Thermoregulated multilayer material characterized in that it comprises at least one substrate and one thermoregulated layer, said thermoregulated multilayer material having: for λ radiation of between 0.25 and 2 μm, an absorption coefficient αm≥0.8; and, for incident λ radiation of between 7.5 and 10 μm, a reflection coefficient ρm: ρm≥0.85, when the temperature T of said multilayer material 1 is ≤100° C.; ρm between 0.3 and 0.85, when the temperature T of said multilayer material is between 0 and 400° C.

A CaTiO.sub.3-based oxide thermoelectric material and a preparation method thereof are disclosed. The CaTiO.sub.3-based oxide thermoelectric material has a chemical formula of Ca.sub.1-xLa.sub.xTiO.sub.3, where 0<x≤0.4. The present disclosure makes it possible to prepare a CaTiO.sub.3-based thermoelectric material with properties comparable to n-type ZnO, CaTiO.sub.3, SrTiO.sub.3 and other oxide thermoelectric materials. Among them, the La15 sample has a power factor reaching up to 8.2 μWcm.sup.−1K.sup.−2 (at about 1000 K), and a power factor reaching up to 9.2 μWcm.sup.−1K.sup.−2 at room temperature (about 300 K); and a conductivity reaching up to 2015 Scm.sup.−1 (at 300 K). The CaTiO.sub.3-based oxide thermoelectric material exhibits the best thermoelectric performance among calcium titanate ceramics. The method for preparing the CaTiO.sub.3-based oxide thermoelectric material of the present disclosure is simple in process, convenient in operation, low in cost, and makes it possible to prepare a CaTiO.sub.3-based ceramic sheet with high thermoelectric performance.

There are provided a new type of crystal laminate of an alkaline earth metal titanate having improved catalytic activity, and a method for producing the same. The crystal laminate is provided having a crystal of the alkaline earth metal titanate as a constitutional unit, wherein the crystal being the constitutional unit is a cubic crystal, a tetragonal crystal or an orthorhombic crystal; the crystal being the constitutional unit has a primary particle diameter of 500 nm or less; and the crystal is layered with an orientation in a {100} plane direction thereof.

The present invention relates to a method of preparing an iron-chromium oxide using an ion-exchange resin. Moreover, the present invention relates to a method of preparing an iron-chromium oxide that can be used as a cathode material for lithium-ion batteries. According to one aspect of the present invention, it has the effect of providing a cathode material for lithium-ion batteries with a high capacitance, while exhibiting a voltage similar to that of a transition-metal oxide (2-4.5 V vs Li.sup.+/Li).

A method of forming a halide perovskite nanocrystal array having a plurality of halide perovskite nanocrystals arranged in a pattern can include coating an array of pens with a first ink comprising at least one first perovskite precursor having the formula AX and at least one second perovskite precursor having the formula BX′.sub.2 dissolved in a solvent. A is a cation, B is a metal, and X and X′ are each a halogen. The method further includes contacting a substrate with the coated pen array to thereby deposit the first ink indias a pattern of printed indicia on the substrate. The printed indicia form nanoreactors on the substrate and a halide perovskite nanocrystal nucleates and grows within each nanoreactor to form the halide perovskite nanocrystal array.

A solvent-free and ligand-free ball milling method for preparation of cesium lead tribromide (CsPbBr.sub.3) quantum dot is provided. First, mixing a Cs source, a Pb source, and a Br source as per a molar ratio of Cs source:Pb source:Br source is 1:1˜6:1˜9, and then adding polymethyl methacrylate (PMMA) to obtain a mixture. The mixture is milled for 1-2 hours at a rotation speed in a range of 360˜630 revolutions per minute (r/min) in a ball milling device, obtaining CsPbBr.sub.3 quantum dot. The method has advantages such as simple process, easy industrial production, no solvent, no organic ligand, low cost, and environmental protection. A quantum yield of product obtained by the method is up to 78%, and the product has a strong environmental stability. A preparation temperature of the product is low, and the reaction can be completed at a room temperature without a high temperature treatment.

Provided is a method of producing fine particulate barium calcium titanate in which calcium forms a homogeneous solid solution. The present invention relates to a method of producing a perovskite compound represented by the following formula (1):

Ba.sub.(1-x)A.sub.xTiO.sub.3  (1)

wherein A represents Ca or Sr, and x is a number satisfying 0.00<x≤0.30,

the method including: a first step of acid washing barium titanate to provide barium titanate having a ratio of barium element to titanium element of lower than 1.00; a second step of mixing the barium titanate obtained in the first step and a calcium salt or a strontium salt and drying the mixture to provide a dry mixture; and a third step of heating the dry mixture obtained in the second step.

Described herein are compositions and methods relating to luminescent structures.

The present disclosure pertains to a color filter for a display device, which has at least one color filter element for generating a predefined color in response to incident light, wherein the at least one color filter element includes a Perovskite material.

A perovskite-type composite oxide powder is a perovskite-type composite oxide powder represented by a general formula ABO.sub.3-δ (where δ represents an amount of deficiency of oxygen and 0≤δ<1), an element contained in an A site is La, elements contained in a B site are Co and Ni and a crystallite size determined by a Williamson-Hall method is equal to or greater than 20 nm and equal to or less than 100 nm. In this way, when the perovskite-type composite oxide powder is used as an air electrode material for a fuel cell, an air electrode in which the resistance thereof is low and the conductivity thereof is high can be obtained.