Crystal structure, oxygen nonstoichiometry, hydration and conductivity BaZr1- xMxO3-d (M=Pr, Nd, Y, Co)

Partially substituted perovskite-like barium zirconates with general formula BaZr1-хМхО3-d possess oxygen-ion and proton conductivity and, therefore, may be promising as electrolytes for intermediate temperature solid oxide fuel cells. The aim of this work was to study the crystal structure, thermal and chemical expansion, water uptake, oxygen nonstoichiometry, total conductivity and Seebeck coefficient of zirconates BaZr1-xMxO3-d (M=Pr, Nd, Y, Co) in the atmospheres with different levels of humidity (log(pH2O/atm.) = -1.75; -2.5; -3.5) as a function of oxygen partial pressure (log(pO2/atm) = -20 - -0.67) and temperature (T = 25 – 1050 °C). Synthesis of the samples was carried out by glycerol-nitrate method. The phase composition of the as-prepared powders was analyzed by the X-ray diffraction (XRD). Room temperature and high temperature XRD studies were carried out using Shimadzu XRD-7000 diffractometer equipped with high temperature chamber HTK 16N (Anton Paar GmbH). Thermal and chemical expansion was also measured using DIL 402 C dilatometer (Netzsch GmbH). Oxygen nonstoichiometry was studied by solid state coulometric titration and thermogravimetry. Electrical conductivity and Seebeck coefficient were measured simultaneously in the same setup. This work was supported by the Russian Science Foundation (project No.18-73-00022)

Nonstoichiometry, Defect Chemistry and Oxygen Transport in Fe-Doped Layered Double Perovskite Cobaltite PrBaCo2−xFexO6−δ (x = 0–0.6) Membrane Materials

Mixed conducting cobaltites PrBaCo2−xFexO6−δ (x = 0–0.6) with a double perovskite structure are promising materials for ceramic semi-permeable membranes for oxygen separation and purification due to their fast oxygen exchange and diffusion capability. Here, we report the results of the detailed study of an interplay between the defect chemistry, oxygen nonstoichiometry and oxygen transport in these materials as a function of iron doping. We show that doping leads to a systematic variation of both the thermodynamics of defect formation reactions and oxygen transport properties. Thus, iron doping can be used to optimize the performance of mixed conducting oxygen-permeable double perovskite membrane materials