Covalently functionalized carbon nanostructures and methods for their separation
US-8980216-B2 · Mar 17, 2015 · US
US9983058B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9983058-B2 |
| Application number | US-201715590397-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 9, 2017 |
| Priority date | May 9, 2016 |
| Publication date | May 29, 2018 |
| Grant date | May 29, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention relates to near-infrared quantum emitters, and in particular carbon nanostructures with chemically incorporated fluorescent defects, and methods of synthesizing near-infrared emitting nanostructures.
Opening claim text (preview).
What is claimed is: 1. A method of synthesizing a near infrared emitter comprising the steps of: reacting a carbon nanostructure with a halogen-containing hydrocarbon precursor and thereby creating sp 3 defects in said carbon nanostructure, wherein covalent functionalization produces fluorescent defects that emit near-infrared radiation having wavelengths between about 800 nm and about 2500 nm. 2. The method of claim 1 , wherein said carbon nanostructure is a carbon nanotube (CNT). 3. The method of claim 2 , wherein said CNT has a diameter of between about 0.5 nm and about 1.6 nm. 4. The method of claim 1 , wherein said sp 3 defects are created in a pristine carbon nanostructure during said reacting step. 5. The method of claim 1 , wherein said halogen-containing hydrocarbon precursor is a chlorine, a bromide, an iodide or a di-halide alkyl precursor. 6. The method of claim 1 , wherein said halogen-containing hydrocarbon precursor is a polymer containing the reactive halogen. 7. The method of claim 6 , wherein said halogen-containing hydrocarbon precursor is a polyoligonucleotide containing the reactive halogen. 8. The method of claim 1 , wherein said halogen-containing hydrocarbon precursor is an alkyl halide. 9. The method of claim 5 , wherein said reacting step further comprises combining said carbon nanostructure with sodium dithionite (Na2S2O4), said sodium dithionite activating said alkyl precursor. 10. The method of claim 1 , wherein said halogen-containing hydrocarbon precursor is an iodide or di-halide aryl precursor. 11. The method of claim 10 , comprising exposing said carbon nanostructure and said aryl precursor to electromagnetic radiation having a wavelength(s) of between about 300 nm and about 1200 nm and resonant with said carbon nanostructures, said electromagnetic radiation activating said aryl precursor. 12. The method of claim 1 , wherein said created sp 3 defects are selected from the group consisting of monovalent alkyl defects, divalent alkyl defects, monovalent aryl defects, and divalent aryl defects. 13. The method of claim 1 , wherein said covalently functionalized carbon nanostructure is functionalized with an alkyl group or an aryl group. 14. The method of claim 1 , wherein said covalently functionalized carbon nanostructure is functionalized with —(CH 2 ) n (CF 2 ) m CF 3 , wherein n is an integer between 0 and 10, and wherein m is an integer between 0 and 10. 15. The method of claim 1 , wherein said covalently functionalized carbon nanostructure is functionalized with —(CH 2 ) n CH 3 , wherein n is an integer between 0 and 17. 16. A synthetic near-infrared emitter, comprising: a carbon nanostructure comprising sp 3 defects in a carbon lattice thereof and created via reaction with a halogen-containing hydrocarbon precursor; and a functional group covalently bonded to said sp 3 defects to produce fluorescent defects that emit near-infrared radiation having wavelengths between about 800 nm and about 2500 nm. 17. The near-infrared emitter of claim 16 , wherein said carbon nanostructure is a carbon nanotube (CNT). 18. The near-infrared emitter of claim 16 , wherein said CNT has a diameter of between about 0.5 nm and about 1.6 nm. 19. The near-infrared emitter of claim 16 , wherein said functional group is selected from the group consisting of a monovalent alkyl group, a divalent alkyl group, a monovalent aryl group, and a divalent aryl group. 20. The near-infrared emitter of claim 16 , wherein said functional group is —(CH 2 ) n (CF 2 ) m X, wherein n is an integer between 0 and 17, and wherein m is an integer between 0 and 17, and wherein X is CH3, CF3, NH2, N+(CH2CH3)2, or COOH. 21. The near-infrared emitter of claim 16 , wherein said functional group is —(CH 2 ) n CH 3 , wherein n is an integer between 0 and 10.
Electricity · mapped topic
Nanooptics, e.g. quantum optics or photonic crystals · CPC title
Electricity · mapped topic
Infrared light · CPC title
for measurement in the infrared range · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.