IP Library Granted Patent US 8,496,844
Granted Patent B1
US 8,496,844 · App. 13/645,876 · Granted Jul 30, 2013

Ion etching of growing InP nanocrystals using microwave

Inventors: Geoffrey F. Strouse (Tallahassee, FL); Derek D. Lovingood (Tallahassee, FL)
Assignee: The Florida State University Research Foundation, Inc.
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Quick Facts
Patent No.
US 8,496,844
App. No.
13/645,876
Granted
Jul 30, 2013
Kind
B1
Abstract

High quantum yield InP nanocrystals are used in the bio-technology, bio-medical, and photovoltaic, specifically IV, III-V and III-VI nanocrystal technological applications. InP nanocrystals typically require post-generation HF treatment. Combining microwave methodologies with the presence of a fluorinated ionic liquid allows Fluorine ion etching without the hazards accompanying HF. Growing the InP nanocrystals in the presence of the ionic liquid allows in-situ etching to be achieved. The optimization of the PL QY is achieved by balancing growth and etching rates in the reaction.

Claims (36)

1. A method of producing nanoparticles exhibiting enhanced photoluminescence quantum yield comprising the steps of:

providing stock solutions of Group III-VI elements;

providing an ionic liquid containing an anion that thermally degrades to form an ion etchant, wherein the anion is BF 4 , PF 6 , F, ClO 4 , PO 4 , chloride, bromide, acetate, or hydroxide;

placing the ionic liquid into a microwave reactor vessel;

dissolving the stock solutions of Group III-VI elements in a solute and injecting the resulting solution into the microwave reactor vessel;

subjecting the solutions in the microwave reactor vessel to microwave irradiation, wherein the microwave irradiation degrades the anion of the ionic liquid into an etchant;

where the etchant is F − , Cl − , Br − , or O − ;

wherein the microwave irradiation is ramped at 300 W for between 1 minute and 25 minutes;

allowing the stock solutions of Group III-VI elements to form nanoparticles, wherein the nanoparticles are etched in situ by the etchant during nanoparticle growth; and

collecting the resulting nanoparticles.

2. The method of claim 1 , wherein the ionic liquid comprises 1-hexyl-3-methyl-imidazolium, 1-butyl-4-methyl-pyridinium, tetrabutylammonium, or their derivatives.

3. The method of claim 2 , wherein the ionic liquid is used at a molar concentration ratio between 1:1 and 1:10, stock solutions of Group III-VI elements to ionic liquid.

4. The method of claim 1 , wherein the resulting nanoparticles are collected by using at least one compound selected from the group consisting of toluene, acetone, and methanol.

5. The method of claim 1 , further comprising the step of cooling the reaction site after formation of the nanoparticles using forced air cooling.

6. The method of claim 1 , wherein stock solutions of Group III-VI elements are indium, indium palmitate, tris-trimethylsilylphosphine, gallium, nitrogen phosphorus, arsenic, or antimony; and

the stock solutions of Group III-VI elements cadmium, zinc, seleium, tellurium, sulfur, or oxygen.

7. The method of claim 6 , wherein stock solutions of Group III-VI elements consist of indium palmitate and tris-trimethylsilylphosphine.

8. The method of claim 1 , wherein the nanoparticles consist of GeS, GeSe, GeTe, SnS, SnSe, SnTe, PbS, PbSe, PbTe, MN, AlP, AlAs, AlSb, GaN, GaP GaAs, GaSb, InN, InP, InAs, InSb, GaS, GaSe, GaTe, InS, InSe, InTe, TlS, TlSe, TlTe, ZnS, ZnSe, ZnTe, CdS, CdSe, CdTe, HgS, HgSe, HgTe, As 2 S 3 , As 4 S 4 , As 2 Se 3 , As 2 Te 3 , Sb 2 S 3 , Sb 2 Se 3 , Sb 2 Te 3 , Bi 2 S 3 , Bi 2 Se 3 , Bi 2 Te 3 , CuO, Cu 2 O, Ag 2 S, CuSe, CuCl, AgBr, AuCl, NiS 2 , PdS, PtSe, CoSe, RhS, IrSe, FeO, FeS, FeSe, RuS, MnO, MnS, MnSe, ReS, Cr 2 S 3 , Cr 2 Se 3 , MoS 2 , VS, VSe, NbS, TiO 2 , TiS 2 , ZrS 2 , BeO, MgS, CaSe, or BaTiO 3 .

9. A method of etching nanoparticles comprising the steps of:

providing stock solutions of Group III-VI elements;

providing an ionic liquid containing an anion that thermally degrades to form an ion etchant, wherein the anion is BF 4 PF 6 , F, ClO 4 , PO 4 , chloride, bromide, acetate, or hydroxide;

placing the ionic liquid into a microwave reactor vessel;

dissolving the stock solutions of Group III-VI elements in a solute and injecting the resulting solution into the microwave reactor vessel;

subjecting the solutions in the microwave reactor vessel to microwave irradiation, wherein the microwave irradiation degrades the anion of the ionic liquid into an etchant;

where the etchant is F − , Cl − , Br − , or O − ;

wherein the microwave irradiation is ramped at 300 W for between 1 minute and 25 minutes;

allowing the stock solutions of Group III-VI elements to form nanoparticles, wherein the nanoparticles are etched in situ by the etchant; and

collecting the resulting nanoparticles.

10. The method of claim 9 , wherein the ionic liquid comprises 1-hexyl-3-methyl-imidazolium, 1-butyl-4-methyl-pyridinium, tetrabutylammonium, or their derivatives.

11. The method of claim 9 , wherein the ionic liquid is used at a molar concentration ratio between 1:1 and 1:10, stock solutions of Group III-VI elements to ionic liquid.

12. The method of claim 9 , wherein the resulting nanoparticles are collected by using at least one compound selected from the group consisting of toluene, acetone, and methanol.

13. The method of claim 9 , further comprising the step of cooling the reaction site after reaction completion using forced air cooling.

14. The method of claim 9 , wherein stock solutions of Group III-VI IV-VI elements are compounds selected from the group consisting of indium, gallium, nitrogen phosphorus, arsenic, indium palmitate, tris-trimethylsilylphosphine, and antimony; and

wherein the stock solutions of Group III-VI elements are cadmium, zinc, seleium, tellurium, sulfur, or oxygen.

15. The method of claim 14 , wherein stock solutions of Group III-VI elements further consist of indium palmitate and tris-trimethylsilylphosphine.

16. The method of claim 9 , wherein the nanoparticles consist of GeS, GeSe, GeTe, SnS, SnSe, SnTe, PbS, PbSe, PbTe, AlN, AlP, AlAs, AlSb, GaN, GaP GaAs, GaSb, InN, InP, InAs, InSb, GaS, GaSe, GaTe, InS, InSe, InTe, TlS, TlSe, TlTe, ZnS, ZnSe, ZnTe, CdS, CdSe, CdTe, HgS, HgSe, HgTe, As 2 S 3 , As 4 S 4 , As 2 Se 3 , As 2 Te 3 , Sb 2 S 3 , Sb 2 Se 3 , Sb 2 Te 3 , Bi 2 S 3 , Bi 2 Se 3 , Bi 2 Te 3 , CuO, Cu 2 O, Ag 2 S, CuSe, CuCl, AgBr, AuCl, NiS 2 , PdS, PtSe, CoSe, RhS, IrSe, FeO, FeS, FeSe, RuS, MnO, MnS, MnSe, ReS, Cr 2 S 3 , Cr 2 Se 3 , MoS 2 , VS, VSe, NbS, TiO 2 , TiS 2 , ZrS 2 , BeO, MgS, CaSe, or BaTiO 3 .

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 23, 2017
From: FLORIDA STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041069/0896 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2013
From: STROUSE, GEOFFREY F.; LOVINGOOD, DEREK D.
To: THE FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC.
Reel/Frame 029739/0561 →
Continuity (2)
Continuation 12201589 · Aug 29, 2008
Provisional Application 61079478 · Jul 10, 2008