A positive electrode active material for a non-aqueous electrolyte secondary battery according to a configuration includes a lithium-transition metal composite oxide containing nickel (Ni) in an amount of greater than or equal to 80 mol %, in which boron (B) is present at least on a particle surface of the lithium-transition metal composite oxide. In the lithium-transition metal composite oxide, when particles having a larger particle size than a volume-based 70% particle size (D70) are first particles and particles having a smaller particle size than a volume-based 30% particle size (D30) are second particles, a coverage ratio of B on surfaces of the first particles is larger than a coverage ratio of B on surfaces of the second particles by 5% or greater.

A method of producing a positive electrode active material, the method includes: contacting first particles that contain a lithium transition metal composite oxide with a solution containing sodium ions to obtain second particles containing the lithium transition metal composite oxide and sodium element, wherein the lithium transition metal composite oxide has a layered structure and a composition ratio of a number of moles of nickel to a total number of moles of metals other than lithium in a range of from 0.7 to less than 1; mixing the second particles and a boron compound to obtain a mixture; and heat-treating the mixture at a temperature in a range of from 100° C. to 450° C.

The present disclosure relates to an anode electrode active material for a secondary battery containing nickel cobalt molybdenum oxide, an anode electrode for a secondary battery including the same, a secondary battery including the anode electrode for a secondary battery, and a method for manufacturing the same. The novel anode electrode material for a sodium secondary battery containing nickel cobalt molybdenum oxide according to the present disclosure allows intercalation/deintercalation reaction of sodium ion during charge/discharge and does not undergo significant volume change during the intercalation reaction because structure is maintained stably during repeated charge/discharge. As a result, electrode damage and electric short circuit are decreased and, thus, improved electrochemical characteristics can be achieved in long-life and high-rate capability.

Provided are processes for the production of particles for use as a precursor material for synthesis of Li-ion cathode active material of a lithium-ion cell comprising: a non-lithiated nickel oxide particle of the formula MO.sub.x wherein M comprises 80 at % Ni or greater and wherein x is 0.7 to 1.2, M optionally excluding boron in the MO.sub.x crystal structure; and a modifier oxide intermixed with, coated on, present within, or combinations thereof the non-lithiated nickel oxide particle, wherein the modifier oxide is associated with the non-lithiated nickel oxide such that a calcination at 500 degrees Celsius for 2 hours results in crystallite growth measured by XRD of 2 nanometers or less.

A method for producing a metal composite hydroxide, which includes a first crystallization process of obtaining first metal composite hydroxide particles by supplying a first raw material aqueous solution containing a metal element and an ammonium ion donor to a reaction tank, adjusting a pH of a reaction aqueous solution in the reaction tank, and performing a crystallization reaction and a second crystallization process of forming a tungsten-concentrated layer on a surface of the first metal composite hydroxide particles and obtaining second metal composite hydroxide particles by supplying a second raw material aqueous solution containing a metal element and a more amount of tungsten than the first raw material aqueous solution and an ammonium ion donor to a reaction aqueous solution containing the first metal composite hydroxide particles, adjusting a pH of the reaction aqueous solution, and performing a crystallization reaction, and the like.

A positive electrode active material for nonaqueous electrolyte secondary batteries comprises a lithium transition metal composite oxide that has secondary particles each formed from aggregated primary particles and a surface modification layer that is formed on the surface of each of the primary particles of the lithium transition metal composite oxide, in which the lithium transition metal composite oxide contains at least Al and Ni in an amount of 80 mol % or more relative to the total number of moles of metal elements excluding Li, the surface modification layer contains W and at least one of Sr and Ca, and the content of W in the surface modification layer is 0.075 mol % or less relative to the total number of moles of the metal elements excluding Li in the lithium transition metal composite oxide.

The present invention provides a method for producing a manganese-doped nickel molybdate electrode material including mixing a nickel salt solution with a manganese salt solution to form a mixture; adding a molybdate solution into the mixture and being subject to a thermal reaction; and obtaining the manganese-doped nickel molybdate electrode material after washing and drying of the reaction product. The nickel salt includes one or more of nickel nitrate, nickel chloride, and nickel acetate; the manganese salt includes one or more of manganese chloride, manganese nitrate, and manganese sulfate; and the molybdate includes one or more of sodium molybdate or ammonium molybdate. The present method utilizes a single reaction to produce a Mn-doped NiMoO.sub.4 electrode material, which does not require using nickel molybdate as an intermediate product. The method simplifies the preparation process and makes it easy to be adjusted, thereby improving the electrochemical properties of the electrode material.

A method of producing a positive electrode active material, the method includes: contacting first particles that contain a lithium transition metal composite oxide with a solution containing sodium ions to obtain second particles containing the lithium transition metal composite oxide and sodium element, wherein the lithium transition metal composite oxide has a layered structure and a composition ratio of a number of moles of nickel to a total number of moles of metals other than lithium in a range of from 0.7 to less than 1; mixing the second particles and a boron compound to obtain a mixture; and heat-treating the mixture at a temperature in a range of from 100° C. to 450° C.

The present invention belongs to the field of materials, and relates to an environment-friendly precursor, a cathode material for a lithium-ion battery, and preparation methods thereof. The method for preparing an environment-friendly precursor provided in the present invention includes: subjecting a metal and/or a metal oxide, an oxidant, water, and a complexing agent to a chemical corrosion crystallization reaction at an electrical conductivity equal to or greater than 200 uS/cm, a redox potential ORP value equal to or less than 100 my, and a complexing agent concentration of 3-50 g/L. The precursor prepared by using the method provided in the present invention has advantages that no waste water is produced during dissolution and crystallization, and that water is constantly consumed, so that the purpose of environmental friendliness can be achieved. Moreover, the first charge and discharge efficiency of a lithium-ion battery can be effectively improved by means of the precursor.

A nickel cobalt manganese composite hydroxide with low impurity content and high reactivity when synthesizing a positive electrode active material, which can be used as a precursor of the positive electrode active material for non-aqueous electrolyte secondary batteries with low irreversible capacity, represented by a general formula: Ni.sub.xCo.sub.yMn.sub.zM.sub.t(OH).sub.2+a (wherein x+y+z+t=1, 0.20≦x≦0.80, 0.10≦y≦0.50, 0.10≦z≦0.90, 0≦t≦0.10, 0≦a≦0.5, and M is at least one additive element selected from Mg, Ca, Al, Ti, V, Cr, Zr, Nb, Mo, W), which includes: spherical secondary particles formed by aggregation of a plurality of plate-shaped primary particles, which have an average particle diameter of 3 μm to 20 μm, a sulfate radical content of 1.0 mass % or less, a chlorine content of 0.5 mass % or less, and a carbonate radical content of 1.0 mass % to 2.5 mass %.