IP Library Granted Patent US 11,552,223
Granted Patent B2
US 11,552,223 · App. 17/332,765 · Granted Jan 10, 2023

Quantum dot films utilizing multi-phase resins

Inventors: Cong-Duan Vo (Manchester, GB); Imad Naasani (Manchester, GB); Amilcar Pillay Narrainen (Manchester, GB)
Assignee: Nanoco Technologies, Ltd.
H01L33/504B32B37/24C09K11/02C09K11/703H01L33/502B32B2037/243B32B2307/418B32B2307/7242B82Y20/00Y10T156/10
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Quick Facts
Patent No.
US 11,552,223
App. No.
17/332,765
Granted
Jan 10, 2023
Kind
B2
Abstract

Multi-phase polymer films containing quantum dots (QDs) are described herein. The films have domains of primarily hydrophobic polymer and domains of primarily hydrophilic polymer. QDs, being generally more stable within a hydrophobic matrix, are dispersed primarily within the hydrophobic domains of the films. The hydrophilic domains tend to be effective at excluding oxygen.

Claims (23)

1. A method of preparing a film, the method comprising:

dispersing a population of quantum dots in a first resin to form a quantum dot dispersion;

mixing the quantum dot dispersion in a second resin to form an emulsion comprising the quantum dot dispersion suspended in the second resin;

depositing the emulsion between gas barrier sheets to form a film; and

curing the first resin and the second resin to form a solid film.

2. The method of claim 1 , wherein the first resin is a resin monomer.

3. The method of claim 2 , wherein the wherein the resin monomer is selected from the group consisting of methyl(meth)acrylate, ethyl(meth)acrylate, n-propyl(meth)acrylate, butyl(meth)acrylate, n-pentyl(meth)acrylate, n-hexyl(meth)acrylate, cyclohexyl(meth)acrylate, 2-ethyl hexyl(meth)acrylate, octyl(meth)acrylate, isooctyl(meth)acrylate, n-decyl(meth)acrylate, isodecyl(meth)acrylate, lauryl(meth)acrylate, hexadecyl(meth)acrylate, octadecyl(meth)acrylate, isobornyl(meth)acrylate, isobutylene, styrene, divinyl benzene, vinyl acetate, isoprene, carbonate, acrylonitrile, a hydrophobic cellulose, a silicone monomer, dimethyl siloxane, vinyl ether, and polyester precursors.

4. The method of claim 2 , wherein the resin monomer further comprises a crosslinker.

5. The method of claim 4 , wherein resin monomer is lauryl methacrylate and the crosslinker is trimethylolpropane trimethacrylate.

6. The method of claim 2 , wherein the resin monomer is lauryl methacrylate and the second resin is an epoxy-based resin or a polyurethane acrylate resin.

7. The method of claim 1 , wherein the second resin is curable using ultraviolet (UV) light.

8. The method of claim 1 , wherein the second resin is selected from the group consisting of an epoxy-based resin, a polyurethane-based resin, a hydrophilic (meth)acrylate, a polyvinyl alcohol, a poly(ethylene-co-vinyl alcohol), a polyvinyl dichloride, a silicone, a polyimide, a polyester, a polyvinyl, a polyamide, an enphenolic, a cyanoacrylate, gelatin, a sodium silicate, and a poly(vinylpyrrolidone) (PVP).

9. The method of claim 1 , wherein the emulsion further comprises one or more of a photoinitiator, a cross-linking agent, a polymerization catalyst, a surfactant and an emulsifying agent.

10. The method of claim 1 , wherein the first resin is a resin polymer.

11. The method of claim 10 , wherein the resin polymer is selected from the group consisting of a poly(methyl(meth)acrylate), a poly(ethyl(meth)acrylate), a poly(n-propyl(meth)acrylate), a poly(butyl(meth)acrylate), a poly(n-pentyl(meth)acrylate), a poly(n-hexyl(meth)acrylate), a poly(cyclohexyl(meth)acrylate), a poly(2-ethyl hexyl(meth)acrylate), a poly(octyl(meth)acrylate), a poly(isooctyl(meth)acrylate), a poly(n-decyl(meth)acrylate), a poly(isodecyl(meth)acrylate), a poly(lauryl(meth)acrylate), a poly(hexadecyl(meth)acrylate), a poly(octadecyl(meth)acrylate), a poly(isobornyl(meth)acrylate), a poly(isobutylene), a polystyrene, a poly(divinyl benzene), a polyvinyl acetate, a polyisoprene, a polycarbonate, a polyacrylonitrile, a hydrophobic cellulose based polymer, a silicone resin, a poly(dimethyl siloxane), a poly(vinyl ether), and a polyester.

12. The method of claim 11 , wherein the resin polymer is a poly(lauryl(meth)acrylate).

13. The method of claim 1 , wherein the second resin is a resin monomer.

14. The method of claim 13 , wherein the resin monomer is glycidyl methacrylate, the glycidyl methacrylate dissolved in polyvinylidene chloride.

15. The method of claim 1 , wherein the second resin is a resin polymer.

16. The method of claim 2 , wherein the second resin is a resin monomer.

17. The method of claim 10 , wherein the second resin is a resin monomer.

18. The method of claim 2 , wherein the second resin is a resin polymer.

19. The method of claim 10 , wherein the second resin is a resin polymer.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE PREVIOUSLY RECORDED ON REEL 062977 FRAME 0157. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT OF ASSIGNORS INTEREST. Recorded Jul 13, 2023
From: NANOCO TECHNOLOGIES LTD
To: SAMSUNG ELECTRONICS CO., LTD.
Reel/Frame 064273/0340 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2023
From: NANOCO TECHNOLOGIES LTD
To: SAMSUNG ELECTRONICS CO. LTD
Reel/Frame 062977/0157 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 27, 2022
From: VO, CONG-DUAN; NAASANI, IMAD; PILLAY NARRAINEN, AMILCAR
To: NANOCO TECHNOLOGIES, LTD
Reel/Frame 062214/0908 →
Continuity (4)
Continuation 15618863 · Jun 9, 2017
Continuation 14460008 · Aug 14, 2014
Provisional Application 61865692 · Aug 14, 2013
Related Publication 20210288229A1 · Sep 16, 2021