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.

Provided is an improved method for forming a battery comprising a cathode and electrolyte. The method of forming the cathode comprises forming a first solution comprising a digestible feedstock of a first metal suitable for formation of a cathode oxide precursor and a multi-carboxylic acid. The digestible feedstock is digested to form a first metal salt in solution wherein the first metal salt precipitates as a salt of deprotonated multi-carboxylic acid thereby forming an oxide precursor and a coating metal is added to the oxide precursor. The oxide precursor is heated to form the coated lithium ion cathode material. The electrolyte is void of salts and additives.

A lithium deficient cathode active material for lithium-ion batteries is described. More particularly, the lithium deficient cathode active material can have multiphase structures, including both a layered or hexagonal structure (e.g., having an R-3m space group) and a spinel structure (e.g., having a .sub.Fd-m space group). Batteries including the cathode active material and methods of preparing the cathode active material are also described.

A positive electrode active material for a nonaqueous electrolyte secondary battery is used for a nonaqueous electrolyte secondary battery. The positive electrode active material includes a composite oxide containing at least lithium, nickel, and manganese and contains aggregated particles of primary particles having an average particle diameter of 1.0 μm or more. The primary particles have a layered crystal structure and a spinel crystal structure.

The invention relates to polyoxometalates represented by the formula (A.sub.n).sup.m+[M′M.sub.12X.sub.8O.sub.yR.sub.zH.sub.q].sup.m− or solvates thereof, corresponding supported polyoxometalates, and processes for their preparation, as well as corresponding metal clusters, optionally in the form of a dispersion in a liquid carrier medium or immobilized on a solid support, and processes for their preparation, as well as their use in reductive conversion of organic substrate.

VO.sub.2 and V.sub.2O.sub.5 nano- or micro-materials. The VO.sub.2 nano-materials and micro-materials have an M1 phase structure and oxygen stoichiometry that deviates 2% or less from theoretical stoichiometry. The VO.sub.2 nano-materials and micro-materials may doped with cation dopants and/or anion dopants. The VO.sub.2 and V.sub.2O.sub.5 nano- or micro-materials can be made by hydrothermal methods starting with V.sub.3O.sub.7.H.sub.2O nano- or micro-material. The VO.sub.2 and V.sub.2O.sub.5 nano- or micro-materials can be used as, for example, thermochromic window coatings.

A chalcogen-containing compound of the following Chemical Formula 1, which may have decreased thermal conductivity and improved power factor in the low temperature region, and thus exhibit an excellent thermoelectric figure of merit, a method for preparing the same, and a thermoelectric element including the same:
V.sub.1Sn.sub.a−xIn.sub.xSb.sub.2Te.sub.a+3  [Chemical Formula 1]
wherein V, a and x are as defined in the specification.

A cathode active material contains a compound having a crystal structure of space group FM-3M and represented by composition formula (1): Li.sub.xMe.sub.yO.sub.2 . . . (1). In the formula, Me represents any of the following: Mn; Mn and one or two or more elements selected from the group consisting of Co, Fe, Sn, Cu, Mo, Bi, V, and Cr; Ni, Mn, and one or two or more elements selected from the group consisting of Co, Fe, Sn, Cu, Mo, Bi, V, and Cr; and one or two or more elements selected from the group consisting of Ni, Co, Fe, Sn, Cu, Mo, Bi, V, and Cr. In addition to this, the following conditions are met: 0.5≦x/y≦3.0; and 1.5≦x+y≦2.3.

A cathode active material contains a compound having a crystal structure of space group FM-3M, represented by composition formula (1), and having a half-width in 2δ of 0.9° or more and 2.4° or less for a (200) diffraction peak in powder X-ray diffraction (XRD): Li.sub.xMe.sub.yO.sub.2. . . (1). In the formula, Me represents one or two or more elements selected from the group consisting of Mn, Nb, Ti, Ni, Co, Fe, Sn, Cu, Mo, Bi, V, and Cr. In addition to this, the following conditions are met: 0.5≦x/y≦3.0; and 1.5≦x+y≦2.3.

Provided is magnetic powder capable of enhancing simultaneously both magnetic characteristics including SNP and durability of a magnetic recording medium. The hexagonal ferrite magnetic powder for a magnetic recording medium has a Ba/Fe molar ratio of 8.0% or more, a Bi/Fe molar ratio of 2.5% or more and an Al/Fe molar ratio of from 3.0 to 6.0%. The magnetic powder preferably has an activation volume Vact of from 1,400 to 1,800 nm.sup.3. The magnetic powder particularly preferably has a coercive force Hc of from 159 to 279 kA/m (which is approximately from 2,000 to 3,500 Oe) and a coercivity distribution SFD of from 0.3 to 1.0. The magnetic powder may contain, as an element that substitutes an Fe site of the hexagonal ferrite, at least one kind selected from divalent transition metals M1 and tetravalent transition metals M2.