Investigation of the state of the electrochemically generated adsorbed O species on Au films interfaced with Y2O3-doped-ZrO2 |
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Authors: | D Tsiplakides S G Neophytides C G Vayenas |
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Institution: | (1) Department of Chemical Engineering, University of Patras, GR-26500 Patras, Greece;(2) Institute of Chemical Engineering and High Temperature Chemical Processes, P.O. Box 1414, GR-26500 Patras, Greece |
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Abstract: | Adsorbed O species on Au interfaced with Y2O3-doped-ZrO2 are generated by electrochemical O2− supply. It was found that two oxygen chemisorbed states are formed, which desorb at 420 °C (state α) and 550 °C (state β)
with activation energies of desorption ranging between 115–145 kJ/mol and 235–270 kJ/mol, respectively. The strong interaction
of the β-state O species with the Au surface causes an over 600 mV increase in Au surface potential and work function while
the α-state O species is formed at even more positive catalyst-electrode potential. State α is attributed to normally adsorbed
atomic O while the more ionic state β is only created electro-chemically and is mainly responsible for the work function increase
of the Au catalyst-electrode surface. Their desorption activation energies of both states decrease linearly with increasing
catalyst-electrode potential with slopes of the order of four.
Paper presented at the 7th Euroconference on Ionics, Calcatoggio, Corsica, France, Oct. 1–7, 2000. |
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