The invention relates to a process for preparing an AFX-structure zeolite comprising at least the following steps: i) mixing, in an aqueous medium, an FAU-structure zeolite having an SiO.sub.2 (FAU)/Al.sub.2O.sub.3 (FAU) molar ratio of between 6.00 and 200, limits included, an organic nitrogenous compound R, at least one source of at least one alkali and/or alkaline-earth metal M, the reaction mixture having the following molar composition: (SiO.sub.2 (FAU))/(Al.sub.2O.sub.3 (FAU)) between 6.00 and 200, H.sub.2O/(SiO.sub.2 (FAU)) between 1.00 and 100, R/(SiO.sub.2 (FAU)) between 0.01 and 0.60, M.sub.2/nO/(SiO.sub.2 (FAU)) between 0.005 and 0.45, limits included, until a homogeneous precursor gel is obtained; ii) hydrothermal treatment of said precursor gel obtained on conclusion of step i) at a temperature of between 120° C. and 220° C., for a time of between 12 hours and 15 days.

A solid electrolyte material contains Li, M, and X. M is at least one selected from metallic elements, and X is at least one selected from the group consisting of Cl, Br, and I. A plurality of atoms of X form a sublattice having a closest packed structure. An average distance between two adjacent atoms of X among the plurality of atoms of X is 1.8% or more larger than a distance between two adjacent atoms of X in a rock-salt structure composed only of Li and X.

The present specification relates to a connecting material for a solid oxide fuel cell, comprising a conductive substrate; and a ceramic protective film provided on one surface of the conductive substrate, in which the ceramic protective film comprises an oxide represented by Formula 1, a manufacturing method thereof, and a solid oxide fuel cell comprising the same.

Nickelate cathode materials are provided, wherein said cathode material has an X-ray diffraction (XRD) pattern comprising a first peak from about 40.0-41.6 2Θ, and a second peak from about 62.6-63.0 2Θ. Methods of preparing such cathode materials are also provided. Alkaline electrochemical cells comprising said cathode materials are also provided.

Composite carbon particles including a porous carbon material and a silicon component, the composite carbon particle having an average aspect ratio of 1.25 or less, and a ratio (I.sub.Si/I.sub.G) of a peak intensity (I.sub.Si) in the vicinity of 470 cm.sup.−1 to a peak intensity (I.sub.G) in the vicinity of 1580 cm.sup.−1 as measured by Raman spectroscopy of 0.30 or less, wherein the porous carbon material satisfies V.sub.1/V.sub.0>0.80 and V.sub.2/V.sub.0<0.10, when a total pore volume at a maximum value of a relative pressure P/P.sub.0 is defined as V.sub.0 and P.sub.0 is a saturated vapor pressure, a cumulative pore volume at a relative pressure P/P.sub.0=0.1 is defined as V.sub.1, a cumulative pore volume at a relative pressure P/P.sub.0=10.sup.−7 is defined as V.sub.2 in a nitrogen adsorption test, and has a BET specific surface area of 800 m.sup.2/g or more.

A core shell quantum dot including a core including a first semiconductor nanocrystal and including zinc, tellurium, and selenium and a semiconductor nanocrystal shell disposed on the core and including a zinc chalcogenide, a method of manufacture thereof, and a device including the same are disclosed, wherein the core shell quantum dot does not include cadmium, lead, mercury, or a combination thereof, wherein in an X-ray photoelectron spectrum of the quantum dot, a peak area for Te oxide to a peak area for Te3d.sub.5/2 as an area percentage is less than or equal to about 25%.

A cathode active material for a lithium secondary battery includes a lithium-transition metal composite oxide particle having a lattice strain (η) of 0.18 or less, which is calculated by applying Williamson-Hall method defined by Equation 1 to XRD peaks measured through XRD analysis, and having an XRD peak intensity ratio of 8.9% or less, which is defined by Equation 2. By controlling the lattice strain and XRD peak intensity ratio of the lithium-transition metal composite oxide particle, a lithium secondary battery with improved life-span characteristics as well as output characteristics is provided.

The present invention relates to composite particles containing silicon and carbon, wherein a domain size region of vacancies of 2 nm or less is 44% by volume or more and 70% by volume or less when volume distribution information of domain sizes obtained by fitting a small-angle X-ray scattering spectrum of the composite particles with a spherical model in a carbon-vacancy binary system is accumulated in ascending order, and a true density calculated by dry density measurement by a constant volume expansion method using helium gas is 1.80 g/cm.sup.3 or more and 2.20 g/cm.sup.3 or less.

A sputtering target comprising a top coat including a composition of lithium cobalt oxide LiyCozOx. x is smaller than or equal to y+z, and the lithium cobalt oxide has an X-Ray diffraction pattern with a peak P2 at 44°±0.2° 2-theta. The X-Ray diffraction pattern is measured with an X-Ray diffractometer with CuKα1 radiation.

A niobate compound is provided that has excellent reactivity with alkali metal salts and can be reacted with alkali metal salts at room temperature. The niobate compound has a ratio (first peak/second peak) of the intensity of a peak (first peak) having the highest intensity at 2θ=9.4°±1.5° to the intensity of a peak (second peak) having the highest intensity at 2θ=29.0°±1.5° being 1.3 or more in the X-ray diffraction pattern.