Publications by authors named "Sergey Y Istomin"

The influence of different synthesis routes on the structure and luminescent properties of KTb(MoO) (KTMO) was studied. KTMO samples were prepared by solid-state, hydrothermal, and Czochralski techniques. These methods lead to the following different crystal structures: a triclinic scheelite-type α-phase is the result for the solid-state method, and an orthorhombic KY(MoO)-type γ-phase is the result for the hydrothermal and Czochralski techniques.

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Two new cerium(IV) phosphates were obtained: cerium(IV) hydroxidophosphate, Ce(OH)PO , and cerium(IV) oxidophosphate, Ce O(PO ) , which were shown to complement the classes of isostructural compounds M(OH)PO and R O(PO ) , where M=Th, U and R=Th, U, Np, Zr. Ce O(PO ) oxidophosphate is formed by elimination of H O from the crystal structure of Ce(OH)PO during its thermal decomposition. The structures of Ce(OH)PO and Ce O(PO ) are related to each other with the same Cmce space group and similar unit cell parameters (a=6.

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Highly textured thin films of undoped, Ce-doped, and Sr-doped PrCuO were synthesized on single crystal YSZ substrates using pulsed laser deposition to investigate their area-specific resistance (ASR) as cathodes in solid-oxide fuel cells (SOFCs). The effects of T' and T* crystal structures, donor and acceptor doping, and a-axis and c-axis orientation on ASR were systematically studied using electrochemical impedance spectroscopy on half cells. The addition of both Ce and Sr dopants resulted in improvements in ASR in c-axis oriented films, as did the T* crystal structure with the a-axis orientation.

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Three different perovskite-related phases were isolated in the SrGa(1-x)Sc(x)O(2.5) system: Sr(2)GaScO(5), Sr(10)Ga(6)Sc(4)O(25), and SrGa(0.75)Sc(0.

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The brownmillerite-type A 2B 2O 5 structure is considered as a parent one, giving rise to different derivatives: layered double perovskites, A-site and anion-vacancy-ordered perovskites, and the perovskite-like compounds with crystallographic shear planes. The structural relationships and synthesis pathways for these classes of materials are discussed with particular attention to the ordering at the A or B sublattices, anion vacancy ordering, and their mutual interaction.

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