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

• Published in: Acta materialia 2013-02, Vol.61 (4), p.1274-1283
• Main Authors: Lim, D.-K., Im, H.-N., Jeon, S.-Y., Park, J.-Y., Song, S.-J.
• Format: Article
• Language: English
• Subjects: Applied sciences; BaZr0.6Ce0.25Y0.15O3-δ; Conductivity relaxation; Exact sciences and technology; Metals. Metallurgy; Proton conductor
• ISSN: 1359-6454; 1873-2453
• DOI: 10.1016/j.actamat.2012.11.003

The electrical properties of BaZr0.6Ce0.25Y0.15O3−δ (BZCY) were studied as a function of both oxygen partial pressure (-2.65⩽log(PO2atm-1)⩽-0.62) and water vapor activity (-3.33⩽log(PH2Oatm-1⩽-1.3)) in the temperature range of 973–1073K. 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±0.1eV. The chemical diffusivity of oxygen at a fixed water vapor activity, D∼vO, 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 PO2 represents the fixed oxygen partial pressure, D∼iH is the hydrogen chemical diffusivity at PO2 and D∼vH is the oxygen chemical diffusivity at PO2, it was observed that D∼iH>D∼vH at all experimental conditions, suggesting that the hydrogen chemical diffusion is always faster than oxygen on hydration/dehydration in the temperature range studied.