Carbon dioxide can be converted into a higher energy product by contacting carbon dioxide with a polarized monocrystalline magnesium oxide producing at least in part carbon. Further a novel crystalline magnesium oxide carbon composite comprising crystalline magnesium oxide and crystalline carbon having graphene structure which are interwoven is provided.

A method for separating a metallofullerene M@C.sub.82, comprises steps of: a) adding a Lewis acid to an extract containing the metallofullerene M@C.sub.82 to react therewith, producing a complex precipitate; b) washing the precipitate, followed by dissolving and filtering to obtain a purified metallofullerene M@C.sub.82 extract, wherein M is one or more selected from the group consisting of lanthanide metals Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb, and Lu; and the Lewis acid is one or more selected from the group consisting of zinc chloride, nickel chloride, copper chloride, zinc bromide, nickel bromide, and copper bromide.

The invention relates to a method for producing functionalised bimodal periodic mesoporous organosilicates (PMOs) by means of pseudomorphic transformation, to functionalised bimodal periodic mesoporous organosilicates (PMOs) that comprise at least one organosilicate and at least one functional component, and to the use of the PMO as a filter material, adsorption means, sensor material or carrier material for pharmaceutical products, insecticides or pesticides.

The invention relates to a method for producing functionalised bimodal periodic mesoporous organosilicates (PMOs) by means of pseudomorphic transformation, to functionalised bimodal periodic mesoporous organosilicates (PMOs) that comprise at least one organosilicate and at least one functional component, and to the use of the PMO as a filter material, adsorption means, sensor material or carrier material for pharmaceutical products, insecticides or pesticides.

The present invention discloses photostable composite of indium gallium nitride and zinc oxide for solar water splitting, comprising Indium content in the range of 1-40 wt %, Ga content in the range of 1 to 15 wt %, nitrogen content in the range of 0.1 to 5 wt %, and the remaining is ZnO. The combustion synthesis comprises the steps of: (a) dissolving 45 to 55 wt % urea, 75 to 80 wt % Zinc nitrate, 3 to 5 wt % Gallium nitrate, and 15 to 20 wt % Indium nitrate in water with stirring until a homogenous solution is formed; and (b) heating the homogenous solution of step (a) at a temperature in the range of 450-550 [deg.]C. for period in the range of 2 to 20 min to obtain the photostable composite.

A nickel (Ni)-based active material precursor for a lithium secondary battery, a preparing method thereof, a Ni-based active material obtained therefrom, and a lithium secondary battery including a positive electrode including the same, are provided. The Ni-based active material precursor includes a secondary particle including a plurality of particulate structures, wherein each of the particulate structures includes a porous core portion; and a shell portion including primary particles radially arranged on the porous core portion. Phosphorus (P) may be present in the porous core portion, between the plurality of primary particles, and on the surface of the secondary particle, and the content of the phosphorus may be in a range of 0.01 wt % to 2 wt % based on a total weight of the Ni-based active material precursor.

A method for generating hydrogen from a mixture of nitrogen containing borane compound and active metal borohydride reactants uses a catalyst-free water vapor driven hydrothermolysis process. The method involves mechanically mixing a selected ratio of nitrogen containing borane compound such as ammonia borane and an active metal borohydride such as sodium borohydride to produce a mixture, combining the mixture with a water vapor source, and heating the mixture and water vapor source to a temperature within a near ambient temperature range of 30° C. to 104° C., until a product gas comprising hydrogen is released. The heating can be at a constant temperature or at increasing temperatures. Water vapor and impurities are removed from the product gas to produce purified hydrogen gas.

Disclosed is a process for coating onto a substrate, including preparing a precursor having a general formula Q.sub.m/nMO.sub.xF.sub.y by a reaction M(OH).sub.x+yHF+m/nQ(OH).sub.n.fwdarw.Q.sup.n+.sub.m/n(MO.sub.xF.sub.y).sup.m−, wherein Q is an onium ion, selected from quaternary alkyl ammonium, quaternary alkyl phosphonium and trialkylsulfonium; M is a metal capable of forming an oxofluorometallate, where M may further comprise one or more additional metal, metalloid, and one or more of phosphorus (P), sulfur (S) and selenium (Se), iodine (I), and arsenic (As) or a combination thereof, and x>0, y>0, m≥1, n≥1; combining the precursor with a lithium ion source and with the substrate, and mixing to form a coating composition comprising a lithium oxofluorometallate having a general formula Li.sub.mMO.sub.xF.sub.y on the substrate. Further disclosed is a core-shell electrode active material including a core capable of intercalating and deintercalating lithium coated with the lithium oxofluorometallate having the general formula Li.sub.mMO.sub.xF.sub.y.

A nuclear fuel element for use in a nuclear reactor may include a plurality of metal fuel sheaths extending along a longitudinal fuel element axis and spaced apart from each other, the plurality of fuel sheaths comprising a first fuel sheath having an inner surface, an opposing outer surface and a hollow interior configured to receive nuclear fuel material. A carbon coating may be on the inner surface of the first fuel sheath. The carbon coating may include more than 99.0% wt of a carbon material including more than 20% wt of carbon nanotubes and less than about 0.01% wt of organic contaminants.

Provided are a metal element-doped positive electrode active material for a high voltage and a preparation method thereof. The positive electrode active material may include a lithium cobalt oxide having a layered crystal structure; and a metal element (M) incorporated into the lithium cobalt oxide in an amount of 0.2 parts by weight to 1 part by weight with respect to 100 parts by weight of the lithium cobalt oxide, wherein the metal element (M) does not form a chemical bond with the elements of the lithium cobalt oxide, and wherein the layered crystal structure in maintained at a positive electrode potential of more than 4.5 V (based on Li potential) when fully charged.