A solid ionic conducting material for use in an electrochemical device comprises an oxyhydroxide or hydrated oxide derived from of an oxide with a perovskite, Brownmillerite, layered oxide, and/or K.sub.4CdCl.sub.6 structure, the elemental composition of the initial oxide being selected to provide suitable conduction properties for the derived anhydrous or hydrated oxyhydroxide or hydrated oxide. A method of making such a solid ionic conducting material, including treatment with water, and an electrochemical device incorporating such a solid ionic conducting material (optionally as an electrolyte) are also disclosed.

A process for producing a lithium-manganese-nickel oxide spinel material includes maintaining a solution comprising a dissolved lithium compound, a dissolved manganese compound, a dissolved nickel compound, a hydroxycarboxylic acid, a polyhydroxy alcohol, and, optionally, an additional metallic compound, at an elevated temperature T.sub.1, where T.sub.1 is below the boiling point of the solution, until the solution gels. The gel is maintained at an elevated temperature until it ignites and burns to form a Li—Mn—Ni—O powder. The Li—Mn—Ni—O powder is calcined to burn off carbon and/or other impurities present in the powder. The resultant calcined powder is optionally subjected 1 to microwave treatment, to obtain a treated powder, which is annealed to crystallize the powder. The resultant annealed material is optionally subjected to microwave treatment. At least one of the microwave treatments is carried out. The lithium-manganese-nickel oxide spinel material is thereby obtained.

The present disclosure relates to a novel ruthenium oxide, a method of preparing the same, and a catalyst for selective hydrogenation of an aromatic compound or an unsaturated compound including the ruthenium oxide.

The present invention is directed to methods of transferring urea from an aqueous solution comprising urea to a MXene composition, the method comprising contacting the aqueous solution comprising urea with the MXene composition for a time sufficient to form an intercalated MXene composition comprising urea.

A new family of crystalline microporous metalloalumino(gallo)phosphosilicate molecular sieves has been synthesized and are designated high charge density (HCD) MeAPSOs. These metalloalumino(gallo)phosphosilicate are represented by the empirical formula of:

R.sup.p+.sub.rA.sup.+.sub.mM.sup.2+.sub.wE.sub.xPSi.sub.yO.sub.z

where A is an alkali metal such as potassium, R is at least one quaternary ammonium cation such as ethyltrimethylammonium, M is a divalent metal such as Zn and E is a trivalent framework element such as aluminum or gallium. This family of metalloalumino(gallo)phosphosilicate materials are stabilized by combinations of alkali and quaternary ammonium cations, enabling unique, high charge density compositions. The HCD MeAPSO family of materials have catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

The invention relates to active electrode materials and to methods for the manufacture of active electrode materials. Such materials are of interest as active electrode materials in lithium-ion or sodium-ion batteries. The invention provides an active electrode material expressed by the general formula M1.sub.aM2.sub.2-aM3.sub.bNb.sub.34-bO.sub.87-c-dQ.sub.d.

To provide a manganese-iridium composite oxide, a manganese-iridium composite oxide and a manganese-iridium composite oxide electrode material, having high catalytic activity produced at low cost, to be used as an anode catalyst for oxygen evolution in water electrolysis, and their production methods.

A manganese-iridium composite oxide, which has an iridium metal content ratio (iridium/(manganese+indium)) of 0.1 atomic % or more and 30 atomic % or less, and has interplanar spacings of at least 0.243±0.002 nm, 0.214±0.002 nm, 0.165±0.002 nm, 0.140±0.002 nm, and a manganese-iridium composite oxide electrode material comprising an electrically conductive substrate constituted by fibers at least part of which are covered with the above manganese-iridium composite oxide.

A cathode active material precursor for a lithium secondary battery has a structure of a nickel composite hydroxide. An oxygen position in a Z-axis direction measured by a Rietveld method in a space group P-3m crystal structure based on an X-ray diffraction (XRD) analysis is 0.200 or more. A cathode active material and a lithium secondary battery having a stabilized crystal structure are provided using the cathode active material precursor.

A cathode active material precursor for a lithium secondary battery has a structure of a nickel composite hydroxide. A first peak intensity ratio represented by Equation 1 is 0.5 or more, and a second peak intensity ratio represented by Equation 2 is 0.7 or more. A cathode active material and a lithium secondary battery having a stabilized crystal structure are provided using the cathode active material precursor.

A lithium secondary battery is produced by employing a charging method where a positive electrode upon charging has a maximum achieved potential of 4.3 V (vs. Li/Li.sup.+) or lower. The lithium secondary battery contains an active material including a solid solution of a lithium transition metal composite oxide having an α-NaFeO.sub.2-type crystal structure. The solid solution has a diffraction peak observed near 20 to 30° in X-ray diffractometry using CuKα radiation for a monoclinic Li[Li.sub.1/3Mn.sub.2/3]O.sub.2-type before charge-discharge. The lithium secondary battery is charged to reach at least a region with substantially flat fluctuation of potential appearing in a positive electrode potential region exceeding 4.3 V (vs. Li/Li.sup.+) and 4.8 V (vs. Li/Li.sup.+) or lower. A dischargeable electric quantity in a potential region of 4.3 V (vs. Li/Li.sup.+) or lower is 177 mAh/g or higher.