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Structure of active phases during the course of electrocatalytic reactions

Journal Article · · Journal of Physical Chemistry B: Materials, Surfaces, Interfaces, amp Biophysical
DOI:https://doi.org/10.1021/jp9917446· OSTI ID:20017302
Structures of ordered adsorbates have been determined during the course of the electrocatalytic reduction of oxygen by using synchrotron surface X-ray scattering techniques. The origin of the catalytic action of Tl adlayers on O{sub 2} reduction on Au has been determined, and a possibility of measuring the adsorption configuration-specific activity in O{sub 2} reduction has been demonstrated in the reaction on Ag(100) with Br adlayer. On the Au(111) electrode surface, the oxidation/redeposition of Tl in catalyzing the four-electron oxygen reduction is revealed from the analysis of X-ray diffraction intensity as a function of the O{sub 2} reduction current for the (3 x {radical}3)-2TlBr adlayer. This indicates that the redox property of the metal adsorbates is responsible for the catalytic effect. On Ag(100) with the c(2 x 2)Br adlayer, the O{sub 2} reduction current resulting solely from adsorption in the end-on configuration through the 3-fold symmetry holes in the c(2 x 2) Br lattice is observed, showing the bridge adsorption may not be necessary for the four-electron O{sub 2} reduction on Ag at large overpotentials.
Research Organization:
Brookhaven National Lab., Upton, NY (US)
Sponsoring Organization:
US Department of Energy
DOE Contract Number:
AC02-98CH10886
OSTI ID:
20017302
Journal Information:
Journal of Physical Chemistry B: Materials, Surfaces, Interfaces, amp Biophysical, Journal Name: Journal of Physical Chemistry B: Materials, Surfaces, Interfaces, amp Biophysical Journal Issue: 5 Vol. 104; ISSN 1089-5647; ISSN JPCBFK
Country of Publication:
United States
Language:
English