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

Non-Faradaic electrochemical modification of catalytic activity. VII. The case of methane oxidation on platinum

Journal Article · · Journal of Catalysis; (United States)
It was found that the catalytic activity of Pt for the oxidation of CH[sub 4] can be increased reversibly by up to 7,000% by depositing polycrystalline Pt films on Y[sub 2]O[sub 3]-doped ZrO[sub 2], an O[sup 2[minus]] conductor, and by polarizing the Pt-solid electrolyte interface. The catalytic rate is enhanced, to a different extent, both by supplying and by removing O[sup 2[minus]] to or from the Pt catalyst through the gas-impervious solid electrolyte. The rate of CH[sub 4] oxidation was found to depend exponentially on catalyst potential and work function e[Phi] over wide (up to 0.8 eV) e[Phi] ranges. Within the same e[Phi] ranges the catalytic activation energy E varies linearly with e[Phi] and can be lowered from 40 kcal/mol to 11 kcal/mol. The observed behavior can be accounted for within the framework of previous NEMCA studies, although in the present case, due to high operating temperatures, the role of direct electrocatalytic reactions is more pronounced. 45 refs., 12 figs., 1 tab.
OSTI ID:
6130589
Journal Information:
Journal of Catalysis; (United States), Journal Name: Journal of Catalysis; (United States) Vol. 140:1; ISSN 0021-9517; ISSN JCTLA5
Country of Publication:
United States
Language:
English