To provide a ferrite sintered magnet having a high residual magnetic flux density (Br), a high coercive force (HcJ), a good production stability, 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. 0.14≤x≤0.22, 11.60≤(12-y)z≤11.99, and 0.13≤yz≤0.17 are satisfied. 0.30≤Mc≤0.63 is satisfied in which Mc is CaO content (mass %) converted from a content of Ca included in the ferrite sintered magnet.

The present disclosure provides a cathode material including multiple composite secondary particles, each of the composite secondary particles including multiple primary cathode material particles, where the composite secondary particles meet: 0.9≤0.1D/A+B*C≤20 (Relation 1). In which A represents a particle size D50 of the primary cathode material particles, unit: μm; B represents a particle size D50 of the composite secondary particles, unit: μm; C represents a specific surface area of the composite secondary particles, unit: m.sup.2/g; and D represents a number of the primary cathode material particles in each of composite secondary particles.

A dielectric material, a device including the same, and a method of preparing the dielectric material are provided. The dielectric material may include a compound represented by the following Formula 1:

K.sub.1+xNaSr.sub.4-2xLa.sub.xNb.sub.10O.sub.30,  Formula 1

wherein, in Formula 1, 0<x<2.

A process for preparing a stable Li.sub.xK.sub.yMn.sub.2-zMe.sub.zO.sub.4 is provided. The general formula of the potassium “A” site and Group VIII Period 4 (Fe, Co and Ni) “B” site modified lithium manganese-based AB.sub.2O.sub.4 spinel is Li.sub.xK.sub.yMn.sub.2-zMe.sub.zO.sub.4 where Me is Fe, Co, or Ni. In addition, a Li.sub.xK.sub.yMn.sub.2-zMe.sub.zO.sub.4 cathode material for electrochemical systems is provided. Furthermore, a lithium or lithium-ion rechargeable electrochemical cell is provided, incorporating the Li.sub.xK.sub.yMn.sub.2-zMe.sub.zO.sub.4 cathode material in a positive electrode.

A sulfide solid electrolyte contains a compound that has a crystal phase having an argyrodite-type crystal structure and that is represented by Li.sub.aPS.sub.bX.sub.c, where X is at least one elemental halogen, a represents a number of 3.0 or more and 6.0 or less, b represents a number of 3.5 or more and 4.8 or less, and c represents a number of 0.1 or more and 3.0 or less. The sulfide solid electrolyte has a ratio of A.sub.Li/(A.sub.Li+A.sub.P+A.sub.S+A.sub.X) to a specific surface area (m.sup.2 g.sup.−1) of 3.40 (m.sup.−2g) or more, where A.sub.Li represents the amount of lithium (atom %) quantitatively determined from the Li 1s peak, A.sub.P represents the amount of phosphorus (atom %) quantitatively determined from the P 2p peak, A.sub.S represents the amount of sulfur (atom %) quantitatively determined from the S 2p peak, and A.sub.X represents the amount of halogen (atom %) quantitatively determined from the halogen peak, the peaks being exhibited in X-ray photoelectron spectroscopy (XPS).

The purpose of the present invention is to provide positive electrode active substance particles for a lithium ion secondary battery, such particles being capable of producing a lithium ion secondary battery having excellent high-speed discharge properties. The present invention is a granulated body of a positive electrode active substance for a lithium ion secondary battery, wherein the primary particle average diameter is 10 to 80 nm and the number of primary particles having a diameter of 100 nm or greater is no more than 5.0%.

A positive electrode active material, a method for producing the same, and a positive electrode and a lithium secondary battery in including the same are disclosed herein. In some embodiments, a method of producing a positive electrode active material includes mixing a lithium transition metal oxide and a carbon-based material having a hollow structure to form a mixture, and mechanically treating the mixture to form a carbon coating layer on the surface of the lithium transition metal oxide, wherein the carbon-based material has a chain shape, and has a specific surface area of 500 m.sup.2/g or greater, a graphitization degree (I.sub.D/I.sub.G) of 1.0 or higher, and a dibutylphthalate (DBP) absorption of 300 mL/100 g or greater.

A method encapsulates nanoscale material by producing a suspension of the nanostructure material in a first solvent using a micelle surrounding the nanostructure material. The micelle surrounding the suspended nanostructure material is swollen by adding to and mixing with the suspension an immiscible phase second solvent containing a precursor. The precursor is then reduced by adding a reducing reactant selectively soluble in the first solvent that reacts to the precursor containing reactant selectively solvated in the second solvent to encapsulate the nanostructure material. A metal-nanostructure composite can be provided by collecting and mixing the metal-shell encapsulated nanostructure product produced by the aforementioned method into a metal matrix.

The present invention relates to a method of preparing a precursor material of a positive electrode active material from a waste lithium secondary battery, to a method of preparing a lithium secondary battery positive electrode active material including a precursor material prepared by the same precursor preparation method, and to a lithium secondary battery positive electrode active material prepared by the same positive electrode active material preparation method.

The present invention provides a PZN-based large-size ternary high-performance single crystal, a growing method and a molten salt furnace. The PZN-based large-size ternary high-performance single crystal is represented by formula (1-x-y)Pb(B′.sub.1/2B″.sub.1/2)O.sub.3-yPb(Zn.sub.1/3Nb.sub.2/3)O.sub.3-xPbTiO.sub.3, wherein B′ is Mg, Fe, Sc, Ni, In, Yb, Lu and/or Ho, B″ is Nb, Ta and/or W, 0.4<x<0.6, 0.1<y<0.4, 0.1<1-x-y<0.4. The present invention adjusts the convective change of the melt through the rotation of the top seed and the bottom crucible, overcoming the problems of serious crystal inclusions and poor crystal quality during the growth process, and can adapt the change of the crystal diameter to the thermal inertia of the heat preservation system, thus effectively reducing crystal inclusions and improving the yield of the crystal.