An object of the present invention is to provide a non-aqueous electrolyte secondary battery that has a large charge/discharge capacity, has a small irreversible capacity, which is the difference between the doping capacity and the de-doping capacity, and is capable of effectively using an active material. The problem described above can be solved by a method for producing a carbonaceous material for a non-aqueous electrolyte secondary battery anode, the method including: (1) an alkali metal compound impregnating step of adding an elemental alkali metal or a compound containing an elemental alkali metal to a carbonaceous precursor to obtain an alkali-impregnated carbonaceous precursor; (2) a heat treatment step of: (a) obtaining a heat-treated product by performing main heat treatment on the alkali-impregnated carbonaceous precursor at 800° C. to 1500° C. in a non-oxidizing gas atmosphere, or (b) obtaining a heat-treated product by performing pre-heat treatment on the alkali-impregnated carbonaceous precursor at a temperature of not lower than 400° C. and lower than 800° C. in a non-oxidizing gas atmosphere and then performing main heat treatment at 800° C. to 1500° C. in a non-oxidizing gas atmosphere; and (3) coating the heat-treated product with pyrolytic carbon.

A nickel-hydrogen secondary battery includes an electrode group comprising a separator, a positive electrode, and a negative electrode, and the positive electrode contains a positive electrode active material including a base particle comprising a nickel hydroxide particle containing Mn in solid solution and a conductive layer comprising a Co compound and covering the surface of the base particle, wherein the X-ray absorption edge energy of Mn detected within 6500 to 6600 eV by measurement with an XAFS method is 6548 eV or higher.

A uniform cluster of nanocompositions suspended in a liquid media is provided. Methods of making such nanocompositions, and uses of such nanocompositions are also provided. The nanocompositions can be used for nucleic acid extraction and diagnostic assays, for immunoassays, for cell separation, identification and modulation, for controlled functional molecule protection and release, for assays used in the clinic (companion diagnostics) or in the therapeutic development process (drug target validation), and in a system for transcatheter arterial chemoembolization, and demonstrate superior performance due to the uniform property or monodispersity.

A carbon nanotube aggregate includes a plurality of carbon nanotubes, a metal compound, and an oxide of the metal compound. The metal compound is contained in a space inside of each of the carbon nanotubes and/or in a space defined between the plurality of carbon nanotubes. When the metal compound is added inside the carbon nanotube aggregate, the metal compound is oxidized by reacting with oxygen or the like during or after a production process of the CNT aggregate, and the oxide is formed in the opening of the space to which the metal compound is added, so that the metal compound is capped with the oxide. Since the metal compound inside the CNT aggregate is shielded from the atmosphere, separation of the metal compound and reaction between the metal compound and oxygen and water in the atmosphere are suppressed, increasing heat resistance of the carbon nanotube aggregate.

There is disclosed a functional lamellar particle including an unconverted portion of the lamellar particle, wherein the unconverted portion includes a first metal, a converted portion of the lamellar particle disposed external to a surface of the unconverted portion, wherein the converted portion includes a chemical compound of the first metal; and a functional coating disposed external to a surface of the converted portion.

Methods and systems are provided for salt-rinse surface doping of electrode materials for lithium-ion batteries. In one example, a method may include dissolving a dopant salt in a solvent to form a dopant salt rinse solution, rinsing an electrode active material with the dopant salt rinse solution to form a coated electrode active material, and heating the coated electrode active material to form a doped electrode active material. In some examples, a surface region of the doped electrode active material may include a uniform distribution of dopants from the dopant salt rinse solution. In this way, the electrode active material may be rinsed and doped via the dopant salt rinse solution in a single-stage process.

There is provided a method of forming a porous particle comprising an electrically conductive continuous shell encapsulating a core, said core comprising an elemental compound that reversibly reduces in the presence of a cation and oxidizes in the absence of said cation, said method comprising the steps of: a) encapsulating an elemental compound precursor with said electrically conductive shell; b) reacting said elemental compound precursor with an oxidation agent to oxidise said elemental compound precursor to form said elemental compound, thereby forming said electrically conductive shell encapsulating said core comprising said elemental compound.

The present invention relates to a positive electrode active material for a lithium secondary battery, and a lithium secondary battery including the same, and the positive electrode active material includes lithium cobalt oxide particles. The lithium cobalt oxide particles include lithium cobalt oxide having a Li/Co molar ratio of less than 1 in the particles. Good rate property and life property may be obtained without worrying on the deterioration of initial capacity property.

Provided is a cathode active material including a core including a compound represented by Formula 1; and a coating layer including a phosphorus-containing compound disposed on a surface of the core:
Li.sub.aZr.sub.αW.sub.βM.sub.1−α−βO.sub.2−bS.sub.b  Formula 1 In Formula 1, M, Zr, W, a, α, β, and b are the same as defined in relation to the present specification.

At least partial substitution of zirconium by hafnium in ion-conducting zirconium-based ceramics provides enhanced chemical stability in alkaline and acid environments.