Surface oxygen exchange kinetics of mixed conducting oxides: Dilatometric vs electrical conductivity relaxation study

The surface oxygen exchange kinetics of mixed ionic-electronic conducting (MIEC) oxides play a crucial role in a variety of applications, including solid oxide fuel/electrolysis cells (SOFCs/SOECs), permeation membranes and sensors. To date, a variety of methods, including isotope exchange, electrical conductivity, optical absorptivity and thermogravimetry relaxation, and impedance spectroscopy have been used to measure the oxygen exchange coefficient of MIEC oxides. Each of these methods have their advantages and limitations, depending on the physical and chemical properties of the investigated materials and their sample dimensions and densities. Here, we demonstrate the ability to precisely measure the surface oxygen exchange coefficient (kchem) of MIEC model material Pr0.1Ce0.9O2-delta (PCO) by use of dilatometric relaxation measurements, particularly of interest for materials that exhibit larger chemical expansion coefficients. This is achieved by use of porous bulk specimens to ensure that the contribution of oxygen exchange to the overall kinetics is dominant. We demonstrate that kchem values extracted from chemical expansion relaxation measurements on PCO are nearly identical to those derived from electrical conductivity relaxation measurements. This provides the opportunity to precisely investigate the oxygen exchange and chemical expansion kinetics of a wide range of materials used in high-temperature applications, particularly where more conventional methods are difficult or inappropriate to apply.

Automated summary

The surface oxygen exchange kinetics of mixed ionic-electronic conducting (MIEC) oxides have important implications in various applications. Different methods have been used to measure the oxygen exchange coefficient, each with its advantages and limitations. The study demonstrates the precise measurement of the surface oxygen exchange coefficient of a model MIEC material using dilatometric relaxation measurements, particularly beneficial for materials with larger chemical expansion coefficients. This provides an opportunity to investigate the oxygen exchange and chemical expansion kinetics of various materials used in high-temperature applications with accuracy, especially in cases where conventional methods are not suitable.