A memristor material is disclosed which has the chemical formula R.sub.1-xA.sub.xB0.sub.3, wherein R is one of Eu, Gd, Tb, Nd, A is one of Ca, Sr, Ba, B is one of Mn, Co, Ni, and x is larger than 0 but smaller than 1, a preferred example being Gd.sub.1-xCa.sub.xMn0.sub.3 (GCMO) with x not less than 0.2 to obtain practical resistance switching ratios. A memristor can be manufactured by pulsed laser deposition using a sintered target of said material.

The purpose of the present invention is to provide an active material for a secondary battery electrode, the active material having excellent rate characteristics and cycle resistance. The present invention is an active material for a secondary battery electrode, the active material having an olivine-type crystal structure, while having a carbon layer on the surface, wherein the ratio of the average thickness of the carbon layer which is present on a plane that is perpendicular to the crystal b-axis to the average thickness of the carbon layer which is present on a plane that is not perpendicular to the b-axis is from 0.30 to 0.80.

A cobalt-free layered positive electrode material, a preparation method thereof, and a lithium-ion battery are provided. The method includes: preparing a layered lithium nickel manganese oxide matrix material; mixing the layered lithium nickel manganese oxide matrix material with a coating agent to obtain a first mixed material; and forming a coating layer on a surface of the layered lithium nickel manganese oxide matrix material by performing a first sintering treatment on the first mixed material to obtain the cobalt-free layered positive electrode material. The coating agent includes a first coating agent including ceramic oxide, and a second coating agent including at least one of phosphate and silicate.

A positive electrode material and a preparation method therefor, a lithium-ion battery, and an electric vehicle. The positive electrode material comprises: matrix particles, materials forming the matrix particles comprising at least one of a lithium-rich manganese-based material, lithium nickel cobalt manganese oxide, lithium nickel cobalt aluminum oxide, lithium iron phosphate, lithium manganate, lithium nickel cobalt manganese aluminate, and lithium nickel manganate; and a housing, the housing covering at least a portion of the outer surfaces of the matrix particles.

A class of compositions that are inclusive of a lithium metal oxide or oxyfluoride compound having a general formula: LiTM[n]OF where TM[n] represents a number of transition metal species inclusive of transitional metal species differentiated by charge or d.sup.0 electron shell conformation, with [n] being at least 4 of said transitional metal species, and wherein said lithium metal oxide or oxyfluoride has a cation-disordered rocksalt (DRX) structure and a mitigated SRO via a high entropy DRX design strategy. Also featured is a method of synthesizing the high entropy DRX lithium metal oxide or oxyfluoride compounds, as well as usage of the same in Li-ion batteries, with particular utility in cathodes of such Li-ion batteries.

Secondary batteries using lithium cobalt oxide as positive electrode active materials have a problem of a decrease in battery capacity due to repeated charging/discharging, for example. A positive electrode active material particle which hardly deteriorates is provided. In a first step, a container in which a lithium oxide and a fluoride are set is placed in a heating furnace, and in a second step, the inside of the heating furnace is heated in an atmosphere containing oxygen. The heating temperature of the second step is from 750° C. to 950° C., inclusive. By the manufacturing method, fluorine can be contained in the positive electrode active material particle to increase the wettability of the surface of the positive electrode active material so that the surface of the positive electrode active material is homogenized and planarized. The crystal structure of the thus manufactured positive electrode active material is unlikely to be broken in repeated high-voltage charging/discharging. Thus, secondary batteries using the positive electrode active material having such a feature have greatly improved cycle characteristics.

A positive electrode active material having a crystal structure that is unlikely to be broken by repeated charging and discharging is provided. A positive electrode active material with high charge and discharge capacity is provided. One embodiment of the present invention is a positive electrode active material containing lithium, cobalt, nickel, and oxygen; in which a molar ratio of lithium, cobalt, and nickel is lithium: cobalt: nickel=1:1−x: x (0.3<x<0.75); in which the average of a bond distance between cobalt and oxygen and a bond distance between nickel and oxygen is longer than or equal to 1.94×10.sup.−10 m and shorter than or equal to 2.1×10.sup.−10 m in a crystal structure of the positive electrode active material; and in which the average of an angle formed between a line connecting cobalt to an adjacent oxygen and a line connecting cobalt to another adjacent oxygen and an angle formed between a line connecting nickel to an adjacent oxygen and a line connecting nickel to another adjacent oxygen is greater than or equal to 86.5° and less than 90°.

Disclosed herein is a stabilised Na-ion oxide P3 phase of formula (I): P3-Na.sub.xM.sub.yO.sub.z Where, x>0.66, 0.8≤y≤1.0, z≤2; and M is selected from one or more of the group consisting of a 3d transition metal, a 4d transition metal, Al, Mg, B, Si, Sn, Sr and Ca. The stabilised Na-ion oxide P3 phase of formula (I) may be particularly useful as an active material in a Na-ion battery.

There is provided a method for collecting and reusing an active material from positive electrode scrap. The method of reusing a positive electrode active material of the present disclosure includes (a-1) immersing a positive electrode scrap comprising an active material layer on a current collector into a basic solution to separate the active material layer from the current collector, (a-2) thermally treating the active material layer in air for thermal decomposition of a binder and a conductive material in the active material layer, and collecting an active material in the active material layer, (b) washing the active material collected from the step (a-2) with a lithium compound solution which is basic in an aqueous solution and drying, and (c) annealing the active material washed from the step (b) with a lithium precursor to obtain a reusable active material.

Provided is alumina material comprising alumina and zirconium, wherein in a radial distribution function obtained by Fourier-transforming an extended X-ray absorption fine structure (EXAFS) spectrum of a K absorption edge of the zirconium in the alumina material, the value of I.sub.B/I.sub.A is 0.5 or less where I.sub.A is a maximum intensity among the intensities of peaks present at 0.1 nm to 0.2 nm, and I.sub.B is a maximum intensity among the intensities of peaks present at 0.28 nm to 0.35 nm.