A positive electrode active material includes a lithium transition metal oxide having a spinel crystal structure, and a coating layer positioned on the surface of the lithium transition metal oxide, wherein the coating layer has an orthorhombic structure, and includes an oxide represented by Formula 1. A method for producing the positive electrode active material, a positive electrode including the positive electrode active material, and a lithium secondary battery, the positive electrode active material.

Systems and methods are disclosed for a rock-salt structure formed from an electrochemically-driven amorphous-to-crystalline (a-to-c) transformation of nanostructured Nb.sub.2O.sub.5, the rock-salt structure including, upon cycling with lithium ions (Li+), an insertion of lithium ions (Li+) into Nb.sub.2O.sub.5 to form the rock-salt structure (RS—Nb.sub.2O.sub.5).

A crystalline titanium and magnesium compound having an X-ray diffraction pattern having interplanar spacing (d-spacing) values at about 5.94, 3.10, 2.97, 2.10, 1.98, 1.82, and 1.74±0.1 angstroms may be used in protective coatings for metal or metal alloy substrates. The coatings exhibit excellent corrosion resistances and provide corrosion protection equal to or better than typical non-chromate coatings.

The present disclosure provides for compositions, methods of making compositions, and methods of using the composition. In an aspect, the composition can be a reactive material that can be used to split a gas such as water or carbon dioxide.

A method for producing mesoporous magnesium hydroxide nanoplates involving solvothermal treatment of a solution of a magnesium salt, a base, a glycol, and water is disclosed. The method does not use a surfactant or template in the solvothermal treatment. The method yields mesoporous nanoparticles of magnesium hydroxide having a plate-like morphology with a diameter of 20 nm to 100 nm, a mean pore diameter of 2 to 10 nm, a surface area of 50 to 70 m.sup.2/g, and a type-III nitrogen adsorption-desorption BET isotherm with a H3 hysteresis loop. An antibacterial composition containing the mesoporous magnesium hydroxide nanoplates is also disclosed. A method for reducing nitroaromatic compounds with a reducing agent and the mesoporous magnesium hydroxide nanoplates as a catalyst is also disclosed.

An oxide superconductor according to an embodiment includes an oxide superconducting layer includes a single crystal having a continuous perovskite structure containing at least one rare earth element selected from the group consisting of yttrium, lanthanum, neodymium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, and lutetium, barium, and copper, containing praseodymium in a part of the site of the rare earth element in the perovskite structure, and having a molar ratio of praseodymium of 0.00000001 or more and 0.2 or less with respect to the sum of the at least one rare earth element and praseodymium; fluorine in an amount of 2.0×10.sup.15 atoms/cc or more and 5.0×10.sup.19 atoms/cc or less; and carbon in an amount of 1.0×10.sup.17 atoms/cc or more and 5.0×10.sup.20 atoms/cc or less.

A main object of the present disclosure is to provide an active material wherein an expansion upon intercalation of a metal ion such as a Li ion is suppressed. The present disclosure achieves the object by providing an active material comprising a silicon clathrate type crystal phase, and the active material includes a Na element, a Si element and a M element that is a metal element with an ion radius larger than the Si element, and a proportion of the M element to a total of the Si element and the M element is 0.1 atm % or more and 5 atm % or less.

A lithium vanadium oxide crystal and usage thereof that can achieve further excellent electrochemical characteristics are provided. New lithium vanadium oxide crystal is a lithium vanadium oxide crystal which is Li.sub.3VO.sub.4 to which tetravalent metal species M is doped, in which the lithium vanadium oxide crystal is represented by a chemical formula of Li.sub.3+1V.sub.1−xM.sub.xO.sub.4 and includes only a single crystal structure with γ-phase as Li.sub.3VO.sub.4 under a temperature environment including normal temperature, and the tetravalent metal species M is included in a ratio of x≥0.2.

A positive electrode active material in which a discharge capacity decrease due to charge and discharge cycles is suppressed and a secondary battery including the positive electrode active material are provided. A positive electrode active material in which a change in a crystal structure, e.g., a shift in CoO.sub.2 layers is small between a discharged state and a high-voltage charged state is provided. For example, a positive electrode active material that has a layered rock-salt crystal structure belonging to the space group R-3m in a discharged state and a crystal structure belonging to the space group P2/m in a charged state where x in Li.sub.xCoO.sub.2 is greater than 0.1 and less than or equal to 0.24 is provided. When the positive electrode active material is analyzed by powder X-ray diffraction, a diffraction pattern has at least diffraction peaks at 2θ of 19.47±0.10° and 2θ of 45.62±0.05°.

The present invention relates to a cathode active material, and a lithium secondary battery comprising the same, the present invention provides a cathode active material, represented by the following Chemical Formula 1, wherein I003/I104 ratio is 1.6 or more, and R-factor value represented by the following Formula 1 is 0.40 to 0.44, and c-axis lattice constant (c) and a-axis lattice constant (a) satisfy 3(a)+5.555≤(c)≤3(a)+5.580:
R-factor=(I102+I006)/(I101)  Formula 1 wherein I003, I006, I101, I102, and I104 are the intensity of diffraction peaks on the (003), (006), (101), (102), and (104) planes by X-ray diffraction analysis using CuKα-rays,
Li.sub.α[(Ni.sub.xCo.sub.y).sub.1-βA.sub.β]O.sub.z  Chemical Formula 1 in the Chemical Formula 1, 0.95≤α≤1.1, 0.75≤x≤0.95, 0.03≤y≤0.25, 0<β≤0.2, and 1.9≤z≤2.1, and A is a dopant metal element, and the average oxidation number N of A is 3.05≤N≤3.35.