Experimental evidence of hydrogen–oxygen decoupled diffusion into BaZr0.6Ce0.25Y0.15O3−δ Original Research Article

The electrical properties of BaZr0.6Ce0.25Y0.15O3−δ (BZCY) were studied as a function of both oxygen partial pressure image and water vapor activity image in the temperature range of 973–1073 K. The total conductivity slightly increased in reducing atmospheres with increasing water vapor activity because of the relative contribution to the total conductivity by the redox reaction at the given thermodynamic conditions. The partial conductivities of protons, holes and oxygen vacancies were successfully calculated, and the activation energy determined for proton transport was 0.3 ± 0.1 eV. The chemical diffusivity of oxygen at a fixed water vapor activity, image, could only be evaluated from Fick’s second law during oxidation and reduction at the fixed water vapor activity. However, twofold nonmonotonic conductivity relaxation behaviors were clearly confirmed in the temperature range investigated during hydration/dehydration. If image represents the fixed oxygen partial pressure, image is the hydrogen chemical diffusivity at image and image is the oxygen chemical diffusivity at image, it was observed that image at all experimental conditions, suggesting that the hydrogen chemical diffusion is always faster than oxygen on hydration/dehydration in the temperature range studied.