Publications by authors named "E P Sadovskaya"

Oxygen and hydrogen mobility are among the important characteristics for the operation of solid oxide fuel cells, permselective membranes and many other electrochemical devices. This, along with other characteristics, enables a high-power density in solid oxide fuel cells due to reducing the electrolyte resistance and enabling the electrode processes to not be limited by the electrode-electrolyte-gas phase triple-phase boundary, as well as providing high oxygen or hydrogen permeation fluxes for membranes due to a high ambipolar conductivity. This work focuses on the oxygen and hydrogen diffusion of mixed ionic (oxide ionic or/and protonic)-electronic conducting materials for these devices, and its role in their performance.

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Synthesis and study of materials based on bismuth cerates and titanates were carried out. Complex oxides BiYTiO were synthesized by the citrate route; BiCeO and BiYCeO-by the Pechini method. The structural characteristics of materials after conventional sintering at 500-1300 °C were studied.

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The mesoporous MgAlO support is promising for the design of efficient and stable to coking catalysts for natural gas and biofuel reforming into syngas. This work aims at doping this support with transition metal cations (Fe, Cr, Ti) to prevent the incorporation of Ni and rare-earth cations (Pr, Ce, Zr), loaded by impregnation, into its lattice along with providing additional sites for CO activation required to prevent coking. Doped MgAlMeO (Me = Fe, Ti, Cr) mesoporous supports prepared by the one-pot evaporation-induced self-assembly method with Pluronic P123 triblock copolymers were single-phase spinels.

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A series of 5%Ni/CeTiO catalysts was prepared with nickel impregnation of mixed Ce-Ti oxides obtained via synthesis in supercritical isopropanol. All oxides have a cubic fluorite phase structure. Ti is incorporated into the fluorite structure.

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MeO/CeO (Me = Fe, Co, Ni) samples were tested in an O temperature-programmed isotope exchange and NO decomposition (deNO). A decrease in the rate of deNO in the presence of oxygen evidences the competitive adsorption of NO and O on the same sites. A study of isotope oxygen exchange revealed dissociative oxygen adsorption with the subsequent formation of surface oxygen species.

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