IP Library Granted Patent US 9,327,314
Granted Patent B2
US 9,327,314 · App. 13/680,749 · Granted May 3, 2016

Core-shell nanoparticles with multiple cores and a method for fabricating them

Inventors: Chuan-Jian Zhong (Endwell, NY); Hye-Young Park (Seoul, KR)
Assignee: The Research Foundation for the State University of New York
B05D7/00B01J13/02B03C1/30B82Y40/00Y10T428/2991
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Quick Facts
Patent No.
US 9,327,314
App. No.
13/680,749
Granted
May 3, 2016
Kind
B2
Abstract

The present invention is directed toward core-shell nanoparticles, each comprising a ligand-capped metal shell surrounding a plurality of discrete, nonconcentric, metal-containing cores. Methods of making and using these nanoparticles are also disclosed.

Claims (27)

1. A method of producing core-shell nanoparticles, each comprising a ligand-capped metal shell surrounding a plurality of discrete metal-containing cores, said method comprising:

providing ligand-capped metal-containing core material nanoparticles;

providing ligand-capped metal shell material nanoparticles; and

reacting the ligand-capped metal-containing core material nanoparticles and the ligand-capped metal shell material nanoparticles to produce the core-shell nanoparticles comprising a ligand-capped metal shell surrounding a plurality of discrete metal-containing cores, wherein said reacting comprises:

combining the ligand-capped metal-containing core material nanoparticles and the ligand-capped metal shell material nanoparticles in a solvent to form a reaction mixture and

heating the reaction mixture to form the core-shell nanoparticles comprising a ligand-capped metal shell surrounding the plurality of metal-containing cores, wherein said heating raises the temperature of the reaction mixture to a temperature of 140-160° C.

2. The method according to claim 1 wherein the core-shell nanoparticles are present in a monodispersion with controlled diameters ranging from 5 nm to 100 nm.

3. The method according to claim 1 , wherein the solvent is selected from the group consisting of toluene, tetraoctylammonium bromide, and decanethiols.

4. The method according to claim 1 , wherein said reacting further comprises:

subjecting the core-shell nanoparticles to at least one sizing operation.

5. The method according to claim 4 , wherein the sizing operation comprises centrifugation.

6. The method according to claim 1 , wherein the ligand-capped metal containing core material nanoparticles are ligand-capped Fe 2 O 3 nanoparticles.

7. The method according to claim 6 , wherein the capping ligand of the ligand-capped Fe 2 O 3 nanoparticles is selected from the group consisting of oleylamine and oleic acid.

8. The method according to claim 1 , wherein the ligand-capped shell material nanoparticles are decanethiolate capped gold nanoparticles.

9. The method according to claim 1 , wherein the core material nanoparticles are magnetic, paramagnetic, or superparamagnetic.

10. The method according to claim 1 , wherein the metal of the core material nanoparticles is selected from the group consisting of iron, magnesium, cobalt, and mixtures thereof.

11. The method according to claim 10 , wherein the metal of the core material nanoparticles is iron.

12. The method according to claim 11 , wherein the core of the core material nanoparticles comprises an iron-oxygen compound selected from the group consisting of Fe 3 O 4 and Fe 2 O 3 .

13. The method according to claim 12 , wherein the core of the core material nanoparticles comprises Fe 2 O 3 .

14. The method according to claim 1 , wherein the metal of the metal shell material nanoparticles is selected from the group consisting of gold, silver, platinum, rhodium, palladium, vanadium, titanium, iron, cobalt, magnesium, ruthenium, chromium, molybdenum, tantalum, zirconium, manganese, tin, and mixtures thereof.

15. The method according to claim 14 , wherein the metal of the metal shell material nanoparticles is gold.

16. The method according to claim 1 , wherein the metal shell material nanoparticles and the metal-containing core material nanoparticles are independently capped with a capping ligand selected from the group consisting of decanethiolate, oleylamine, oleic acid, acrylates, N,N-trimethyl(undecylmercapto)ammonium (TUA), tetrabutylammonium tetrafluoroborate (TBA), tetramethylammonium bromide (TMA), cetyltrimethylammonium bromide (CTAB), citrates, poly methacrylate, ascorbic acid, DNA, 2-mercaptopropionic acid (MPA), 3-mercaptopropionic acid (MPA), 11-mercaptoundecanoic acid (MUA), 10-mercaptodecane-1-sulfonic acid, 16-mercaptohexadecanoic acid, diimide, N-(2-mercaptopropionyl)glycine (tiopronin), 2-mercaptoethanol, 4-mercapto-1-butanol, dodecyl sulfate, amino acids, homocysteine, homocystine, cysteine, cystine, glutathione, mercaptobenzoic acid (MBA), Protein A, bovine serum albumin (BSA), and anti-rabbit-IgG (Ab).

17. The method according to claim 16 , wherein the capping ligand is selected from the group consisting of decanethiolate, oleylamine, and oleic acid.

18. The method according to claim 17 , wherein the capping ligand is decanethiolate.

19. The method according to claim 17 , wherein the capping ligand is oleylamine.

20. The method according to claim 17 , wherein the capping ligand is oleic acid.

21. The method according to claim 1 , wherein the core-shell nanoparticles each comprises a ligand-capped metal shell surrounding a plurality of discrete, non-concentric metal-containing cores.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jun 11, 2015
From: STATE UNIVERSITY OF NEW YORK, BINGHAMTON
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 035890/0244 →
Continuity (3)
Division 12034155 · Feb 20, 2008
Provisional Application 60890699 · Feb 20, 2007
Related Publication 20130071558A1 · Mar 21, 2013