IP Library Granted Patent US 11,637,256
Granted Patent B2
US 11,637,256 · App. 16/546,486 · Granted Apr 25, 2023

Quantum dots with charge-transporting ligands

Inventors: Christian Ippen (Cupertino, CA); Daekyoung Kim (Santa Clara, CA); Emma Rose Dohner (Redwood City, CA); Jesse Manders (Mountain View, CA); David Olmeijer (San Francisco, CA); Ruiqing Ma (Morristown, NJ)
Assignee: Nanosys, Inc.
H01L51/502B82Y40/00C09K11/06H01L51/0035H01L51/5056
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Quick Facts
Patent No.
US 11,637,256
App. No.
16/546,486
Granted
Apr 25, 2023
Kind
B2
Abstract

The present invention provides nanostructure compositions and methods of producing nanostructure compositions. The nanostructure compositions comprise a population of nanostructures comprising charge-transporting ligands. The present invention also provides nanostructure films comprising the nanostructure compositions and methods of making nanostructure films using the nanostructure compositions.

Claims (180)

1. A nanostructure composition comprising:

(a) at least one population of nanostructures; and

(b) at least one charge-transporting ligand bound to the surface of the nanostructures, the charge-transporting ligand comprising:

(i) a hole-transporting ligand of formula (I)

wherein:

R 1 is hydrogen or carboxy;

R 2 is

R 3 is hydrogen;

X 1 -X 8 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

X 9 -X 13 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 4 is an unsubstituted or substituted aryl or heteroaryl group;

X 14 -X 17 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 5 is an unsubstituted or substituted aryl or heteroaryl group;

R 6 is hydrogen; or

R 5 and R 6 together form:

X 18 -X 22 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 7 is an unsubstituted or substituted aryl or heteroaryl group; or

R 2 and R 3 together form:

X 23 -X 26 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 8 is an unsubstituted or substituted aryl or heteroaryl group;

R 9 is an unsubstituted or substituted aryl or heteroaryl group;

R 10 is hydrogen or an unsubstituted or substituted aryl or heteroaryl group; or

R 9 and R 10 together form:

or

(ii) an electron-transporting ligand of formula (X)

wherein:

R 11 is

R 12 is hydrogen or is

R 13 and R 17 independently are a substituted or unsubstituted aryl or heteroaryl group;

R 14 and R 18 independently are hydrogen, or

R 15 and R 19 independently are a substituted or unsubstituted aryl or heteroaryl group;

R 16 and R 20 independently are a substituted or unsubstituted aryl or heteroaryl group;

R 21 is a substituted or unsubstituted aryl or heteroaryl group;

R 22 is a substituted or unsubstituted aryl or heteroaryl group;

R 23 is H or a substituted or unsubstituted aryl or heteroaryl group; and

R 24 is H or a substituted or unsubstituted aryl or heteroaryl group;

or

(iii) a combination thereof.

2. The nanostructure composition of claim 1 , wherein the nanostructures comprise a core selected from the group consisting of InP, InZnP, InGaP, CdSe, CdS, CdSSe, CdZnSe, CdZnS, ZnSe, ZnTe, ZnSeTe, ZnS, ZnSSe, InAs, InGaAs, and InAsP.

3. The nanostructure composition of claim 1 , wherein the nanostructures comprises an InP core, a ZnSe shell, and a ZnS shell.

4. The nanostructure composition of claim 1 , wherein the hole-transporting ligand has formula II:

wherein:

X 1 -X 8 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl; and

R 1 is hydrogen or carboxy.

5. The nanostructure composition of claim 4 , wherein X 1 , X 2 , X 4 , X 5 , X 7 , and X 8 are hydrogen, X 3 and X 6 independently are hydrogen, methyl, tert-butyl, methoxy, dimethylamino, or trifluoromethyl, and R 1 is hydrogen.

6. The nanostructure composition of claim 1 , wherein the hole-transporting ligand has the structure of formula III:

wherein:

X 9 -X 13 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 1 is hydrogen or carboxy; and

R 4 is an unsubstituted or substituted aryl or heteroaryl group.

7. The nanostructure composition of claim 1 , wherein the hole-transporting ligand has the structure of formula IV:

wherein:

X 14 -X 17 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 1 is hydrogen or carboxy;

R 5 is an unsubstituted or substituted aryl or heteroaryl group; and

R 6 is hydrogen.

8. The nanostructure composition of claim 1 , wherein the hole-transporting ligand has the structure of formula V:

wherein:

X 14 -X 17 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl; and

R 1 is hydrogen or carboxy.

9. The nanostructure composition of claim 1 , wherein the hole-transporting ligand has the structure of formula VI:

wherein:

X 18 -X 22 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 1 is hydrogen or carboxy; and

R 7 is an unsubstituted or substituted aryl or heteroaryl group.

10. The nanostructure composition of claim 1 , wherein the hole-transporting ligand has the structure of formula VII:

wherein:

X 23 -X 26 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 1 is hydrogen or carboxy; and

R 8 is an unsubstituted or substituted aryl or heteroaryl group.

11. The nanostructure composition of claim 1 , wherein the hole-transporting ligand has the structure of formula VIII:

wherein:

R 1 is hydrogen or carboxy; and

R 9 is an unsubstituted or substituted aryl or heteroaryl group; and

R 10 is an unsubstituted or substituted aryl or heteroaryl group.

12. The nanostructure composition of claim 1 , wherein the hole-transporting ligand has the structure of formula IX:

wherein:

R 1 is hydrogen or carboxy.

13. The nanostructure composition of claim 1 , wherein the electron-transporting ligand has the structure of formula XII:

14. The nanostructure composition of claim 1 , wherein the electron-transporting ligand has the structure of formula XIII:

wherein:

R 14 is a substituted or unsubstituted aryl or heteroaryl group.

15. The nanostructure composition of claim 1 , wherein the electron-transporting ligand has the structure of formula XIV:

wherein:

R 17 is a substituted or unsubstituted aryl or heteroaryl group.

16. The nanostructure composition of claim 15 , wherein R 17 is an unsubstituted phenyl group.

17. The nanostructure composition of claim 1 , wherein the electron-transporting ligand has the structure of formula XV:

wherein:

R 18 is a substituted or unsubstituted aryl or heteroaryl group.

18. The nanostructure composition of claim 1 , wherein the electron-transporting ligand has the structure of formula XVI:

wherein:

R 19 is a substituted or unsubstituted aryl or heteroaryl group; and

R 20 is a substituted or unsubstituted aryl or heteroaryl group.

19. The nanostructure composition of claim 1 , wherein the electron-transporting ligand has the structure of formula XVIII:

wherein:

R 14 is a substituted or unsubstituted aryl or heteroaryl group; and

R 15 is a substituted or unsubstituted aryl or heteroaryl group.

20. A nanostructure film layer comprising the nanostructure composition of claim 1 .

21. The nanostructure film layer of claim 20 , wherein the at least one population of nanostructures comprises a core selected from the group consisting of InP, InZnP, InGaP, CdSe, CdS, CdSSe, CdZnSe, CdZnS, ZnSe, ZnTe, ZnSeTe, ZnS, ZnSSe, InAs, InGaAs, and InAsP.

22. A method of replacing a first ligand on a nanostructure with a second ligand, the method comprising admixing a reaction mixture comprising a population of nanostructures having the first ligand bound to the nanostructure and a charge-transporting ligand which is the second ligand, such that the second ligand displaces the first ligand and becomes bound to the nanostructure, wherein the charge-transporting ligand comprises:

(i) a hole-transporting ligand of formula (I)

wherein:

R 1 is hydrogen or carboxy;

R 2 is

R 3 is hydrogen;

X 1 -X 8 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

X 9 -X 13 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 4 is an unsubstituted or substituted aryl or heteroaryl group;

X 14 -X 17 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 5 is an unsubstituted or substituted aryl or heteroaryl group;

R 6 is hydrogen; or

R 5 and R 6 together form:

X 18 -X 22 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 7 is an unsubstituted or substituted aryl or heteroaryl group;

or

R 2 and R 3 together form:

X 23 -X 26 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 8 is an unsubstituted or substituted aryl or heteroaryl group;

R 9 is an unsubstituted or substituted aryl or heteroaryl group;

R 10 is hydrogen or an unsubstituted or substituted aryl or heteroaryl group; or

R 9 and R 10 together form:

or

(ii) an electron-transporting ligand of formula (X)

wherein:

R 11 is

R 12 is hydrogen or is

R 13 and R 17 independently are a substituted or unsubstituted aryl or heteroaryl group;

R 14 and R 18 independently are hydrogen, or

R 15 and R 19 independently are a substituted or unsubstituted aryl or heteroaryl group;

R 16 and R 20 independently are a substituted or unsubstituted aryl or heteroaryl group;

R 21 is a substituted or unsubstituted aryl or heteroaryl group;

R 22 is a substituted or unsubstituted aryl or heteroaryl group;

R 23 is H or a substituted or unsubstituted aryl or heteroaryl group; and

R 24 is H or a substituted or unsubstituted aryl or heteroaryl group;

or

(iii) a combination thereof.

23. A light emitting diode comprising:

(a) a first conductive layer;

(b) a second conductive layer; and

(c) an emitting layer between the first conductive layer and the second conductive layer, wherein the emitting layer comprises at least one population of nanostructures comprising a charge-transporting ligand bound to the nanostructures, wherein the charge-transporting ligand comprises:

(i) a hole-transporting ligand of formula (I)

wherein:

R 1 is hydrogen or carboxy;

R 2 is

X 1 -X 8 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

X 9 -X 13 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 4 is an unsubstituted or substituted aryl or heteroaryl group;

X 14 -X 17 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 5 is an unsubstituted or substituted aryl or heteroaryl group;

R 6 is hydrogen; or

R 5 and R 6 together form:

X 18 -X 22 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 7 is an unsubstituted or substituted aryl or heteroaryl group;

or

R 2 and R 3 together form:

X 23 -X 26 independently are hydrogen, carboxy, C 1-10 alkyl, C 1-10 alkoxy, C 1-10 haloalkyl, halogen, C 1-10 alkylamino, or cycloalkyl;

R 8 is an unsubstituted or substituted aryl or heteroaryl group;

R 9 is an unsubstituted or substituted aryl or heteroaryl group;

R 10 is hydrogen or an unsubstituted or substituted aryl or heteroaryl group; or

R 9 and R 10 together form:

or

(ii) an electron-transporting ligand of formula (X)

wherein:

R 11 is

is hydrogen or is

R 13 and R 17 independently are a substituted or unsubstituted aryl or heteroaryl group;

R 14 and R 18 independently are hydrogen, or

R 15 and R 19 independently are a substituted or unsubstituted aryl or heteroaryl group;

R 16 and R 20 independently are a substituted or unsubstituted aryl or heteroaryl group;

R 21 is a substituted or unsubstituted aryl or heteroaryl group;

R 22 is a substituted or unsubstituted aryl or heteroaryl group;

R 23 is H or a substituted or unsubstituted aryl or heteroaryl group; and

R 24 is H or a substituted or unsubstituted aryl or heteroaryl group;

or

(iii) a combination thereof.

24. The light emitting diode of claim 23 , wherein the at least one population of nanostructures comprises a core selected from the group consisting of InP, InZnP, InGaP, CdSe, CdS, CdSSe, CdZnSe, CdZnS, ZnSe, ZnTe, ZnSeTe, ZnS, ZnSSe, InAs, InGaAs, and InAsP.

25. The light emitting diode of claim 23 , wherein the first conductive layer comprises indium tin oxide, indium zinc oxide, tin dioxide, zinc oxide, magnesium, aluminum, aluminum-lithium, calcium, magnesium-indium, magnesium-silver, silver, gold, or mixtures thereof.

26. The light emitting diode of claim 23 , wherein the second conductive layer comprises indium tin oxide, indium zinc oxide, titanium dioxide, tin oxide, zinc sulfide, silver, or mixtures thereof.

27. The light emitting diode of claim 23 , wherein the first conductive layer comprises indium tin oxide, the second conductive layer comprises aluminum, further comprising a semiconductor polymer layer, wherein the semiconductor polymer layer comprises PEDOT/PSS, further comprising a first transport layer, wherein the first transport layer comprises N,N′-di(naphthalen-1-yl)-N,N′-bis(4-vinylphenyl)-4,4′-diamine, and further comprising a second transport layer, wherein the second transport layer comprises ZnMgO.

28. The light emitting diode of claim 23 , wherein the first conductive layer comprises indium tin oxide, the second conductive layer comprises gold, further comprising a semiconductor polymer layer, wherein the semiconductor polymer layer comprises PEDOT/PSS, and further comprising a first transport layer, wherein the first transport layer comprises N,N′-di(naphthalen-1-yl)-N,N′-bis(4-vinylphenyl)-4,4′-diamine.

Assignments (5)
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 →
TERMINATION AND RELEASE OF PATENT SECURITY AGREEMENT RECORDED AT REEL 059569 / FRAME 0840 Recorded Sep 7, 2023
From: FORTRESS CREDIT CORP.,
To: NANOSYS, INC.
Reel/Frame 064836/0263 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2023
From: IPPEN, CHRISTIAN; KIM, DAEKYOUNG; DOHNER, EMMA ROSE; MANDERS, JESSE; OLMEIJER, DAVID; MA, RUIQUING
To: NANOSYS, INC.
Reel/Frame 062481/0310 →
SECURITY INTEREST Recorded Apr 1, 2022
From: NANOSYS, INC.
To: FORTRESS CREDIT CORP., AS AGENT
Reel/Frame 059569/0840 →