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Molecular Electrocatalysts for the Oxidation of Hydrogen and the Production of Hydrogen - The Role of Pendant Amines as Proton Relays

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume -, Issue 7, Pages 1017-1027

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201001081

Keywords

Hydrogen; Electrochemistry; Hydrides; Homogeneous catalysis; Proton transport

Funding

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences

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Electrocatalysts for efficient conversion between electricity and chemical bonds will play a vital role in future systems for storage and delivery of energy. Our research on functional models of hydrogenase enzymes uses nickel and cobalt, abundant and inexpensive metals, in contrast to platinum, a precious metal used in fuel cells. A key feature of our research is a focus on the use of pendant amines incorporated into diphosphane ligands. These pendant amines function as proton relays, lowering the barrier to proton transfers to and from the catalytically active metal site. The hydride acceptor ability of metal cations, along with the basicity of pendant amines, are key thermochemical values that determine the thermodynamics of addition of H-2 to a metal complex with a pendant amine incorporated into its ligand. Nickel catalysts for oxidation of H-2 have turnover frequencies up to 50 s(-1) (at 1 atm H-2 and room temperature). Nickel and cobalt catalysts for production of H-2 by reduction of protons were studied; one of them has a turnover frequency over 1000 s(-1).

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