A process for producing a surface-modified particulate lithium nickel metal oxide material is provided. The process comprises the addition of a controlled quantity of a coating liquid to lithium nickel metal oxide particles followed by a calcination step.

A cathode composition for a lithium-ion cell or battery of the general formula: Li.sub.1+xMn.sub.1−xO.sub.2, wherein the composition is in the form of a single phase having a rock salt crystal structure such that an x-ray diffraction pattern of the composition has an absence of peaks below a 20 value of 35; and the value of x is greater than 0, and equal to or less than 0.3. The compound is also formulated into a positive electrode, or cathode, for use in an electrochemical cell.

The present invention belongs to the field of battery materials, and relates to a process for preparing a particulate lithium manganese nickel spinel compound, and materials produced by the process. The process of the invention uses Mn-containing precursors, Ni-containing precursors, Li-containing precursors and optionally M-containing precursor which form substantially no NOx ases during calcination. The particulate lithium manganese nickel spinel compound product of the process may find use in a lithium ion battery.

A positive electrode active material for a non-aqueous electrolyte secondary battery, according to an example of this embodiment, includes a lithium transition metal composite oxide which has a layered structure and contains at least Ni, Al, and Ca. The lithium transition metal composite oxide has a Ni content of 85-95 mol %, an Al content of at most 8 mol %, and a Ca content of at most 2 mol % with respect to the total amount of metal elements other than Li. In addition, the proportion of metal elements other than Li present in a Li layer is 0.6-2.0 mol % with respect to the total amount of metal elements other than Li contained in the composite oxide.

The invention relates to active electrode materials and to methods for the manufacture of active electrode materials. Such materials are of interest as active electrode materials in lithium-ion or sodium-ion batteries. The invention provides an active electrode material expressed by the general formula [M][Nb].sub.y[O].sub.z; wherein the active electrode material is oxygen deficient; wherein M consists of one of Mg, Cr, W, Mo, Cu, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Sb, Y, La, Hf, Ta, Zn, In, or Cd; y satisfies 0.5≤y≤49; and z satisfies 4≤z≤124.

An alumina grain has a single-crystal structure and has an approximate regular octahedral stereoscopic morphology. Eight sides of the alumina grain belong to the {111} family of crystal planes of γ-state alumina, and the grain size is 5-100 μm. The alumina grain is unique in crystal plane exposure and distribution, simple and feasible in preparation, and low in cost, and has higher operability, and thus has good application prospect in the field of catalysis and adsorption.

A zirconia powder in which when a stabilizer is Y.sub.2O.sub.3, a content thereof is 1.4 mol % or more and less than 2.0 mol %; when the stabilizer is Er.sub.2O.sub.3, a content thereof is 1.4 mol % or more and 1.8 mol % or less; when the stabilizer is Yb.sub.2O.sub.3, a content thereof is 1.4 mol % or more and 1.8 mol % or less; and when the stabilizer is CaO, a content thereof is 3.5 mol % or more and 4.5 mol % or less; and in a range of 10 nm or more and 200 nm or less in a pore distribution, a peak top diameter of a pore volume distribution is 20 nm or more and 120 nm or less, a pore volume is 0.2 ml/g or more and less than 0.5 ml/g, and a pore distribution width is 30 nm or more and 170 nm or less.

Passivated Li.sub.7La.sub.3Zr.sub.2O.sub.12 (LLZO) particles, tape casting powders and slip compositions including the particles, methods of forming the particles, methods of tape casting using the particles, green tapes including the particles, cast LLZO films formed from the particles, and lithium batteries including the cast LLZO film. A passivated LLZO particle includes an LLZO core, wherein the LLZO is optionally doped with one or more elements. The passivated LLZO particle also includes a shell including H-LLZO, H.sub.3O.sup.+-LLZO, and/or Li.sub.2CO.sub.3.

A preparation method of fluorocarbon-coated VSe.sub.2 composite (VSe.sub.2@CF) anode electrode material, including: weighting and dissolving an acetylacetone oxovanadium (VO(acac).sub.2) and a selenium dioxide in a solvent to prepare a first solution with a concentration of 0.5-2 mol/L, and stirring the first solution for 0.5 h to obtain a dark green solution; adding the dark green solution with an organic acid to obtain a second solution; transferring the second solution to a polytetrafluoroethylene-lined high-pressure hydrothermal reactor, and holding at a heat insulation temperature for 15-30 h to obtain a third solution; after the third solution is cooled, suction filtering the cooled third solution, and washing the filtered third solution repeatedly to obtain a precipitate; drying the precipitate to obtain a black powder; co-mixing a citric acid solution with the black powder, stirring, ball milling, and drying; and heating up, holding, and finally cooling naturally to room temperature under inert atmosphere.

A membrane electrode assembly of an electrochemical device includes a proton conductive solid electrolyte membrane and an electrode including Ni and an electrolyte material which contains as a primary component, at least one of a first compound having a composition represented by BaZr.sub.1-x1M.sup.1.sub.x1O.sub.3 (M.sup.1 represents at least one element selected from trivalent elements each having an ion radius of more than 0.720 A° to less than 0.880 A°, and 0<x.sub.1<1 holds) and a second compound having a composition represented by BaZr.sub.1-x2Tm.sub.x2O.sub.3 (0<x.sub.2<0.3 holds).