IP Library Granted Patent US 11,760,926
Granted Patent B2
US 11,760,926 · App. 16/742,875 · Granted Sep 19, 2023

Quantum dot, curable composition comprising the same, cured layer using the composition, color filter including the cured layer, and display device including the cured layer

Inventors: Yonghee Kang (Suwon-si, KR); Jonggi Kim (Suwon-si, KR); Dongjun Kim (Suwon-si, KR); Misun Kim (Suwon-si, KR); Minjee Park (Suwon-si, KR); Bumjin Lee (Suwon-si, KR); Jihyeon Yim (Suwon-si, KR); Mi Jeong Choi (Suwon-si, KR)
Assignee: Samsung SDI Co., Ltd.
C09K11/025C08F220/18G02B5/20B82Y20/00B82Y40/00G02B2207/101
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Quick Facts
Patent No.
US 11,760,926
App. No.
16/742,875
Granted
Sep 19, 2023
Kind
B2
Abstract

A quantum dot surface-modified with a specific compound, a non-solvent curable composition including the quantum dot, a solvent based curable composition including the quantum dot, a cured layer manufactured utilizing the curable composition, a color filter including the cured layer, and a display device including the cured layer are disclosed.

Claims (65)

1. A quantum dot surface-modified with a compound represented by Chemical Formula 1:

wherein, in Chemical Formula 1,

R 1 is a substituted or unsubstituted C1 to C10 alkyl group or a substituted or unsubstituted C6 to C20 aryl group,

L 1 to L 3 are each independently a substituted or unsubstituted C1 to C10 alkylene group, an ester group, or an ether group, and

n is an integer of 3 to 20,

provided that when L 2 is an ester group and when L 3 is an unsubstituted C7 to C10 alkylene group:

n is an integer of 4 to 20,

provided that when L 2 is an ester group and when L 3 is an unsubstituted C1 to C6 alkylene group:

n is an integer of 4 to 20 and R 1 is selected from the group consisting of a substituted or unsubstituted C11 to C20 aryl group, a moiety represented by Formula 3-1, and a moiety represented by Formula 3-2, and

provided that when L 2 is a substituted or unsubstituted C1 to C10 alkylene group or an ether group and when L 3 is a substituted or unsubstituted C2 alkylene group:

L 1 is an ester group or an ether group, or R 1 is a substituted or unsubstituted C15 to C20 aryl group:

wherein in Formulae 3-2 and 3-2, * represents a binding site to a neighboring oxygen atom.

2. The quantum dot of claim 1 , wherein

L 1 and L 3 are each independently a substituted or unsubstituted C1 to C10 alkylene group, and

L 2 is an ester group or an ether group.

3. The quantum dot of claim 1 , wherein the quantum dot has a maximum fluorescence emission wavelength at about 500 nm to about 680 nm.

4. A quantum dot surface-modified with a compound represented by Chemical Formula 1:

wherein, in Chemical Formula 1,

R 1 is a substituted or unsubstituted C1 to C10 alkyl group or a substituted or unsubstituted C6 to C20 aryl group,

L 1 to L 3 are each independently a substituted or unsubstituted C1 to C10 alkylene group, an ester group, or an ether group, and

n is an integer of 3 to 20,

provided that when L 2 is an ester group and when L 3 is an unsubstituted C7 to C10 alkylene group:

n is an integer of 4 to 20,

provided that when L 2 is an ester group and when L 3 is an unsubstituted C1 to C6 alkylene group:

n is an integer of 4 to 20 and R 1 is selected from the group consisting of a substituted or unsubstituted C11 to C20 aryl group, a moiety represented by Formula 3-1, and a moiety represented by Formula 3-2, and

provided that when L 2 is a substituted or unsubstituted C1 to C10 alkylene group or an ether group and when L 3 is a substituted or unsubstituted C2 alkylene group:

L 1 is an ester group or an ether group, or R 1 is a substituted or unsubstituted C15 to C20 aryl group:

wherein in Formulae 3-2 and 3-2, * represents a binding site to a neighboring oxygen atom,

wherein the compound represented by Chemical Formula 1 comprises at least one selected from compounds represented by Chemical Formula 1-4 to Chemical Formula 1-5:

5. A non-solvent curable composition comprising

a quantum dot surface-modified with a compound represented by Chemical Formula 1,

a polymerizable monomer having a carbon-carbon double bond at a terminal end, and

a light diffusing agent,

wherein the polymerizable monomer is about 35 wt % to about 80 wt % in amount based on a total weight of the non-solvent curable composition, and

the non-solvent curable composition does not contain any solvent:

wherein, in Chemical Formula 1,

R 1 is a substituted or unsubstituted C1 to C10 alkyl group or a substituted or unsubstituted C6 to C20 aryl group,

L 1 to L 3 are each independently a substituted or unsubstituted C1 to C10 alkylene group, an ester group, or an ether group, and

n is an integer of 3 to 20,

provided that when L 2 is an ester group and when L 3 is an unsubstituted C7 to C10 alkylene group:

n is an integer of 4 to 20, and

provided that when L 2 is an ester group and when L 3 is an unsubstituted C1 to C6 alkylene group:

n is an integer of 4 to 20 and R 1 is selected from the group consisting of a substituted or unsubstituted C11 to C20 aryl group, a moiety represented by Formula 3-1, and a moiety represented by Formula 3-2:

wherein in Formulae 3-2 and 3-2, * represents a binding site to a neighboring oxygen atom.

6. The non-solvent curable composition of claim 5 , wherein the polymerizable monomer has a molecular weight of about 220 g/mol to about 1,000 g/mol.

7. The non-solvent curable composition of claim 5 , wherein the polymerizable monomer is represented by Chemical Formula 2:

wherein, in Chemical Formula 2,

R 2 and R 3 are each independently a hydrogen atom or a substituted or unsubstituted C1 to C10 alkyl group,

L 4 and L 6 are each independently a substituted or unsubstituted C1 to C10 alkylene group, and

L 5 is a substituted or unsubstituted C1 to C10 alkylene group or an ether group.

8. The non-solvent curable composition of claim 5 , wherein the quantum dot is about 1 wt % to about 60 wt % in amount based on the total weight of the non-solvent curable composition.

9. The non-solvent curable composition of claim 5 , wherein the light diffusing agent comprises barium sulfate, calcium carbonate, titanium dioxide, zirconia, or a combination thereof.

10. The non-solvent curable composition of claim 5 , wherein the non-solvent curable composition further comprises a polymerization initiator.

11. The non-solvent curable composition of claim 5 , wherein the non-solvent curable composition further comprises a polymerization inhibitor; malonic acid; 3-amino-1,2-propanediol; a silane-based coupling agent; a leveling agent; a fluorine-based surfactant; or a combination thereof.

12. A solvent based curable composition comprising the quantum dot of claim 1 ;

a binder resin; and

a solvent.

13. The solvent based curable composition of claim 12 , further comprising a polymerizable monomer, a polymerization initiator, a light diffusing agent, or a combination thereof.

14. The solvent based curable composition of claim 12 , wherein the solvent based curable composition is a photosensitive resin composition.

15. A curing layer manufactured utilizing the composition of claim 5 .

16. A curing layer manufactured utilizing the composition of claim 12 .

17. A color filter comprising the cured layer of claim 15 .

18. A color filter comprising the cured layer of claim 16 .

19. A display device comprising the color filter of claim 17 .

20. A display device comprising the color filter of claim 18 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 12, 2020
From: KANG, YONGHEE; KIM, JONGGI; KIM, DONGJUN; KIM, MISUN; PARK, MINJEE; LEE, BUMJIN; YIM, JIHYEON; CHOI, MI JEONG
To: SAMSUNG SDI CO., LTD.
Reel/Frame 052098/0551 →
Priority Claims (1)
KR 10-2019-0091233 · Jul 26, 2019 · national
Continuity (1)
Related Publication 20210024819A1 · Jan 28, 2021
Cited By (1)
US 12,410,365