IP Library Granted Patent US 9,983,058
Granted Patent B2
US 9,983,058 · App. 15/590,397 · Granted May 29, 2018

Tunable near-infrared emitters and methods

Inventors: YuHuang Wang (Laurel, MD); Hyejin Kwon (Greenbelt, MD); Mijin Kim (Silver Spring, MD)
Assignee: University of Maryland, College Park
G01J3/108B01J19/128H01L49/006H01L51/5262B82Y20/00
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Quick Facts
Patent No.
US 9,983,058
App. No.
15/590,397
Granted
May 29, 2018
Kind
B2
Abstract

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.

Claims (25)

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.

Assignments (2)
CONFIRMATORY LICENSE Recorded Oct 11, 2019
From: UNIVERSITY OF MARYLAND, COLLEGE PARK
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 050711/0986 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 5, 2018
From: WANG, YUHUANG; KWON, HYEJIN; KIM, MIJIN
To: UNIVERSITY OF MARYLAND, COLLEGE PARK
Reel/Frame 045452/0077 →
Continuity (2)
Provisional Application 62333372 · May 9, 2016
Related Publication 20170322081A1 · Nov 9, 2017