C07C211/65

MOLYBDENUM(0) PRECURSORS FOR DEPOSITION OF MOLYBDENUM FILMS

Molybdenum(0) and coordination complexes are described. Methods for depositing molybdenum-containing films on a substrate are described. The substrate is exposed to a molybdenum precursor and a reactant to form the molybdenum-containing film (e.g., elemental molybdenum, molybdenum oxide, molybdenum carbide, molybdenum silicide, molybdenum disulfide, molybdenum nitride). The exposures can be sequential or simultaneous.

METHOD FOR PRODUCING METAL CARBONATE AND CATALYST FOR PRODUCING THE SAME
20170217786 · 2017-08-03 ·

A method for producing metal carbonate is disclosed. The method includes the following steps of providing a first mixture of metal and a catalyst containing iron, NO groups, and N-containing ligands first; then introducing carbon dioxide to the first mixture to form a second mixture and obtaining a product. The method described here can improve the yield and decrease the cost of metal carbonate production.

METHOD FOR PRODUCING METAL CARBONATE AND CATALYST FOR PRODUCING THE SAME
20170217786 · 2017-08-03 ·

A method for producing metal carbonate is disclosed. The method includes the following steps of providing a first mixture of metal and a catalyst containing iron, NO groups, and N-containing ligands first; then introducing carbon dioxide to the first mixture to form a second mixture and obtaining a product. The method described here can improve the yield and decrease the cost of metal carbonate production.

ORGANIC-INORGANIC HYBRID COMPOUND, AMINE HYDROGEN IODIDE SALT, COMPOSITION FOR PHOTOELECTRIC CONVERSION ELEMENT, AND PHOTOELECTRIC CONVERSION ELEMENT
20170260125 · 2017-09-14 ·

The present invention provides a novel compound to be used in a solar cell. The compound of the present invention is an organic-inorganic hybrid compound represented by Formula (I).


R.sup.1CH.sub.2N.sup.+H.sub.3M.sup.1X.sup.1.sub.3   (I)

where, R.sup.1 is a C1-C5 alkyl group or C2-C5 alkenyl group substituted with at least one halogen atom; M.sup.1 is a divalent metal ion; X.sup.1 is a monovalent halogen atom ion; and X.sup.1.sub.3 is formed from one type of halogen atom ion or a combination of two or more types of halogen atom ions.

ORGANIC-INORGANIC HYBRID COMPOUND, AMINE HYDROGEN IODIDE SALT, COMPOSITION FOR PHOTOELECTRIC CONVERSION ELEMENT, AND PHOTOELECTRIC CONVERSION ELEMENT
20170260125 · 2017-09-14 ·

The present invention provides a novel compound to be used in a solar cell. The compound of the present invention is an organic-inorganic hybrid compound represented by Formula (I).


R.sup.1CH.sub.2N.sup.+H.sub.3M.sup.1X.sup.1.sub.3   (I)

where, R.sup.1 is a C1-C5 alkyl group or C2-C5 alkenyl group substituted with at least one halogen atom; M.sup.1 is a divalent metal ion; X.sup.1 is a monovalent halogen atom ion; and X.sup.1.sub.3 is formed from one type of halogen atom ion or a combination of two or more types of halogen atom ions.

OCTAHEDRAL PEROVSKITE MATERIALS WITH SMALL RADIUS METAL CENTER AND USES THEREOF

Ge-centered octahedral perovskites have heretofore not been achievable due to collapse of the perovskite structure into non-octahedral units due to a lack of B site support from the small-radius Ge atom, which breaks Goldschmidt’s rules for constructing octahedral perovskites. To overcome this shortcoming, a strategy was developed to form a strong cage with the A sites in which the octahedron is forced to remain intact. Strong intermolecular interaction between the organic A site cations were used to stabilize the symmetric Ge octahedral perovskite beyond the Goldschmidt’s rules. The molecules used based on Y-PMA (Y: F, Cl, Br, I) that facilitated strong halogen bonding to form the cage around the octahedral. Octahedral Ge perovskites exhibit a direct bandgap in contrast to the indirect bandgap of non-octahedral Ge perovskites are demonstrated. In addition, the octahedral Ge perovskite exhibited a dramatic increase in the carrier mobility. A photodetector made with the stabilized octahedral perovskite material exhibited a vastly better responsivity than non-octahedral Ge perovskites.

Molybdenum(0) precursors for deposition of molybdenum films

Molybdenum(0) and coordination complexes are described. Methods for depositing molybdenum-containing films on a substrate are described. The substrate is exposed to a molybdenum precursor and a reactant to form the molybdenum-containing film (e.g., elemental molybdenum, molybdenum oxide, molybdenum carbide, molybdenum silicide, molybdenum disulfide, molybdenum nitride). The exposures can be sequential or simultaneous.

Asphalt emulsion composition and method of treating a pavement surface

Compositions and methods are provided for treating a pavement such as by microsurfacing or slurry sealing. The compositions contain iron chelants that are effective in reducing discoloration of the pavement surface.

Compositions, methods, and devices for capturing phosphate from water

The present disclosure provides compositions, methods, and devices for sensing, detecting, and/or selectively capturing phosphate from water. An exemplary method includes: contacting a ligand or a rare earth metal complex of a ligand as described herein with an aqueous phosphate-containing medium at a pH of 5 to 12 under conditions sufficient to bind phosphate (e.g., reversibly bind phosphate). In certain embodiments, the method further includes releasing the bound phosphate by contacting the bound phosphate complex with an aqueous medium at a pH of 0 to 4 under conditions sufficient to release the bound phosphate.

Compositions, methods, and devices for capturing phosphate from water

The present disclosure provides compositions, methods, and devices for sensing, detecting, and/or selectively capturing phosphate from water. An exemplary method includes: contacting a ligand or a rare earth metal complex of a ligand as described herein with an aqueous phosphate-containing medium at a pH of 5 to 12 under conditions sufficient to bind phosphate (e.g., reversibly bind phosphate). In certain embodiments, the method further includes releasing the bound phosphate by contacting the bound phosphate complex with an aqueous medium at a pH of 0 to 4 under conditions sufficient to release the bound phosphate.