A -sialon phosphor represented by general formula: Si.sub.6zAl.sub.zO.sub.zN.sub.8z (0<z<4.2) has as a host crystal, a crystal structure identical to that of a -sialon crystal phase and having a bulk density of 0.80 g/cm.sup.3 or more and 1.60 g/cm.sup.3 or less. Also, a light-emitting element includes the -sialon phosphor and a semiconductor light-emitting element capable of exciting the -sialon phosphor.

According to one embodiment, an active material is provided. The active material includes particles of a monoclinic niobium titanium composite oxide. The particles include primary particles. The primary particles have an average aspect ratio of 5 or more.

Disclosed is a method of preparing a sulfide-based solid electrolyte for an all-solid battery having an argyrodite-type crystal structure through a solution process. The method including obtaining a precursor solution by dissolving lithium sulfide, phosphorus sulfide and a halogen compound in a solvent, obtaining a precursor powder by removing the solvent from the precursor solution. Solid electrolyte for an all-solid battery can be produced by such method.

A process for preparing a nanometric zeolite Y of FAU structural type with a crystal size of less than 100 nm and an A/B ratio of greater than 2, by mixing, in aqueous medium, of at least one source AO.sub.2 of at least one tetravalent element A chosen from silicon, germanium and titanium, of at least one source BO.sub.b of at least one trivalent element B chosen from aluminum, boron, iron, indium and gallium, of at least one source C.sub.2/mO of an alkali metal or alkaline-earth metal C chosen from lithium, sodium, potassium, calcium and magnesium, where source C.sub.2/mO also includes at least one source of hydroxide ions, to obtain a gel, maturation and hydrothermal treatment of the gel.

A sulfide-based solid electrolyte particle having a crystal phase of a cubic argyrodite-type crystal structure composed of Li, P, S and a halogen (Ha. The proposed sulfide-based solid electrolyte particle has a feature such that the ratio (Z.sub.Ha2/Z.sub.Ha1) of an element ratio Z.sub.Ha2 of the halogen (Ha) at the position of 5 nm in depth from the particle surface to an element ratio Z.sub.Ha1 of the halogen (Ha) at the position of 100 nm in depth from the particle surface is 0.5 or lower, as measured by XPS; and the ratio (Z.sub.O2/Z.sub.A2) of an element ratio Z.sub.O2 of oxygen to the total Z.sub.A2 of element ratios of phosphorus (P), sulfur (S), oxygen (O) and the halogen (Ha) at the position of 5 nm in depth from the particle surface is 0.5 or higher, as measured by XPS.

The disclosure herein relates to rechargeable batteries and solid electrolytes therefore which include lithium-stuffed garnet oxides, for example, in a thin film, pellet, or monolith format wherein the density of defects at a surface or surfaces of the solid electrolyte is less than the density of defects in the bulk. In certain disclosed embodiments, the solid-state anolyte, electrolyte, and catholyte thin films, separators, and monoliths consist essentially of an oxide that conducts Li.sup.+ ions. In some examples, the disclosure herein presents new and useful solid electrolytes for solid-state or partially solid-state batteries. In some examples, the disclosure presents new lithium-stuffed garnet solid electrolytes and rechargeable batteries which include these electrolytes as separators between a cathode and a lithium metal anode.

A method for producing a sulfide solid electrolyte having an argyrodite-type crystal structure may involve: mixing a raw material containing elemental phosphorus at an integrated power of 0.5 kWh/kg or more, and heat-treating a precursor obtained in the mixing at 350 to 500 C.

The present invention is to provide an electron or hydride ion intake/release material comprising a lanthanoid oxyhydride represented by the formula Ln(HO) (in the formula, Ln represents a lanthanoid element) or an electron or hydride ion intake/release composition comprising at least one kind of lanthanoid oxyhydride; a transition metal-supported material wherein a transition metal is supported by the above electron or hydride ion intake/release material or electron or hydride ion intake/release composition; and a catalyst comprising the transition metal-supported material. The electron or hydride ion intake/release material or electron or hydride ion intake/release composition according to the present invention has a higher ability for intake/release of electron or hydride ion than that of a conventional hydride-containing compound, and can be used effectively as a catalyst such as a catalyst having excellent ammonia synthesis activity by supporting a transition metal thereon.

Disclosed are basic copper chloride particulate matter and a preparation method therefor. The basic copper chloride particulate matter is mainly composed of basic copper chloride particles, and the basic copper chloride particles, with a particle size of 60-250 m, in the basic copper chloride particulate matter comprise 97% or more of the total mass of the basic copper chloride particulate matter.

A basic zinc chloride particulate matter and a preparation method therefor. The basic zinc chloride particulate matter mainly consists of basic zinc chloride particles. In the basic zinc chloride particulate matter, D.sub.10>100 m, and D.sub.95>450 m. The basic zinc chloride particles do not contain adhesives. The basic zinc chloride particles contained in the basic zinc chloride particulate matter are approximately spherical, and the basic zinc chloride particles with the particle diameter >500 m in the basic zinc chloride particulate matter accounts for 1% or less of the total mass of the basic zinc chloride particulate matter.