IP Library Granted Patent US 11,926,776
Granted Patent B2
US 11,926,776 · App. 17/846,357 · Granted Mar 12, 2024

Films comprising bright silver based quaternary nanostructures

Inventors: Ravisubhash Tangirala (Fremont, CA); Jay Yamanaga (Campbell, CA); Wenzhou Guo (San Jose, CA); Christopher Sunderland (San Jose, CA); Ashenafi Damtew Mamuye (Milpitas, CA); Chunming Wang (Milpitas, CA); Eunhee Hwang (Suwon-si, KR); Nahyoung Kim (Incheon, KR)
Assignee: SHOEI CHEMICAL INC.
C09K11/621C08J5/18C09K11/025G02B1/002G02F1/133603G02F1/133614B82Y20/00B82Y30/00B82Y40/00C08J2329/10G02F2202/36
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Quick Facts
Patent No.
US 11,926,776
App. No.
17/846,357
Granted
Mar 12, 2024
Kind
B2
Abstract

Disclosed are films comprising Ag, In, Ga, and S (AIGS) nanostructures and at least one ligand bound to the nanostructures. In some embodiment, the AIGS nanostructures have a photon conversion efficiency of greater than 32% and a peak wavelength emission of 480-545 nm. In some embodiments, the nanostructures have an emission spectrum with a FWHM of 24-38 nm.

Claims (32)

1. A method of preparing a film comprising Ag, In, Ga, and S (AIGS) nanostructures, comprising:

admixing at least one organic resin with AIGS nanostructures and at least one ligand to form an admixture;

preparing a first film comprising the admixture on a first barrier layer;

curing the film by UV irradiation and/or baking; and

encapsulating the first film between the first barrier layer and a second barrier layer;

wherein the encapsulated film exhibits a photon conversion efficiency (PCE) of greater than 32% at a peak emission wavelength of about 480-545 nm, when excited using a blue light source with a wavelength of about 450 nm;

wherein the nanostructures have an emission spectrum with a full width half maximum (FWHM) of less than 40 nm, and wherein the average diameter of the nanostructures is less than 10 nm by TEM.

2. The method of claim 1 , further comprising:

addition of at least one oxygen reactive material to the admixture,

forming a second film comprising at least one oxygen reactive material on top of the first film; or

forming a sacrificial barrier layer on the first film that temporarily blocks oxygen and/or water; measuring the PCE of the film, then removing the sacrificial barrier layer.

3. The method of claim 1 , wherein the method is configured to yield a film comprising AIGS nanostructures having an emission spectrum with a FWHM of 24-38 nm.

4. The method of claim 1 , wherein the method is configured to yield a film comprising AIGS nanostructures having a quantum yield (QY) of 80-99.9%.

5. The method of claim 4 , wherein the method is configured to yield a film comprising AIGS nanostructures having a QY of 85-95%.

6. The method of claim 1 , wherein the method is configured to yield a film comprising AIGS nanostructures having an OD 450 /mass greater than or equal to 0.8 mL mg −1 cm −1 , where OD 450 is the optical density of the film when irradiated with electromagnetic energy having of wavelength of 450 nm.

7. The method of claim 6 , wherein the method is configured to yield a film comprising AIGS nanostructures have an OD 450 /mass in the inclusive range 0.8-2.5 mL mg −1 cm −1 .

8. The method of claim 1 , wherein the method is configured to yield a film comprising AIGS nanostructures have an average diameter of about 5 nm.

9. The method of claim 1 , wherein the method is configured to yield a film comprising AIGS nanostructures such that at least about 80% of the emission is band-edge emission.

10. The method of claim 9 , wherein the method is configured to yield a film comprising AIGS nanostructures such that 92-98% of the emission is band-edge emission.

11. The method of claim 1 , wherein the admixing at least one ligand comprises admixing a polyamino ligand.

12. The method of claim 11 , wherein the admixing a polyamino ligand comprises admixing a polyamino alkane, a polyamino-cycloalkane, a polyamino heterocyclic compound, a polyamino functionalized silicone, or a polyamino substituted ethylene glycol.

13. The method of claim 11 , wherein the admixing a polyamino ligand comprises admixing a C 2-20 alkane or C 2-20 cycloalkane substituted by two or three amino groups and optionally containing one or two amino groups in place of a carbon group.

14. The method of claim 13 , wherein the admixing a polyamino ligand comprises admixing 1,3-cyclohexanebis(methylamine), 2,2-dimethyl-1,3-propanediamine, tris(2-aminoethyl)amine, or 2-methyl-1,5-diaminopentane.

15. The method of claim 1 , wherein the admixing at least one ligand comprises admixing a compound of Formula I:

wherein:

x is 1 to 100;

y is 0 to 100; and

R 2 is C 1-20 alkyl.

16. The method of claim 15 , wherein x=19, y=3, and R 2 ═—CH 3 .

17. The method of claim 1 , wherein the admixing a polyamino ligand comprises admixing (3-aminopropyl)trimethoxysilane); (3-mercaptopropyl)triethoxysilane; DL-α-lipoic acid; 3,6-dioxa-1,8-octanedithiol; 6-mercapto-1-hexanol; methoxypolyethylene glycol amine; poly(ethyleneglycol) methyl ether thiol; diethyl phenylphosphonite; dibenzyl N,N-diisopropylphosphoramidite; di-tert-butyl N,N-diisopropylphosphoramidite; tris(2-carboxyethyl)phosphine hydrochloride; poly(ethylene glycol) methyl ether thiol; methoxypolyethylene glycol amine; acrylamide; or polyethylenimine.

18. The method of claim 1 , wherein the admixing a polyamino ligand comprises admixing a combination of amino-polyalkylene oxide and methoxypolyethylene glycol amine; amino-polyalkylene oxide and 6-mercapto-1-hexanol; amino-polyalkylene oxide and (3-mercaptopropyl)triethoxysilane; or 6-mercapto-1-hexanol and methoxypolyethylene glycol amine.

19. The method of claim 1 , wherein the method is configured to yield a film that is 5-15 μm thick.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2023
From: TANGIRALA, RAVISUBHASH; YAMANAGA, JAY; GUO, WENZHOU; SUNDERLAND, CHRISTOPHER; MAMUYE, ASHENAFI DAMTEW; WANG, CHUNMING; HWANG, EUNHEE; KIM, NAHYOUNG
To: NANOSYS, INC.
Reel/Frame 065422/0037 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ADDRESS OF THE ASSIGNEE TO BE: 2-1-1, NISHI-SHINJUKU SHINJUKU-KU TOKYO, JAPAN 163-0043 PREVIOUSLY RECORDED AT REEL: 065114 FRAME: 0769. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Oct 9, 2023
From: NANOSYS, INC.
To: SHOEI CHEMICAL INC.
Reel/Frame 065271/0540 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2023
From: NANOSYS, INC.
To: SHOEI CHEMICAL INC.
Reel/Frame 065114/0769 →