Indium Oxide (indium + oxide)

Distribution by Scientific Domains


Selected Abstracts


ChemInform Abstract: Nano Indium Oxide as a Recyclable Catalyst for C,S Cross-Coupling of Thiols with Aryl Halides under Ligand Free Conditions.

CHEMINFORM, Issue 35 2009
Vutukuri Prakash Reddy
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


Growth of Nano- and Microstructured Indium Nitride Crystals by the Reaction of Indium Oxide with Ammonia.

CHEMINFORM, Issue 52 2005
Woo-Sik Jung
Abstract For Abstract see ChemInform Abstract in Full Text. [source]


Inorganic Macroporous Films from Preformed Nanoparticles and Membrane Templates: Synthesis and Investigation of Photocatalytic and Photoelectrochemical Properties,

ADVANCED FUNCTIONAL MATERIALS, Issue 10 2003
D.G. Shchukin
Abstract Colloidal dispersions of titania, zirconia, tin oxide, indium oxide, and ceria have been successfully used to impregnate membrane templates and form the respective metal oxide (MO) porous films. The use of alumina and iron oxide sols in the same procedure, however, resulted in compact structures. By mixing different nanoparticle solutions before impregnation, final inorganic films containing two metal oxides, of variable metal oxide ratios, were obtained. The porous inorganic materials were analyzed in terms of surface area, pore size, film thickness, and crystallinity. The mechanism of nanoparticle infiltration and particle adsorption to the template walls is proposed based on the stability of the inorganic film and a study of the influence of either the sol concentration or washing times on the amount of inorganic substance incorporated in the hybrid material. The photocatalytic decomposition of an organic pollutant, 2-chlorophenol, was demonstrated for the porous titania material along with the structures containing mixtures of titania with zirconia, indium oxide, and tin oxide. A ratio of 9:1 TiO2/MO gave the highest photocatalytic activity, which was higher than the activity of Degussa P25 for the TiO2/In2O3 and TiO2/SnO2 systems under the same conditions. The titania films have also been attached to substrates,glass or indium tin oxide (ITO) surfaces,and the photoelectrochemical properties of the porous film attained. A comparison with a spin-coated titania film (prepared from the same colloidal dispersion) showed that the structured porous inorganic film has two times the photoelectrochemical efficiency as the spin-coated film. [source]


Preparation of lithium indium oxide via a rheological phase route and its electrochemical characteristics in LiOH and Li2SO4 solutions

PHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 1 2010
Guo-Qing Zhang
Abstract Submicrometer-sized lithium indium oxide (LiInO2) powder via a rheological phase method using trilithium citrate tetra hydrate (C6H5Li3O7,·,4H2O) and indium oxide (In2O3) has been prepared in this work for the first time. The optimal pyrolyzing temperature range to prepare crystalline LiInO2 is between 650 and 900,°C, which was confirmed by thermal gravimetric and differential thermogravimetric analysis of the precursor and X-ray diffraction analysis. The pure phase LiInO2 sample obtained has a uniform particle morphology and submicrosize, which was observed by scanning electron microscopy. The electrochemical studies show that a new pair of cathodic and anodic peaks at 0.23 and 0.38,V (vs. saturated calomel electrode) was obviously observed from the cyclic voltammetry curve of LiInO2 in 1,M LiOH solution, indicating a battery characteristic of the material in this electrolyte. While in 1,M Li2SO4 solution, the sample presents a supercapacitive characteristic within the same potential range. The reasons for different electrochemical behaviors in these two electrolytes can be attributed to the fact that the reaction of lithium ion insertion/extraction into/out of a LiInO2 electrode takes place in the bulk material in LiOH electrolyte solution, whereas it takes place on the electrode/electrolyte interface for Li2SO4 electrolyte case. [source]


Optical properties of pure and transition metal-doped indium oxide

PHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 5 2009
H. A. Rahnamaye Aliabad
Abstract The band structure, the dielectric function, the reflectivity, the refractive index and the oscillator strength sum rule were calculated for pure In2O3 and alloyed In1.5T0.5O3 (where T represents Sc, Y, La and Ac) using density functional theory (DFT). The full potential linearized augmented plane wave (FP-LAPW) method was used with the local density approximation (LDA + U). Calculations of the optical spectra were performed for the energy range 0,30 eV. The calculated results indicate that the upper valance bands of In2O3 show a small dispersion and the value of the band gap increases for Sc and Y dopants and decreases for Ac and La dopants. The calculations indicate that there are two band gaps for In2O3. The first shows a strong optical absorption, as a direct band gap occurs from a 0.81 eV energy level below the top of valence band. The second shows a much weaker absorption from the top of the valence band to the bottom of the conduction band. The refractive index for In2O3 is 1.69 nm at 800 nm, near the visible region. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


Structure of cubic polytype indium nitride layers on top of modified sapphire substrates

PHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 2 2008
F. M. Morales
Abstract The occurrence of cubic indium nitride thin layers grown by molecular beam epitaxy on top of c-plane sapphire substrates modified by an intermediate layer of cubic indium oxide is reported. An orientation relationship between the (0001) plane of Al2O3 and both (001) surfaces of body-centered cubic In2O3 and zinc-blende InN is demonstrated by means of electron and X-ray diffraction and by transmission electron microscopy. We propose that the demonstrated approach is able to stabilize the non equilibrium phase of InN (i. e., the cubic polytype) due to a low lattice mismatch together with a four fold surface atomic arrangement of the indium oxide-indium nitride interface. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


A stacked chalcopyrite thin-film tandem solar cell with 1.2,V open-circuit voltage

PROGRESS IN PHOTOVOLTAICS: RESEARCH & APPLICATIONS, Issue 4 2003
S. Nishiwaki
Abstract CuGaSe2 (CGS) thin films were prepared on tin-doped indium oxide (ITO) coated soda-lime glass substrates by thermal co-evaporation to fabricate transparent solar cells. The films consisted of columnar grains with a diameter of approximately 1,,m. Some deterioration of the transparency of the ITO was observed after deposition of the CGS film. The CGS solar cells were electrically connected in series with Cu(In,Ga)Se2 (CIGS) solar cells and mechanically stacked on the CIGS cells to construct tandem cells. The tandem solar cell with the CGS cell as the top cell showed an efficiency of 7.4% and an open-circuit voltage of 1.18,V (AM,1.5, total area). Copyright © 2003 John Wiley & Sons, Ltd. [source]


Ageing in granular aluminium insulating thin films

ANNALEN DER PHYSIK, Issue 12 2009
J. Delahaye
Abstract We present a new set of electrical field effect measurements on granular aluminium insulating thin films. We have explored how the conductance relaxations induced by gate voltage changes depend on the age of the system, namely the time elapsed since its quench at low temperature. A clear age dependence of the relaxations is seen, qualitatively similar to ageing effects seen in other well studied glassy systems such as spin glasses or polymers. We explain how our results differ from the previous ones obtained with different protocols in indium oxide and granular aluminium thin films. Our experimental findings bring new information on the dynamics of the system and put new constraints on the theoretical models that may explain slow conductance relaxations in disordered insulators. [source]


Metastability of Corundum-Type In2O3

CHEMISTRY - A EUROPEAN JOURNAL, Issue 11 2008
Aleksander Gurlo Dr.
Abstract The description of structural relations between bixbyite- and corundum-type structures is of particular interest because of the common occurrence of both structures. One of the representative examples of the bixbyite to corundum transition is the high-pressure high-temperature synthesis of the corundum-type indium oxide. The wet chemistry synthesis and stabilisation of the corundum-type In2O3 under ambient pressure conditions calls for a re-interpretation of the InO phase diagram as well as for the clarification of the phase transitions in In2O3. One of the questions to be clarified is the stability of the corundum-type In2O3. In the present work we studied the stability of the corundum-type In2O3 both theoretically (by density-functional calculations) and experimentally. The synthesis of the corundum-type In2O3 was performed by the modified non-alkoxide sol,gel method based on the ammonia-induced hydrolysis of indium nitrate in methanol. The corundum-type In2O3 was subjected to thermal analysis (STA) as well as to structural studies, that is, it was examined using X-ray powder diffraction (XRPD) including in situ XRPD characterisation upon thermal treatment. For the first time we have undoubtedly demonstrated, both theoretically and experimentally, the metastability of the corundum-type In2O3 polymorph. The In2O3 polymorph appears to be metastable throughout the entire enthalpy,pressure phase diagram. Upon heating, corundum-type In2O3 transforms irreversibly into cubic bixbyite-type In2O3 as shown by STA as well as in situ heating XRPD experiments. Computations indicate the existence of another high-pressure modification of In2O3 with orthorhombic structure, iso-typic to Rh2O3 -II. We predict this new phase to form at pressures exceeding 15,GPa from both the cubic bixbyite-type and the corundum-type modification of In2O3. [source]