Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Electrocatalysis of anodic oxygen-transfer reactions: Evolution of ozone

Journal Article · · Journal of the Electrochemical Society; (United States)
DOI:https://doi.org/10.1149/1.2059184· OSTI ID:6992849
;  [1]; ;  [2]
  1. Ames Lab., IA (United States)
  2. Environmental Sciences/HAEL, Rochester, NY (United States). Kodak Research Labs.
Current efficiencies are compared for the generation of O[sub 3] simultaneously with O[sub 2] during anodic discharge of H[sub 2]O at pure and iron(III)-doped [beta]-lead dioxide film electrodes in phosphate buffer (pH 7.5, 10 C) containing 2.5 mM KF. Also examined is the effect of applied current density. A current efficiency of 14.6% was obtained for the Fe(III)-doped PbO[sub 2] film electrode deposited on a internally cooled (10 C) tubular titanium substrate at a current density of 200 mA cm[sup [minus]2] as compared to only 6.1% at the undoped PbO[sub 2] electrode under the same conditions. This result is tentatively explained on the basis of a mechanism involving the transfer of oxygen from hydroxyl radicals adsorbed on Pb(IV) sites adjacent to Fe(III) sites to O[sub 2] adsorbed at the Fe(III) sites in the surface of the Fe(III)-doped PbO[sub 2] electrodes.
DOE Contract Number:
W-7405-ENG-82
OSTI ID:
6992849
Journal Information:
Journal of the Electrochemical Society; (United States), Journal Name: Journal of the Electrochemical Society; (United States) Vol. 141:10; ISSN JESOAN; ISSN 0013-4651
Country of Publication:
United States
Language:
English