A main object of the present disclosure is to provide an active material wherein a volume variation due to charge/discharge is small. The present disclosure achieves the object by providing an active material comprising a silicon clathrate II type crystal phase, including a void inside a primary particle, and a void amount A of the void with a fine pore diameter of 100 nm or less is more than 0.15 cc/g and 0.40 cc/g or less.

Provided is a polycrystalline SiC molded body wherein the resistivity is not more than 0.050 Ωcm and, when the diffraction peak strength in a diffraction angle 2θ range of 33-34° in an X-ray diffraction pattern is regarded as “A” and the diffraction peak strength of the SiC(111) plane in the X-ray diffraction pattern is regarded as “B”, then the ratio (A/B) is not more than 0.018.

Provided are a composite oxide powder from which dense solid electrolyte objects having a high ion conductivity can be produced and a method for producing the composite oxide powder. The composite oxide powder is composed of particles comprising lithium (Li), lanthanum (La), zirconium (Zr), and oxygen (O) and having a cubic garnet-type crystal structure, and has a volume particle size distribution in which the 50% diameter (D50) is 1,000 nm or smaller, the composite oxide powder having a pyrochlore phase content of 10 mass % or less.

A molybdenum trioxide powder contains an aggregate of primary particles having a β crystal structure of molybdenum trioxide. The molybdenum trioxide powder has a MoO.sub.3 content ratio of 99.6% or more measured by X-ray fluorescence (XRF), and has an average particle diameter of the primary particles of 1 μm or less. A method for producing the above molybdenum trioxide powder includes vaporizing a molybdenum oxide precursor compound to form molybdenum trioxide vapor, and cooling the molybdenum trioxide vapor.

A cobalt oxide for a lithium secondary battery, a method of preparing the cobalt oxide; a lithium cobalt oxide for a lithium secondary battery formed from the cobalt oxide; and a lithium secondary battery having a positive electrode including the lithium cobalt oxide, the cobalt oxide having a tap density of about 2.8 g/cc to about 3.0 g/cc, and an intensity ratio of about 0.8 to about 1.2 of a second peak at 2θ of about 31.3±1° to a first peak at 2θ of about 19±1° in X-ray diffraction spectra, as analyzed by X-ray diffraction.

The present invention provides a method for producing a nitrogen-doped highly graphitic porous carbon body, and a nitrogen-doped highly graphitic porous carbon body produced according to the same. Also, the present invention provides a method for producing a sulfur and nitrogen double-doped highly graphitic porous carbon body, a sulfur and nitrogen double-doped highly graphitic porous carbon body produced according to the same, and an electrode catalyst for a fuel cell and/or a water electrolysis reaction comprising the carbon body.

Provided are a cathode active material for a lithium secondary battery, a method of preparing the same, and a lithium secondary battery containing a cathode including the cathode active material, in which the cathode active material includes nickel-based lithium metal oxide containing single-crystal particles, and a particle size of the single-crystal particles is about 1 μm to about 8 μm, and a particle size distribution of the single-crystal particles expressed by (D90-D10)/D50 is 1.4 or less.

The present application relates to copper-doped double perovskites, for example, copper-doped double perovskites of the formula (I) and to uses thereof, for example as low-bandgap materials such as a semiconducting material in a device. The present application also relates to methods of tuning the bandgap of a Cs.sub.2SbAgZ.sub.6 double perovskite (for example, wherein Z is Cl) comprising doping the double perovskite with copper.
Cs.sub.2Sb.sub.1-aAg.sub.1-bCu.sub.2xZ.sub.6  (I)

A positive-electrode active material contains a lithium composite oxide containing manganese. The crystal structure of the lithium composite oxide belongs to a space group Fd-3m. The integrated intensity ratio I.sub.(111)/I.sub.(400) of a first peak I.sub.(111) on the (111) plane to a second peak I.sub.(400) on the (400) plane in an XRD pattern of the lithium composite oxide satisfies 0.05≤I.sub.(111)/I.sub.(400)≤0.90.

This invention relates to particulate electroactive materials consisting of a plurality of composite particles, wherein the composite particles comprise: (a) a porous conductive particle framework including micropores and/or mesopores having a total volume of at least 0.4 to 2.2 cm.sup.3/g; (b) an electroactive material disposed within the porous conductive particle framework; and (c) a lithium-ion permeable filler penetrating the pores of the porous conductive particle framework and disposed intermediate the nanoscale silicon domains and the exterior of the composite particles.