These authors contributed equally to this work.
Communication
Enhancing the Alkaline Hydrogen Evolution Reaction Activity through the Bifunctionality of Ni(OH)2/Metal Catalysts†
Article first published online: 5 NOV 2012
DOI: 10.1002/anie.201204842
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Angewandte Chemie International Edition
Volume 51, Issue 50, pages 12495–12498, December 7, 2012
Additional Information
How to Cite
Danilovic, N., Subbaraman, R., Strmcnik, D., Chang, K.-C., Paulikas, A. P., Stamenkovic, V. R. and Markovic, N. M. (2012), Enhancing the Alkaline Hydrogen Evolution Reaction Activity through the Bifunctionality of Ni(OH)2/Metal Catalysts . Angew. Chem. Int. Ed., 51: 12495–12498. doi: 10.1002/anie.201204842
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This work was supported by the Office of Science, Office of Basic Energy Sciences, Division of Materials Science, U.S. Department of Energy, under contract number DE-AC0-06CH11357. N.D. would like to thank the Chemical Sciences and Engineering Division at Argonne National Laboratory for funding.
- ‡
These authors contributed equally to this work.
Publication History
- Issue published online: 4 DEC 2012
- Article first published online: 5 NOV 2012
- Manuscript Revised: 10 OCT 2012
- Manuscript Received: 21 JUN 2012
Funded by
- Office of Science, Office of Basic Energy Sciences, Division of Materials Science, U.S. Department of Energy. Grant Number: DE-AC0-06CH11357
- Chemical Sciences and Engineering Division at Argonne National Laboratory
Keywords:
- electrocatalysis;
- electrochemistry;
- hydrogen;
- hydrogen evolution reaction;
- surface chemistry
Active in alkaline environment: The activity of nickel, silver, and copper catalysts for the electrochemical transformation of water to molecular hydrogen in alkaline solutions was enhanced by modification of the metal surfaces by Ni(OH)2 (see picture; I=current density and η=overpotential). The hydrogen evolution reaction rate on a Ni electrode modified by Ni(OH)2 nanoclusters is about four times higher than on a bare Ni surface.

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