Disclosed are a precursor for preparation of a lithium composite transition metal oxide, a method for preparing the same and a lithium composite transition metal oxide obtained from the same. More particularly, the transition metal precursor which has a composition represented by Formula 1 below and is prepared in an aqueous transition metal solution, mixed with a transition metal-containing salt, including an alkaline material, the method for preparing the same and the lithium composite transition metal oxide obtained from the same are disclosed.
Mn.sub.aM.sub.b(OH.sub.1-x).sub.2-yA.sub.y(1) wherein M is at least one selected form the group consisting of Ni, Ti, Co, Al, Cu, Fe, Mg, B, Cr, Zr, Zn and Period II transition metals; A is at least one selected form the group consisting of anions of PO.sub.4, BO.sub.3, CO.sub.3, F and NO.sub.3, and 0.5a1.0; 0b0.5; a+b=1; 0<x<1.0; and 0y0.02.

Li-ion battery materials, such as Li-ion cathodes, are provided that have spinels characterized by a close-packed face-centered-cubic rocksalt-type structure and spinel-like ordered TM (the TM preferably occupying one of the two octahedral sites 16c and 16d) that favor fast Li transport kinetics. Such spinels have a larger deviation from a normal spinel and have a formula. Li.sub.1+xTM.sub.2-yO.sub.4-zF.sub.z where 0.2x1, 0.2y0.6, and 0z0.8; and TM is Mn, Ni, Co, Al, Sc, Ti, Zr, Mg, Nb, or a mixture thereof. The spinels achieve a higher gravimetric energy density than traditional spinels while still retaining high capacity at an extremely fast charging/discharging rate.

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 m to 20 m, and at least 80% of the primary particles exposed on surfaces of the secondary particles each have a polyhedral shape having at least one plane that is adjacent to two planes.

A method for making a catalyst for ozone decomposition includes: adding a reducing agent into a water solution of a permanganate salt to obtain a first reaction liquid, and heating the first reaction liquid under continuous stirring to form a birnessite-type manganese dioxide; and adding the birnessite-type manganese dioxide into a water solution of an ammonium salt to obtain a second reaction liquid, and heating the second reaction liquid under continuous stirring to form the catalyst.

A positive electrode active material includes a lithium composite oxide and a covering material that covers a surface of the lithium composite oxide. The covering material has an electron conductivity of 10.sup.6 S/m or less. The lithium composite oxide is a multiphase mixture including a first phase having a first crystal structure that belongs to a space group Fm-3m and a second phase having a second crystal structure that belongs to a space group other than a space group Fm-3m. The ratio I.sub.(18-20)/I.sub.(43-46) of a first integrated intensity I.sub.(18-20) of a first maximum peak present at a first diffraction angle 2 of 18 or more and 20 or less to a second integrated intensity I.sub.(43-46) of a second maximum peak present at a second diffraction angle 2 of 43 or more and 46 or less in an XRD pattern of the lithium composite oxide satisfies 0.05I.sub.(18-20)/I.sub.(43-46)0.90.

A ceramic member comprising a compound oxide of La, E and Mn, wherein AE is (i) Ca, or (ii) contains Ca and at least one of Sr and Ba with a total amount of Sr and Ba to a total of Ca, Sr and Ba of not more than 5 mol %, and a crystal system in a surface of the ceramic member is a monoclinic system.

A catalyst for decomposing an organic substance, the catalyst having a body which has a plurality of pores and the body contains a perovskite-type composite oxide represented by A.sub.xB.sub.yM.sub.zO.sub.w, where the A contains at least one selected from Ba and Sr, the B contains Zr, the M is at least one selected from Mn, Co, Ni, and Fe, 1.001x1.1, 0.05z0.2, y+z=1, and w is a positive value that satisfies electrical neutrality. The average pore diameter of the plurality of pores is 49 nm to 260 nm and the pore volume of each of the plurality of pores is 0.08 cm.sup.3/g to 0.37 cm.sup.3/g.

A method for producing lithium manganese oxide that is a precursor of a lithium adsorbent under atmospheric pressure is provided. The method for producing a precursor of a lithium adsorbent comprises tire following steps (1) to (3): (1) A 1.sup.st mixing step of mixing a manganese salt and alkali hydroxide, so as to obtain a 1.sup.st slurry containing manganese hydroxide; (2) a 2.sup.nd mixing step of adding lithium hydroxide to the 1.sup.st slurry and then mixing the mixture to obtain a 2.sup.nd slurry; and (3) an oxidation step of adding an oxidizing agent to the 2.sup.nd slurry, so as to obtain a precursor of a lithium adsorbent.
The method for producing a precursor of a lithium adsorbent comprises these steps, so that a precursor of a lithium adsorbent can be produced under atmospheric pressure. Therefore, a precursor of a lithium adsorbent can be produced at a limited cost.

A method for synthesizing mesoporous lithium manganese dioxide micro/nanostructures, in accord with an implementation, includes preparing an aqueous metal salt solution by dissolving a lithium ion source and a manganese ion source in water, and subjecting the aqueous metal salt solution to an anodic electrodeposition process. The anodic electrodeposition process may include transferring the aqueous metal salt solution to an electrodeposition bath comprising an anode electrode and a cathode electrode, such that the anode electrode and the cathode electrode are immersed in the transferred aqueous metal salt solution, and applying a pulse reverse current through the electrodeposition bath to obtain lithium manganese dioxide deposited on a surface of the anode electrode.

Vessels such as crucibles, pans, open cups and saggars, containing a monolithic ceramic material, and a ceramic matrix composite, wherein the monolithic ceramic material is an inner part. A method for making oxide materials that can be utilized in the contact with corrosive materials and that allows for higher conversions in a given heating process.