To understand the kinetics controlling the SOFC cathode processes, a model mixed conducting perovskite materials system, SrTi_(1-x)Fe_xO_(3-δ), was selected, offering the ability to systematically control both the levels of electronic and ionic electrical conductivity as well as the energy band structure. This, in combination with considerably simplified electrode geometry, served to demonstrate that the rate of oxygen exchange at the surface of SrTi_(1-x)Fe_xO_(3-δ) is only weakly correlated with either high electronic or ionic conductivity, in apparent contradiction with common expectations. On the other hand, evidence was found suggesting the importance of minority electronic species in determining the rate of oxygen exchange. Furthermore, the enrichment of Sr to the surface of the electrodes was found to reduce the oxygen exchange rate constant; this effect becoming more evident with increasing values of x. The observed trends are discussed in relation to the cathodic behavior of MIEC electrodes
