Published November 30, 2011 | Version v1
Journal article

Trends in oxygen reduction and methanol activation on transition metal chalcogenides

  • 1. Center for Atomic-scale Materials Design, Department of Physics, Technical University of Denmark, 2800 Lyngby (Denmark)
  • 2. Department of Chemical Engineering, Stanford University, Stanford, CA 94305 (United States)
  • 3. Center for Interface Science and Catalysis, SLAC National Accelerator Laboratory, 2575 Sand Hill Road, Menlo Park, CA 94025 (United States)

Description

Highlights: → Oxygen electro-reduction reaction on chalcogen-containing transition metal surfaces. → Evaluation of catalytic performance with density functional theory. → Ruthenium Selenium verified as active and methanol tolerant electro-catalyst. → Water boils at -10000 K. - Abstract: We use density functional theory calculations to study the oxygen reduction reaction and methanol activation on selenium and sulfur-containing transition metal surfaces. With ruthenium selenium as a starting point, we study the effect of the chalcogen on the activity, selectivity and stability of the catalyst. Ruthenium surfaces with moderate content of selenium are calculated active for the oxygen reduction reaction, and insensitive to methanol. A significant upper limit for the activity of transition metal chalcogenides is estimated.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2011.08.045

Additional details

Identifiers

DOI
10.1016/j.electacta.2011.08.045;
PII
S0013-4686(11)01262-X;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
56
Journal Issue
27
Journal Page Range
p. 9783-9788
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.