Light conversion film and image display device
US-2020264461-A1 · Aug 20, 2020 · US
US11762289B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11762289-B2 |
| Application number | US-201816155691-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 9, 2018 |
| Priority date | Oct 27, 2017 |
| Publication date | Sep 19, 2023 |
| Grant date | Sep 19, 2023 |
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A photosensitive resin composition includes: (A) a binder resin; (B) a photopolymerizable monomer; (C) a photopolymerization initiator; (D) a quantum dot surface-modified with a compound having a thiol group at one terminal end and an alkoxy group, a cycloalkyl group, a carboxyl group, or a hydroxy group at the other terminal end; and (E) a solvent. A curable composition includes: (A′) a resin; (B′) a quantum dot surface-modified with a compound represented by Chemical Formula 1 or Chemical Formula 2; and (C′) a solvent. A method of manufacturing the surface-modified quantum dot, and a color filter manufactured using the photosensitive resin composition or the curable composition are also disclosed.
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What is claimed is: 1. A curable composition comprising: (A′) a resin; (B′) a quantum dot surface-modified with a compound represented by Chemical Formula 1 or Chemical Formula 2; and (C′) a solvent: wherein, in Chemical Formula 1 and Chemical Formula 2, R 1 is a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C1 to C20 alkoxy group, a substituted or unsubstituted C3 to C20 cycloalkyl group, a substituted or unsubstituted C6 to C20 aryl group, or a substituted or unsubstituted lactone ring, L 1 and L 2 are independently a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C1 to C20 oxyalkylene group, or a combination thereof, and n is an integer of 1 or 2, and wherein the curable composition comprises 1 wt % to 30 wt % of the resin, 1 wt % to 40 wt % of the surface-modified quantum dot, and 20 wt % to 80 wt % of the solvent based on the total amount of the curable composition, and wherein the curable composition further comprises a diffusion agent. 2. The curable composition of claim 1 , wherein the lactone ring is a 5-membered ring or a 6-membered ring. 3. The curable composition of claim 1 , wherein in Chemical Formula 2, L 2 is a C1 to C20 alkylene group substituted with a thiol group. 4. The curable composition of claim 1 , wherein the substituted or unsubstituted C1 to C20 oxyalkylene group is a substituted or unsubstituted oxymethylene group, a substituted or unsubstituted oxyethylene group, or a combination thereof. 5. The curable composition of claim 4 , wherein the oxymethylene group is represented by Chemical Formula 3 and the oxyethylene group is represented by Chemical Formula 4: wherein, in Chemical Formula 3 and Chemical Formula 4, m is an integer of 1 to 5. 6. The curable composition of claim 1 , wherein Chemical Formula 1 is represented by one of Chemical Formula 1-1 to Chemical Formula 1-7 and Chemical Formula 2 is represented by Chemical Formula 2-1: in Chemical Formula 1-3 to Chemical Formula 1-6, m is an integer of 1 to 5, 7. The curable composition of claim 1 , wherein the surface-modified quantum dot has a core-shell structure wherein the shell comprises Zn, and the thiol group at the terminal end of the compound represented by Chemical Formula 1 or Chemical Formula 2 is bonded with Zn of the shell. 8. The curable composition of claim 1 , wherein the quantum dot has a maximum fluorescence wavelength in a wavelength range of 500 nm to 680 nm. 9. The curable composition of claim 1 , wherein the solvent comprises propylene glycol monomethylether acetate, dipropylene glycol methylether acetate, ethanol, ethylene glycoldimethylether, ethylene diglycolmethylethylether, diethylene glycoldimethylether, dimethyl acetamide, 2-butoxyethanol, N-methylpyrrolidine, N-ethylpyrrolidine, propylene carbonate, γ-butyrolactone, or a combination thereof. 10. The curable composition of claim 1 , wherein the resin comprises at least one of a binder resin and an reactive unsaturated compound. 11. The curable composition of claim 10 , wherein the binder resin comprises an acryl-based resin, an epoxy resin, or a combination thereof. 12. The curable composition of claim 1 , wherein the diffusion agent is included in an amount of 0.1 wt % to 20 wt % based on the total amount of the curable composition. 13. The curable composition of claim 1 , wherein the diffusion agent comprises barium sulfate, calcium carbonate, titanium dioxide, zirconia, or a combination thereof. 14. The curable composition of claim 1 , wherein the curable composition further comprises a polymerization initiator. 15. The curable composition of claim 14 , wherein the polymerization initiator comprises a cation initiator. 16. The curable composition of claim 1 , wherein the curable composition further comprises malonic acid; 3-amino-1,2-propanediol; a silane-based coupling agent; a leveling agent; a fluorine-based surfactant; a polymerization inhibitor; or a combination thereof. 17. A method of manufacturing a pixel for a color filter, comprising: coating the curable composition of claim 1 on a substrate utilizing an inkjet spraying method to form a pattern; and curing the pattern. 18. A color filter comprising a pixel for a color filter manufactured according to the method of manufacturing the pixel of claim 17 .
non-luminescent particle coatings or suspension media · CPC title
characterised by the solvents or agents facilitating spreading, e.g. tensio-active agents · CPC title
Nanotechnology for materials or surface science, e.g. nanocomposites · CPC title
characterised by additives for obtaining a metallic or ceramic pattern, e.g. by firing · 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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