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Electrocatalysis of anodic oxygen-transfer reactions at modified lead dioxide electrodes

Technical Report ·
DOI:https://doi.org/10.2172/6562056· OSTI ID:6562056
The electrocatalytic activities were compared for pure and chloride-doped beta-PbO{sub 2} (Cl-PbO{sub 2}) films on gold and platinum substrates. Rate constants were increased significantly for oxidations of Mn{sup 2+}, toluene, benzyl alcohol, dimethylsulphoxide (DMSO) and benzaldehyde in acidic media by the incorporation of Cl{sup {minus}} into the oxide films. These reactions are concluded to occur by the electrocatalytic transfer of oxygen from H{sub 2}O to the reaction products. Results of x-ray diffraction studies indicate the Cl-PbO{sub 2} film continues to have the slightly distorted rutile structure of pure beta-PbO{sub 2}. The observed electrocatalytic phenomena are concluded to be the beneficial consequence of surface defects generated when Cl{sup {minus}} serves for charge compensation within the surface matrix and, thereby, increases the number of surface sites capable of adsorbing hydroxyl radicals which are transferred in the electrocatalytic O-transfer reactions. 91 refs., 44 figs., 10 tabs.
Research Organization:
Ames Lab., IA (USA)
Sponsoring Organization:
DOE/ER
DOE Contract Number:
W-7405-ENG-82
OSTI ID:
6562056
Report Number(s):
IS-T-1451; ON: DE91000664
Country of Publication:
United States
Language:
English

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