of chalcogenide chemistry, precise control over the active sulfur sites and enhancement of electronic conductivity need to be achieved. This study develops a highly active HER catalyst with an optimized active site-controlled cobalt molybdenum sulfide (CoMo3S13) chalcogel/graphene oxide aerogel heterostructure. The highly active CoMo3S13 chalcogel catalyst was achieved by the synergetic catalytic sites of [Mo3S13](2-) and the Mo-S-Co bridge. The optimized GO/CoMo3S13 chalcogel heterostructure catalyst exhibited high catalytic HER performance with an overvoltage of 130 mV, a current density of 10 mA cm(-2), a small Tafel slope of 40.1 mV dec(-1), and remarkable stability after 12 h of testing. This study presents a successful example of a synergistic heterostructure exploiting both the appealing electrical functionality of GO and catalytically active [Mo3S13](2-) sites.

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