A metal oxide catalyst involved in a hydrogenation reaction in which a ketone is converted into an alcohol, a method of preparing the metal oxide catalyst, and a method of preparing an alcohol using the same are provided. The metal oxide catalyst has a spinel structure represented by the following Formula 1:
XAl.sub.2O.sub.4,<Formula 1> wherein X represents nickel or copper.

A metal oxide catalyst involved in a hydrogenation reaction in which a ketone is converted into an alcohol, a method of preparing the metal oxide catalyst, and a method of preparing an alcohol using the same are provided. The metal oxide catalyst has a spinel structure represented by the following Formula 1:
XAl.sub.2O.sub.4,<Formula 1> wherein X represents nickel or copper.

Cu-based nanostructures have excellent catalytic, electronic, and plasmonic performance due to their unique chemical and physical properties. A range of Cu materials including foil, spherical nanoparticles, nanowires, and nanocubes have been explored for catalyzing CO.sub.2 electroreduction. However, practical application of the CO.sub.2 electroreduction reaction requires Cu catalysts hold a high percentage of exposed surface atoms for improved product selectivity. The present disclosure describes a high temperature reduction method to prepare Cu nanosheets with size range from about 40 nm to about 13 m in a hydrophobic system. The purity of trioctyphosphine (TOP) plays an important role for shape-controlled synthesis of Cu nanosheets. The morphology evolution was investigated by adjusting the feeding molar ratio of TOP/Cu-tetradecylamine complex. The Cu nanosheets formed by the methods of the present disclosure have high surface area and stability in solution for more than three months. These Cu nanosheets have applications in reducing CO.sub.2 to fuels.

A negative electrode active material includes a compound represented by a composition formula of Mg.sub.xMe.sub.1-xO.sub.1-xH.sub.2x, where Me is at least one selected from the group consisting of Mn, Fe, Co, Ni, and Cu, and 0.5x0.9.

An oxide superconducting thin film material includes: a metal substrate having a surface with a biaxially oriented crystal orientation structure; an intermediate layer biaxially oriented and formed on the metal substrate; and an oxide superconducting thin film formed on the intermediate layer and composed of a RE123-based oxide superconductor represented by REBa.sub.2Cu.sub.3O.sub.y. The oxide superconducting thin film includes Br (bromine).

An oxide superconducting thin film material includes: a metal substrate having a surface with a biaxially oriented crystal orientation structure; an intermediate layer biaxially oriented and formed on the metal substrate; and an oxide superconducting thin film formed on the intermediate layer and composed of a RE123-based oxide superconductor represented by REBa.sub.2Cu.sub.3O.sub.y. The oxide superconducting thin film includes Br (bromine).

A copper microparticle with antibacterial and/or biocidal activity, wherein each microparticle has a regular, crystalline and microstructured composition that comprises 5 different copper compounds: Antlerite Cu.sub.3.sup.+2(SO.sub.4)(OH).sub.4, Brochantite Cu.sub.4.sup.+2SO.sub.4(OH).sub.6, Chalcantite Cu.sup.+2SO.sub.4.5H.sub.2O, Natrochalcite NaCu.sub.2.sup.+2(SO.sub.4).sub.2OH.H.sub.2O and Hydrated copper sulfate hydroxide Cu.sub.3(SO.sub.4).sub.2(OH).sub.2.4H.sub.2O/2CuSO.sub.4.Cu(OH).sub.2, with the microparticle having a size of between 5 and 50 m. A process for preparing copper microparticles with antibacterial and/or biocidal activity. A concentrated polymeric composition (masterbatch) with antibacterial and/or biocidal activity that is incorporated during the extrusion process to molten polymers for forming rigid or flexible products such as fibers, filaments, and sheets. A use of a copper microparticle with antibacterial and/or biocidal activity. A use of a concentrated polymeric composition (masterbatch) with antibacterial and/or biocidal activity.

A thermoelectric material containing a dichalcogenide compound represented by Formula 1 and having low thermoelectric conductivity and high Seebeck coefficient:
R.sub.aT.sub.bX.sub.2-nY.sub.n(1)
wherein R is a rare earth element, T includes at least one element selected from the group consisting of Group 1 elements, Group 2 elements, and a transition metal, X includes at least one element selected from the group consisting of S, Se, and Te, Y is different from X and includes at least one element selected from the group consisting of S, Se, Te, P, As, Sb, Bi, C, Si, Ge, Sn, B, Al, Ga and In, a is greater than 0 and less than or equal to 1, b is greater than or equal to 0 and less than 1, and n is greater than or equal to 0 and less than 2.

A thermoelectric material containing a dichalcogenide compound represented by Formula 1 and having low thermoelectric conductivity and high Seebeck coefficient:
R.sub.aT.sub.bX.sub.2-nY.sub.n(1)
wherein R is a rare earth element, T includes at least one element selected from the group consisting of Group 1 elements, Group 2 elements, and a transition metal, X includes at least one element selected from the group consisting of S, Se, and Te, Y is different from X and includes at least one element selected from the group consisting of S, Se, Te, P, As, Sb, Bi, C, Si, Ge, Sn, B, Al, Ga and In, a is greater than 0 and less than or equal to 1, b is greater than or equal to 0 and less than 1, and n is greater than or equal to 0 and less than 2.

Compositions comprising high levels of high specific activity copper-64, and process for preparing said compositions. The compositions comprise from about 2 Ci to about 15 Ci of copper-64 and have specific activities up to about 3800 mCi copper-64 per microgram of copper. The processes for preparing said compositions comprise bombarding a nickel-64 target with a low energy, high current proton beam, and purifying the copper-64 from other metals by a process comprising ion exchange chromatography or a process comprising a combination of extraction chromatography and ion exchange chromatography.