A thermal method of forming ferric oxide nano/microparticles with predominant morphology is described using different solvents. Methods of using the Fe.sub.3O.sub.4 nano/microparticles as catalysts in the reduction of nitro compounds with sodium borohydride to the corresponding amines and decomposition of ammonium salts.

The cathode active material for a lithium secondary battery according to embodiments of the present invention includes lithium-transition metal composite oxide particles including a plurality of primary particles, and the lithium-transition metal composite oxide particles have a lithium-potassium-containing portion formed between the primary particles. Thereby, it is possible to improve life-span properties and capacity properties by preventing the layer structure deformation of the primary particles and removing residual lithium.

A positive electrode active material that can achieve high thermal stability at low cost is provided.

Provided is a positive electrode active material for a lithium ion secondary battery, the positive electrode active material containing a lithium-nickel-manganese composite oxide, in which metal elements constituting the lithium-nickel-manganese composite oxide include lithium (Li), nickel (Ni), manganese (Mn), cobalt (Co), titanium (Ti), niobium (Nb), and optionally zirconium (Zr), an amount of substance ratio of the elements is represented as Li:Ni:Mn:Co:Zr:Ti:Nb=a:b:c:d:e:f:g (provided that, 0.97≤a≤1.10, 0.80≤b≤0.88, 0.04≤c≤0.12, 0.04≤d≤0.10, 0≤e≤0.004, 0.003<f≤0.030, 0.001<g≤0.006, and b+c+d+e+f+g=1), in the amount of substance ratio, (f÷g)≤0.030 and f>g are satisfied, and an amount of lithium to be eluted in water when the positive electrode active material is immersed in water is 0.20% by mass or less with respect to the entire positive electrode active material.

This positive electrode material comprises a lithium transition metal complex oxide which contains at least 80 mol % Ni in terms of the total mol number of metal elements excluding Li, and which has a total Co content of less than 5 mol %. The lithium transition metal complex oxide is formed as secondary particles obtained by aggregating primary particles, wherein at least one element A selected from Ca and Sr is present on the surface of the primary particles in the amount of 0.01-1 mol %, inclusive, in terms of the total mol number of the metal elements excluding Li. In addition, at least one element B selected from B, Zr, W, Al, Nb, Mo, and Ti is present on the surface of the secondary particles in the amount of 0.05-2 mol %, inclusive, in terms of the total mol number of the Ni in the complex oxide.

The present invention relates to an anode active material for lithium secondary battery and a lithium secondary battery including the same, and more specifically it relates to an anode active material for lithium secondary battery in which the a lithium ion diffusion path in the primary particles is formed to exhibit specific directivity, and a lithium secondary battery including the same. The cathode active material for lithium secondary battery of the present invention has a lithium ion diffusion path exhibiting specific directivity in the primary particles and the secondary particles, thus not only the conduction velocity of the lithium ion is fast and the lithium ion conductivity is high but also the cycle characteristics are improved as the crystal structure hardly collapses despite repeated charging and discharging.

Provided is a cathode active material for a lithium ion secondary battery in which the secondary particles constituting the powder have a high breaking strength and a good coatability, and a method for manufacturing same. The cathode active material for a lithium ion secondary battery includes a primary particle of a lithium composite compound; and secondary particles formed by an aggregation of primary particles, wherein a ratio between an average particle size of the primary particles and an average particle size of the secondary particles is 0.006 or more and 0.25 or less, an amount of lithium carbonate is 0.4% by mass or less, and a breaking strength of the secondary particles is 30 MPa or more.

Positive electrode active material particle powder includes: lithium manganese oxide particle powder having Li and Mn as main components and a cubic spinel structure with an Fd-3m space group. The lithium manganese oxide particle powder is composed of secondary particles, which are aggregates of primary particles, an average particle diameter (D50) of the secondary particles being from 4 μm to 20 μm, and at least 80% of the primary particles exposed on surfaces of the secondary particles each have a polyhedral shape having at least one (110) plane that is adjacent to two (111) planes.

Core particles produced in situ or introduced as preformed core particles are coated with a layer of carbon. Non-carbon as well as some carbon-based core materials can be utilized. The resulting carbon coated particles can find applications in rubber products, for instance as reinforcement for tire components.

A nickel composite hydroxide containing reduced amounts of sulfate radicals and chlorine as impurities. The nickel composite hydroxide is represented by Ni.sub.1-x-yCo.sub.xAl.sub.y(OH).sub.2+α(0.05≦x≦0.01≦y≦0.2, x+y<0.4, and 0≦α<0.5), and includes spherical secondary particles formed by aggregation of plurality of plate-shaped primary particles, secondary particles have an average particle diameter of 3-20 μm, sulfate radical content of 1.0 mass % or less, chlorine content of 0.5 mass % or less, and carbonate radical content of 1.0-2.5 mass %. The nickel composite hydroxide is obtained by a process including a crystallization step in which crystallization is performed in reaction solution obtained by adding alkali solution to aqueous solution containing mixed aqueous solution containing nickel and cobalt, ammonium ion supplier, and aluminum source. The alkali solution is mixed aqueous solution of alkali metal hydroxide and carbonate, and ratio of carbonate to alkali metal hydroxide in mixed aqueous solution represented by [C0.sub.3.sup.2−]/[OH.sup.−]=0.002 or more but 0.050 or less.

To provide a composition for a three-dimensional integrated circuit capable of forming a filling interlayer excellent in thermal conductivity also in a thickness direction, using agglomerated boron nitride particles excellent in the isotropy of thermal conductivity, disintegration resistance and kneading property with a resin. A composition for a three-dimensional integrated circuit, comprising agglomerated boron nitride particles which have a specific surface area of at least 10 m.sup.2/g, the surface of which is constituted by boron nitride primary particles having an average particle size of at least 0.05 μm and at most 1 μm, and which are spherical, and a resin (A) having a melt viscosity at 120° C. of at most 100 Pa.Math.s.