A positive electrode active material particle with little deterioration is provided. A power storage device with little deterioration is provided. A highly safe power storage device is provided. The positive electrode active material particle includes a first crystal grain, a second crystal grain, and a crystal grain boundary positioned between the crystal grain and the second crystal grain; the first crystal grain and the second crystal grain include lithium, a transition metal, and oxygen; the crystal grain boundary includes magnesium and oxygen; and the positive electrode active material particle includes a region where the ratio of the atomic concentration of magnesium in the crystal grain boundary to the atomic concentration of the transition metal in first crystal grain and the second crystal grain is greater than or equal to 0.010 and less than or equal to 0.50.

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.

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°.

Thermoregulated multilayer material characterized in that it comprises at least one substrate and one thermoregulated layer, said thermoregulated multilayer material having: for λ radiation of between 0.25 and 2 μm, an absorption coefficient αm≥0.8; and, for incident λ radiation of between 7.5 and 10 μm, a reflection coefficient ρm: ρm≥0.85, when the temperature T of said multilayer material 1 is ≤100° C.; ρm between 0.3 and 0.85, when the temperature T of said multilayer material is between 0 and 400° C.

A positive-electrode material for a lithium ion secondary battery contains a lithium complex compound that is represented by the formula: Li.sub.1+aNi.sub.bMn.sub.cCo.sub.dTi.sub.eM.sub.fO.sub.2+α, and has an atomic ratio Ti.sup.3+/Ti.sup.4+ between Ti.sup.3+ and Ti.sup.4+, as determined through X-ray photoelectron spectroscopy, of greater than or equal to 1.5 and less than or equal to 20. In the formula, M is at least one element selected from the group consisting of Mg, Al, Zr, Mo, and Nb, and a, b, c, d, e, f, and a are numbers satisfying −0.1≤a≤0.2, 0.7<b≤0.9, 0≤c<0.3, 0≤d<0.3, 0<e≤0.25, 0≤f<0.3, b+c+d+e+f=1, and −0.2≤α≤0.2.

A lithium cobalt-based oxide cathode active material powder having: —a primary phase comprising Li, Co, and O, and —a secondary phase comprising LiNaSO.sub.4, wherein the content of said LiNaSO.sub.4 secondary phase in said powder is of at least 0.4 wt. % and inferior or equal to 1.1 wt. % with respect to a total weight of the cathode active material powder, said cathode active material powder being characterized in that it has a S/Na atomic ratio superior or equal to 0.80 and inferior or equal to 1.20.

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

An object of the present invention is to provide a positive electrode active substance for a lithium secondary battery, the positive electrode active substance, when being used as a positive electrode active substance for a lithium secondary battery, being little in deterioration of cycle characteristics and being high in the energy density retention rate, even in repetition of charge and discharge at high voltages, and a lithium secondary battery little in deterioration of cycle characteristics and high in the energy density retention rate, even in repetition of charge and discharge at high voltages. The positive electrode active substance for a lithium secondary battery comprises a lithium cobalt-based composite oxide particle having a Ti-containing compound and an Mg-containing compound adhered on at least part of the particle surface.

A positive-electrode active material contains a lithium composite oxide containing at least one selected from the group consisting of F, Cl, N, and S. The crystal structure of the lithium composite oxide belongs to a space group C2/m. An XRD pattern of the lithium composite oxide comprises a first peak within the first range of 44 degrees to 46 degrees of a diffraction angle 2θ and a second peak within the second range of 18 degrees to 20 degrees of the diffraction angle 2θ. The ratio of the second integrated intensity of the second peak to the first integrated intensity of the first peak is within a range of 0.05 to 0.90.

An iron-based oxide magnetic particle powder has a narrow particle size distribution a small content of fine particles that do not contribute to magnetic recording characteristics, and a narrow coercive force distribution, to enhance magnetic recording medium density. Neutralizing an aqueous solution containing a trivalent iron ion and an ion of the metal substituting a part of the Fe sites by adding an alkali to make pH of 1.5 or more and 2.5 or less, adding a hydroxycarboxylic acid, and further neutralizing by adding an alkali to make pH of 8.0 or more and 9.0 or less are performed at 5° C. or more and 25° C. or less. A formed iron oxyhydroxide precipitate containing the substituting metal element is rinsed with water, then coated with silicon oxide, and then heated thereby providing e-type iron-based oxide magnetic particle powder. The rinsed precipitate may be subjected to a hydrothermal treatment.