Ligand-exchangeable nanoparticles and methods of making the same

Patent metadata

Field	Value
Publication number	US-10544168-B2
Application number	US-201715623910-A
Country	US
Kind code	B2
Filing date	Jun 15, 2017
Priority date	Jun 15, 2016
Publication date	Jan 28, 2020
Grant date	Jan 28, 2020

Abstract

An aspect of the present disclosure is a nanocrystal that includes a nanocrystal core and a ligand coordinated to a surface of the nanocrystal core, where the ligand includes a functionalized aromatic molecule. In some embodiments of the present disclosure, the functionalized aromatic molecule may include at least one of cinnamic acid (CAH) and/or a functionalized CAH molecule.

First claim

What is claimed is:

1. A nanocrystal comprising:
a nanocrystal core comprising lead sulfide; and
a ligand coordinated to a surface of the nanocrystal core, wherein:
the ligand comprises at least one of cinnamic acid (CAH) or a functionalized CAH molecule.

2. The nanocrystal of claim 1 , wherein the functionalized CAH molecule comprises at least one of cinnamic acid, 2,3,4,5,6-pentafluorocinnamic acid, 3,5-bis(trifluoromethyl)cinnamic acid, 4-(2,2-dicyanovinyl)cinnamic acid, 4-nitrocinnamic acid, 4-cyanocinnamic acid, 3,5-difluoro-4-trifluoromethyl cinnamic acid, 4-formylcinnamic acid, 4-trifluoromethylcinnamic acid, 3,5-difluorocinnamic acid, 4-chlorocinnamic acid, 4-bromocinnamic acid, 4-iodocinnamic acid, 4-fluorocinnamic acid, 4-mercaptocinnamic acid, 4-carboxycinnamic acid, 4-hydroxycinnamic acid, 3,5-dimethoxy-4-hydroxycinnamic acid, 4-methylcinnamic acid, 4-ethylcinnamic acid, 4-tertbutylcinnamic acid, 2,6-difluorocinnamic acid, 4-methoxycinnamic acid, 2,6-difluoro-4-methoxycinnamic acid, 4-dimethylaminocinnamic acid, 4-aminocinnamic acid, alpha-cyano-4-dimethylaminocinnamic acid, 4-(di-(4-methoxyphenyl)amino)cinnamic acid, or 3,4-(2,5-pyrrolidinedione)cinnamic acid.

3. The nanocrystal of claim 1 , wherein the nanocrystal core has an average particle size between 1 nm and 100 nm.

4. The nanocrystal of claim 2 , further comprising an optical absorbance enhancement between 1.1 and 2.0.

5. The nanocrystal of claim 4 , further comprising an ionization energy between 6.5 eV and 4.0 eV.

6. The nanocrystal of claim 5 , further comprising a work function between 5.5 eV and 3.0 eV.

7. The nanocrystal of claim 1 , wherein the nanocrystal core comprises at least one of a uniformly mixed alloy type nanocrystal core, a core-shell type nanocrystal core, a dot-in-rod type nanocrystal core, a dot-on-rod type nanocrystal core, or a Janus particle type nanocrystal core.

8. The nanocrystal of claim 1 , wherein the ligand is coordinated to the surface by at least one of a covalent bond, an ionic bond, a van der Waals interaction, dipole-dipole interactions, or a hydrogen-bond.

9. The nanocrystal of claim 8 , wherein the ligand is coordinated to the surface of the nanocrystal core by an ionic bond.

10. The nanocrystal of claim 1 , wherein the functionalized CAH molecule comprises at least one of 2,3,4,5,6-pentafluorocinnamic acid, 3,5-bis(trifluoromethyl)cinnamic acid, 4-(2,2-dicyanovinyl)cinnamic acid, 4-cyanocinnamic acid, 3,5-difluoro-4-trifluoromethyl cinnamic acid, 4-formylcinnamic acid, 4-trifluoromethylcinnamic acid, 3,5-difluorocinnamic acid, 4-iodocinnamic acid, 4-mercaptocinnamic acid, 4-carboxycinnamic acid, 3,5-dimethoxy-4-hydroxycinnamic acid, 4-methylcinnamic acid, 4-ethylcinnamic acid, 4-tertbutylcinnamic acid, 2,6-difluorocinnamic acid, 2,6-difluoro-4-methoxycinnamic acid, 4-aminocinnamic acid, alpha-cyano-4-dimethylaminocinnamic acid, 4-(di-(4-methoxyphenyl)amino)cinnamic acid, or 3,4-(2,5-pyrrolidinedione)cinnamic acid.

11. A mixture comprising:
a nanocrystal comprising a nanocrystal core and a ligand; and
a solvent, wherein:
the nanocrystal core comprises lead sulfide;
the ligand comprises at least one of cinnamic acid (CAH) or a functionalized CAH molecule,
the ligand is coordinated to a surface of the nanocrystal core, and
the solvent, the nanocrystal, and the ligand form at least one of a stable solution-phase colloid or a stable ink.

12. The mixture of claim 11 , wherein the solvent comprises at least one of a polar solvent or a non-polar solvent.

13. The mixture of claim 12 , wherein the solvent comprises at least one of toluene, benzene, chlorobenzene, dichlorobenzene, nitrobenzene, dichloromethane, tetrachoroethylene, chloroform, carbon tetrachloride, acetone, acetonitrile, methyl acetate, ethyl acetate, tetrahydrofuran, diethyl ether, methanol, ethanol, propanol, butanol, N-methylformamide, N,N-dimethylformamide, dimethyl sulfoxide, or water.

14. A method comprising:
adding an exchange ligand to a solution comprising a first solvent, a nanocrystal core, and a starting ligand, wherein:
the exchange ligand comprises at least one of cinnamic acid (CAH) or a functionalized CAH molecule,
the nanocrystal core comprises lead sulfide,
the starting ligand is coordinated to a surface of the nanocrystal core to form a starting nanocrystal,
the exchange ligand replaces at least a portion of the starting ligand coordinated to the surface, and
the exchange ligand coordinates to the surface to produce a ligand-exchanged nanocrystal in the solution.

15. The method of claim 14 , wherein the solution is maintained at a temperature between 20° C. and 30° C.

16. The method of claim 14 , wherein the first solvent comprises at least one of a polar solvent or a non-polar solvent.

17. The method of claim 16 , wherein the first solvent comprises at least one of dichloromethane, pentane, cyclohexane, hexane, heptane, octane, toluene, tetrachoroethylene, chloroform, or carbon tetrachloride.

18. The method of claim of claim 14 , wherein the starting ligand comprises at least one of an alkyl carboxylate, an alkyl amine, an alkyl phosphine, an alkyl phosphonate, or an alkyl thiolate.

19. The method of claim 18 , wherein the starting ligand is oleate.

Assignees

• Alliance Sustainable Energy
• Colorado School Of Mines
• Univ Colorado Regents

Inventors

• Beard Matthew C
• Kroupa Daniel McCray
• Sellinger Alan

Classifications

• C09D11/03

  characterised by features other than the chemical nature of the binder · CPC title

• C09K11/06 Primary

  containing organic luminescent materials · CPC title

• C09D11/50

  Sympathetic, colour changing or similar inks · CPC title

• C09K11/661

  Chalcogenides · CPC title

• C09K2211/188

  of other metals not provided for in one of the previous groups · CPC title