A positive-electrode active material for a non-aqueous electrolyte secondary battery is provided. The positive-electrode active material contains a lithium transition metal composite oxide having a spinel structure and containing nickel and manganese. The lithium transition metal composite oxide has a surface region containing niobium as a solid solution. A mole ratio of an amount of niobium to a total amount of nickel and manganese in the surface region decreases according to a distance from a surface in a depth direction in a region from the surface to a distance of 0.3 nm in the depth direction.

The present application discloses a positive electrode active material, comprising a lithium nickel manganese oxide modified material and a coating layer on the surface of the lithium nickel manganese oxide modified material. The lithium nickel manganese oxide modified material is a primary particle with a core-shell-like structure comprising a spinel phase and a rocksalt-like structure phase. The spinel phase is an inner core, and the rocksalt-like structure phase constitutes an outer shell. The rocksalt-like structure phase is further doped with a phosphorus element and the phosphorus element is distributed in a gradient from the outer surface to the interior of the rocksalt-like structure phase. The present application further discloses a preparation method of the positive electrode active material, a positive electrode containing the positive electrode active material for lithium-ion secondary batteries, and a lithium ion secondary battery.

A process for producing a cathode or anode material adapted for use in the manufacture of fast rechargeable ion batteries. The process may include the steps of Selecting an precursor material that, upon heating in a gas stream, releases volatile compounds to create porous materials to generate a material compound suitable for an electrode in an ion battery. Grinding the precursor material to produce a powder of particles with a first predetermined particle size distribution to form a precursor powder. Calcining the precursor powder in a flash calciner reactor segment with a first process gas at a first temperature to produce a porous particle material suitable for an electrode in an ion battery, and having the pore properties, surface area and nanoscale structures for applications in such batteries. Processing the hot precursor powder in a second calciner reactor segment with a second process gas to complete the calcination reaction, to anneal the material to optimise the particle strength, and to modify the oxidation state of the product for maximising the charge density when the particle is activated in a battery cell to form a second precursor powder. Quenching the second precursor powder. Activating the particles of the second precursor powder in an electrolytic cell by the initial charging steps to intercalate electrolyte ions in the particles.

A spinel-type nickel-manganese-lithium-containing composite oxide, a preparation method thereof, and a secondary battery and an electric apparatus containing the same are provided. A body material of the spinel-type nickel-manganese-lithium-containing composite oxide is represented by a general formula Li.sub.xNi.sub.yMn.sub.zM.sub.mO.sub.4Q.sub.q, and both element P and one or more elements selected from elements Nb, W, and Sb are doped in the body material, where based on mass of the spinel-type nickel-manganese-lithium-containing composite oxide, doping content k of the element P satisfies 0.48 wt %≤k≤3.05 wt %, doping content g of the one or more elements selected from the elements Nb, W, and Sb satisfies 0.05 wt %≤g≤0.31 wt %, and 2≤k/g≤20. The secondary battery provided in this application has good high-temperature storage performance and high-temperature cycling performance.

Disclosed are a method for preparing lithium nickel cobalt manganese oxide by reverse positioning of a power battery and use thereof. The method first mixes and grinds a positive electrode tab and a slagging agent, then dries, cools, adds an aluminum powder, mixes well, conducts a self-propagating reaction to the mixed material, cools, takes a lower layer of rough nickel cobalt manganese alloy, grinds the rough nickel cobalt manganese alloy, adds an alkali liquor, then immerses, filters, takes the filter residue for washing and then dries, to obtain a nickel cobalt manganese alloy powder, adds a lithium salt solution to the porous nickel cobalt manganese alloy powder, mixes and drips an alkali liquor, ages, filters, takes a filter residue for washing and then dries, to obtain a mixed powder of precursor, sinters the mixed powder of precursor and cools, to obtain a lithium nickel cobalt manganese oxide.

Provided is an improved method for forming a coated lithium ion cathode materials specifically for use in a battery. The method comprises forming a first solution comprising a digestible feedstock of a first metal suitable for formation of a cathode oxide precursor and a multi-carboxylic acid. The digestible feedstock is digested to form a first metal salt in solution wherein the first metal salt precipitates as a salt of deprotonated multi-carboxylic acid thereby forming an oxide precursor and a coating metal is added to the oxide precursor. The oxide precursor is heated to form the coated lithium ion cathode material.

This positive electrode active material for nonaqueous electrolyte secondary batteries comprises: a lithium transition metal composite oxide which is represented by general formula Li.sub.xM1.sub.2−yM2.sub.yM3.sub.zO.sub.wF.sub.v (wherein 1≤x≤1.2, 0<y<1, 0.001≤z≤0.1, 0≤v≤0.2, 3.8≤w+v≤4.2, M1 represents one or more elements selected from the group consisting of Ni, Co and Mn, M2 represents one or more elements selected from the group consisting of Ti, Fe, Al, Ge and Si, and M3 represents one or more elements selected from the group consisting of Ca and Sr), while containing M1 and M2; and a coating layer which is formed on at least a part of the surface of the lithium transition metal composite oxide, while containing M2 and M3.

Disclosed are a method for preparing lithium nickle cobalt manganese oxide by reverse positioning of a power battery and use thereof. The method first mixes and grinds a positive electrode tab and a slagging agent, then dries, cools, adds an aluminum powder, mixes well, conducts a self-propagating reaction to the mixed material, cools, takes a lower layer of rough nickel cobalt manganese alloy, grinds the rough nickel cobalt manganese alloy, adds an alkali liquor, then immerses, filters, takes the filter residue for washing and then dries, to obtain a nickel cobalt manganese alloy powder, adds a lithium salt solution to the porous nickel cobalt manganese alloy powder, mixes and drips an alkali liquor, ages, filters, takes a filter residue for washing and then dries, to obtain a mixed powder of precursor, sinters the mixed powder of precursor and cools, to obtain a lithium nickle cobalt manganese oxide.

A lithium positive electrode active material intermediate including less than 80 wt % spinel phase and a net chemical composition of Li.sub.xNi.sub.yMn.sub.2-yO.sub.4-δ wherein 0.9≤x≤1.1; 0.4≤y≤0.5; and 0.1≤δ. Further, a process for the preparation of a lithium positive electrode active material with high tap density for a high voltage secondary battery where the cathode is fully or partially operated above 4.4 V vs. Li/Li+, comprising the steps of a)heating a precursor in a reducing atmosphere at a temperature of from 300° C. to 1200° C. to obtain a lithium positive electrode active material intermediate; b)heating the product of step a. in a non-reducing atmosphere at a temperature of from 300° C. to 1200° C.; wherein the mass of the product of step b. increases by at least 0.25% compared to the mass of the product of step a.

A method of producing a positive-electrode active material for a non-aqueous electrolyte secondary battery is provided. The method includes obtaining a precipitate containing nickel and manganese from a solution containing nickel and manganese, heat-treating the resulting precipitate at a temperature of from 850° C. to less than 1100° C. to obtain a first heat-treated product, mixing the first heat-treated product and a lithium compound, and heat-treating the resulting lithium-containing mixture at a temperature of from 550° C. to 1000° C. to obtain a second heat-treated product. The second heat-treated product contains a group of lithium transition metal composite oxide particles having an average particle diameter D.sub.SEM of from 0.5 μm to less than 3 μm and D.sub.50/D.sub.SEM of 1 to 2.5. The lithium transition metal composite oxide particles have a spinel structure based on nickel and manganese.