Patent classifications
C01P2004/38
CZTS PRECURSOR INKS AND METHODS FOR PREPARING CZTS THIN FILMS AND CZTS-BASED-DEVICES
The present disclosure relates to compositions comprising quaternary metal chalcogenide nanoparticles stabilized by an inorganic metal-chalcogenide stabilizing agent, wherein the nanoparticles are dispersible in a polar solvent. More particularly, the disclosure relates to compositions of CZTS nanoparticles. This disclosure provides processes for manufacturing these compositions. The disclosure also provides coated substrates, thin films and devices comprising the compositions, and processes for manufacturing the same.
Iron pyrite nanocrystals
An apparatus includes a nanocrystal. The nanocrystal includes a core including FeS.sub.2; and a coating including a ligand component capable of chemically interacting with both an iron atom and a sulfur atom on a surface of the core.
Proton-conductive complex oxide and fuel cell using same as electrolyte
Provided is a complex oxide that has a high hydrogen content, contains almost no impurity phase, and is suitable for proton conductivity. The complex oxide is represented by a chemical formula Li.sub.7-xH.sub.xLa.sub.3M.sub.2O.sub.12 (M represents Zr and/or Hf, and 3.2<x7) and is a single phase of a garnet type structure belonging to a cubic system. A method for producing the complex oxide includes an exchange step of bringing a raw material complex oxide represented by a chemical formula Li.sub.7-xH.sub.xLa.sub.3M.sub.2O.sub.12 (M represents Zr and/or Hf, and 0x3.2) and a compound having a hydroxy group or a carboxyl group into contact with each other to exchange at least some of lithium of the raw material complex oxide and hydrogen of the compound having a hydroxy group or a carboxyl group.
SOLID ELECTROLYTE AND ELECTRICITY STORAGE DEVICE USING THE SAME
Provided is a solid electrolyte containing a crystal phase having a chemical composition Li.sub.7(1+x).sub.2+aO.sub.12+3.5x+b, where a includes Pr, includes Zr, 0.05x0.35, 0.5a0.5, and 0.5b0.5.
Zeolite compositions and methods for tailoring zeolite crystal habits with growth modifiers
Embodiments of the invention generally provide compositions of crystalline zeolite materials with tailored crystal habits and the methods for forming such crystalline zeolite materials. The methods for forming the crystalline zeolite materials include binding one or more zeolite growth modifiers (ZGMs) to the surface of a zeolite crystal, which results in the modification of crystal growth rates along different crystallographic directions, leading to the formation of zeolites having a tailored crystal habit. The improved properties enabled by the tailored crystal habit include a minimized crystal thickness, a shortened internal diffusion pathlength, and a greater step density as compared to a zeolite having the native crystal habit prepared by traditional processes. The tailored crystal habit provides the crystalline zeolite materials with an aspect ratio of about 4 or greater and crystal surfaces having a step density of about 25 steps/m.sup.2 or greater.
Method and system for producing crystalline calcium carbonate by the combined use of two gases with different CO.SUB.2 .content
The invention relates to a particularly energy efficient, two-step method and to a system for the continuous or semicontinuous production of crystalline calcium carbonate (precipitated calcium carbonate, PCC) by reacting calcium hydroxide with CO.sub.2, the calcium hydroxide being lime milk. In the first step of the germination, the CO.sub.2-source is exclusively flue gas having a CO.sub.2-content of between 4-25% <sb/><sb/>. In the second step, the complete conversion of the lime milk reacted in the first step to a maximum of 90%, preferably between 10-90%, is carried out exclusively using a rich gas which comprises 30-99% CO.sub.2, preferably using biogas.
HIGH TEMPERATURE SUPERCONDUCTING MATERIAL AND A METHOD FOR PRODUCTION
A process for producing a process for producing a LnM.sub.2Cu.sub.3O.sub.x high-temperature superconductive powder, the process comprising: i) providing an aqueous solution of Ln, M and Cu and at least one mineral acid; ii) adding at least one sequestrating agent and, optionally, at least one dispersant to the solution to form a precipitate; iii) recovering the precipitate from the solution; and iv) heating the precipitate in a flow of oxygen to form the LnM.sub.2Cu.sub.3O.sub.x powder, wherein Ln is a rare earth element, preferably Y, Ce, Dy, Er, Gd, La, Nd, Pr, Sm, Sc, Yb, or a mixture of two or more thereof, and wherein M is selected from Ca, Sr, and Ba.
Method for forming lanthanum hydroxycarbonate nanoparticles
A hydrothermal method of preparing uniform, monodisperse ceramic lanthanum hydroxyl carbonate (LaCO.sub.3OH) having cherry-blossom-like nanogears and/or nanocubes is described. The method produced a hexagonal crystal with a crystal lattice in which at least on lanthanum ion is substituted with calcium ion. The ceramic nanoparticles produced by the method are good catalyst for the reduction of nitrogen oxides with a hydrocarbon. A method of reducing exhaust gases is described.
Dendronized metallic oxide nanoparticles, a process for preparing the same and their uses
Dendronized metallic oxide nanoparticles, a process for preparing the same and their uses.
Systems And Methods For Improved Solid-State Electrolytes
Disclosed are system and methods for manufacturing a solid-state electrolyte to be used in an electrochemical cell. The method can include forming a solid-state electrolyte from a material having a compositional property and a structural property, the material having been selected by: (i) providing material properties of a material, wherein the material properties comprise both compositional and structural information; (ii) calculating a first distortion parameter of a material, wherein the first distortion parameter represents the degree of lattice distortion of the material; (iii) determining an estimated ionic mobility value of the material using the one or more distortion parameters; (iv) varying the provided material properties using isovalent substitution and determining a second ionic mobility value from a second distortion parameter by repeating steps (i)-(iii); and (v) comparing the first and second ionic mobility values to select the superior material derivative.