A. Kaloyannis et Cg. Vayenas, NON-FARADAIC ELECTROCHEMICAL MODIFICATION OF CATALYTIC ACTIVITY .11. ETHANE OXIDATION ON PT, Journal of catalysis, 171(1), 1997, pp. 148-159
The rate of ethane oxidation on polycrystalline Pt catalyst films depo
sited on 8 mol% Y2O3-stabilized ZrO2, an O2- conductor, can be reversi
bly enhanced by up to a factor of 20 by varying the potential of the P
t film. The rate increase is typically a factor of 200 higher than the
electrochemically controlled rate of supply of promoting oxide ions.
Electrochemical oxygen removal from the Pt catalyst surface also enhan
ces the catalytic rate by up to a factor of 7. In this case the rate i
ncrease is typically a factor of 20 higher than the electrochemically
controlled rate of oxygen removal. The ethane oxidation activation ene
rgy varies linearly by a factor of 3 with varying catalyst potential,
leading to the appearance of the compensation effect. The observed pro
nounced promotional phenomena are discussed on the basis of the reacti
on mechanism, previous electrochemical promotion studies and recent TP
D and XPS investigations. (C) 1997 Academic Press.