Patent classifications
C01G51/00
METHOD FOR DECOMPOSING WATER INTO H2 AND O2
A CoVO.sub.x composite electrode and method of making is described. The composite electrode comprises a substrate with an average 0.5-5 μm thick layer of CoVO.sub.x having pores with average diameters of 2-200 nm. The method of making the composite electrode involves contacting the substrate with an aerosol comprising a solvent, a cobalt complex, and a vanadium complex. The CoVO.sub.x composite electrode is capable of being used in an electrochemical cell for water oxidation.
SECONDARY BATTERY, ELECTRONIC DEVICE, AND VEHICLE
A positive electrode active material with high charge and discharge capacity is provided. A positive electrode active material with high charge and discharge voltage is provided. A power storage device that hardly deteriorates is provided. A highly safe power storage device is provided. A novel power storage device is provided. A positive electrode active material containing lithium, a plurality of transition metals, oxygen, and an impurity element. The positive electrode active material includes a first region including a surface portion and a second region provided inward from the first region, and the concentration of a transition metal is higher in the first region than in the second region. An impurity region is included between the first region and the second region.
Lithium cobalt-based positive electrode active material, preparation method thereof, positive electrode and secondary battery including the same
A lithium cobalt-based positive electrode active material is provided. The lithium cobalt-based positive electrode active material includes a core portion including a lithium cobalt-based oxide represented by Formula 1 and a shell portion including a lithium cobalt-based oxide represented by Formula 2, wherein the lithium cobalt-based positive electrode active material includes 2500 ppm or more, preferably 3000 ppm or more of a doping element M based on the total weight of the positive electrode active material. An inflection point does not appear in a voltage profile measured during charging/discharging a secondary battery including the lithium cobalt-based positive electrode active material.
Positive-electrode active material and battery
A positive-electrode active material containing a compound that has a crystal structure belonging to the space group FM-3M and is represented by the composition formula (1):
Li.sub.xMe.sub.yO.sub.αF.sub.β (1) wherein Me denotes one or two or more elements selected from the group consisting of Mn, Co, Ni, Fe, and Al, and the following conditions are satisfied. 1.3≤x≤2.2, 0.8≤y≤1.3, 1≤α≤2.93, 0.07≤β≤2.
Positive electrode material for lithium secondary battery, method of preparing the same, and positive electrode for lithium secondary battery and lithium secondary battery which include the positive electrode material
The present disclosure relates to a positive electrode material which includes a first positive electrode active material and a second positive electrode active material, wherein the second positive electrode active material has an electrical conductivity of 0.1 μS/cm to 150 μS/cm, which is measured after the second positive electrode active material is prepared in the form of a pellet by compressing the second positive electrode active material at a rolling load of 400 kgf to 2,000 kgf, a method of preparing the positive electrode material, and a positive electrode for a lithium secondary battery and a lithium secondary battery which include the positive electrode material.
Ruthenium doped Z-type hexaferrite
In an aspect, a ferrite composition comprises a Ru—Co.sub.2Z ferrite having the formula: (Ba.sub.3-xM.sub.x)Co.sub.2(M′Ru).sub.yFe.sub.24-2y-zO.sub.41, wherein M is at least one of Sr, Pb, or Ca; M′ is at least one of Co, Zn, Mg, or Cu; x is 1 to 3; y is greater than 0 to 2; and z is −4 to 4. In another aspect, an article comprises the ferrite composition. In yet another aspect, method of making the ferrite composition comprises mixing ferrite precursor compounds comprising Fe, Ba, Co, and Ru; and sintering the ferrite precursor compounds in an oxygen atmosphere to form the Ru—Co.sub.2Z ferrite.
Ferrite sintered magnet and rotating electric machine
To provide a ferrite sintered magnet having a high residual magnetic flux density (Br) and a high coercive force (HcJ), and also able to produce at a low cost. The ferrite sintered magnet includes a hexagonal M-type ferrite including A, R, Fe, and Co in an atomic ratio of A.sub.1-xR.sub.x(Fe.sub.12-yCo.sub.y).sub.zO.sub.19. A is at least one selected from Sr, Ba, and Pb. R is La only or La and at least one selected from rare earth elements. 0.13≤x≤0.23, 10.80≤(12−y)z≤12.10, and 0.13≤yz≤0.20 are satisfied.
Ferrite sintered magnet
A ferrite sintered magnet including ferrite grains having a hexagonal crystal structure. The ferrite grains satisfy 0.56≤W≤0.68 where W is an average value of circularities of the ferrite grains in a cross section parallel to an axis of easy magnetization.
CATHODE COMPOSITE MATERIAL FOR LITHIUM-ION BATTERY (LIB), AND PREPARATION METHOD THEREOF
The present disclosure discloses a cathode composite material for a lithium-ion battery (LIB), and a preparation method thereof. The cathode composite material for an LIB is composed of a lithium-containing matrix and a three-layer coating layer coated on a surface of the matrix, where the three-layer coating layer includes a lithium-deficient matrix material layer, a lithium-deficient lithium cobalt phosphate (LCP) layer, and a cobalt phosphate layer in sequence from inside to outside. The cathode composite material of the present disclosure can reduce the oxidation of a highly-delithiated cathode material to an electrolyte under high voltage, and has a high energy density.
Perovskite compound, a catalyst comprising the same, and an electrochemical device comprising the same
The perovskite compound according to the invention has a cubic perovskite structure, has high catalytic activity in oxygen reduction and evolution reactions, and has excellent durability, and thus, can be used as a catalyst of electrochemical devices, particularly as a fuel cell catalyst.