Positive electrode active material particle powder includes: lithium manganese oxide particle powder having Li and Mn as main components and a cubic spinel structure with an Fd-3m space group. The lithium manganese oxide particle powder is composed of secondary particles, which are aggregates of primary particles, an average particle diameter (D50) of the secondary particles being from 4 μm to 20 μm, and at least 80% of the primary particles exposed on surfaces of the secondary particles each have a polyhedral shape having at least one (110) plane that is adjacent to two (111) planes.

A method of preparing an octahedral-structured lithium manganese-based positive electrode active material includes mixing a manganese raw material, a raw material including doping element M.sup.1, wherein the doping element M.sup.1 is at least one element selected from the group consisting of Mg, Al, Li, Zn, B, W, Ni, Co, Fe, Cr, V, Ru, Cu, Cd, Ag, Y, Sc, Ga, In, As, Sb, Pt, Au, and Si, and a lithium raw material and sintering the mixture in an oxygen atmosphere to prepare a lithium manganese oxide having an octahedral structure and doped with the doping element M.sup.1, wherein the sintering includes performing first sintering at 400° C. to 700° C. for 3 hours to 10 hours and performing second sintering at 700° C. to 900° C. for 10 hours to 20 hours. Also provided is an octahedral-structured lithium manganese-based positive electrode active material prepared by the above preparation method.

Provided is an improved method for forming a battery comprising a cathode and electrolyte. The method of forming the cathode 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. The electrolyte is void of salts and additives.

Provided is a method for manufacturing a slurry for a positive electrode of a nonaqueous electrolyte secondary battery containing an alkali metal complex oxide, the method making it possible to reliably deaerate surplus carbonic acid gas after an alkali component of a slurry containing the alkali metal complex oxide is neutralized within a short period of time. The method for manufacturing a slurry for a positive electrode of a nonaqueous electrolyte secondary battery includes a step of manufacturing an electrode slurry including a step of performing a neutralization treatment on an alkali component in the slurry by using inorganic carbon dissolved in a solvent of the slurry and a step of deaerating the inorganic carbon in the slurry as carbonic acid gas by causing cavitation.

The present disclosure relates to a cathode active material, and more particularly, to a cathode active material doped with a trivalent metal (Me) and a lithium secondary battery comprising the same. According to one aspect, there is provided the cathode active material doped with the trivalent metal (Me), represented by the formula Li.sub.xMn.sub.2Me.sub.yO.sub.4 (here, x is from 0.5 to 1.3, and y is from 0.01 to 0.1). According to the present disclosure, release of manganese ions of the cathode active material greatly reduces, and consequently, capacity and cycle life of the battery may be significantly improved.

The present disclosure provides a positive electrode active material which can impart an excellent low temperature output characteristic to a nonaqueous electrolyte secondary battery, and can suppress an increase in resistance after cycle charging and discharging. The positive electrode active material herein disclosed includes a core part including a lithium transition metal composite oxide, and a coating part including a titanium-containing compound on at least a partial surface of the core part. The coating part includes brookite type TiO.sub.2 and a lithium titanium (LiTi) composite oxide including lithium (Li) and titanium (Ti) as titanium-containing compounds, and at least part of titanium (Ti) of the titanium-containing compound is incorporated in a solid solution in the surface of the core part.

This invention provides a membrane electrode material and its preparation method, as well as the application of the material into lithium extraction by adsorption-electrochemical coupling method. The membrane electrode material is described as MnO@C. The preparation steps are as follows: LiMn.sub.2O.sub.4 is firstly obtained by calcining lithium carbonate and manganese carbonate, which is then dispersed in hydrochloric acid solution. After stirring and separating, the solid products are dried to obtain λ-MnO.sub.2. The λMnO.sub.2 is added to the raw material of Mn-MOF-74, and then the Mn-MOF-74 coated λ-MnO.sub.2 can be obtained by hydrothermal reaction. By further calcining Mn-MOF-74 coated λ-MnO.sub.2 in nitrogen atmosphere, the membrane capacitor/electrode material can be obtained as MnO@C. The material is fabricated into an adsorption film electrode plate and assembled into an adsorption-electrochemical coupling lithium extraction device. The pure lithium solution can be obtained in the recovery pool through the combined lithium extraction and lithium recovery process. In this invention, the thickness of the carbon coating layer in the electrode material is adjustable. Adsorption-electrochemical coupling technology takes the advantages of both adsorption and electrochemical lithium intercalation, which can extract and recover lithium resources with high capacity. Thus, this invention not only achieves high-efficiency separation of lithium resources, but also opens up a new way for the extraction of lithium resources.

A method of forming an inorganic nano-material by thermally treating metal-infused organic polymers to remove the organics to leave an inorganic nano-material where the metal-infused organic polymer precursor may be formed by a polymer synthesis reaction of organic monomers with a metal-containing precursor and by combining a metal containing precursor with at least one organic monomer to obtain a mixture and initiating a polymerization reaction of the mixture to form a metal-infused organic polymer precursor.

A material synthesis method may comprise: adding at least one liquid precursor solution to an atomizer device; generating by the atomizer device an aerosol comprising liquid droplets; transporting the aerosol to a reactive zone for evaporating one or more solvents from the aerosol; and collecting particles synthesized from at least evaporating the aerosol.

A LiMnO.sub.2 production method includes generating cubic crystal LiMnO.sub.2 nanoparticles by adding an organic solvent, manganese oxide nanoparticles, and lithium amide in a reaction vessel and heating in an inert atmosphere. and a washing and recovering the generated particles. Wurtzite type MnO nanoparticles are preferably used as the manganese oxide. As a result, LiMnO.sub.2 nanoparticles that have a substantially similar particle size to wurtzite type MnO nanoparticles can be obtained from an Mn raw material. Nanoparticles having a hollow structure can be obtained by controlling the reaction temperature.