The effect of applied potential on the oxygen transport around gold / gadolinium doped ceria (GDC) or yttria stabilized zirconia (YSZ) was investigated by using oxygen isotope exchange and secondary ion mass spectrometry (SIMS). The active area of oxygen exchange was clearly observed along Au / YSZ / O 2 triple phase boundary (TPB) treated under an applied potential (cathodic polarization) of E = -0.3 V at T = 773 K in dry O 2 , whereas no obvious activation was observed at E = 0 V. On the other hand, the activation of oxygen exchange was broadly observed on GDC surface around Au/GDC boundary, and it was remarkably enhanced by applying the electric potential of E = -0.3 V. The difference of oxygen transport path between Au/YSZ system and Au/GDC system was discussed in relation to the difference in chemical properties of electrolyte materials.
IntroductionThe oxygen transport around the interfaces between electron conducting metal or oxide electrodes / ion conducting oxide electrolytes is very important to realize the kinetics in surface reactions of oxygen permeation membrane, sensors and cathode reactions in solid oxide fuel cells (SOFC). Concerning the cathode reaction in SOFC, it consists of several reaction steps:1. Adsorption of oxygen molecule on electrode surface, 2. Surface diffusion of adsorbed oxygen to the triple phase boundary (TPB) of gas / electron conducting metal or oxide (electrolyte) / ion conducting oxide (electrolyte), 3. Reduction of oxygen by charge transfer process between adsorbed oxygen and oxide ion in electrolyte, 4. Dissolution of oxygen as oxide ion into electrolyte.The reaction processes on simplified interfaces with metal electrode / electrolyte, for examples, platinum / YSZ (1-4) or gold / YSZ (5,6) have been intensively investigated by using a conventional electrochemical method, such as current interruption, complex impedance spectroscopy. Those electrochemical methods have been well established. By these methods, it is easy to obtain the information of charge carrier migration along current path but it is not easy to interpret the observed data because all information is obtained as the changes of current and voltage in which the local transport of oxygen atom and oxide ion are neglected or are not well taken into account. In the actual electrode / electrolyte interfaces, the reaction does not always proceed homogenously, and there will be some inhomogeneous distribution of reaction active sites which will be influenced by many parameters, that is, physical properties of electrode and electrolyte materials and their combination, temperature, magnitude of cathodic polarization etc.To obtain information about the local oxygen transport in the vicinity of interface, we have adopted the experimental approaches for visualizing the tracks of oxygen transport at interfaces by using the oxygen isotope ( 18 O) labeling and subsequent secondary ion mass spectrometry analyses (SIMS). Kawada et al. firstly reported that the oxygen exchange was activated at those very restricted areas of pla...