Processes for preparing a niobate material include the following steps: (i) providing a niobium-containing source; (ii) providing a transitional metal source (TMS), a post-transitional metal source (PTMS), or both; (iii) dissolving (a) the niobium-containing source, and (b) the TMS, the PTMS, or both in an aqueous medium to form an intermediate solution; (iv) forming an intermediate paste by admixing an inert support material with the intermediate solution; (v) optionally coating the intermediate paste on a support substrate; and (vi) removing the inert support material by subjecting the intermediate paste to a calcination process and providing a transition-metal-niobate (TMN) and/or a post-transition-metal-niobate (PTMN). Anodes including a TMN and/or PTMN are also provided.

An object of the present invention is to provide an AFX zeolite having a novel structure. An AFX zeolite having a lattice spacing d of a (004) plane being not less than 4.84 Å and not greater than 5.00 Å, and a molar ratio of silica to alumina being not less than 10 and not higher than 32. Such an AFX zeolite can be produced by a production method comprising a crystallization step of crystallizing a composition at a temperature of not lower than 160° C.; the composition containing a silicon source, an aluminum source, a 1,3-di(1-adamantyl)imidazolium cation, and an alkali metal; a molar ratio of hydroxide ions to silica being less than 0.25 or a molar ratio of silica to alumina being not higher than 27; and a molar ratio of the 1,3-di(1-adamantyl)imidazolium cation to silica being less than 0.20.

The invention relates to a fluorination process consisting in bringing an inorganic compound M into contact with an atmosphere comprising difluorine gas, the inorganic compound M being a garnet based on the elements Li, La, Zr, A and O and for which the relative composition of the Li, La, Zr and A cations corresponds to the formula (I): Li.sub.xLa.sub.3Zr.sub.zA.sub.w.

A positive electrode active material for a lithium ion secondary battery including a coating layer, wherein, a substance quantity ratio is represented by Li:Ni:Co:M=t:1−x−y:x:y (wherein, M is at least one element selected from Mg and else, 0.95≤t≤1.20, 0<x≤0.22, and 0≤y≤0.15), the coating layer includes a lithium zirconium compound, and a ratio of a sum of substance quantities of Ni, Co, Zr and a substance quantity of Zr existing on a surface of the positive electrode active material is 0.80 or more and 0.97 or less.

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.

A method of preparing a lithium lanthanum zirconate (LLZO) cubic garnet material is provided which comprises the following steps: (a) milling a slurry comprising one or more precursor compounds in an aqueous medium, wherein the one or more precursor compounds comprise lithium, lanthanum, zirconium and optionally one or more dopant elements, to provide a milled slurry; (b) spray drying the milled slurry to provide a spray-dried powder; and (c) annealing the spray-dried powder. The resultant LLZO cubic garnet material may be used as a lithium ion conductive solid electrolyte in secondary lithium-ion batteries.

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.

A SCM-33 molecular sieve has a schematic chemical composition as shown in the formula “SiO.sub.2.Math.1/x XO.sub.1.5.Math.m MO.sub.0.5”, wherein X is a framework trivalent element, the Si/X molar ratio x is ≥5, M is a framework equilibrium cation, and the M/Si molar ratio is 0 <m≤1. The molecular sieve is a novel molecular sieve with RTE topology and the molecular sieve requires short preparation time, involves a low synthesis cost and can be used as adsorbent or catalyst.

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.

Positive electrode active material particle powder includes: lithium manganese oxide particle powder having Li and Mn as main components and a cubic spinel structure with an Fd-3m space group. The lithium manganese oxide particle powder is composed of secondary particles, which are aggregates of primary particles, an average particle diameter (D50) of the secondary particles being from 4 μm to 20 μm, and at least 80% of the primary particles exposed on surfaces of the secondary particles each have a polyhedral shape having at least one (110) plane that is adjacent to two (111) planes.