Quantum dot, curable composition comprising the same, cured layer using the composition, and color filter including the cured layer
US-2022213380-A1 · Jul 7, 2022 · US
US11760926B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11760926-B2 |
| Application number | US-202016742875-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 14, 2020 |
| Priority date | Jul 26, 2019 |
| Publication date | Sep 19, 2023 |
| Grant date | Sep 19, 2023 |
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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.
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What is claimed is: 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 .
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containing inorganic luminescent materials · CPC title
Photosensitive materials (G03F7/12, G03F7/14 take precedence) · CPC title
Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds (G03F7/075 takes precedence) · CPC title
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