Patent classifications
C01P2002/74
CATHODE ACTIVE MATERIAL, PREPARATION METHOD THEREFOR AND LITHIUM SECONDARY BATTERY COMPRISING SAME
The present exemplary embodiments relate to a cathode active material, a manufacturing method thereof, and a lithium secondary battery including the same. A cathode active material according to an exemplary embodiment is a lithium metal oxide particle in the form of a secondary particle including a primary particle, a coating layer including a boron compound is positioned on at least a portion of a surface of the primary particle, and the boron compound includes an amorphous structure.
Lithium Battery Positive Electrode Material Precursor, Preparation Method Therefor and Application Thereof
A lithium battery positive active material precursor, a preparation method therefor and the use thereof are provided. The precursor has a chemical formula of Ni.sub.xCo.sub.yM.sub.z(OH).sub.2, wherein M is at least one metal selected from the group consisting of Fe, Cr, Cu, Ti, Mg, W, Mo, Nb, Zn, Sn, Zr, Ga, Mn and Al, 0.3≤x≤1, 0<y≤0.5, 0<z≤0.3; and the precursor comprises aggregates of platy monocrystals and polyhedral monocrystal particles. In the XRD pattern of the precursor, I(001), I(100) and I(101) satisfy the following relationship: I(001)/I(100) is not less than about 1.5, and I(001)/I(101) is not less than about 1.2.
COMPOSITE CATHODE ACTIVE MATERIAL, METHOD OF PREPARING THE SAME, CATHODE INCLUDING THE SAME, AND LITHIUM SECONDARY BATTERY INCLUDING CATHODE
A composite cathode active material, a method of preparing the composite cathode active material, and a lithium secondary battery including a cathode including the composite cathode active material are provided. The composite cathode active material includes: a nickel-based active material including about 60 mol % or more of nickel; and a coating layer on a surface of the nickel-based active material, the coating layer including a lanthanide composite. The composite cathode active material includes or is in the form of single crystal particles having an average particle diameter in a range of about 2 μm to about 8 μm.
Positive electrode for rechargeable lithium battery, preparing method thereof, and rechargeable lithium battery comprising positive electrode
A positive electrode for a rechargeable lithium battery includes a positive active material for a rechargeable lithium battery that includes a first positive active material including a secondary particle including at least two agglomerated primary particles, where at least a portion of the primary particles has a radial arrangement structure, and a second positive active material having a monolith structure, wherein the first and second positive active materials each include a nickel-based positive active material, and an X-ray diffraction (XRD) peak intensity ratio (I(003)/I(104)) of the positive electrode is greater than or equal to about 3. Further embodiments provide a method of manufacturing the positive electrode for rechargeable lithium battery, and a rechargeable lithium battery including the same.
METHOD FOR PREPARING 3D CARBONITRIDE COATED VSE2 COMPOSITE (3D-VSe2@CN)
The disclosure relates to a method for preparing a 3D sponge structured carbonitride coated VSe.sub.2 composite (3D-VSe.sub.2@CN), belonging to the technical fields of electrode materials and preparation of batteries. In the disclosure, carbon, nitrogen and VSe.sub.2 are composited by using NaCl as a template so as to construct a 3D sponge structured carbonitride coated VSe.sub.2 composite. The 3D sponge structure can increase the structure stability of the material in the cyclic process, and the carbocanitride can increase the electron conductivity and activity sites of the material, so as to allow easier diffusion of potassium ions. Meanwhile, the stable structure can cause the clustering of VSe.sub.2 all the time. Thus, the prepared composite has good and stable rate capability and cycle stability. The process method is simple, low in cost, environmental-friendly, and suitable for large-scale industrial production.
PROCESS FOR MAKING PRECURSORS FOR CATHODE ACTIVE MATERIALS, PRECUSORS, AND CATHODE ACTIVE MATERIALS
Process for making a manganese composite (oxy)hydroxide with a mean particle diameter D50 in the range from 2 to 16 μm comprising the step(s) of combining (a) an aqueous solution containing salts of nickel and of manganese, and, optionally, at least one of Al, Mg, or transition metals other than nickel and manganese wherein at least 50 mole-% of the metal is manganese, (b) with an aqueous solution of an alkali metal hydroxide and (c) an organic acid or its alkali or ammonium salt wherein said organic acid bears at least two functional groups per molecule and at least one of the functional groups is a carboxylate group.
POSITIVE ELECTRODE ACTIVE MATERIAL, POSITIVE ELECTRODE, SECONDARY BATTERY, AND MANUFACTURING METHOD THEREOF
A positive electrode active material that has high capacity and excellent charge and discharge cycle performance for a secondary battery is provided. The positive electrode active material includes a group of particles including a first group of particles and a second group of particles. The group of particles includes lithium, cobalt, nickel, aluminum, magnesium, oxygen, and fluorine. When the number of cobalt atoms included in the group of particles is taken as 100, the number of nickel atoms is greater than or equal to 0.05 and less than or equal to 2, the number of aluminum atoms is greater than or equal to 0.05 and less than or equal to 2, and the number of magnesium atoms is greater than or equal to 0.1 and less than or equal to 6. When particle size distribution in the group of particles is measured by a laser diffraction and scattering method, the first group of particles has a first peak and the second group of particles has a second peak; the first peak has a local maximum value at longer than or equal to 2 μm and shorter than or equal to 4 μm, and the second peak has a local maximum value at longer than or equal to 9 μm and shorter than or equal to 25 μm.
SiC material and SiC composite material
The present invention relates to an SiC material and an SiC composite material and, more particularly, to an SiC material and an SiC composite material having a diffraction intensity ratio (I) of an X-ray diffraction peak, calculated by formula 1 down below, of less than 1.5. The present invention can provide an SiC material and an SiC composite material which can be etched evenly when exposed to plasma and thereby reduce the occurrence of cracks, holes and so forth. [Formula 1] Diffraction intensity ratio (I)=(peak intensity of plane (200)+peak intensity of plane (220))/peak intensity of plane (111).
Ceramic particle composite material
To provide a ceramic particle separable composite material having a calcium phosphate sintered body particle with which bioaffinity reduction and solubility change are suppressed as much as possible and which has a smaller particle diameter. A ceramic particle separable composite material comprising a ceramic particle and a substrate, wherein: the ceramic particle and the substrate are chemically bonded to each other, or the ceramic particle physically adheres to or is embedded in the substrate; the ceramic particle has a particle diameter within a range of 10 nm to 700 nm; the ceramic particle is a calcium phosphate sintered body particle; and the ceramic particle contains no calcium carbonate.
Thermoplastic resin composition and molded article produced from same
The present invention is characterized by including an aromatic vinyl-based copolymer, glass fiber, and zinc oxide, wherein the zinc oxide has an average particle size (D50) of about 0.5 to 3 μm as measured by a particle size analyzer, and a size ratio (B/A) of peak B, spanning the range of 450 to 600 nm, to peak A, spanning the range of 370 to 390 nm, of about 0.01 to 1.0 when measuring photoluminescence. The thermoplastic resin composition exhibits excellent rigidity, antibacterial properties, weather resistance, external appearance and the like.