Patent classifications
C01G39/006
Cathode material for a lithium-ion rechargeable battery
A positive electrode for a rechargeable battery, comprising a lithium metal oxide powder having a layered crystal structure and having the formula Li.sub.xTm.sub.yHm.sub.zO.sub.6, with 3x4.8, 0.60y2.0, 0.60z2.0, and x+y+z=6, wherein Tm is one or more transition metals of the group consisting of Mn, Fe, Co, Ni, and Cr; wherein Hm is one or more metals of the group consisting of Zr, Nb, Mo and W. The lithium metal oxide powder may comprise dopants and have the formula Li.sub.xTm.sub.yHm.sub.zM.sub.mO.sub.6 A, wherein A is either one or more elements of the group consisting of F, S or N; and M is either one or more metal of the group consisting of Ca, Sr, Y, La, Ce and Zr, with either >0 or m>0, 0.05, m0.05 and x+y+z+m=6.
Positive electrode active material for secondary battery, and secondary battery including the same
A method for positive electrode active material for a secondary battery includes preparing a precursor by reacting a nickel raw material, a cobalt raw material and an M1 raw material; forming a first surface-treated layer including an oxide of Formula 2 below, on a surface of a core including a lithium composite metal oxide of Formula 1 below, by mixing the precursor with a lithium raw material and an M3 raw material, firing the resultant mixture; and forming a second surface-treated layer including a lithium compound of Formula 3 below, on the core with the first surface-treated layer formed thereon,
Li.sub.aNi.sub.1xyCo.sub.xM1.sub.yM3.sub.zM2.sub.wO.sub.2[Formula 1]
Li.sub.mM4O.sub.(m+n)/2[Formula 2]
Li.sub.pM5.sub.qA.sub.r[Formula 3]
wherein, in Formulae 1 to 3, A, M1 to M5, a, x, y, z, w, m, n, p, and q are the same as those defined in the specification.
Active material, active material composite material, electrode, secondary battery, battery pack, and vehicle
According to one embodiment, an active material is provided. The active material includes particles of a monoclinic niobium titanium composite oxide. The particles include primary particles. The primary particles have an average aspect ratio of 5 or more.
MN-ACTIVATED OXIDOHALIDES AS CONVERSION LUMINESCENT MATERIALS FOR LED-BASED SOLID STATE LIGHT SOURCES
The present invention relates to Mn-activated luminescent materials, to a process for preparation thereof and to the use thereof as luminophores or conversion luminophores in light sources. The present invention further relates to a radiation-converting mixture comprising the luminescent material of the invention and a light source comprising the luminescent material of the invention or the radiation-converting mixture. The present invention further provides light sources, especially LEDs, and lighting units comprising a primary light source and the luminescent material of the invention or the radiation-converting mixture. The Mn-activated luminescent materials of the invention are especially suitable for creation of warm white light in LEDs.
Active material, nonaqueous electrolyte battery, battery pack, and vehicle
According to one embodiment, an active material is provided. This active material includes active material particles containing orthorhombic Na-containing niobium titanium composite oxide, and satisfies the following formula (1):
1A5/A0(1) where A5 is a mole content ratio of a Li mole content L5 to a total of a Ti mole content T5 and a Nb mole content N5, and A0 is a mole content ratio of a Li mole content L0 to a total of a Ti mole content T0 and a Nb mole content N0.
Cathodes and electrolytes for rechargeable magnesium batteries and methods of manufacture
The invention relates to Chevrel-phase materials and methods of preparing these materials utilizing a precursor approach. The Chevrel-phase materials are useful in assembling electrodes, e.g., cathodes, for use in electrochemical cells, such as rechargeable batteries. The Chevrel-phase materials have a general formula of Mo.sub.6Z.sub.8 and the precursors have a general formula of M.sub.xMo.sub.6Z.sub.8. The cathode containing the Chevrel-phase material in accordance with the invention can be combined with a magnesium-containing anode and an electrolyte.
Mo-doped Co.SUB.2.Z-type ferrite composite material for use ultra-high frequency antennas
A Co.sub.2Z hexaferrite composition is provided containing molybdenum and one or both of barium and strontium, having the formula (Ba.sub.2Sr.sub.(3-Z)Co.sub.(2+X))Mo.sub.xFe.sub.(y-2x)O.sub.41 where x=0.01 to 0.20; y=20 to 24; and z=0 to 3. The composition can exhibit high permeabilities and equal or substantially equal values of permeability and permittivity while retaining low magnetic and dielectric loss tangents and loss factors. The composition is suitable for high frequency applications such as ultrahigh frequency and microwave antennas and other devices.
Mask free methods of depositing compositions to form heterostructures
The present disclosure provides methods of preparing heterostructures of two or more transition metal dichalcogenides on a surface in a pattern in which the method does not require a mask or blocking agent to create a pattern on the surface. Also provided herein are ink compositions which are used in the methods described herein and include precursor materials that generate these transition metal dichalcogenides.
Multimetal oxide compositions comprising Mo, Bi, Fe and Cu
Multimetal oxide composition comprising Mo, Bi, Fe, Cu and one or more than one of the elements Co and Ni and use thereof.
PREPARATION METHOD FOR HOLLOW MOLYBDATE COMPOSITE MICROSPHERES AND THEIR APPLICATION
A method of preparing hollow molybdate composite microspheres includes steps of: (1) dissolving 1-4 mmol of MCl.sub.2 in 20 ml of water to obtain a solution A and dissolving 1-4 mmol. of molybdic acid in 20 ml of water to obtain a solution B, followed by mixing the solution A and the solution B, in which M is Co, Ni, or Cu; (2) dissolving 10-40 mmol of urea in 40 ml of water, adding the mixed solution of step (1) and stirring uniformly; (3) placing the mixed solution of step (2) into a reaction vessel and reacting at 120-160 C. for 6-12 hours; (4) suction filtrating and water washing, followed by drying in a vacuum oven at 40-60 C.; (5) calcination at 350-500 C. for 2-4 hours in a Muffle furnace.