The present invention relates to a chalcogenide device and particularly to a metal chalcogenide device using transition metal chalcogenides as electrodes and a production method therefor. The metal chalcogenide device according to the present invention may comprise: a substrate; an oxide layer positioned on the substrate; a first conductive metal chalcogenide layer positioned on the oxide layer; and first and second electrodes, which are positioned apart from one another on the metal chalcogenide layer and comprise metal chalcogenides.

An object of the present invention is to provide a novel sulfur-based positive electrode active material for a lithium-ion secondary battery which is excellent in cyclability and can largely improve a charging and discharging capacity, a positive electrode comprising the positive electrode active material and a lithium-ion secondary battery made using the positive electrode. The sulfur-based positive electrode active material is obtainable by subjecting a starting material comprising a polymer, sulfur and an organometallic compound dispersed in a form of fine particles to heat-treatment under a non-oxidizing atmosphere, wherein the particles of metallic sulfide resulting from sulfurization of the organometallic compound are dispersed in the heat-treated material, and particle size of the metallic sulfide particles is not less than 10 nm and less than 100 nm.

An object of the present invention is to provide a novel sulfur-based positive electrode active material for a lithium-ion secondary battery which is excellent in cyclability and can largely improve a charging and discharging capacity, a positive electrode comprising the positive electrode active material and a lithium-ion secondary battery made using the positive electrode. The sulfur-based positive electrode active material is obtainable by subjecting a starting material comprising a polymer, sulfur and an organometallic compound dispersed in a form of fine particles to heat-treatment under a non-oxidizing atmosphere, wherein the particles of metallic sulfide resulting from sulfurization of the organometallic compound are dispersed in the heat-treated material, and particle size of the metallic sulfide particles is not less than 10 nm and less than 100 nm.

The disclosure is directed to a sulfidizing agent obtainable by mixing M.sub.yS.sub.x and ZSH in a weight ratio of from about 90:10 to about 10:90, wherein M is chosen from Li.sup.+, Na.sup.+, K.sup.+, Rb.sup.+, Cs.sup.+, NH.sub.4.sup.+, Mg.sup.2+ and Ca.sup.2+, y is about 1 or about 2, x is from about 1.1 to about 5, and Z is independently chosen from Li.sup.+, Na.sup.+, K.sup.+, Rb.sup.+, Cs.sup.+ and NH.sub.4.sup.+, and a process for using the sulfidizing agent in the recovery of one or more metal ores and/or polymetallic minerals from gangue.

Provided is a magnesium secondary battery including a positive electrode member 23 including at least a positive electrode active material layer 23B, a separator 24 disposed facing the positive electrode member 23, a negative electrode member 25 containing magnesium or a magnesium compound disposed facing the separator 24, and an electrolytic solution containing a magnesium salt. The positive electrode active material layer 23B includes magnesium sulfide having a zinc blende type crystal structure.

A positive electrode active material contains a composite sulfide containing Mg and at least one element selected from the group consisting of Ti, V, Cr, Mn, Fe, Ni, Cu, Zr, Nb, Mo, Ta, and W. The positive electrode active material has a crystal structure belonging to space group Fm-3m.

In one aspect, the disclosure relates to compositions comprising a surface-modified phosphor material comprising a phosphor material and a silane, methods of making same, and articles comprising same. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.

A method of treating mercury-contaminated material to obtain a treated product having reduced mercury leachability includes the steps of (a) admixing the mercury-contaminated material with a reagent system comprising calcium sulfide (CaS) and trisodium phosphate (TNaP), wherein the calcium sulfide and trisodium phosphate are preferably provided at a CaS:TNaP ratio of from 2:1 to 1:2, on a dry weight reagent basis, and the reagent system is preferably provided in an amount equal to 0.4% to 5% by weight of the contaminated material; and (b) adding water as needed to achieve a moisture content of at least 5% by weight of the contaminated material.

Embodiments of the present application relate to a solid electrolyte and a preparation method thereof, and an electrochemical device and an electronic device comprising the same. The solid electrolyte of the present application includes a solid electrolyte material being represented by the chemical formula of Li.sub.1+2x−2yM.sub.yGa.sub.2+xP.sub.1−xS.sub.6, where M is selected from the group consisting of Sr, Ba, Zn, Cd and a combination thereof, 0≤x≤0.2 and 0≤y≤0.05. Embodiments of the present application provides a solid electrolyte having good stability with lithium and ionic conductivity by forming the solid electrolyte using lower cost solid electrolyte materials and optimizing the material composition and a crystal structure thereof. At the same time, this also reduces the manufacturing costs of the solid electrolyte, and improves the structural stability of the solid electrolyte.

Embodiments of the present application relate to a solid electrolyte and a preparation method thereof, and an electrochemical device and an electronic device comprising the same. The solid electrolyte of the present application includes a solid electrolyte material being represented by the chemical formula of Li.sub.1+2x−2yM.sub.yGa.sub.2+xP.sub.1−xS.sub.6, where M is selected from the group consisting of Sr, Ba, Zn, Cd and a combination thereof, 0≤x≤0.2 and 0≤y≤0.05. Embodiments of the present application provides a solid electrolyte having good stability with lithium and ionic conductivity by forming the solid electrolyte using lower cost solid electrolyte materials and optimizing the material composition and a crystal structure thereof. At the same time, this also reduces the manufacturing costs of the solid electrolyte, and improves the structural stability of the solid electrolyte.