Related Experiment Video
Updated: Jul 13, 2026

Probing and Mapping Electrode Surfaces in Solid Oxide Fuel Cells
Published on: September 20, 2012
The p(O2) dependence of oxygen surface coverage and exchange current density of mixed conducting oxide electrodes:
J Fleig1, Rotraut Merkle, Joachim Maier
1Institute of Chemical Technologies and Analytics, Vienna University of Technology, Getreidemarkt 9-164/EC, 1060, Vienna, Austria. j.fleig@tuwien.ac.at
Abstract:
The charge of adsorbed oxygen species such as O, O or O electrostatically affects the kinetics of the oxygen exchange reaction (1/2O2+2e-<-->O2-) taking place on mixed conducting oxides. For a model assuming a homogeneous double layer of adsorbed ions and counter charges in the mixed conducting electrode it is calculated how the surface coverage theta of the different species depends on the oxygen partial pressure p(O2). Mixed conducting "electron rich" oxides with high electronic carrier concentrations are considered. Models with p(O2) independent hole concentration or p(O2) independent vacancy concentration are discussed as limiting cases. It is quantified how strongly the electrostatic repulsion of adsorbed ions flattens the theta-p(O2) relationships compared to Langmuir's case; even situations can occur in which the surface coverage of some oxygen species decreases with increasing p(O2). In a second step the p(O2)-dependence of the equilibrium exchange rate of the surface reaction 1/2O2+2e-<-->O2- is deduced for several possible rate limiting steps. These relations may serve as a basis for future mechanistic interpretations of the p(O2) dependence of SOFC electrode polarization and of effective surface rate constants kdelta, k* in oxygen stoichiometry change or 18O tracer exchange experiments, respectively.
More Related Videos
Related Concept Videos
Processes at Electrodes
The Electrical Double Layer
Debye–Huckel–Onsager Conductance Equation
Current Density
Interfacial Electrochemical Methods: Overview
Electrochemical Systems

