Organic light-emitting display apparatus and method of manufacturing the same
US-10326111-B2 · Jun 18, 2019 · US
US12069890B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12069890-B2 |
| Application number | US-202117551016-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 14, 2021 |
| Priority date | Dec 16, 2020 |
| Publication date | Aug 20, 2024 |
| Grant date | Aug 20, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A light-emitting device includes: a first electrode; a second electrode facing the first electrode; an interlayer between the first electrode and the second electrode and including an emission layer; and a first capping layer and a second capping layer outside the second electrode, wherein the first capping layer includes at least one compound selected from compounds represented by Formulae 1-1 to 1-3, as defined herein, and the second capping layer includes at least one compound selected from compounds represented by Formulae 2-1 to 2-6, as defined herein.
Opening claim text (preview).
What is claimed is: 1. A light-emitting device comprising: a first electrode; a second electrode facing the first electrode; an interlayer between the first electrode and the second electrode and comprising an emission layer; and a first capping layer and a second capping layer outside the second electrode, wherein the first capping layer comprises at least one compound selected from compounds represented by Formulae 1-1 to 1-3, and the second capping layer comprises at least one compound selected from compounds represented by Formulae 2-1 to 2-6: wherein, in Formulae 1-1, 2-2, and 2-6, n8 is 0 or 1, when n8 is 0, (A 8 ) n8 is represented by *—R 8 , when n8 is 1, (A 8 ) n8 is represented by Formula 1A, n45 is 1 or 2, when n45 is 1, A 45 is: *—O—*′; *—S—*′; *—Se—*′; *—N(R 45a )—*; *—C(R 45a )(R 45b )—*′; *—Si(R 45a )(R 45b )—*; *—S(═O) 2 —*; *—P(═O)(R 45a )—*′; a C 3 -C 60 carbocyclic group unsubstituted or substituted with at least one R 10a , or a C 1 -C 60 heterocyclic group unsubstituted or substituted with at least one R 10a , when n45 is 2, A 45 is a C 3 -C 60 carbocyclic group unsubstituted or substituted with at least one R 10a or a C 1 -C 60 heterocyclic group unsubstituted or substituted with at least one R 10a , n89 is 0 or 1, when n89 is 0, A 89 is *—N(R 89a )(R 89b ), a C 3 -C 60 carbocyclic group unsubstituted or substituted with at least one R 10a , or a C 1 -C 60 heterocyclic group unsubstituted or substituted with at least one R 10a , when n89 is 1, A 89 is: *—O—*′; *—S—*′; *—Se—*′; *—N(R 89a )—*′; *—C(R 89a )(R 89b )—*′; *—Si(R 89a )(R 89b )—*′; *—S(═O) 2 —*′; *—P(═O)(R 89a )—*′; a C 3 -C 60 carbocyclic group unsubstituted or substituted with at least one R 10a , or a C 1 -C 60 heterocyclic group unsubstituted or substituted with at least one R 10a , wherein, in Formulae 1-1, 1-A, 1-2, 1-3, 1-1-1, 2-1, 2-2, 2-3, 2-4, 2-5, and 2-6, X 1 is C-(L 1 ) a1 -R 1 or N, X 2 is C-(L 2 ) a2 -R 2 or N, X 3 is C-(L 3 ) a3 -R 3 or N, X 4 is C-(L 4 ) a4 -R 4 or N, X 1a is C-(L 1a ) a1a -R 1a or N, X 2a is C-(L 2a ) a2a -R 2a or N, X 3a is C-(L 3a ) a3a -R 2a or N, X 4a is C-(L 4a ) a4a -R 4a or N, X 81 is C(R 81a )(R 81b ), Si(R 81a )(R 81b ), N(R 81a ), O, S, or Se, X 82 is C(R 82a ) or N, X 83 is C(R 83a )(R 83b ), Si(R 83a )(R 83b ), N(R 83a ), O, S, or Se, X 84 is C(R 84a ) or N, ring A 1 is a substituted or unsubstituted benzene ring, ring A 2 is a 5-membered ring represented by Formula 2A, wherein, in Formula 2A, X 74 is C(R 74a )(R 74b ), Si(R 74a )(R 74b ), N(R 74a ), O, S, or Se, L 1 to L 8 , L 1a to L 7a , L 11 to L 13 , L 21 to L 25 , L 31 to L 33 , L 41 to L 44 , L 51 to L 52 , L 61 , L 66 , L 67 , L 71 , L 85 , and L 86 are each, independently from one another: *—O—*′; *—S—*′; *—Se—*′; *—N(R 10 )—*′; *—C(R 10 )(R 20 )—*′; *—Si(R 10 )(R 20 )—*′; *—S(═O) 2 —*′; *—P(═O)(R 10 )—*′; a C 3 -C 60 carbocyclic group unsubstituted or substituted with at least one R 10a , or a C 1 -C 60 heterocyclic group unsubstituted or substituted with at least one R 10a , a1 to 8, a1a to a7a, a11 to a13, a21 to a25, a31 to a33, a41 to a45, a51 to a52, a61, a66, a67, a71, a85, and a86 are each, independently from one another, an integer from 1 to 5, R 1 to R 8 , R 1a to R 7a , R 10 , R 20 , R 11 to R 13 , R 21 to R 24 , R 31 to R 33 , R 41 to R 44 , R 45a , R 45b , R 51 to R 54 , R 61 to R 66 , R 71 to R 73 , R 74a , R 74b , R 81a , R 81b , R 82a , R 83a , R 83b , R 84a , R 87 , R 88 , R 89a , and R 89b are each independently selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, a C 1 -C 60 alkyl group unsubstituted or substituted with at least one R 10a , a C 2 -C 60 alkenyl group unsubstituted or substituted with at least one R 10a , a C 2 -C 60 alkynyl group unsubstituted or substituted with at least one R 10a , a C 1 -C 60 alkoxy group unsubstituted or substituted with at least one R 10a , a C 3 -C 60 carbocyclic group unsubstituted or substituted with at least one R 10a , a C 1 -C 60 heterocyclic group unsubstituted or substituted with at least one R 10a , a C 6 -C 60 aryloxy group unsubstituted or substituted with at least one R 10a , a C 6 -C 60 arylthio group unsubstituted or substituted with at least one R 10a , —Si(Q 1 )(Q 2 )(Q 3 ), —N(Q 1 )(Q 2 ), —B(Q 1 )(Q 2 ), —C(═O)(Q 1 ), —S(═O) 2 (Q 1 ), and —P(═O)(Q 1 )(Q 2 ), b53, b54, b62, b65, b72, b73, b87, and b88 are each, independently from one another, an integer from 0 to 4, b63 and b64 are each, independently from one another, an integer from 0 to 3, two neighboring groups among R 1 to R 8 , R 1a to R 7a , R 10 , R 20 , R 11 to R 13 , R 21 to R 24 , R 31 to R 33 , R 41 to R 44 , R 45a , R 45b , R 51 to R 54 , R 61 to R 66 , R 71 to R 73 , R 74a , R 74b , R 81a , R 81b , R 82a , R 83a , R 83b , R 84a , R 87 , R 88 , R 89a , and R 89b are optionally linked to each other, via a single bond, a C 1 -C 5 alkylene group unsubstituted or substituted with at least one R 10a , or a C 2 -C 5 alkenylene group unsubstituted or substituted with at least one R 10a , to form a C 3 -C 60 carbocyclic group unsubstituted or substituted with at least one R 10a or a C 1 -C 60 heterocyclic group substituted or unsubstituted at least one R 10a , R 10a is: deuterium (-D), —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, or a nitro group; a C 1 -C 60 alkyl group, a C 2 -C 60 alkenyl group, a C 2 -C 60 alkynyl group, or a C 1 -C 60 alkoxy group, each, independently from one another, unsubstituted or substituted with deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, a C 3 -C 60 carbocyclic group, a C 1 -C 60 heterocyclic group, a C 6 -C 60 aryloxy group, a C 6 -C 60 arylthio group, —Si(Q 11 )(Q 12 )(Q 13 ), —N(Q 11 )(Q 12 ), —B(Q 11 )(Q 12 ), —C(═O)(Q 11 ), —S(═O) 2 (Q 11 ), —P(═O)(Q 11 )(Q 12 ), or any combination thereof, a C 3 -C 60 carbocyclic group, a C 1 -C 60 heterocyclic group, a C 6 -C 60 aryloxy group, or a C6-C 60 arylthio group, each, independently from one another, unsubstituted or substituted with deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, a C 1 -C 60 alkyl group, a C 2 -C 60 alkenyl group, a C 2 -C 60 alkynyl group, a C 1 -C 60 alkoxy group, a C 3 -C 60 carbocyclic group, a C 1 -C 60 heterocyclic group, a C 6 -C 60 aryloxy group, a C 6 -C 60 arylthio group, —Si(Q 21 )(Q 22 )(Q 23 ), —N(Q 21 )(Q 22 ), —B(Q 21 )(Q 22 ), —C(═O)(Q 21 ), —S(═O) 2 (Q 21 ), —P(═O)(Q 21 )(Q 22 ), or any combination thereof; or —Si(Q 31 )(Q 32 )(Q 33 ), —N(Q 31 )(Q 32 ), —B(Q 31 )(Q 32 ), —C(═O)(Q 31 ), —S(═O) 2 (Q 31 ), or —P(═O)(Q 31 )(Q 32 ), wherein Q 1 to Q 3 , Q 11 to Q 13 , Q 21 to Q 23 , and Q 31 to Q 33 are each, independently from one another: hydrogen; deuterium; —F; —Cl; —Br; —I; a hydroxyl group; a cyano group; a nitro group; a C 1 -C 60 alkyl group; a C 2 -C 60 alkenyl group; a C 2 -C 60 alkynyl group; a C 1 -C 60 alkoxy group; or a C 3 -C 60 carbocyclic group or a C 1 -C 60 heterocyclic group, each, independently from one another unsubstituted or substituted with deuterium, —F, a cyano group, a C 1 -C 60 al
Active-matrix OLED [AMOLED] displays · CPC title
comprising refractive means, e.g. lenses · CPC title
Containers · CPC title
comprising refractive means, e.g. lenses · CPC title
Encapsulations · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.