Carbon nanostructure and method for preparing the same

US9944850B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9944850-B2
Application numberUS-201615165115-A
CountryUS
Kind codeB2
Filing dateMay 26, 2016
Priority dateSep 2, 2015
Publication dateApr 17, 2018
Grant dateApr 17, 2018

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Abstract

Official abstract text for this publication.

Provided is a carbon nanostructure including a plurality of organic molecules that are decomposition products of an organic solvent. The carbon nanostructure includes a carbon nanostructure core and a plurality of organic molecules bound to and grown on the carbon nanostructure core, wherein the carbon nanostructure core is a combination of the organic molecules.

First claim

Opening claim text (preview).

What is claimed is: 1. A carbon nanostructure comprising: a carbon nanostructure core; and, a plurality of organic molecules bound to and grown on the carbon nanostructure core, wherein the carbon nanostructure core is a combination of the organic molecules, wherein the organic molecules are decomposition products of an organic solvent selected from the group consisting of acetone, benzene, N-methyl-2-pyrrolidone (NMP), dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), n-hexane, benzene, carbon tetrachloride, liquid carbon dioxide, carbon disulfide, liquid ammonia, and mixtures thereof wherein the carbon nanostructure is obtained by placing the organic solvent in a reactor and applying sufficient temperature and pressure to the organic solvent to carry out decomposition thereof, wherein the temperature to carry out decomposition is within the range of 40-800° C. and the pressure to carry out decomposition is within the range of 1-500 atm. 2. The carbon nanostructure according to claim 1 , which is doped with a heteroatom. 3. The carbon nanostructure according to claim 2 , wherein the heteroatom is at least one selected from the group consisting of nitrogen (N), fluorine (F), oxygen (O), phosphorus (P), boron (B), sulfur (S), chlorine (CI), bromine (Br) and iodine (I), other than carbon (C). 4. The carbon nanostructure according to claim 1 , wherein the organic solvent further comprises a metal or metal precursor, and the organic molecules are metal-organic molecules formed through the binding of a decomposition product of the metal or metal precursor with a decomposition product of the organic solvent. 5. The carbon nanostructure according to claim 4 , which comprises a metal-carbon nanostructure core and the metal-organic molecules bound to and grown on the metal-carbon nanostructure core, wherein the metal-carbon nanostructure core is a combination of the metal-organic molecules. 6. The carbon nanostructure according to claim 4 , which is a decomposition product of a metal-carbon precursor, wherein the metal-carbon precursor is a combination of the metal-organic molecules. 7. The carbon nanostructure according to claim 4 , wherein the metal is at least one selected from the group consisting of platinum (Pt), ruthenium (Ru), copper (Cu), iron (Fe), nickel (Ni), cobalt (Co), palladium (Pd), tungsten (W), iridium (Ir), rhodium (Rh), strontium (Sr), cesium (Ce), praseodymium (Pr), neodymium (Nd), samarium (Sm), rhenium (Re), magnesium (Mg), boron (B) and aluminum (Al), and the metal precursor is at least one selected from the group consisting of CuCl 2 , CoCl 2 , OsCl 3 , CrCl 3 , (NH 3 ) 6 RuCl 3 , FeCl 3 , NiCl 2 , PdCl 2 , RuCl 3 , H 2 PtCl 6 , Pd(NO 3 ) 2 , (NH 3 ) 4 Pt(NO 3 ) 2 , Fe(NO 3 ) 3 , Ni(NO 3 ) 2 , iron acetylacetonate, ferrocene and Pt(acac) 2 . 8. The carbon nanostructure according to claim 1 , wherein the solvent is NMP, and the organic molecule is at least one selected from the group consisting of methyl 5-oxo-L-prolinate, 1-methyl-5-oxo-2-pyrrolidinyl)methyl acetate, (2S)-2-(Methoxymethyl)-1-pyrrolidinecarbaldehyde, 5-(hydroxymethyl)-1-methyl-2-pyrrolidinone, 5-(hydroxymethyl)-1-methyl-2-pyrrolidinone, (2E)-N-Hydroxy-4-methyl-3-penten-2-imine, 1-butylpyrrolidin-2-one, 1-methyl-2-pyrrolidinone, 1-ethyl-2-pyrrolidinyl)methanol, 1-(1-ethyl-2-pyrrolidinyl)methanamine, 1-[(2R)-1-ethyl-2-pyrrolidinyl]methanamine, (5E)-7-vinyl-5-undecene, (2E,9E)-2,9-undecadiene, N-ethyl-1-propanamine, N-methyl-N-nitro-1-(1-piperidinyl)methanamine, 3-(2-methyl-1-piperidinyl)-1-propanamine, 1,5-dimethyl-2-pyrrolidinone, (2S)-2-(methoxymethyl)-1-pyrrolidinecarbaldehyde, 1-(2-hydroxyethyl)-2-pyrrolidinone, 5-methyl-2-octyl-3(2H)-furanone, 3-hydroxy-3-phenylpropyl carbamate, 2-hydroxypropanoic acid, 4-penten-2-ol, N-(2-aminoethyl)acetamide, N-acetyl-N-methylacetamide, N-ethylformamide, 1-(3-hydroxypropyl)-2-pyrrolidinone and 1-ethyl-N-(2-formylphenyl)prolinamide. 9. The carbon nanostructure according to claim 1 , which has a size of 0.1-100 nm.

Assignees

Inventors

Classifications

  • C09K11/65Primary

    containing carbon (in organic compounds C09K11/06) · CPC title

  • containing chromium, molybdenum or tungsten · CPC title

  • containing neodynium · CPC title

  • Nano-sized carbon materials · CPC title

  • containing platina group metals · CPC title

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What does patent US9944850B2 cover?
Provided is a carbon nanostructure including a plurality of organic molecules that are decomposition products of an organic solvent. The carbon nanostructure includes a carbon nanostructure core and a plurality of organic molecules bound to and grown on the carbon nanostructure core, wherein the carbon nanostructure core is a combination of the organic molecules.
Who is the assignee on this patent?
Korea Inst Sci & Tech
What technology area does this patent fall under?
Primary CPC classification C09K11/65. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).