A multistage centrifugal atomizer comprises an outer shell that contains an inlet port and an outlet port and that encloses a tundish, a first inclined rotating surface and a second inclined rotating surface. The first inclined rotating surface is opposedly disposed to the second inclined rotating surface. The inlet is used to introduce a molten material into the multistage atomizer and the outlet is used to remove ultrafine particles having a D50 of less than 20 micrometers.

The present disclosure provides a cathode material and a method for preparing the cathode material, a cathode, a lithium ion battery and a vehicle. The cathode material comprises a matrix particle, wherein the matrix particle is a monocrystal particle comprising nickel lithium manganate and nickel cobalt lithium manganate. A position in the matrix particle close to a surface layer is provided with a buffer layer. A content of at least one of elements Ni, Co and Mn in the buffer layer is lower than contents thereof in other positions of the matrix particle. The cathode material has at least one of advantages of relatively high specific capacity, cycling stability, better safety performance and the like, and the buffer layer can alleviate erosion by an electrolyte and inhibit separation of active oxygen.

The solid electrolyte material consists essentially of Li, Ti, M, and F. Here, M is at least one selected from the group consisting of Al and Y.

Preparing MAX phase structures includes forming a gel including a transition metal M, a Group 3A or Group 4A metal or semimetal A, and an acidic chelating agent or gelling agent X. X includes one or both of carbon and nitrogen. Preparing the MAX phase structures further includes shaping the gel to yield a shaped gel and heating the shaped gel to yield carbonaceous MAX phase structures with a composition represented by M.sub.n+1AX.sub.n, wherein n is 1, 2, 3, or 4. The MAX phase structures can be thick films, microspheres, or microwires.

Embodiments of the present disclosure generally relate to carbon materials for battery electrodes and methods for preparing such carbon materials. More specifically, embodiments relate to methods for coating a carbon film onto nano-ordered carbon particles to produce carbon-coated particles which can be used as an anode material within a battery, such as a lithium-ion battery, a sodium-ion battery, other types of batteries. In one or more embodiments, a method for producing carbon-coated particles is provided and includes positioning nano-ordered carbon particles within a processing region of a processing chamber, purging the processing region containing the nano-ordered carbon particles with an inert gas, heating the nano-ordered carbon particles to a temperature of about 700° C. or greater during an annealing process, and depositing a carbon film on the nano-ordered carbon particles to produce carbon-coated particles during a vapor deposition process.

Exemplary embodiments of positive electrode active materials in the form of single particles, and a method of preparing each of them, are provided. The single particles of the exemplary embodiments include single particles of a nickel-based lithium composite metal oxide, having a plurality of crystal grains, each having a size of 180 nm to 300 nm, as analyzed by a Cu Kα X-ray (X-rα). The single particles include a metal doped in the crystal lattice thereof. One embodiment includes a surface coating. The total content of the metal doped in the crystal lattice thereof and the metal of the metal oxide coated on the surface thereof is controlled in the range of 2500 ppm to 6000 ppm.

The invention relates to Chevrel-phase materials and methods of preparing these materials utilizing a precursor approach. The Chevrel-phase materials are useful in assembling electrodes, e.g., cathodes, for use in electrochemical cells, such as rechargeable batteries. The Chevrel-phase materials have a general formula of Mo.sub.6Z.sub.8 (Z=sulfur) or Mo.sub.6Z.sup.1.sub.8-yZ.sup.2.sub.y (Z.sup.1=sulfur; Z.sup.2=selenium), and partially cuprated Cu.sub.1Mo.sub.6S.sub.8 as well as partially de-cuprated Cu.sub.1-xMg.sub.xMo.sub.6S.sub.8 and the precursors have a general formula of M.sub.xMo.sub.6Z.sub.8 or M.sub.xMo.sub.6Z.sup.1.sub.8-yZ.sup.2.sub.y, M=Cu. The cathode containing the Chevrel-phase material in accordance with the invention can be combined with a magnesium-containing anode and an electrolyte.

The present invention provides alumina hydrate particles, a flame retardant and a resin composition that are each for an electric wire/cable covering material improvable in flame retardancy and mechanical properties while the covering material keeps acid resistance; such an electric wire/cable; and producing methods thereof. The alumina hydrate particles of the present invention for electric wire/cable covering material have an average particle size of 0.5 to 2.5 μm, and having a primary particle variation R of 24% or less, the variation R being represented by the following expression:
primary particle variation R (%)=“standard deviationσ(μm) of major axis diameters of the primary particles”/“average value(μm) of the major axis diameters of the primary particles”×100.

Disclosed herein are a nickel oxide fine powder that is suitable as a material for electronic parts and has a controlled sulfur content, a low chlorine content, and a fine particle size and a method for industrially and stably producing such a nickel oxide fine powder.

Nickel hydroxide obtained by neutralizing an aqueous nickel sulfate solution with an alkali is heat-treated in a non-reducing atmosphere at a temperature higher than 650° C. but lower than 1050° C. to form nickel oxide particles, and a sintered compact of nickel oxide particles that may be formed during the heat treatment is pulverized by preferably allowing the nickel oxide particles to collide with one another. The thus obtained nickel oxide fine powder has a sulfur content of 400 mass ppm or less, a chlorine content of 50 mass ppm or less, a sodium content of 100 mass ppm or less, and a specific surface area of 3 m.sup.2/g or more but less than 6 m.sup.2/g.

A cathode active material for a lithium secondary battery includes lithium transition metal oxide particles, wherein the lithium transition metal oxide particles may include first lithium transition metal oxide particles (first particles) including an interparticular pore and second lithium transition metal oxide particles (second particles) having an average particle diameter within a range of a diameter of the interparticular pore, measured by mercury intrusion porosimetry. By including first particles including an interparticular pore and second particles having an average particle diameter within a range of a diameter of the interparticular pore measured by mercury intrusion porosimetry, the cathode active material may have a reduced interparticular pore present therein. Accordingly, the cathode active material may have an improved pellet density. Consequently, when a lithium secondary battery is manufactured using the cathode active material, the energy density thereof may improve.