II. Structure of Perovskites 1982 A. Crystal Structure 1982 B. Nonstoichiometry in Perovskites 1983 1. Oxygen Nonstoichiometry 1983 2. Cation Nonstoichiometry 1984 C. Physical Properties 1985 D. Adsorption Properties 1986 1. CO and NO Adsorption 1986 2. Oxygen Adsorption 1987 E. Specific Surface and Porosity 1987 F. Thermal Stability in a Reducing Atmosphere 1989 III. Acid−Base and Redox Properties 1990 A. Acidity and Basicity 1990 B. Redox Processes 1991 1. Kinetics and Mechanisms 1992 2. Reduction−Oxidation Cycles 1993 C. Ion Mobility 1993 1. Oxygen Transport 1993 2. Cation Transport 1994 IV. Heterogeneous Catalysis 1995 A. Oxidation Reactions 1995 1. CO Oxidation 1995 2. Oxidation of Hydrocarbons 1996 B. Pollution Abatement 2001 1. NOx Decomposition 2001 2. Exhaust Treatment 2002 3. Stability 2004 C. Hydrogenation and Hydrogenolysis Reactions 2004 1. Hydrogenation of Carbon Oxides 2004 2. Hydrogenation and Hydrogenolysis Reactions 2006

Chemical structures and performance of perovskite oxides.

We have investigated carrier transport in a crystalline oxide semiconductor InGaO3(ZnO)5 using single-crystalline thin films. When carrier concentration is less than 2×1018cm−3, logarithm of electrical conductivity decreases in proportion to T−1∕4 and room-temperature Hall mobility was as low as ∼1cm2(Vs)−1. When carrier concentration was increased to 4×1018cm−3, the conduction mechanism changed to degenerate conduction and room-temperature Hall mobility was steeply increased to >10cm2(Vs)−1, showing metal–insulator transition behavior. These results are explained by percolation conduction over distribution of potential barriers formed around conduction band edge. The potential distribution is a consequence of potential modulation originating from random distribution of Ga3+ and Zn2+ ions in the crystal structure of InGaO3(ZnO)5.

Carrier transport in transparent oxide semiconductor with intrinsic structural randomness probed using single-crystalline InGaO3(ZnO)5 films

In the paragraph following eq 28, the average bond valence was incorrectly referred to as V/R. It has been corrected to V/N. The paper originally posted to the web on September 3, 2009, and was reposted on September 24, 2009.

http://pubs.acs.org/doi/pdf/10.1021/cr900053k

Recent developments in the methods and applications of the bond valence model.

Oxidation into CO2 is a major solution to CO abatement in air depollution treatments. The development of catalytic converters led to an extraordinary high number of publications on metal catalysts during the last fifty years. Due to the increasing price of noble metals and to remarkable progresses in oxide syntheses, catalytic oxidation of carbon monoxide over oxide catalysts has recently gained in interest, even if some oxides are known to present remarkable activity since the beginning of the 20th century. In this Review, the kinetics and mechanism of CO oxidation on single and mixed oxides are examined, alongside the catalyst structures

Catalytic Oxidation of Carbon Monoxide over Transition Metal Oxides

Perovskite oxides with formula ABO3 or A2BO4 are a very important class of functional materials that exhibit a range of stoichiometries and crystal structures. Because of the structural features, they could accommodate around 90% of the metallic natural elements of the Periodic Table that stand solely or partially at the A and/or B positions without destroying the matrix structure, offering a way of correlating solid state chemistry to catalytic properties. Moreover, their high thermal and hydrothermal stability enable them suitable catalytic materials either for gas or solid reactions carried out at high temperatures, or liquid reactions carried out at low temperatures. In this review, we addressed the preparation, characterization, and application of perovskite oxides in heterogeneous catalysis. Preparation is an important issue in catalysis by which materials with desired textural structure and physicochemical property could be achieved; characterization is the way to explore and understand the textura...

Perovskite Oxides: Preparation, Characterizations, and Applications in Heterogeneous Catalysis

Perovskite-type (La 1-x Sr x )MnO 3 (0≤x≤0.3) was synthesized through the sol-gel process at low temperature (400 o to 500 o C). Poly(acrylic acid) (PAA) was used to make a gel from an aqueous solution of lanthanum, strontium, and manganese nitrates. The particle-diameter distribution of the manganites had a maximum value of 0.3 to 0.7 μm, and a specific surface area of about 17.5 to 23.5 m 2 /g

Hideki Taguchi

Papers

Synthesis of Perovskite‐Type (La1−xSrx)MnO3 (O X 0.3) at Low Temperature

Metal-insulator transition and thermoelectric properties in the system (R1−xCax)MnO3−δ (R: Tb, Ho, Y)

Synthesis of LaMnO3+δby Firing Gels Using Citric Acid

Tetradentate Schiff base–oxovanadium(IV) complexes: structures and reactivities in the solid state

High-temperature phase transition of CaMnO3−δ