4.8 Article

Activating MoS2 for pH-Universal Hydrogen Evolution Catalysis

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 45, 页码 16194-16200

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b07450

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  1. CCDM, an EFRC - U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences (BES) [DE-SC0012575]
  2. DOE, Office of Science, BES, Materials Sciences and Engineering Division [DE-SC0012704]
  3. State of North Carolina
  4. National Science Foundation
  5. U.S. Department of Energy (DOE) [DE-SC0012575] Funding Source: U.S. Department of Energy (DOE)

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MoS2 presents a promising catalyst for the hydrogen evolution reaction (HER) in water splitting, but its worse catalytic performance in neutral and alkaline media than in acidic environment may be problematic for practical application. This is because the other half reaction of water splitting, i.e., oxygen evolution reaction, often needs to be implemented in alkaline environment. Here we demonstrate a universal strategy that may be used to significantly improve the HER catalysis of MoS2 in all kinds of environments from acidic to alkaline, proton intercalation. Protons may be enabled to intercalate between monolayer MoS2 and underlying substrates or in the interlayer space of thicker MoS2 by two processes: electrochemically polarizing MoS2 at negative potentials (vs RHE) in acidic media or immersing MoS2 into certain acid solutions like TFSI. The improvement in catalytic performance is due to the activity enhancement of the active sites in MoS2 by the intercalated protons, which might be related with the effect of the intercalated protons on electrical conductance and the adsorption energy of hydrogen atoms. The enhancement in catalytic activity by the intercalated proton is very stable even in neutral and alkaline electrolytes.

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