Abstract: There are provided a method of manufacturing a ceramic powder having a perovskite structure and a ceramic powder having a perovskite structure manufactured by the same. The method includes: mixing a compound of an element corresponding to site A in an ABO3 perovskite structure as well as a compound of an element corresponding to site B in the same structure, with supercritical water in a continuous mode to form seed crystals; and mixing the seed crystals in a batch mode to conduct grain growth thereof.

Abstract: A scintillation device includes a free-standing ceramic scintillator body that includes a polycrystalline ceramic scintillating material comprising a rare earth element, wherein the polycrystalline ceramic scintillating material is characterized substantially by a cation-deficient perovskite structure. A method of producing a free-standing ceramic scintillator body includes preparing a precursor solution including a rare earth element precursor, a hafnium precursor and an activator (Ac) precursor, obtaining a precipitate from the solution, and calcining the precipitate to obtain a polycrystalline ceramic scintillating material including a rare earth hafnate doped with the activator and having a cation-deficient perovskite structure.

Abstract: A method of: dissolving salts of a first metal ion and a second metal ion in water to form a solution; heating the solution to a temperature of about 80-90° C.; and adding a base to the solution to precipitate nanoparticles of an oxide of the first metal ion and the second metal ion.

Abstract: The present invention provides an ammonium perrhenate containing less than 5 ppm of potassium.

Abstract: A compound MjXp which is particularly suitable for use in a battery prepared by the complexometric precursor formulation methodology wherein: Mj is at least one positive ion selected from the group consisting of alkali metals, alkaline earth metals and transition metals and j is an integer representing the moles of said positive ion per moles of said MjXp; and Xp, a negative anion or polyanion from Groups IIIA, IV A, VA, VIA and VIIA and may be one or more anion or polyanion and p is an integer representing the moles of said negative ion per moles of said MjXp.

Abstract: A battery with improved properties is provided. The battery has a cathode material prepared by the complexometric formulation methodology comprising MjXp wherein: Mj is at least one positive ion selected from the group consisting of alkali metals, alkaline earth metals and transition metals and n represents the moles of said positive ion per mole of said MjXp; and Xp is a negative anion or polyanion selected from Groups IIIA, IV A, VA, VIA and VIIA and may be one or more anion or polyanion and p representing the moles of said negative ion per moles of said MjXp. The battery has a discharge capacity at the 1000th discharge cycle of at least 120 mAh/g at room temperature at a discharge rate of 1 C when discharged from at least 4.6 volts to at least 2.0 volts.

Abstract: The paste composition for forming a back electrode of solar cell 10 provided by the present invention contains, as solids, an aluminum powder, a glass powder and a composite powder composed of a particulate composite of a metal oxide with a silicon-containing organic or inorganic compound. This composite powder is contained in an amount of at least 0.01 mass % but less than 0.45 mass % given 100 mass % as the total of the composite powder, the aluminum powder and the glass powder.

Abstract: Disclosed is a reactor for preparing a precursor of lithium composite transition metal oxide for lithium secondary batteries, the reactor having a closed structure including a stationary hollow cylinder; a rotary cylinder having the same axis as the stationary hollow cylinder and an outer diameter smaller than an inner diameter of the stationary hollow cylinder, an electric motor to generate power, enabling rotation of the rotary cylinder, a rotation reaction area disposed between the stationary hollow cylinder and the rotary cylinder, wherein ring-shaped vortex pairs that are uniformly arranged in a rotation axis direction and rotate in opposite directions are formed in the rotation reaction area, and an inlet through which a reactant fluid is fed into the rotation reaction area and an outlet through which the reactant fluid is discharged from the rotation reaction area.

Abstract: A composition comprising: a metal oxide of a first metal ions and second metal ions; an electrically conductive material; and a binder material. The second metal ions have a higher oxidation state than the first metal ions. The presence of the second metal ion increases the number of metal cation vacancies. A method of: dissolving salts of a first metal ion and a second metal ion in water to form a solution; heating the solution to a temperature of about 80-90° C.; and adding a base to the solution to precipitate nanoparticles of a metal oxide of the first metal ion and the second metal ion.

Abstract: A luminescent nanosheet has perovskite octahedral crystal units combined together in a planar configuration. The octahedral crystal units each have a multistacked crystal sheet structure. The octahedral crystal units are multistacked over at least 3 high in a direction vertical to a sheet plane, and an element providing a luminescence center is solid-solubilized between the multistacked octahedral crystal units.

Abstract: Disclosed are a method of producing fine particulate alkali metal niobate in a liquid phase system, wherein the size and shape of the particulate alkali metal niobate can be controlled; and fine particulate alkali metal niobate having a controlled shape and size. One of specifically disclosed is a method of producing a substantially rectangular cuboid particulate alkali metal niobate represented by MNbO3 (1), wherein M represents one element selected from alkaline metals, including specific four steps. Another one of specifically disclosed is particulate alkali metal niobate represented by the formula (1) having a substantially rectangular cuboid shape, wherein the substantially rectangular cuboid shape has a longest side and a shortest side, the length of the longest side represented by an index Lmax is 0.10 to 25 ?m, and the length of the shortest side represented by an index Lmin is 0.050 to 15 ?m.

Abstract: A method for extracting tungsten from scheelite by: 1) adding a mixed acid including H2SO4 and H3PO4 to a decomposition reactor; 2) heating the mixed acid to a temperature of 70-100° C.; adding scheelite while controlling the mixed acid present in an amount of 3-8 L per kg of scheelite; allowing the components in the decomposition reactor to react for 1-6 h, and filtering the resulting mixture to obtain a filtrate; 3) supplementing the filtrate with sulfuric acid consumed in the reaction; 4) crystallizing the filtrate to obtain phosphotungstic acid crystals and mother liquor; 5) dissolving the phosphotungstic acid crystals in water to obtain a phosphotungstic acid solution; 6) transforming the phosphotungstic acid solution into an ammonium tungstate solution for the purpose of preparing ammonium paratungstate; and 7) supplementing the mother liquor with phosphoric acid and water to an initial level and reusing the mother liquor for ore leaching.

Abstract: A method for preparing nanotubes by providing nanorods of a piezoelectric material having an asymmetric crystal structure and by further providing hydroxide ions to the nanorods to etch inner parts of the nanorods to form the nanotubes.

Abstract: The present invention describes a solid-solution synthesis method for producing porous Fe-containing active material (74) wherein Fe is interwoven with supporting oxide(s) by the following steps: mixing (64) Fe-containing specie (?) (60) and a supporting specie (?) (62) containing element of X, to provide a mixture (66), high-temperature treatment (68) to provide a Fe—X—O solid solution (70), and reducing (72) the solid solution to provide the Fe-containing active material wherein Fe is interwoven with X oxide(s) (74).

Abstract: A method for making a metal oxide material and catalyzing the oxidative coupling of methane, including mixing a metal cation-containing oxidizer portion and a reducing fuel portion with water to define an aqueous solution, evaporatively removing water from the aqueous solution to yield a concentrated liquid, burning the concentrated liquid yield an homogeneous metal oxide powder, flowing methane from a first source and oxygen from a second source over the homogeneous metal oxide powder, and catalyzing an oxidative coupling of methane reaction with the homogeneous metal oxide powder. The homogeneous metal oxide powder contains metal oxides selected from the group including LaSrAlO4, LaAlO3, Sr3Al2O6, Na2WO4—Mn/SiO2, and combinations thereof.

Abstract: Provided are an apparatus for preparing a cathode active material precursor for lithium secondary batteries including a cylindrical outer chamber, an inner cylinder that has the same central axis as the outer chamber and is mounted to rotatably move along the central axis, an electric motor to transfer power to rotate the inner cylinder, a reactant inlet disposed on the outer chamber, to add reactants to a space between the outer chamber and the inner cylinder, and an outlet disposed in the outer chamber, to obtain reaction products after reaction in the space between the outer chamber and the inner cylinder, and a method for preparing a cathode active material precursor for lithium secondary batteries using the apparatus.

Abstract: The invention is directed to a solid ion conductor which has a garnet-like crystal structure and has the stoichiometric composition L7+xAxG3?xZr2O12, wherein L is in each case independently a monovalent cation, A is in each case independently a divalent cation, G is in each case independently a trivalent cation, 0?x?3 and O can be partly or completely replaced by divalent or trivalent anion.

Abstract: The present invention relates to a method for producing a tungsten oxide photocatalyst having titanium oxide and copper ion supported thereon, comprising dissolving urea in a solution in which copper-ion supporting tungsten oxide particles are uniformly dispersed in a titanium oxide sol, thermally decomposing the urea to thereby allow the titanium oxide to precipitate on the surface of copper ion-supporting tungsten oxide and to be supported thereon; and a tungsten oxide photocatalyst modified by both titanium oxide and copper ion obtained by the method, wherein the rate of change of diffuse reflectivity (at wavelength of 700 nm) is less than 3% before and after the irradiation of ultraviolet and the titanium oxide is supported on the tungsten oxide in an island shape of 1 to 100 nm in size. The tungsten oxide photocatalyst having titanium oxide and copper ion supported thereon of the present invention exhibits high catalyst activity under visible light irradiation.

Abstract: A device includes a back contact, an absorber layer coupled to the back contact, a buffer layer coupled to the absorber layer; and an amorphous transparent conductive layer coupled to the buffer layer, wherein the amorphous transparent conductive phase is characterized by, as a function of composition, i) a range of band gaps and ii) a range of work functions.

Abstract: Porous metal oxides are provided. The porous metal oxides are prepared by heat treating a coordination polymer. A method of preparing the porous metal oxide is also provided. According to the method, the shape of the particles of the metal oxide can be easily controlled, and the shape and distribution of pores of the porous metal oxide can be adjusted.

Abstract: An oxide evaporation material according to the present invention includes a sintered body containing indium oxide as a main component thereof and cerium with a Ce/In atomic ratio of 0.001 to 0.110. The L* value in the CIE 1976 color space is 62 to 95. The oxide evaporation material with the L* value of 62 to 95 has an optimal oxygen amount. Accordingly, even when a small amount of an oxygen gas is introduced into a film-formation vacuum chamber, a transparent conducting film having a low resistance and a high transmittance in the visible to near-infrared region is formed by vacuum deposition methods. Since the amount of the oxygen gas introduced is small, the difference in composition between the film and the evaporation material is made small. This reduces the variations in composition and characteristics among films formed in large quantities.

Abstract: The present invention is directed to a method of making metal oxide and mixed metal oxide particles. The method includes treating a mixture formed from a metal source, such as metal alkoxide, a surfactant, and a first alcohol in an aqueous media at a very high metal oxide yield. The mixture is reacted using a catalyst to form metal oxide particles having a desired particle size in said mixture. The method is particularly suitable for forming silica particles. The metal oxide particles can then be heat treated to form synthetic fused metal oxides such as, for example, synthetic fused silica.

Abstract: A method for the fabrication of nanostructured semiconducting, photoconductive, photovoltaic, optoelectronic and electrical battery thin films and materials at low temperature, with no molecular template and no organic contaminants. High-quality metal oxide semiconductor, photovoltaic and optoelectronic materials can be fabricated with nanometer-scale dimensions and high dopant densities through the use of low-temperature biologically inspired synthesis routes, without the use of any biological or biochemical templates.

Abstract: The disclosed subject concerns nanometric-sized ceramic materials in the form of multiple crystalline structures, composites, or solid solutions, the process for their synthesis, and uses thereof. These materials are mainly obtained by detonation of two water-in-oil (W/O) emulsions, one of which is prepared with precursors in order to present a detonation regime with temperature lower than 2000° C., and they present a high chemical and crystalline phase homogeneity, individually for each particle, as well as a set of complementary properties adjustable according to the final applications, such as a homogeneous distribution of the primary particles, very high chemical purity level, crystallite size below 50 nm, surface areas by mass unit between 25 and 500 m2/g, and true particle densities higher than 98% of the theoretical density.

Abstract: A biotemplated nanomaterial can include a crystalline perovskite.

Abstract: According to example embodiments, a hybrid metal oxide having a network structure includes an oxygen atom that is covalently bonded to a first metal and a second metal. At least one of the first metal and the second metal has two or more oxidation states. A solar cell may have an interlayer including the hybrid metal oxide. According to example embodiments, a hybrid metal oxide may be formed using a sol-gel process from a solution including a first metal precursor and a second metal precursor.

Abstract: A cathode material for a solid oxide fuel cell comprising a complex oxide having a perovskite structure expressed by the general formula ABO3 with a standard deviation value of no more than 10.3 for the atomic percentage of respective elements in the A site measured using energy dispersive X-ray spectroscopy at 10 spots in a single field.

Abstract: Disclosed is a new thermoelectric conversion material represented by the chemical formula 1: Bi1-xCu1-yO1-zTe, where 0?x<1, 0?y<1, 0?z<1 and x+y+z>0. A thermoelectric conversion device using said thermoelectric conversion material has good energy conversion efficiency.

Abstract: A composition comprising an extruded inorganic support comprising an oxide of a metal or metalloid, and at least one catalytically active metal, wherein the extruded inorganic support has pores, a total pore volume, and a pore size distribution, wherein the pore size distribution displays at least two peaks of pore diameters, each peak having a maximum, wherein a first peak has a first maximum of pore diameters of equal to or greater than about 120 nm and a second peak has a second maximum of pore diameters of less than about 120 nm, and wherein greater than or equal to about 5% of a total pore volume of the extruded inorganic support is contained within the first peak of pore diameters.

Abstract: A method for synthesizing strontium cerate (SrCeO3) nanoparticles is disclosed. Initially, ammonium cerium(IV) nitrate ((NH4)2Ce(NO3)6) and n-butanol (C4H10O) are reacted to synthesize cerium-n-butoxide (Ce(OBu)4). Next, the cerium-n-butoxide, strontium acetate (Sr(CH3COO)2), and stearic acid (C18H36O2) are reacted to form a homogenous product including the strontium cerate nanoparticles. Finally, the strontium cerate nanoparticles are isolated from the homogenous product.

Abstract: An adsorbent for carbon dioxide may include a composite metal oxide including a divalent first metal (M1), a trivalent second metal (M2), and an element (A) with an electronegativity of about 2.0 to about 4.0. The composite metal oxide may have an amorphous structure. A method of manufacturing the adsorbent for carbon dioxide and a capture module for carbon dioxide including the adsorbent for carbon dioxide are also disclosed.

Abstract: Provided is a cathode active material which is lithium transition metal oxide having an ?-NaFeO2 layered crystal structure, wherein the transition metal is a blend of Ni and Mn, an average oxidation number of the transition metals except lithium is more than +3, and lithium transition metal oxide satisfies the Equation m(Ni)?m(Mn) (in which m (Ni) and m (Mn) represent an molar number of manganese and nickel, respectively). The lithium transition metal oxide has a uniform and stable layered structure through control of oxidation number of transition metals to a level higher than +3, thus advantageously exerting improved overall electrochemical properties including electric capacity, in particular, superior high-rate charge/discharge characteristics.

Abstract: Disclosed herein is a cathode active material for a lithium secondary battery, in particular, including a lithium transition metal oxide with a layered crystalline structure in which the transition metal includes a transition metal mixture of Ni, Mn and Co, and an average oxidation number of all transition metals other than lithium is more than +3, and specific conditions represented by the following formulae (1) and (2), 1.1<m(Ni)/m(Mn)<1.5 and 0.4<m(Ni2+)/m(Mn4+)<1, are satisfied. The inventive cathode active material has a more uniform and stable layered structure by controlling the oxidation number of transition metals contained in a transition metal oxide layer to form the layered structure, compared to conventional substances. Accordingly, the active material exhibits improved overall electrochemical characteristics including battery capacity and, in particular, excellent high rate charge-discharge features.

Abstract: Nanowires useful as heterogeneous catalysts are provided. The nanowire catalysts are useful in a variety of catalytic reactions, for example, the oxidative coupling of methane to C2 hydrocarbons. Related methods for use and manufacture of the same are also disclosed.

Abstract: Nanowires useful as heterogeneous catalysts are provided. The nanowire catalysts are prepared by polymer templated methods and are useful in a variety of catalytic reactions, for example, the oxidative coupling of methane to ethane and/or ethylene. Related methods for use and manufacture of the same are also disclosed.

Abstract: A composition comprising: a metal oxide of a first metal ions and second metal ions; an electrically conductive material; and a binder material. The second metal ions have a higher oxidation state than the first metal ions. The presence of the second metal ion increases the number of metal cation vacancies. A method of: dissolving salts of a first metal ion and a second metal ion in water to form a solution; heating the solution to a temperature of about 80-90° C.; and adding a base to the solution to precipitate nanoparticles of a metal oxide of the first metal ion and the second metal ion.

Abstract: Provided is a lithium transition metal oxide having an ?-NaFeO2 layered crystal structure, as a cathode active material for lithium secondary battery, wherein the transition metal includes a blend of Ni and Mn, an average oxidation number of the transition metals except lithium is +3 or higher, and the lithium transition metal oxide satisfies Equations 1 and 2 below: 1.0<m(Ni)/m(Mn)??(1) m(Ni2+)/m(Mn4+)<1??(2) wherein m(Ni)/m(Mn) represents a molar ratio of nickel to manganese and m (Ni2+)/m(Mn4+) represents a molar ratio of Ni2+ to Mn4+. The cathode active material of the present invention has a uniform and stable layered structure through control of oxidation number of transition metals to a level higher than +3, in contrast to conventional cathode active materials, thus advantageously exerting improved overall electrochemical properties including electric capacity, in particular, superior high-rate charge/discharge characteristics.

Abstract: Disclosed is a superconducting compound which has a structure obtained by partially substituting oxygen ions of a compound, which is represented by the following chemical formula; LnTMOPh [wherein Ln represents at least one element selected from Y and rare earth metal elements (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu), TM represents at least one element selected from transition metal elements (Fe, Ru, Os, Ni, Pd and Pt), and Pn represents at least one element selected from pnictide elements (N, P, As and Sb)] and has a ZrCuSiAs-type crystal structure (space group P4/nmm), with at least one kind of monovalent anion (F?, Cl? or Br?). The superconducting compound alternatively has a structure obtained by partially substituting Ln ions of the compound with at least one kind of tetravalent metal ion (Ti4+, Zr4+, Hf4+, C4+, Si4+, Ge4+, Sn4+ or Pb4+) or a structure obtained by partially substituting Ln ions of the compound with at least one kind of divalent metal ion (Mg2+, Ca2+, Sr2+ or Ba2+).

Abstract: A method for producing ammonium metatungstate from ammonium paratungstate includes preparing an ammonium paratungstate mixture including solid ammonium paratungstate and water. The mixture is contacted with a cation exchange material to lower a pH of the mixture to a pH range wherein metatungstate ion is stable and an insoluble tungstic acid is not formed. The pH of the mixture may be maintained in the pH range until the ammonium paratungstate mixture is converted into an ammonium metatungstate solution.

Abstract: Hopcalite-type catalysts for oxidation of CO are formed by preparing a mixed-metal oxide precursor by firstly preparing a solution of a mixture of metal precursor compounds in a solvent, followed by contacting the solution with a supercritical antisolvent to precipitate the mixed-metal oxide precursor. A mixed-metal oxide may then be prepared from the precursor by oxidation, for example by calcination. The mixed-metal oxide is then collected and optionally activated for use as a catalyst. The activated or calcined catalyst contains a nano-structured mixed-phase composition comprising phase-separated intimately mixed nanoparticles of copper and manganese oxide.

Abstract: A process for producing a piezoelectric oxide having a composition (A, B, C)(D, E, F)O3, where each of A, B, C, D, E, and F represents one or more metal elements. The composition is determined so as to satisfy the conditions (1), (2), (3), and (4), 0.98?TF(P)?1.01,??(1) TF(ADO3)>1.0,??(2) TF(BEO3)<1.0, and??(3) TF(BEO3)<TF(CFO3)<TF(ADO3),??(4) where TF(P) is the tolerance factor of the perovskite oxide, and TF(ADO3), TF(BEO3), and TF(CFO3) are respectively the tolerance factors of the compounds ADO3, BEO3, and CFO3.

Abstract: The mixed oxide of the invention mainly consists of cerium oxide and of at least one oxide of another rare earth. It has a specific surface area of at least 20 m2/g after calcining at 1000° C. for 5 hours. It is obtained by forming a liquid medium comprising a cerium compound; by heating this medium; by adding to the precipitate obtained a compound of the other rare earth, by heating the medium thus obtained and by bringing its pH to a basic value and by calcining the precipitate. The mixed oxide may be used as a catalyst support.

Abstract: A method for preparing ammonium heptamolybdate with the steps of: i) adding a molybdenum-containing organic phase to a liquid-liquid reextraction apparatus or to a desorption apparatus, and ii) directly cold-crystallization ammonium heptamolybdate by cooling the resulting reextraction or desorption solution.

Abstract: An optical information recording medium includes a recording layer capable of recording information signals on the basis of application of light, wherein the recording layer contains an oxide of metal X and an oxide of metal Y, the metal X is at least one type selected from the group consisting of tungsten and molybdenum, and the metal Y is at least one type selected from the group consisting of copper, manganese, nickel, and silver.

Abstract: Provided is a transition metal precursor comprising a composite transition metal compound represented by Formula I, as a transition metal precursor used in the preparation of a lithium-transition metal composite oxide: M(OH1?x)2??(1) wherein M is two or more selected from the group consisting of Ni, Co, Mn, Al, Cu, Fe, Mg, B, Cr and transition metals of period 2 in the Periodic Table of the Elements; and 0<x<0.5.

Abstract: A method of recovering rhenium (Re) and other metals from Re-bearing materials in the form of ammonium perrhenate having at least the step of adding Re-bearing materials into a leaching slurry. Additionally, the method has the step of adjusting the pH of the slurry to obtain Re in soluble form in a metal salt solution and insoluble residues; filtering the metal salt solution to remove the insoluble residues; selectively precipitating Re from the metal salt solution; filtering the Re precipitate from the metal salt solution to obtain a Re filtercake; and formulating and drying the Re filtercake to obtain a Re sulfide product. The method further has the step of combining the Re sulfide product with a Molybdenum (Mo) concentrate containing Re to obtain a Mo/Re concentrate; roasting the Mo/Re concentrate to obtain Mo oxide product and a flue gas containing Re; and treating the flue gas containing Re to obtain ammonium perrhenate.

Abstract: An agent for treating ulcer containing, as an effective component, a particulate composite hydrotalcite obtained by solidly dissolving a small amount of zinc in the particulate hydrotalcite, exhibiting excellent effect for treating the peptic ulcer and, further, working as a Zn-supplying agent. The agent for treating the ulcer is represented by the following formula (1), (MgaZnb)1-xAlx(OH)2(An?)x/n.mH2O??(1) wherein An? is CO32?, SO42? or Cl?, n is 1 or 2, and x, a, b and m are values that satisfy the following conditions, 0.18?x?0.4, 0.1?a<1, 0<b?0.5, 0?m<1.

Abstract: A thermistor based on a composition having the general formula (I): Re2-x-yCraMnbMcEyOz wherein Re is a rare earth metal or a mixture of two or more rare earth metals, M is a metal selected from the group consisting of nickel, cobalt, copper, magnesium and mixtures thereof, E is a metal selected from the group consisting of calcium, strontium, barium and mixtures thereof, x is the sum of a+b+c and is a number between 0.1 and 1, and the relative ratio of the molar fractions a, b and c is in an area bounded by points A, B, C and D in a ternary diagram, wherein point A is, if y<0.006, at (Cr=0.00, Mn=0.93+10?y, M=0.07?10?y), and, if y?0.006, at (Cr=0?00, Mn=0.99, M=0.01), point B is, if y<0.006, at (Cr=0.83, Mn=0.10+10?y, M=0.07?10?y), and, if y?0.006, at (Cr=0.83, Mn=0.16, M=0.01), point C is at (Cr=0.50, Mn=0.10, M=0.40) and point D is at (Cr=0.00, Mn=0.51, M=0.49), y is a number between 0 and 0.5?x, and z is a number between 2.5 and 3.5.

Abstract: Single crystal and polycrystal oxoruthenates having the generalized compositions (Baz,Sr1?z)FexCoyRu6?(x+y)O11 (1?(x+y)?5; 0?z?1) and (Ba,Sr)M2±xRu4?xO11 (M=Fe,Co) belong to a novel class of ferromagnetic semiconductors with applications in spin-based field effect transistors, spin-based light emitting diodes, and magnetic random access memories.

Abstract: Disclosed is an oxide for a semiconductor layer of a thin film transistor, which, when used in a thin film transistor that includes an oxide semiconductor in the semiconductor layer, imparts good switching characteristics and stress resistance to the transistor. Specifically disclosed is an oxide for a semiconductor layer of a thin film transistor, which is used for a semiconductor layer of a thin film transistor and contains at least one element selected from the group consisting of In, Ga and Zn and at least one element selected from the group X consisting of Al, Si, Ni, Ge, Sn, Hf, Ta and W.