4.7 Article

Identification of an Electrode-Adsorbed Intermediate in the Catalytic Hydrogen Evolution Mechanism of a Cobalt Dithiolene Complex

Journal

INORGANIC CHEMISTRY
Volume 56, Issue 4, Pages 1988-1998

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.6b02586

Keywords

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Funding

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0015303]
  2. University of North Carolina at Chapel Hill
  3. Packard Fellowship for Science and Engineering
  4. Alfred P. Sloan Foundation
  5. National Science Foundation of the National Nanotechnology Coordinated Infrastructure (NNCI) [ECCS-1542015]
  6. U.S. Department of Energy (DOE) [DE-SC0015303] Funding Source: U.S. Department of Energy (DOE)

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Analysis of a cobalt bis(dithiolate) complex reported to mediate hydrogen evolution under electrocatalytic conditions in acetonitrile revealed that the cobalt complex transforms into an electrode-adsorbed film upon addition of acid prior to application of a potential. Subsequent application of a reducing potential to the film results in desorption of the film and regeneration of the molecular cobalt complex in solution, suggesting that the adsorbed species is an intermediate in catalytic H-2 evolution. The electroanalytical techniques used to examine the pathway by which H-2 is generated, as well as the methods used to probe the electrode -adsorbed species, are discussed. Tentative mechanisms for catalytic H-2 evolution via an electrode-adsorbed intermediate are proposed.

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