The present invention addresses the problem of providing a method for producing a fibrous carbon nanohorn aggregate with higher efficiency. According to one embodiment of the present invention, a method for producing a carbon nanohorn aggregate comprising a fibrous carbon nanohorn aggregate, is provided, which includes a step (a) of fixing the end of a rod-shaped carbon target to a fixing jig, and a step (b) of irradiating the rod-shaped carbon target with a laser light, and moving the irradiation position of the laser light in the longitudinal direction of the rod-shaped carbon target without rotating the rod-shaped carbon target.

Provided is a positive electrode active material for a non-aqueous electrolyte secondary battery, the active material including a lithium-transition metal composite oxide containing lithium, nickel, cobalt, and manganese, having a layered structure, having a ratio D.sub.50/D.sub.SEM of from 1 to 4, and having a ratio of a number of moles of nickel to a total number of moles of metals other than lithium of greater than 0.8 and less than 1, a ratio of a number of moles of cobalt to the total number of moles of metals other than lithium of less than 0.2, a ratio of a number of moles of manganese to the total number of moles of metals other than lithium of less than 0.2, and a ratio of the number of moles of manganese to a sum of the number of moles of cobalt and the number of moles of manganese of less than 0.58.

A nickel-based hydroxide powder is provided which has an average crystallite size, as determined by Scherrer fitting of the (00I) reflections of an XRD powder diffraction pattern of the nickel-based hydroxide powder, of at most 10 nm, together with a process for producing nickel-based hydroxide powders. The nickel-based hydroxide powders find utility as precursors for the formation of lithium transition metal oxide active electrode materials.

Disclosed are novel precursor particles for preparing a cathode active material including transition metal precursor particles containing one or more transition metals, and one or more of an alkali metal and an alkaline earth metal, wherein the alkali metal and the alkaline earth metal are contained in one or more of inner and outer parts of the transition metal precursor particles, and a novel precursor powder including the novel precursor particles.

The present disclosure relates to the technical field of lithium ion battery, and discloses a Lithium-Manganese-rich material and a preparation method and a use thereof.

The present technology provides an adsorbent material that includes a silicate composition, wherein the silicate composition includes a crystalline phase; wherein the silicate composition may have an interconnected porous scaffold having a total mercury (Hg) pore volume of about 0.005 cc/g to about 0.25 cc/g for pores having a diameter of about 20-10,000 Å and a total nitrogen (N) pore volume of about 0.02 cc/g to about 0.1 cc/g for pores having a diameter of about 20-600 Å.

A compound comprising phosphorus atoms and sulfur atoms as constituent elements and having a peak in Raman spectroscopy, the peak being attributable to a disulfide bond bonding between two phosphorus atoms.

The present invention provides an aerogel blanket including a blanket base, aerogel coupled on the surface of the blanket base, and aerogel located at a space between the blanket bases, the aerogel coupled on the surface of the blanket base is 50 wt % based on the total weight of aerogel, wherein the aerogel blanket has the number of aerogel particles separated from the aerogel blanket ranging from 13,600 to 90,000 per ft.sup.3, when vibrating the aerogel blanket at a frequency of 1 Hz to 30 Hz for 2 hours to 10 hours.

The positive electrode active material is capable of reducing positive electrode resistance, exhibiting better output characteristics, and having high mechanical strength when the positive electrode active material is used in a lithium ion secondary battery. Secondary particles have a d50 of 3.0 to 7.0 μm, a BET specific surface area of 2.0 to 5.0 m.sup.2/g, a tap density of 1.0 to 2.0 g/cm.sup.3, and an oil absorption amount of 30 to 60 ml/100 g. In each of a plurality of primary particles having a primary particle size of 0.1 to 1.0 μm, a coefficient of variation of the concentration of an additive element M is 1.5 or less. The volume of a linking section between the primary particles per primary particle, obtained from the total volume of the linking section and the number of primary particles constituting the secondary particles, is 5×10.sup.5 to 9×10.sup.7 nm.sup.3.

A polycrystalline cubic boron nitride includes a cubic boron nitride particle group. The ratio of a second length to a first length is 0.99 or less. Here, each of the first length and the second length is a value measured on a surface of the polycrystalline cubic boron nitride with an indentation formed by a Knoop hardness test under conditions specified in ISO4545-1 and ISO4545-4. The second length represents the length of the longer diagonal of the indentation. The first length represents the sum of the second length and the length of the streaky indentation.