Patent classifications
C01G53/66
ANNEALING SEPARATOR COMPOSITION FOR GRAIN-ORIENTED ELECTRICAL STEEL SHEET, GRAIN-ORIENTED ELECTRICAL STEEL SHEET, AND MANUFACTURING METHOD THEREFOR
An annealing separator composition for a grain-oriented electrical steel sheet according to an exemplary embodiment of the present invention contains a composite metal oxide containing Mg and a metal M, wherein the metal M is one or more of Be, Ca, Ba, Sr, Sn, Mn, Fe, Co, Ni, Cu, and Zn.
POSITIVE ELECTRODE ACTIVE MATERIAL, SECONDARY BATTERY, ELECTRONIC DEVICE, AND VEHICLE
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°.
Positive electrode active material for secondary battery, and secondary battery comprising the same
In one embodiment, a positive electrode active material for a secondary battery, the positive electrode active material being a primary particle having a monolithic structure that includes a lithium composite metal oxide of Formula 1 below, wherein the primary particle has an average particle size (D.sub.50) of 2 μm to 20 μm and a Brunauer-Emmett-Teller (BET) specific surface area of 0.15 m.sup.2/g to 0.5 m.sup.2/g, and wherein the positive electrode active material has a rolling density of 3.0 g/cc or higher under a pressure of 2 ton.Math.f:
Li.sub.aNi.sub.1-x-yCo.sub.xM1.sub.yM3.sub.zM2.sub.wO.sub.2 [Formula 1] in Formula 1, M1 is at least one selected from the group consisting of Al and Mn, M2 is any one or two or more elements selected from the group consisting of Zr, Ti, Mg, Ta, and Nb, M3 is any one or two or more elements selected from the group consisting of W, Mo, and Cr, and 1.0≤a≤1.5, 0≤x≤0.5, 0≤y≤0.5, 0.005≤z≤0.01, 0≤w≤0.04, 0<x+y≤0.7.
POSITIVE ELECTRODE ACTIVE MATERIAL FOR NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY, AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY
This positive electrode active material for a non-aqueous electrolyte secondary battery contains a lithium-transition metal composite compound. The lithium-transition metal composite compound is represented by general formula Li.sub.xMn.sub.yNi.sub.zMe.sub.αO.sub.aF.sub.b (in the formula, 1≤x≤1.2, 0.4≤y≤0.8; 0≤z≤0.4, x+y+z=2, 0<α<0.05, 1.8≤a≤2, and 1.8≤a±b≤2.2 are satisfied, and Me represents at least two kinds of elements selected from metal elements other than Li, Mn, and Ni) and Me includes at least one kind of element having an ion radius of 0.6 Å or more.
LITHIUM COMPLEX OXIDE FOR LITHIUM SECONDARY BATTERY POSITIVE ACTIVE MATERIAL AND METHOD OF PREPARING THE SAME
Disclosed is a lithium complex oxide and method of manufacturing the same, more particularly, a lithium complex oxide effective in improving the characteristics of capacity, resistance, and lifetime with reduced residual lithium and with different interplanar distances of crystalline structure between a primary particle locating in a internal part of secondary particle and a primary particle locating on the surface part of the secondary particle, and a method of preparing the same.
LAYERED-OXIDE POSITIVE ELECTRODE ACTIVE MATERIAL AND POSITIVE ELECTRODE PLATE, SODIUM-ION BATTERY, AND ELECTRIC APPARATUS CONTAINING SAME
A layered-oxide positive electrode active material may have a molecular formula of Na.sub.xMn.sub.aFe.sub.bNi.sub.cM.sub.dN.sub.eO.sub.2-δQ.sub.f, where a doping element M is selected from at least one of Cu, Li, Ti, Zr, K, Sb, Nb, Mg, Ca, Mo, Zn, Cr, W, Bi, Sn, Ge, or Al, a doping element N is selected from at least one of Si, P, B, S, or Se, a doping element Q is selected from at least one of F, Cl, or N, 0.66≤x≤1, 0<a≤0.70, 0<b≤0.70, 0<c≤0.23, 0≤d<0.30, 0≤e≤0.30, 0≤f≤0.30, 0≤δ≤0.30, a+b+c+d+e=1, 0<e+f≤0.30, 0<(e+f)/a≤0.30, 0.20≤d+e+f≤0.30, and (b+c)/a≤1.5.
METHOD OF FORMING POSITIVE ELECTRODE ACTIVE MATERIAL, KILN, AND HEATING FURNACE
To provide a method of forming a positive electrode active material with high productivity. To provide a manufacturing apparatus capable of forming a positive electrode active material with high productivity. Provided is a method of forming a positive electrode active material including lithium, a transition metal, oxygen, and fluorine. An adhesion preventing step is performed during heating of an object. Examples of the adhesion preventing step include stirring by rotating a furnace during the heating, stirring by vibrating a container containing an object during the heating, and crushing performed between the plurality of heating steps. By these manufacturing methods, a positive electrode active material having favorable distribution of an additive at the surface portion can be formed.
METHOD FOR MANUFACTURING POSITIVE ELECTRODE ACTIVE MATERIAL, AND SECONDARY BATTERY
A positive electrode active material has a small difference in a crystal structure between the charged state and the discharged state. For example, the crystal structure and volume of the positive electrode active material, which has a layered rock-salt crystal structure in the discharged state and a pseudo-spinel crystal structure in the charged state at a high voltage of approximately 4.6 V, are less likely to be changed by charging and discharging as compared with those of a known positive electrode active material. In order to form the positive electrode active material having the pseudo-spinel crystal structure in the charged state, it is preferable that a halogen source such as a fluorine and a magnesium source be mixed with particles of a composite oxide containing lithium, a transition metal, and oxygen, which is synthesized in advance, and then the mixture be heated at an appropriate temperature for an appropriate time.
METHOD FOR MANUFACTURING POSITIVE ELECTRODE ACTIVE MATERIAL, AND SECONDARY BATTERY
A positive electrode active material has a small difference in a crystal structure between the charged state and the discharged state. For example, the crystal structure and volume of the positive electrode active material, which has a layered rock-salt crystal structure in the discharged state and a pseudo-spinel crystal structure in the charged state at a high voltage of approximately 4.6 V, are less likely to be changed by charging and discharging as compared with those of a known positive electrode active material. In order to form the positive electrode active material having the pseudo-spinel crystal structure in the charged state, it is preferable that a halogen source such as a fluorine and a magnesium source be mixed with particles of a composite oxide containing lithium, a transition metal, and oxygen, which is synthesized in advance, and then the mixture be heated at an appropriate temperature for an appropriate time.
PROCESS FOR PRODUCING A SURFACE-MODIFIED PARTICULATE LITHIUM NICKEL METAL OXIDE MATERIAL
A process for producing a surface-modified particulate lithium nickel metal oxide material is provided. The process comprises the dry mixing lithium nickel metal oxide particles with at least one metal-containing compound using acoustic energy and then calcining the mixture at a temperature of less than or equal to 800 # C.