High-temperature proton conductors are promising as electrolytes for intermediate-temperature solid oxide fuel cells. Among them, BaCeO 3 -based materials have high proton conductivity but rather poor chemical stability. In contrast, barium zirconates are rather stable, but have poorly reproducible densities and conductivities. In this study, the investigation of BaCe 1ÀxÀy Zr x Y y O 3Àd solid solutions (x ¼ 0, 0.10, 0.20, 0.30, 0.40; y ¼ 0.15, 0.20) was undertaken, with the final aim of finding a composition having both high conductivity and good stability. The influence of the modified sol-gel Pechini synthetic approach on the powder morphology, and of a barium excess on the densification were demonstrated. Single-phase perovskite powders were prepared and high density pellets were obtained at temperatures lower than those commonly employed. Stability tests demonstrated that the Zr introduction into doped barium cerate greatly enhanced the chemical stability, particularly for Zr $ 20%. The proton conductivities, measured in a humidified H 2 /Ar atmosphere by impedance spectroscopy, were only slightly influenced by the Zr amount. Overall, BaCe 1ÀxÀy Zr x Y y O 3Àd solid solutions having Zr z 20-40% and Y z 15-20% showed good chemical stability and high conductivity.

No abstract

No abstract

Proton conducting perovskite oxides have been widely investigated because of their potential as electrolytes for intermediate temperature solid oxide fuel cells. Among them, BaCeO3‐ based materials exhibit good proton conductivity under a humidified hydrogen‐containing atmosphere, but rather poor chemical stability in CO2 atmosphere. The substitution with Zr for Ce improves the chemical stability but reduces proton conductivity due to difficulties in fabricating dense materials. In the present work, single phase nanostructured powders of Ba1+xCe0.65Zr0.20Y0.15O3–δ (x = 0, 0.05, 0.10) solid solutions have been prepared by a modified sol–gel Pechini method with the final aim of evaluating the role of barium on their chemical and electrical properties. A significant influence of barium excess on the preparation and on properties of these materials has been demonstrated. In fact, density measurements evidenced that a 5 or 10 mol% nominal barium excess sensibly favoured the sintering process. Impedance analyses of sintered pellets confirmed the necessity of barium excess in order to avoid the lowering of proton conductivity, which has been evidenced for samples having stoichiometric barium content. Moreover, an unforeseen increase in chemical stability in CO2‐containing atmosphere with the growth of the barium excess was detected by thermogravimetric analyses.

No abstract