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Electrocatalytic reactivity of hydrocarbons on a zirconia electrolyte surface

Journal Article · · J. Electrochem. Soc.; (United States)
DOI:https://doi.org/10.1149/1.2109027· OSTI ID:7143671
An experimental survey of the electrochemical reactivity of five common fuel species was made employing a solid oxide electrolyte galvanic cell with porous Au and Pt electrodes in the temperature range 700/sup 0/-850/sup 0/C. The electrolyte used was Sc/sub 2/O/sub 3/-stabilized ZrO/sub 2/(SSZ). The fuel species electro-oxidized at the anode were: H/sub 2/ CO, CH/sub 4/, CH/sub 3/OH, and C/sub 2/H/sub 5/OH. Rates of reaction were determined coulometrically so that species other than H/sub 2/ could have undergone an undetermined amount of thermal dissociation during electro-oxidation. The concomitant reactivity of O/sub 2/, which is reduced at the cathode, was also investigated. The current-overpotential behavior at both the cathode and anode was found to be similar whether Au or Pt was used to form the porous electrodes. In the low overpotential range, the rate of charge transfer is found to be rate determining for both the cathodic and anodic reactions.
Research Organization:
Dept. of Chemical Engineering, Stanford Univ., Stanford, CA 94305
OSTI ID:
7143671
Journal Information:
J. Electrochem. Soc.; (United States), Journal Name: J. Electrochem. Soc.; (United States) Vol. 133:9; ISSN JESOA
Country of Publication:
United States
Language:
English