Articles, such as components for high temperature turbomachinery components, include one or more coatings bearing certain perovskite compositions resistant to incursion by liquid calcium-magnesium-aluminum-silicon-oxide (CMAS) materials during service. The CMAS-reactive material includes a perovskite-structured oxide, which comprises a) a rare earth element, b) niobium, tantalum or a combination of tantalum and niobium, and c) oxygen. The CMAS-reactive material is present in an effective amount to react with a CMAS composition at an operating temperature, thereby forming a reaction product having one or both of melting temperature and viscosity greater than that of the CMAS composition.

Articles, such as components for high temperature turbomachinery components, include one or more coatings bearing certain perovskite compositions resistant to incursion by liquid calcium-magnesium-aluminum-silicon-oxide (CMAS) materials during service. The CMAS-reactive material includes a perovskite-structured oxide, which comprises a) a rare earth element, b) niobium, tantalum or a combination of tantalum and niobium, and c) oxygen. The CMAS-reactive material is present in an effective amount to react with a CMAS composition at an operating temperature, thereby forming a reaction product having one or both of melting temperature and viscosity greater than that of the CMAS composition.

A production method of a battery active material of the present embodiment includes a step of obtaining a coprecipitated product containing Ti and Nb by mixing a solution with a pH of 5 or lower, in which a Ti compound is dissolved, and a solution with a pH of 5 or lower, in which a Nb compound is dissolved, such that molar ratio of Ti and Nb (Nb/Ti) is adjusted within a range of 1≦Nb/Ti≦28, and then further mixing with an alkali solution with a pH of 8 or higher; and a step of burning the coprecipitated product under condition of 635° C. or higher and 1200° C. or lower.

A production method of a battery active material of the present embodiment includes a step of obtaining a coprecipitated product containing Ti and Nb by mixing a solution with a pH of 5 or lower, in which a Ti compound is dissolved, and a solution with a pH of 5 or lower, in which a Nb compound is dissolved, such that molar ratio of Ti and Nb (Nb/Ti) is adjusted within a range of 1≦Nb/Ti≦28, and then further mixing with an alkali solution with a pH of 8 or higher; and a step of burning the coprecipitated product under condition of 635° C. or higher and 1200° C. or lower.

Products derived from and methods of micelle tem plating that allow for orthogonal control over structural features.

Products derived from and methods of micelle tem plating that allow for orthogonal control over structural features.

Provided is a precursor of transition metal oxide represented by chemical formula 1 below.

Ni.sub.aMn.sub.bCo.sub.1−(a+b+c+d)Zr.sub.cM.sub.d[OH.sub.(1-x)2-y]A.sub.(y/n)   [Chemical formula 1]

A method of forming a thermal barrier coating is disclosed. The method may include providing a solution containing strontium and niobium and applying the solution to a substrate via a chemical solution deposition process to form a first film layer on the substrate. The method may further include pyrolyzing the first film layer and annealing the first film in an air atmosphere to form a strontium niobate coating.

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.

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.