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Molecular Electrocatalysts for the Oxidation of Hydrogen and the Production of Hydrogen – The Role of Pendant Amines as Proton Relays
Article first published online: 4 JAN 2011
DOI: 10.1002/ejic.201001081
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

European Journal of Inorganic Chemistry
Special Issue: Hydrogenases (Cluster Issue)
Volume 2011, Issue 7, pages 1017–1027, March 2011
Additional Information
How to Cite
DuBois, D. L. and Bullock, R. M. (2011), Molecular Electrocatalysts for the Oxidation of Hydrogen and the Production of Hydrogen – The Role of Pendant Amines as Proton Relays. Eur. J. Inorg. Chem., 2011: 1017–1027. doi: 10.1002/ejic.201001081
Publication History
- Issue published online: 21 FEB 2011
- Article first published online: 4 JAN 2011
- Manuscript Received: 11 OCT 2010
Funded by
- Center for Molecular Electrocatalysis, an Energy Frontier Research Center
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Biosciences and Geosciences
- Abstract
- Article
- References
- Cited By
Keywords:
- Hydrogen;
- Electrochemistry;
- Hydrides;
- Homogeneous catalysis;
- Proton transport
Abstract
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 H2 to a metal complex with a pendant amine incorporated into its ligand. Nickel catalysts for oxidation of H2 have turnover frequencies up to 50 s–1 (at 1 atm H2 and room temperature). Nickel and cobalt catalysts for production of H2 by reduction of protons were studied; one of them has a turnover frequency over 1000 s–1.

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