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.

Core particles produced in situ or introduced as preformed core particles are coated with a layer of carbon. Non-carbon as well as some carbon-based core materials can be utilized. The resulting carbon coated particles can find applications in rubber products, for instance as reinforcement for tire components.

The present invention comprises: an overlithiated layered oxide represented by chemical formula 1 below; and an ion-conductive coating layer on the overlithiated layered oxide represented by chemical formula 1: [chemical formula 1] .sub.rLi.sub.2MnO.sub.3.Math.(1-r)Li.sub.aNi.sub.xCo.sub.yMn.sub.zM1.sub.1−(x+y+z)O.sub.2 (in chemical formula 1, 0<r≤0.6, 0<a≤1, 0≤x≤1, 0≤y<1, 0≤z<1, and 0<x+y+z<1, and M1 is at least one selected from among Na, K, Mg, Al, Fe, Cr, Y, Sn, Ti, B, P, Zr, Ru, Nb, W, Ba, Sr, La, Ga, Mg, Gd, Sm, Ca, Ce, Fe, Al, Ta, Mo, Sc, V, Zn, Cu, In, S, B, Ge, Si, and Bi).

Single-phase manganese oxide particles having a wurtzite crystal structure. The particles can be obtained by thermally decomposing a compound containing manganese. In this procedure, a reducing agent consisting of at least one of a polyol-based material and an ethylene glycol stearate-based material is added as an additive to the reaction system. It is heated at a first temperature (200° C. or lower) under a reduced pressure atmosphere, then the temperature is raised, and the product is heated at a temperature higher than the first temperature under an inert gas atmosphere.

A graphite anode material, an anode, a lithium ion battery and preparation methods thereof. The graphite anode material includes a natural graphite core, a carbon coating layer, and a graphitizing filler. The natural graphite core has pores. The graphitizing filler is filled in the pores inside the natural graphite core. The graphitizing filler further forms the carbon coating layer. The preparation method includes: mixing natural graphite with a filler, and then pulverizing to obtain a graphite powder body; and graphitizing the graphite powder body in a protective atmosphere to obtain a graphite anode material. The preparation method reduces material turnover and residual loss, and achieves simple process and high production efficiency. The anode and lithium ion battery prepared have high first efficiency and excellent cycling performance.

The present disclosure relates to the technical field of lithium ion battery, and discloses a Lithium-Manganese-rich material and a preparation method and a use thereof.

Methods of preparing graphene/graphene oxide particulates under mild conditions, comprising reacting pristine graphene with hydrogen peroxide and a source of iron to oxidize the outer surface of the pristine graphene particulates in solution and yield graphene/graphene oxide particulates. Methods and articles incorporating the same are also disclosed.

A positive electrode active material precursor for a secondary battery, which is a secondary particle in which primary particles are aggregated, includes a core portion including nickel (Ni), cobalt (Co), and manganese (Mn), and a shell portion surrounding a surface of the core portion and including nickel (Ni), cobalt (Co), manganese (Mn), and aluminum (Al), wherein the core portion and the shell portion has rod-shaped primary particles, and an average major axis length of the primary particles of the shell portion is smaller than an average major axis length of the primary particles of the core portion. A method of preparing the positive electrode active material precursor, and a positive electrode active material prepared by using the positive electrode active material precursor are also provided.

Provided are a cathode active material for a lithium secondary battery, a method of preparing the same, and a lithium secondary battery containing a cathode including the cathode active material, in which the cathode active material includes nickel-based lithium metal oxide containing single-crystal particles, and a particle size of the single-crystal particles is about 1 μm to about 8 μm, and a particle size distribution of the single-crystal particles expressed by (D90-D10)/D50 is 1.4 or less.

The present application provides a high-nickel ternary positive electrode active material, which comprises a core Li.sub.1+a[LixCoyMn.sub.zM.sub.b]O.sub.2, a fast ionic conductor Li.sub.αAl.sub.XSi.sub.YO.sub.4 of a first shell layer, an oxide of an element R of a second shell layer, and a transition layer Li.sub.pR.sub.qO.sub.w formed between the first shell layer and the second shell layer. In the high-nickel ternary positive electrode active material of the present application, the surface impurity lithium amount is significantly reduced, and by creatively converting the surface impurity lithium into effective components in the fast ionic conductors Li.sub.αAl.sub.XSi.sub.YO.sub.4 and Li.sub.pR.sub.qO.sub.w which accelerate the intercalation/deintercalation of lithium ions in the core material, the decomposition and gas production of an electrolyte solution caused by the surface impurity lithium is greatly improved, such that a high-nickel ternary lithium-ion battery has high energy density as well as good cycle performance and safety performance.