A positive active material for a lithium secondary battery and a lithium secondary battery including the same are provided, wherein the positive active material includes lithium, nickel, cobalt, manganese, and a doping element, and the doping element may include Zr, Al, and Ti.

A ferrite composition includes a main component and a sub-component. The main component includes 10.0 to 38.0 mol % of a Fe compound in terms of Fe.sub.2O.sub.3, 3.0 to 11.0 mol % of a Cu compound in terms of CuO, 39.0 to 80.0 mol % (excluding 39.0 mol %) of a Zn compound in terms of ZnO, and a balance of a Ni compound. The sub-component includes 10.0 to 23.0 parts by weight of a Si compound in terms of SiO.sub.2, 0 to 3.0 parts by weight (including 0 parts by weight) of a Co compound in terms of Co.sub.3O.sub.4, and 0.1 to 3.0 parts by weight of a Bi compound in terms of Bi.sub.2O.sub.3 with respect to 100 parts by weight of the main component.

Provided are 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. Also provided are processes of forming electrochemically active particles using the precursors nickel oxides.

The present disclosure provides core-shell nickel ferrite, a nickel ferrite@C material and preparation methods and application thereof. The preparation method of the core-shell nickel ferrite includes: preparing nickel iron glycerate ball powder by a solvothermal method; and under an air condition, heating the nickel iron glycerate ball powder at a heating rate of lower than 1.5° C./min to not less than 350° C. for performing calcination to obtain the core-shell nickel ferrite. The preparation method of the nickel ferrite@C material includes: performing a phenolic resin condensation reaction on the core-shell nickel ferrite, resorcinol and formaldehyde to obtain a phenolic resin (RF) coated core-shell nickel ferrite@RF composite material; and in an inert atmosphere, calcining and carbonizing the nickel ferrite@RF composite material to obtain the nickel ferrite@C material.

The disclosure discloses a nickel cobalt lithium manganate cathode material, a preparation method thereof and a lithium ion battery. The nickel cobalt lithium manganate includes a core and an outer layer covering the outside of the core, the core comprises flaky particles, a D50 particle diameter of the flaky particles in the core is 5-10 μm, and a D50 particle diameter of particles in the outer layer is 0.1-4.5 μm.

A nickel complex oxide having a carbon content of 0.15% by mass or lower.

An NTC compound, a thermistor and a method for producing a thermistor are disclosed. In an embodiment an NTC compound includes a ceramic material of a Mn—Ni—O system as a main constituent, wherein the Mn—Ni—O system has a general composition Ni.sub.xMn.sub.2O.sub.4-δ, wherein y corresponds to a molar fraction of Ni of a total metal content of the ceramic material of the Mn—Ni—O system, which is defined as c(Ni):(c(Ni)+c(Mn)), and wherein the following applies: 0.500<x<0.610 and 0.197<y<0.240.

A hydroprocessing catalyst has been developed. The catalyst is a crystalline transition metal tungstate material or metal sulfides derived therefrom, or both. The hydroprocessing using the crystalline transition metal tungstate material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking. A data system comprising at least one processor; at least one memory storing computer-executable instructions; and at least one receiver configured to receive data of a conversion process comprising at least one reaction catalyzed by the catalyst or a metal sulfide decomposition product of the catalyst has been developed.

Described herein is a nanocrystalline ferrite having the formula Ni.sub.1-x-y M.sub.yCo.sub.xFe.sub.2+zO.sub.4, wherein M is at least one of Zn, Mg, Cu, or Mn, x is 0.01 to 0.8, y is 0.01 to 0.8, and z is −0.5 to 0.5, and wherein the nanocrystalline ferrite has an average grain size of 5 to 100 nm. A method of forming the nanocrystalline ferrite can comprise high energy ball milling.

Electrocatalytic materials and methods of making the electrocatalytic materials are provided. Such a method may comprise forming precursor nanosheets comprising a precursor metal on a surface of a substrate; exposing the precursor nanosheets to a modifier solution comprising a polar, aprotic solvent and a metal salt at a temperature and for a period of time, the metal salt comprising a metal cation and an anion, thereby forming modified precursor nanosheets; and calcining the modified precursor nanosheets for a period of time to form an electrocatalytic material comprising structurally modified nanosheets and the substrate, each nanosheet extending from the surface of the substrate and having a solid matrix. The solid matrix defines pores distributed throughout the solid matrix and comprises a precursor metal oxide and domains of another metal oxide distributed throughout the precursor metal oxide; or the solid matrix comprises the precursor metal oxide and nanoparticles of the another metal oxide distributed on a surface of the solid matrix.