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Perovskite Oxides (perovskite + oxide)
Selected AbstractsBarium Holmium Zirconate, A New Complex Perovskite Oxide: I, Synthesis, Characterization, and Potential Use as a Substrate for High-Critical-Temperature SuperconductorsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2002Rajan Jose Barium holmium zirconate, a new complex perovskite ceramic oxide, has been synthesized through liquid-phase sintering for the first time. The conventional solid-state reaction method using constituent oxides and carbonates was found to be inadequate for the synthesis of Ba2HoZrO5.5 material. During high-temperature annealing, the development of stable BaZrO3 and BaHoO2.5 phases prevented the formation of Ba2HoZrO5.5 as a single-phase material, even at 1650°C. However, an addition of a small amount of CuO (1 wt%) in the reaction mixture has resulted in the formation of an ordered complex perovskite Ba2HoZrO5.5 phase during the heating process. The structure of Ba2HoZrO5.5 was studied by X-ray diffraction and found to have a cubic perovskite structure with a lattice constant of a= 8.482 Å. Dielectric constant and loss factor values of Ba2HoZrO5.5 are also in the range suitable for use as a substrate for microwave applications. The X-ray diffraction and resistivity measurements have shown that there is no detectable chemical reaction in YBa2Cu3O7,,,Ba2HoZrO5.5 and Bi(2212),Ba2HoZrO5.5 composites, even under extreme processing conditions. Dip-coated and melt-textured YBa2Cu3O7,, and Bi(2212) thick films developed on polycrystalline Ba2HoZrO5.5 gave zero-resistivity transition temperatures of Tc(0) = 92 and 85 K, respectively. [source] Barium Holmium Zirconate, A New Perovskite Oxide: II, Synthesis as Nanoparticles through a Modified Combustion ProcessJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2002Rajan Jose Nanoparticles of barium holmium zirconate, a new complex perovskite ceramic oxide, has been synthesized using a modified self-propagating combustion process. The solid combustion products obtained were characterized by X-ray diffraction (XRD), electron diffraction, differential thermal analysis, thermogravimetric analysis, infrared spectroscopy, particle size analysis, surface area determination, and high-resolution transmission electron microscopy. The XRD and electron diffraction studies have shown that the as-prepared powder is phase pure Ba2HoZrO5.5 and has a complex cubic perovskite (A2BB,O6) structure with a lattice constant a= 8.428 Å. The transmission electron microscopic investigation has shown that the particle size of the as-prepared powder was in the range 4,16 nm with a mean grain size of 8.2 nm. The nanoparticles of Ba2HoZrO5.5 obtained by the present method could be sintered to 98% theoretical density at 1500°C. [source] From Chelating Precursor to Perovskite Oxides and Hollow Fiber MembranesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2007S. Liu Perovskite Ba0.5Sr0.5Co0.8Fe0.2O3-, (BSCF) is a promising mixed-conducting ceramic membrane material in addition to being a good electrode catalyst for solid oxide fuel cells. In this study, BSCF powder was synthesized via a chelated water-soluble complex method at relatively low temperatures. The combined ethylenediaminetetraacetic acid and citric acid was used for the synthesis of a complex-based precursor, followed by thermal decomposition of the precursor at high temperatures. Thermal behavior, crystal phases, and structures of the prepared powders were characterized by thermogravimetric analysis/differential scanning calorimetry, XRD, and scanning electron microscopic (SEM) techniques, respectively. Pure and single-phase perovskite could be obtained after sintering at a temperature higher than 800°C for 5 h. The soft precursor powder synthesized at lower temperatures, i.e., 600°C, is water insoluble and more appropriate for use as a membrane material to prepare gas-tight tubular or hollow fiber ceramic membranes. By contrast, the hollow fibers prepared via the traditional techniques where the perovskite powder is used as the starting membrane materials display gas leakage. The fibers were characterized by SEM, XRD, and tested for air separation at ambient pressure and temperatures between 700° and 950°C. The oxygen flux measured in this work reached 3.90 mL·(min·cm2),1 and compares favorably with any experimental values reported in the open literature. [source] Effect of pH on synthesis and properties of perovskite oxide via a citrate processAICHE JOURNAL, Issue 2 2006Zhentao Wu Abstract A series of La0.6Sr0.4Co0.4Fe0.6O3-, (LSCF) perovskite-type oxides were synthesized using a modified citrate process under various pH conditions (pH =1, 3, 5, 7, and 9, respectively). The effect of pH on the chelate process, crystal development, morphology, and oxygen permeability of LSCF oxides were investigated. FT-IR analysis showed that the chelate processes for pH = 1 and 3 were different from those for pH = 5, 7, and 9. XRD and SEM observations revealed that the crystal formation and morphology of LSCF oxides were dependent on the precursors with different pH conditions. The LSCF membranes derived from the precursors with lower pH values (pH = 1 and 3) exhibited larger apparent activation energy for oxygen permeation than the other samples (pH = 5, 7, and 9) in the range of 1073-1123K. This study indicated that properties such as crystallinity and oxygen permeability of LSCF oxide could be tailored by controlling the pH values in the synthesis process. © 2005 American Institute of Chemical Engineers AIChE J, 2006 [source] Low-Temperature Facile Template Synthesis of Crystalline Inorganic Composite Hollow SpheresCHEMISTRY - AN ASIAN JOURNAL, Issue 7 2007Huifang Xu Abstract This report presents a facile approach for the low-temperature synthesis of crystalline inorganic-oxide composite hollow spheres by employing the bulk controlled synthesis of inorganic-oxide nanocrystals with polymer spheres as templates. The sulfonated polystyrene gel layer can adsorb the target precursor and induce inorganic nanocrystals to grow on the template in,situ. The crystalline phase and morphology of the composite shell is tunable. By simply adjusting the acidity of the titania sol, crystalline titania composite hollow spheres with tunable crystalline phases of anatase, rutile, or a mixture of both were achieved. The approach is general and has been extended to synthesize the representative perovskite oxide (barium and strontium titanate) composite hollow spheres. The traditional thermal treatment for crystallite transformation is not required, thus intact shells can be guaranteed. The combination of oxide properties such as high refractive index, high dielectric constant, and catalytic ability with the cavity of the hollow spheres is promising for applications such as opacifiers, photonic crystals, high- , -gate dielectrics, and photocatalysis. [source] Barium Non-Stoichiometry Role on the Properties of Ba1+xCe0.65Zr0.20Y0.15O3,, Proton Conductors for IT-SOFCsFUEL CELLS, Issue 5 2008S. Barison 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,, (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. [source] Novel Multifunctional Properties Induced by Interface Effects in Perovskite Oxide HeterostructuresADVANCED MATERIALS, Issue 45 2009Kui-juan Jin Abstract Multilayer structures have emerged as a leading research topic and researchers expect that multilayers may lead to interesting artificial materials with novel properties. In this Research News we show that the introduction of interfaces into perovskite oxides can induce a series of novel properties including an unusual positive magnetoresistance, great enhancement of lateral photovoltage in La0.9Sr0.1MnO3/SrNb0.01Ti0.99O3, and an electrical modulation of the magnetoresistance in multi-p-n heterostructures of SrTiO3,,/La0.9Sr0.1MnO3/SrTiO3,,/La0.9Sr0.1MnO3/Si. This novel positive magnetoresistance is attributed to the creation of a space charge region at the interface where the spin of the carriers is anti-parallel to that of the carriers in the region far from the interface of manganese oxide in the heterostructures. [source] Lanthanum Chromite-Based Interconnects as Key Materials for SOFC Stack DevelopmentINTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 1 2004Natsuko Sakai The historical investigations on the physicochemical and transport properties of lanthanum chromite-based perovskite oxides are reviewed to evaluate the compatibility as interconnects in solid oxide fuel cells. These materials improve sinterability in air. This has led to investigations on other physicochemical properties of these materials, such as thermal expansion, mechanical strength, and chemical stability. Lanthanum and chromium ion can be substituted by alkaline earths or transition metals, and this translates into a large flexibility in physicochemical properties. However, the formation of oxygen vacancies in a reducing atmosphere can result in an undesirable isothermal expansion or oxygen permeation. The chemical stability of these materials is governed by the fast cation diffusion at the grain boundary of the polycrystals. [source] 4d Electronic structure analysis of ruthenium in the perovskite oxides by Ru K - and L -edge XASJOURNAL OF SYNCHROTRON RADIATION, Issue 2 2001Jong-Young Kim The 4d electronic structure of ruthenium in the perovskite oxides, La2MRuIVO6 (M = Zn, Mg, and Li) and Ba2YRuVO6, has been investigated by the Ru K-and L-edge XANES and EXAFS analyses. Such X-ray absorption spectroscopic results clarify that the RuIV (d4) and RuV (d3) ions are stabilized in nearly regular Oh site. Comparing the Ru L-edge XANES spectra of perovskites containing isovalent ruthenium, it has been found that the t2g state is mainly influenced by A site cation, whereas the eg is mainly affected by neighboring B site cation. The experimental EXAFS spectra in the range of R ,,4.5 Å are well reproduced by ab-initio calculation based on crystallographic data, which supports the long-range structure presented by Rietveld refinement. [source] | |||||||||||||