Abstract: Thin-film lithium-based batteries and electrochromic devices (10) are fabricated with positive electrodes (12) comprising a nanocomposite material composed of lithiated metal oxide nanoparticles (40) dispersed in a matrix composed of lithium tungsten oxide.

Abstract: A procedure for obtaining mixed multimetallic oxides derived from hydrotalcite type compounds, characterized in that the laminar metallic hydroxides obtained are constituted by three or four metallic cations, forming part of the sheets of the hydrotalcite type material represented by the formula: [M(II)1?x?y?zM(II)?xM(III)yM(III)?z(OH)2](An?y+z/n).mH2O. by a process comprising: (1) preparing an aqueous or organic solution containing three or more cations; (2) preparing an alkaline solution; (3) slowly combining solutions (1) and (2) to cause the co-precipitation of the cations in the form of hydroxides; (4) washing the precipitate containing the hydrotalcites with water, until removal of the non-precipitated ions; (5) drying; and (6) calcining the hydrotalcites.

Abstract: There is provided Lithium-manganese oxides expressed as the following chemical formula 1, Li1+xMn1?x?yMyO2+z,??[Chemical Formula 1] wherein 0.01?x?0.5, 0?y?0.3, ?0.2?z?0.2, and M is a metal selected from the group consisting of Ti, Mn, V, Cr, Fe, Co, Ni, Cu, Zn, Zr, Nb, Mo, W, Ag, Sn, Ge, Si, Al, and alloy thereof.

Abstract: The present invention provides for a process of making a Ni-based lithium transition metal oxide cathode active materials used in lithium ion secondary batteries. The cathode active materials are substantially free of Li2CO3 impurity and soluble bases.

Abstract: The present invention provides for Ni-based lithium transition metal oxide cathode active materials used in lithium ion secondary batteries. The cathode active materials are substantially free of Li2CO3 impurity and soluble bases.

Abstract: The present invention provides for lithium ion secondary batteries that use Ni-based lithium transition metal oxide cathode active materials. The cathode active materials are substantially free of Li2CO3 impurity and soluble bases.

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: In a lithium transition metal oxide having a layered structure, one is provided, which is particularly excellent as a positive electrode active material of a battery on board of an electric vehicle or a hybrid vehicle in particular. A lithium transition metal oxide having a layered structure is proposed, wherein the ratio of the crystallite diameter determined by Measurement Method 1 according to the Rietveld method with respect to the mean powder particle diameter (D50) determined by the laser diffraction/scattering-type particle size distribution measurement method is 0.05 to 0.20.

Abstract: A lithium mixed metal oxide containing Li, Mn and M (M represents at least one metal element, and is free from Li or Mn), and having a peak around 1.5 ? (peak A), a peak around 2.5 ? (peak B), and the value of IB/IA is not less than 0.15 and not more than 0.9 in a radial distribution function obtained by subjecting an extended X-ray absorption fine structure (EXAFS) spectrum at K absorption edge of Mn in the oxide to the Fourier transformation, wherein IA is the intensity of peak A and IB is the intensity of peak B.

Abstract: The present invention provides a process for making a complex metal oxide comprising the formula AxByOz. The process comprises the steps of: (a) reacting in solution at a temperature of between about 75° C. to about 100° C. at least one water-soluble salt of A, at least one water-soluble salt of B and a stoichiometric amount of a carbonate salt or a bicarbonate salt required to form a mole of a carbonate precipitate represented by the formula AxBy(CO3)n, wherein the reacting is conducted in a substantial absence of carbon dioxide to form the carbonate precipitate and wherein the molar amount of carbonate salt or bicarbonate salt is at least three times the stoichiometric amount of carbonate or bicarbonate salt required to form a mole of the carbonate precipitate; and (b) reacting the carbonate precipitate with an oxygen containing fluid under conditions to form the complex metal oxide.

Abstract: An insulating target material for obtaining a conductive complex oxide film represented by a general formula ABO3. The insulating target material includes: an oxide of an element A; an oxide of an element B; an oxide of an element X; and at least one of an Si compound and a Ge compound, the element A being at least one element selected from La, Ca, Sr, Mn, Ba, and Re, the element B being at least one element selected from Ti, V, Sr, Cr, Fe, Co, Ni, Cu, Ru, Ir, Pb, and Nd, and the element X being at least one element selected from Nb, Ta, and V.

Abstract: Disclosed is a positive electrode active material for a nonaqueous electrolyte secondary battery having at least a lithium-transition metal composite oxide of a layer structure, in which an existence ratio of at least one selected from the group consisting of elements which may become tetravalent and magnesium is 20% or more on a surface of the lithium-transition metal composite oxide. By use of this positive electrode active material, a nonaqueous electrolyte secondary battery having excellent battery characteristics, specifically, having excellent high rate characteristics, cycle characteristics, low-temperature characteristics, thermal stability, and the like, under the even more harsh environment for use can be realized.

Abstract: The invention relates to materials for use as electrodes in an alkali-ion secondary (rechargeable) battery, particularly a lithium-ion battery. The invention provides transition-metal compounds having the ordered-olivine, a modified olivine, or the rhombohedral NASICON structure and the polyanion (PO4)3? as at least one constituent for use as electrode material for alkali-ion rechargeable batteries.

Abstract: Anitrate-nitrogen-reducing agent for a farm product, comprising as an active ingredient a hydroxide solid solution represented by the formula (1), [(M12+)1-x(M22+)x]1-z(M3+)z(OH)2(An?)z/n·mH2O??(1) wherein M12+ represents Ca and/or Mg, M22+ represents at least one essential mineral selected from Fe, Mn, Zn, Cu, Ni and Co, M3+ represents at least one trivalent metal, An? represents an anion having a valence of n, x is a positive number in the range of 0<x<0.5, m is 0 or a positive number in the range of 0?m<10, z is a positive number in the range of 0<z<0.4, and n is a positive number in the range of 1?n?10, and/or the formula (2), (M12+)1-x(M22+)x(OH)2??(2) wherein M12+, x and M22+ are as defined in the formula (1).

Abstract: Disclosed herein is a method for producing a lithium composite oxide for use as a positive electrode active material for lithium secondary batteries by a spray pyrolysis process. The method comprises the steps of: subjecting an inorganic acid salt solution of metal elements constituting a final composite oxide other than lithium to a spray pyrolysis process to obtain an intermediate composite oxide powder; and solid state-mixing the intermediate composite oxide powder and a hydroxide salt of lithium, followed by thermally treating the mixture.

Abstract: Disclosed is a process for producing a secondary battery cathode material by calcining raw materials. The process is characterized by calcining the raw materials together with one or more substances, which are selected from the group consisting of hydrogen, water and water vapor, and conductive carbon and/or a substance, which can form conductive carbon by pyrolysis, added thereto. As crystals of the secondary battery cathode material obtained by this process have been controlled fine sizes, the secondary battery cathode material promotes movements of ions of an alkali metal led by lithium between the interiors of grains of the cathode material and an electrolyte to suppress polarization in an electrode reaction, and further, increases an area of contact between the positive material and a conductivity-imparting material to provide improved conductivity so that improvements are assured in voltage efficiency and specific battery capacity.

Abstract: Oxygen is reduced in the presence of a catalyst at the cathode of an alkaline-electrolyte fuel cell. Catalysts of the formula Sr3?xA1+xCo4?yByO10.5?z wherein ?0.6?x?1.0; 0?y?3; and ?1.5?z?0.5; wherein A represents Eu, Gd, Tb, Dy, Ho, or Y; and wherein B represents Fe, Ga, Cu, Ni, Mn, and Cr, demonstrate high catalytic activity and high chemical stability when used as the oxygen-reduction catalyst in alkaline fuel cells.

Abstract: Coagulated particles of nickel-cobalt-manganese hydroxide wherein primary particles are coagulated to form secondary particles are synthesized by allowing an aqueous solution of a nickel-cobalt-manganese salt, an aqueous solution of an alkali-metal hydroxide, and an ammonium-ion donor to react under specific conditions; and a lithium-nickel-cobalt-manganese-containing composite oxide represented by a general formula, LipNixMn1-x-yCoyO2-qFq (where 0.98?p?1.07, 0.3?x?0.5, 0.1?y?0.38, and 0?q?0.05), which is a positive electrode active material for a lithium secondary cell having a wide usable voltage range, a charge-discharge cycle durability, a high capacity and high safety, is obtained by dry-blending coagulated particles of nickel-cobalt-manganese composite oxyhydroxide formed by making an oxidant to act on the coagulated particles with a lithium salt, and firing the mixture in an oxygen-containing atmosphere.

Abstract: The present invention relates to a powderous electrode active material of lithium transition metal oxide LiaMbO2, wherein 0.9 < a < 1.1, 0.9 < b < 1.1 and M is dominantly transition metal chosen from Mn, Co and Nickel, having particles with a distribution of sizes, where the composition M varies with the size of the particles, and a preparation method thereof. The present invention also relates to an electrochemical cell, particularly rechargeable lithium battery, using the powderous electrode active material.

Abstract: To provide a transition metal compound granule serving as a raw material for a cathode active material for a lithium secondary battery, which has high packing density, large volume capacity density and high safety and which is excellent in durability for charge and discharge cycles. A transition metal compound granule serving as a raw material for a positive electrode material for a lithium ion secondary battery, which comprises particles containing at least one element selected from the group consisting of nickel, cobalt and manganese and having an average particle size of the primary particles being at most 1 ?m and which is substantially spherical and has an average particle size D50 of from 10 to 40 ?m and an average pore size of at most 1 ?m.

Abstract: A method for preparing lithium transitional metal oxides, comprises the steps of: preparing a carbonate precursor using the following substeps: forming a first aqueous solution containing a mixture of at least two of the ions of the following metal elements (“Men+”): cobalt (Co), nickel (Ni), and manganese (Mn); forming a second aqueous solution containing ions of CO32?; and mixing and reacting the first solution and the second solution to produce the carbonate precursor, Ni1-x-yCoxMnyCO3; and preparing the lithium transition metals oxide from the carbonate precursors using the following substeps: evenly mixing Li2CO3 and the carbonate precursor; calcinating the mixed material in high temperature; and cooling and pulverizing the calcinated material to obtain the lithium transition metal oxide, Li Ni1-x-yCoxMnyO2.

Abstract: A spinel structure compound of the formula LiNi0.4Mn1.6O4-?, wherein ?>0, has a lattice parameter of from 8.179 to 8.183 ?. The compound may be prepared by mixing carbonated precursors under stoichiometric conditions to produce a mixture, subjecting the mixture to a first heat treatment at a temperature of from 500 to 700° C., and then subjecting the mixture to one or more annealing treatments at a temperature of from 700 to 950° C., followed by cooling in a medium containing oxygen. The spinel structure compound may be used as an electrochemically active material in an electrode, for example an electrode of a battery.

Abstract: The present invention is directed to pigment compositions, thick film black pigment compositions, conductive single layer thick film compositions, black electrodes made from such black conductive compositions and methods of forming such electrodes, and to the uses of such compositions, electrodes, and methods in flat panel display applications, including alternating-current plasma display panel devices (AC PDP).

Abstract: To provide a process for producing a lithium-containing composite oxide for a positive electrode for a lithium secondary battery, which is excellent in the volume capacity density, safety, charge and discharge cycle durability and low temperature characteristics. A process for producing a lithium-containing composite oxide represented by the formula LipNxMmOzFa (wherein N is at least one element selected from the group consisting of Co, Mn and Ni, M is at least one element selected from the group consisting of Al, alkaline earth metal elements and transition metal elements other than N, 0.9?p?1.2, 0.97?x<1.00, 0<m?0.03, 1.9?z?2.2, x+m=1 and 0?a?0.

Abstract: Provided is a method for preparing an electroconductive mayenite type compound with good properties readily and stably at low cost. A production method of an electroconductive mayenite type compound comprising a step of subjecting a precursor to heat treatment, is a method for preparing an electroconductive mayenite type compound, comprising a step of subjecting a precursor to heat treatment; wherein the precursor is a vitreous or crystalline material, which contains Ca and Al, in which a molar ratio of (CaO:Al2O3) is from (12.6:6.4) to (11.7:7.3) as calculated as oxides, and in which a total amount of CaO and Al2O3 is at least 50 mol %, and wherein the heat treatment is heat treatment comprising holding the precursor at a heat treatment temperature T of from 600 to 1415° C. and in an inert gas or vacuum atmosphere with an oxygen partial pressure PO2 in a range of PO2?105×exp [{?7.9×l04/(T+273)}+14.4] in the unit of Pa.

Abstract: Disclosed is a method for regulating terminal voltage of a cathode during overdischarge. Also disclosed is a lithium secondary battery, which is low in capacity loss after overdischarge, having excellent capacity restorability after overdischarge and shows an effect of preventing a battery from swelling at a high temperature.

Abstract: Disclosed are primary materials, precursor materials and final materials as well as methods to prepare these materials. The final materials are mixed lithium transition metal oxides, useful as performance optimized cathode materials for rechargeable lithium batteries. The transition metal is a solid solution mixture of manganese, nickel and cobalt, M=(Mn1-uNiu)1-u-yCoy, with 0.2.

Abstract: A new set of additives to be sued in the preparation of inorganic materials; especially of perovskite nature is proposed. The chemical compositions of the perovskites prepared in the presence of the mentioned additives are found to be more homogenous, leading to better catalytic behavior, including higher selectivity and yields as compared to catalysts of identical formulations prepared through the conventional method of using EDTA/citrate (or other organic additive) method.

Abstract: A positive active material is provided which can give a battery having a high energy density and excellent high-rate discharge performance and inhibited from decreasing in battery performance even in the case of high-temperature charge. Also provided is a non-aqueous electrolyte battery employing the positive active material. The positive active material contains a composite oxide which is constituted of at least lithium (Li), manganese (Mn), nickel (Ni), cobalt (Co), and oxygen (O) and is represented by the following chemical composition formula: LiaMnbNicCodOe (wherein 0<a?1.3, |b?c|?0.05, 0.6?d<1, 1.7?e?2.3, and b+c+d=1). The non-aqueous electrolyte battery has a positive electrode containing the positive active material, a negative electrode, and a non-aqueous electrolyte.

Abstract: The present invention provides a high-capacity and low-cost non-aqueous electrolyte secondary battery, comprising: a negative electrode containing, as a negative electrode active material, a substance capable of absorbing/desorbing lithium ions and/or metal lithium; a separator; a positive electrode; and an electrolyte, wherein the positive electrode active material contained in the positive electrode is composed of crystalline particles of an oxide containing two kinds of transition metal elements, the crystalline particles having a layered crystal structure, and oxygen atoms constituting the oxide forming a cubic closest packing structure.

Abstract: The present invention includes compositions, surface and bulk modifications, and methods of making of (1?x)Li[Li1/3Mn2/3]O2.xLi[Mn0.5-yNi0.5-yCo2y]O2 cathode materials having an O3 crystal structure with a x value between 0 and 1 and y value between 0 and 0.5, reducing the irreversible capacity loss in the first cycle by surface modification with oxides and bulk modification with cationic and anionic substitutions, and increasing the reversible capacity to close to the theoretical value of insertion/extraction of one lithium per transition metal ion (250-300 mAh/g).

Abstract: The invention provides a process for production of an oxide fine particle powder including a heating step in which a dry powder of a metal complex gel is heat treated to obtain an oxide fine particle powder, wherein the heating step is carried out in two stages with different oxygen concentrations, or at least part of the heating step is carried out in a water vapor-containing atmosphere.

Abstract: Provided is a method for preparing an electroconductive mayenite type compound with good properties readily and stably at low cost without need for expensive facilities, a reaction at high temperature and for a long period of time, or complicated control of reaction. A method for preparing an electroconductive mayenite type compound comprises a step of subjecting a precursor to heat treatment, wherein the precursor contains Ca and/or Sr, and Al, a molar ratio of (a total of CaO and SrO:Al2O3) is from (12.6:6.4) to (11.7:7.3) as calculated as oxides, a total content of CaO, SrO and Al2O3 in the precursor is at least 50 mol %, and the precursor is a vitreous or crystalline material; and the method comprises a step of mixing the precursor with a reducing agent and performing the heat treatment of holding the mixture at 600-1,415° C. in an inert gas or vacuum atmosphere with an oxygen partial pressure of at most 10 Pa.

Abstract: The present invention provides a powderous lithium transition metal oxide with the composition as represented by the below Formula and prepared by solid state reaction in air from a mixed transition metal precursor and Li2CO3, with being practically free of Li2CO3 impurity: LixMyO2 wherein M=M?1?kAk, where M?=Ni1?a?b(Ni1/2Mn1/2)aCob on condition of 0.65?a+b?0.85 and 0.1?b?0.4; A is a dopant; and 0?k?0.05; and x+y=2 on condition of 0.95?x?1.05. The Ni-based lithium transition metal oxide according to the present invention has a well-layered structure, and also improved safety, cycling stability and stability against aging and low gas evolution during storage, when used as an active material for cathode of lithium secondary batteries, because it has a high sintering stability and is substantially free of soluble bases.

Abstract: This invention relates to a Polyoxometalate (POM) represented by the formula: (An)m+[HqM16X8W48O184(OH)32]m? or solvates thereof, wherein: A represents a cation, n is the number of the cations A, m is the charge of the polyoxoanion, q is the number of protons and varies from 0 to 12, M represents a transition metal, and X represents a heteroatom selected from P, As and mixtures thereof. This invention also relates to a process to produce such POMs and to a process for the homogeneous or heterogeneous oxidation of organic substrates comprising contacting the organic substrate with such POMs.

Abstract: An active material for positive electrode for a non-aqueous electrolyte secondary battery comprises a lithium-metal composite oxide that is expressed by the general formula of Lix(Ni1-yCoy)1-zMzO2 (where 0.98?x?1.10, 0.05?y?0.4, 0.01?z?0.2, and where M is at least one metal element selected from the group of Al, Mg, Mn, Ti, Fe, Cu, Zn and Ga), and where the SO4 ion content is in the range from 0.4 weight % to 2.5 weight %, and the occupancy rate of lithium found from the X-ray diffraction chart and using Rietveld analysis is 98% or greater, and the carbon amount measured by way of the high frequency heating-infrared adsorption method is 0.12 weight % or less, and that the Karl Fischer water content due to heating at 180° C. be 0.2 weight % or less.

Abstract: An electrode material for a lithium secondary battery which includes particles each having a central portion and a surface portion covering the surface of the central portion. The central portion occupies 80 to 99% of a distance from a center to an outermost surface of the particle and the surface portion occupies 20 to 1% of the distance. The central portion includes LiM1-aDaO2 (M represents Co or Ni, D represents a transition metal element or Al replacing a part of Co or Ni as M, and M is not the same as D) having an ?-NaFeO2 structure. The surface portion includes LiM1-bEbO2 (M represents Co or Ni, E represents a metal element replacing a part of Co or Ni as M, and M is not the same as E) having an ?-NaFeO2 structure. The content of element E in the central portion satisfies the relation of E/(M+D+E)<0.05 in terms of an atomic ratio, and the content of element D in the surface portion satisfies the relation of D/(M+D+E)<0.05 in terms of an atomic ratio.

Abstract: The present invention relates to a novel composite metal oxide catalyst, a method of making the catalyst, and a process for producing synthesis gas using the catalyst. The catalyst may be a nickel and cobalt based dual-active component composite metal oxide catalyst. The catalyst may be used to produce synthesis gas by the carbon dioxide reforming reaction of methane. The catalyst on an anhydrous basis after calcinations has the empirical formula: M a m + ? N b n + ? Al c 3 + ? Mg d 2 + ? O ( am 2 + bn 2 + 3 2 ? c + d ) Mm+ and Nn+ are two transition metals serving as dual-active components and selected from the group consisting of Ni, Co, Fe, Mn, Mo, Cu, Zn or mixtures thereof, a+b+c+d=1, and 0.001?a?0.8, 0.001?b?0.8, 0.1?c?0.99, 0.01?d?0.99.

Abstract: This invention relates to a process for preparing zirconium oxide, in its various forms, including zirconium-based mixed oxides. There is described a process for preparing a zirconium oxide in the absence of a cerium salt which comprises precipitating a zirconium hydroxide from an aqueous solution of a zirconium salt by reaction with an alkali in the presence of a controlled amount of sulphate anions at a temperature not greater than 50° C. and then calcining the hydroxide to form an oxide, wherein the oxide thus formed is essentially sulphate free. Catalysts and ceramics can be produced from the product oxides having improved thermal stability and improved sinterability, respectively. A particular use of the product oxide is as a promoter or catalyst support in automobile exhaust systems.

Abstract: A lithium-transition metal complex compound has an nth order hierarchical structure in which n type structures represented by at least one unit of ath order units in a range of 1×10?(a+5) m to 10×10?(a+5) m exist in a complex form, wherein n is a natural number that is 2 or greater, and a is a natural number in a range of 1 to 5. The lithium-transition metal complex may be prepared by heat-treating a mixture including a lithium source, a transition metal source, and solvent in contact with a natural material having a hierarchical structure. A lithium battery includes an electrode including the lithium-transition metal complex compound having the nth order hierarchical structure. The lithium battery can have improved rapid charging characteristics, high power characteristics, and cycle characteristics.

Abstract: A lithium secondary battery that is highly safe and has long life. The battery, which is a nonaqueous lithium secondary battery, utilizes a cathode active material comprising a complex oxide material having a layered structure containing at least Li and Ni and being represented by the chemical formula LixNia(MnyM1-y)b(COzM?1-z)cO2(0<x<1.2, 0<y<1, 0<z<1, a+b+c=1, 9b?5a+2.7, 0<a<1, 0<b<1, 0<c<1, M: quadrivalent element other than Mn, and M?: trivalent element other than Co).

Abstract: A method for preparing Li1+xNi1?yCoyO2 cathode materials is disclosed, wherein ?0.2?x?0.2 and 0.05?y?0.5. The method includes the following steps: (A) adding a first solution into a second solution to form a mixed solution, wherein the first solution is a saturated lithium hydroxide solution, the second solution contains nickel salt and cobalt salt, the mole ratio of the lithium ion in the first solution to nickel ion and cobalt ion in the second solution ranges from 1.5:1 to 5:1, and the molar ratio of nickel ion to cobalt ion in the second solution is 1?y:y; (B) stirring the mixed solution; (C) filtering the mixed solution and obtaining a co-precipitated precursor, wherein the molar ratio of lithium ion:nickel ion:cobalt ion is 1+x:1?y:y; and (D) heating the co-precipitated precursor at a temperature higher than 600° C.

Abstract: A process for preparing nickel hydroxide by alkaline precipitation from nickel salt solutions in the presence of complexing agents, in which the precipitation is carried out at at least two different locations in the same mother liquor with different precipitation kinetics at the different locations and the mother liquor is mixed prior to agglomeration of the precipitated primary crystals, is described.

Abstract: It is an object to provide a method for producing stable alkaline metal oxide sols having a uniform particle size distribution. The method comprises the steps of: heating a metal compound at a temperature of 60° C. to 110° C. in an aqueous medium that contains a carbonate of quaternary ammonium; and carrying out hydrothermal processing at a temperature of 110° C. to 250° C. The carbonate of quaternary ammonium is (NR4)2CO3 or NR4HCO3 in which R represents a hydrocarbon group, or a mixture thereof. The metal compound is one, or two or more metal compounds selected from a group of compounds based on a metal having a valence that is bivalent, trivalent, or tetravalent.

Abstract: Composite cathode active materials comprising a composite oxide and an acid treated with an organic solvent are provided. The composite cathode active materials are prepared by treating mixtures of nickel-based composite oxides and organic acids with organic solvents. The active materials suppress gelation of the electrode slurries for a long period of time, even when the active materials are mixed with fluorine-based polymers, by decreasing the basicity of the slurries and the amount of lithium present on the surfaces of the active materials. As a result, electrode slurries having high stability can be prepared. Cathodes and lithium batteries comprising the slurries have excellent charge-discharge characteristics, including high capacity and excellent high rate discharge characteristics.

Abstract: There is provided Lithium-manganese oxides expressed as the following chemical formula 1, Li1+xMn1?x?yMyO2+z, ??[Chemical Formula 1] wherein 0.01?x?0.5, 0?y?0.3, ?0.2?z?0.2, and M is a metal selected from the group consisting of Ti, Mn, V, Cr, Fe, Co, Ni, Cu, Zn, Zr, Nb, Mo, W, Ag, Sn, Ge, Si, Al, and alloy thereof.

Abstract: Disclosed is a fabrication method for an electrode active material, and a lithium battery comprising an electrode active material fabricated therefrom. The fabrication method for an electrode active material comprises preparing an aqueous solution by dissolving a precursor that can simultaneously undergo positive ion substitution and surface-reforming processes in water; mixing and dissolving raw materials for an electrode active material with a composition ratio for a final electrode active material in the aqueous solution, thereby preparing a mixed solution; removing a solvent from the mixed solution, thereby forming a solid dry substance; thermal-processing the solid dry substance; and crushing the thermal-processed solid dry substance.

Abstract: A positive electrode material for a nonaqueous lithium secondary battery and a lithium secondary battery that has superior cycle life and safety and reduced internal resistance of the battery at low temperature is provided. The positive electrode material for a nonaqueous lithium secondary battery comprise a layered structured complex oxide expressed by a composition formula LiaMnxNiyCozM?O2, where 0<a?1.2, 0.1?x?0.9, 0?y?0.44, 0.1?z?0.6, 0.01???0.1, and x+y+z+?=1. A diffraction peak intensity ratio between the (003) plane and the (104) plane (I(003)/I(104)) in an X-ray powder diffractometry using a Cu—K? line in the X-ray source is not less than 1.0 and not more than 1.5.

Abstract: A positive active material composition for a rechargeable lithium battery includes at least one lithiated compound, and at least one additive compound selected from the group consisting of a thermal-absorbent element-included hydroxide, a thermal-absorbent element-included oxyhydroxide, a thermal-absorbent element-included oxycarbonate, and a thermal-absorbent element-included hydroxycarbonate.

Abstract: Single-phase lithium-transition metal oxide compounds containing cobalt, manganese and nickel can be prepared by wet milling cobalt-, manganese-, nickel- and lithium-containing oxides or oxide precursors to form a finely-divided slurry containing well-distributed cobalt, manganese, nickel and lithium, and heating the slurry to provide a lithium-transition metal oxide compound containing cobalt, manganese and nickel and having a substantially single-phase O3 crystal structure. Wet milling provides significantly shorter milling times than dry milling and appears to promote formation of single-phase lithium-transition metal oxide compounds. The time savings in the wet milling step more than offsets the time that may be required to dry the slurry during the heating step.