A lithium-rich manganese-based positive electrode material and a preparation method therefor and an application thereof. The positive electrode material comprises a matrix (10) and a coating layer (20). The coating layer (20) coats the matrix (10). The matrix (10) comprises Li.sub.1+αNi.sub.βM.sub.μO.sub.2-νF.sub.ν and Li.sub.2+α′M′O.sub.3-ν′F.sub.ν′. The coating layer (20) comprises M″.sub.μ′O.sub.ν″ and M″′.sub.μ″O.sub.ν″′. The lithium-rich manganese-based positive electrode material can improve both the rate performance and cycle life of the positive electrode material.

The present application discloses a positive electrode active material including a lithium nickel cobalt manganese oxide, the molar content of nickel in the lithium nickel cobalt manganese oxide accounts for 60%-90% of the total molar content of nickel, cobalt and manganese, and the lithium nickel cobalt manganese oxide has a layered crystal structure of a space group R 3m; a transition metal layer of the lithium nickel cobalt manganese oxide includes a doping element, and the local mass concentration of the doping element in particles of the positive electrode active material has a relative deviation of 20% or less; and in a differential scanning calorimetry spectrum of the positive electrode active material in a 78% delithiation state, an initial exothermic temperature of a main exothermic peak is 200° C. or more, and an integral area of the main exothermic peak is 100 J/g or less.

Systems and methods for direct recycling and upcycling of spent cathode materials using Flame-Assisted Spray Pyrolysis Technology (FAST). In illustrative embodiments, cathode layers are separated and collected from spent battery cells. The cathode laminate is ground to a powdered form and treated to remove contaminants by sifting into a hot stream of air which heats the powders, burning off contaminants. After cooling and particle collection, the powders may be dispersed into leaching solution to dissolve metal oxides and create an acid metal solution or ground into nano-sized primary particles and mixed with dispersing liquids to form a solution. The solution may be mixed with glycerol and additional metal salts to create a final precursor solution, which may undergo spray pyrolysis followed by drying and calcination to create cathode materials with high consistency and repeatability, or mixed with an alkaline metal salt solution and undergo electrodeposition to recover desired metal salts.

Provided are a lithium nickel manganese oxide composite material, a preparation method thereof and a lithium ion battery. The preparation method includes: a first calcining process is performed on a nano-oxide and a nickel-manganese precursor, to obtain an oxide-coated nickel-manganese precursor; and a second calcining process is performed on the precursor and a lithium source material, to obtain the lithium nickel manganese oxide, and a temperature of the first calcining process is lower than the second calcining process. At a lower temperature, the nano-oxide may be melted, a denser nano-oxide coating layer is formed on the surface of the precursor, so the oxide-coated nickel-manganese precursor is obtained. At a higher temperature, the nano-oxide, a nickel-manganese material and a lithium element may be more deeply combined. A problem that the nano-oxide layer is easy to fall off is solved, and cycle performance of the lithium nickel manganese oxide is greatly improved.

A method of producing an inorganic material (S10) according to the present invention includes a vitrification step (S12) of applying shearing stress and compressive stress to a mixed powder (MP) of a plurality of kinds of inorganic compound powders by using a ring ball mill mechanism (70) to vitrify at least a part of the mixed powder (MP); and a dispersion step (S13) of dispersing the vitrified mixed powder (MP) after the vitrification step (S12), where a combined step of the vitrification step (S12) and the dispersion step (S13) is performed a plurality of times to obtain a vitrified inorganic material powder from the mixed powder.

A positive electrode active material precursor for a lithium secondary battery containing at least Ni, in which S/D.sub.50 that is a ratio of a BET specific surface area S to a 50% cumulative volume particle size D.sub.50 is 2×10 to 20×10.sup.6 m/g, and, in powder X-ray diffraction measurement using a CuKα ray, A/B that is a ratio of an integrated intensity A of a diffraction peak within a range of 2θ=37.5±1° to an integrated intensity B of a diffraction peak within a range of 2θ=62.8±1° is more than 0.80 and 1.33 or less.

There is provided a method for collecting and reusing an active material from positive electrode scrap. The positive electrode active material reuse method of the present disclosure includes (a) thermally treating positive electrode scrap comprising a lithium composite transition metal oxide positive electrode active material layer on a current collector in air at 300 to 650° C. for 1 hour or less for thermal decomposition of a binder and a conductive material in the active material layer, to separate the current collector from the active material layer, and collecting an active material in the active material layer, and (b) annealing the collected active material with an addition of a lithium precursor to obtain a reusable active material.

Provided in the present disclosure are a lithium-rich manganese-based positive electrode material for use in a lithium-ion battery, a preparation method for the material, a positive electrode tab, the lithium-ion battery, and an electric vehicle. The lithium-rich manganese-based positive electrode material provides increased structural stability in a charging-discharging cycle, is not prone to experiencing an expansion or contraction that causes grain boundary stress imbalance, is not prone to undergoing a side reaction with an electrolytic solution, and is easy to industrialize; moreover, the lithium-ion battery made with the material provides great cycle performance, great rate performance, and great commercial prospect.

An active material is provided for use in a solid-state battery. The active material exhibits at least one peak in the range of 0.145 to 0.185 nm and at least one peak in the range of 0.280 to 0.310 nm in a radial distribution function obtained through measurement of an X-ray absorption fine structure thereof. In the particle size distribution, by volume, of the active material obtained through a particle size distribution measurement by laser diffraction scattering method, the ratio of the absolute value of the difference between the mode diameter of the active material and the D.sub.10 of the active material (referred to as the “mode diameter” and the “D.sub.10” respectively) to the mode diameter in percentage terms, (|mode diameter - D.sub.10 / mode diameter) x 100, satisfies 0% < (( | mode diameter - D.sub.10| / mode diameter) x 100) ≤ 58.0%.

A method of manufacturing a secondary battery cathode material includes preparing Li.sub.2O powder by separating CO.sub.2 from Li.sub.2CO.sub.3 powder, forming a mixed powder by mixing the Li.sub.2O powder with nickel-cobalt-manganese (NCM) precursor powder, and firing the mixed powder using a rotary kiln.