4.6 Article Proceedings Paper

New Cobalt-Bisterpyridyl Catalysts for Hydrogen Evolution Reaction

Journal

CHEMCATCHEM
Volume 9, Issue 12, Pages 2099-2105

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.201700428

Keywords

catalysis; density functional calculation; electrochemistry; hydrogen; terpyridines

Funding

  1. Foundation de l'Orangerie
  2. French National Research Agency (ANR, Carbiored) [ANR-12-BS07-0024-03]
  3. Deutsche Forschungsgemeinschaft
  4. GENCI (TGCC) [2017-810082]
  5. French National Research Agency (ANR, PhotoCarb) [ANR-16-CE05-0025-01]
  6. French National Research Agency (ANR, Grant Labex DYNAMO) [ANR-11-LABX-0011]

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Preparation of a series of terpyridyl ligands bearing different substituents recently led to the synthesis of new cobalt-bisterpyridyl complexes spanning over a wide range of redox potentials. In this work, we describe the catalytic properties of these complexes for the electroreduction of protons into hydrogen ( hydrogen evolution reaction (HER)) in acetonitrile. The substituents of the ligands were found to greatly affect the catalytic performances of the systems, in terms of stability and overpotential. Interestingly, systems based on dimethylaminoterpyridine derivatives perform HER with high efficiency, low overpotential and excellent stability. Density functional theory calculations were used to provide insights into the reaction mechanism of HER catalyzed by these systems, highlighting the role of the ligand for proton activation.

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