A black material of the present invention consists of a zirconium nitride powder containing yttrium. The amount of the yttrium is 1.0% by mass to 12.0% by mass with respect to a total 100% by mass of the zirconium nitride powder and the yttrium. In a transmission spectrum obtained from a dispersion in which the concentration of the zirconium nitride powder containing yttrium is 50 ppm, assuming that the light transmittance at a wavelength of 550 nm is denoted by X.sub.1, and the light transmittance at a wavelength of 365 nm is denoted by X.sub.2, X.sub.1 is 7.5% or less, X.sub.2 is 25% or more, and X.sub.2/X.sub.1 is 3.5 or more.

A black material of the present invention consists of a zirconium nitride powder containing yttrium. The amount of the yttrium is 1.0% by mass to 12.0% by mass with respect to a total 100% by mass of the zirconium nitride powder and the yttrium. In a transmission spectrum obtained from a dispersion in which the concentration of the zirconium nitride powder containing yttrium is 50 ppm, assuming that the light transmittance at a wavelength of 550 nm is denoted by X.sub.1, and the light transmittance at a wavelength of 365 nm is denoted by X.sub.2, X.sub.1 is 7.5% or less, X.sub.2 is 25% or more, and X.sub.2/X.sub.1 is 3.5 or more.

Provided is a novel solid electrolyte material of high density and high ionic conductivity, and an all-solid-state lithium ion secondary battery that utilizes the solid electrolyte material. The solid electrolyte material has a chemical composition represented by Li.sub.7-3xGa.sub.xLa.sub.3Zr.sub.2O.sub.12 (0.08≤x<0.5), has a relative density of 99% or higher, belongs to space group I-43d, in the cubic system, and has a garnet-type structure. The lithium ion conductivity of the solid electrolyte material is 2.0×10.sup.−3 S/cm or higher. The solid electrolyte material has a lattice constant a such that 1.29 nm≤a≤1.30 nm, and lithium ions occupy the 12a site, the 12b site and two types of 48e site, and gallium occupies the 12a site and the 12b site, in the crystal structure. The all-solid-state lithium ion secondary battery has a positive electrode, a negative electrode, and a solid electrolyte. The solid electrolyte is made up of the solid electrolyte material of the present invention.

A method for preparing a solid-state electrolyte powder includes the following steps. An oxygen-free sintering process is performed at a first sintering temperature, such that a refined salt mixture forms a solid-state electrolyte powder precursor mixture. An oxygen-containing sintering process is performed at a second sintering temperature, such that the solid-state electrolyte powder precursor mixture forms a solid-state electrolyte powder, in which the second sintering temperature is higher than the first sintering temperature.

Provided is a battery comprising a cathode, an anode, and an electrolyte layer. The electrolyte layer includes a first electrolyte layer and a second electrolyte layer. The first electrolyte layer includes a first solid electrolyte material. The second electrolyte layer includes a second solid electrolyte material which is different from the first solid electrolyte material. The first solid electrolyte material includes lithium, at least one kind selected from the group consisting of metalloid elements and metal elements other than lithium, and at least one kind selected from the group consisting of chlorine and bromine. The first solid electrolyte material does not include sulfur.

A lithium battery includes: a positive electrode having a positive active material; a negative electrode including lithium metal; and a solid electrolyte disposed therebetween. The solid electrolyte contains at least one oxide represented by Li.sub.4±xM.sub.1-x′M′.sub.x′O.sub.4 (Formula 1), Li.sub.4-yM″O.sub.4-yA′.sub.y (Formula 2), or Li.sub.4+4zM′″.sub.1-zO.sub.4 (Formula 3), wherein and 0≤x23 1 and 0≤x′≤1, M is a Group 4 element, and M′ is an element of Group 2, 3, 5, 12, or 13, a vacancy, or a combination thereof, with the proviso that when M is Zr, then x≠0, x′≠0 and M′ is Be, Ca, Sr, Ba, Ra, Cd, Hg, Cn, Ga, In, TI, an element of Group 3 or 5, or a combination thereof; 0≤y≤1, M″ is a Group 4 element, and A′ includes at least one halogen, with the proviso that when M″ is Zr, then y≠0; and 0<z<1, and M′″ is a Group 4 element.

A reducing agent for use in production of a product gas containing carbon monoxide, the reducing agent being brought into contact with a raw material gas containing carbon dioxide to reduce the carbon dioxide to produce the product gas; the reducing agent containing an oxygen carrier having oxygen ionic conductivity, and a basic oxide supported on the oxygen carrier. In addition, the basic oxide preferably contains at least one selected from the group consisting of lithium (Li), sodium (Na), potassium (K), magnesium (Mg), manganese (Mn), cobalt (Co), strontium (Sr), and rubidium (Rb). The reducing agent has a high conversion efficiency of carbon dioxide to carbon monoxide, and can be used, for example, in a chemical looping method, and a method for producing a gas using such a reducing agent.

The disclosure relates to porous garnet ribbons and methods of making such porous garnet ribbons.

A semiconductor nanocrystal particle including a transition metal chalcogenide represented by Chemical Formula 1, the semiconductor nanocrystal particle having a size of less than or equal to about 100 nanometers, and a method of producing the same:
M.sup.1M.sup.2Cha.sub.3  Chemical Formula 1 wherein M.sup.1 is Ca, Sr, Ba, or a combination thereof, M.sup.2 is Ti, Zr, Hf, or a combination thereof, and Cha is S, Se, Te, or a combination thereof.

The invention belongs to the field of electronic ceramics and its manufacturing, in particular to the modified NiTa.sub.2O.sub.6-based microwave dielectric ceramic material co-sintered at low temperature and its preparation method. Based on the low melting point characteristics of CuO and B.sub.2O.sub.3, and the radius of Cu.sup.2+ ions is similar to that of Ni.sup.2+ and Ta.sup.5+ ions, the chemical general formula of the invention is designed as xCuO-(1-x)NiO-[7.42y+(xy/14.33)]B.sub.2O.sub.3—Ta.sub.2O.sub.5, and the molar content of each component is adjusted from raw materials. The main crystalline phase of NiTa.sub.2O.sub.6 is synthesized at a lower pre-sintering temperature, and NiTa.sub.2O.sub.6-based ceramic material with low-temperature sintering characteristics and excellent microwave dielectric properties are directly synthesized at one time, which broadened the application range in LTCC field.