Organic light-emitting display apparatus and method of manufacturing the same

US10326111B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10326111-B2
Application numberUS-201514884183-A
CountryUS
Kind codeB2
Filing dateOct 15, 2015
Priority dateApr 16, 2015
Publication dateJun 18, 2019
Grant dateJun 18, 2019

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Abstract

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Provided are an organic light-emitting diode display apparatus and a method of manufacturing the same. In an exemplary embodiment, an organic light-emitting diode (OLED) display apparatus includes a substrate, an OLED device on the substrate, and a capping layer on the organic light-emitting device. The capping layer includes a first capping layer and a second capping layer. The second capping layer includes a first material and a second material. The first material and the second material are different from each other.

First claim

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What is claimed is: 1. An organic light-emitting diode (OLED) display apparatus, comprising: a substrate; an OLED device on the substrate; and a capping layer on the OLED device, wherein the capping layer comprises a first capping layer and a second capping layer, the second capping layer consists of a first material and a second material, and the first material and the second material are different from each other, wherein the first material is selected from the group consisting of an organic low molecular weight compound and an organic polymer compound, wherein the second material is an organic low molecular weight compound wherein a weight ratio of the first material to the second material is in a range of about 50:50 to about 99:1, and wherein a thickness of the second capping layer is in a range of about 30 nm to about 100 nm. 2. The OLED display apparatus of claim 1 , wherein the first material has a refractive index in a range of about 1.7 to about 2.7. 3. The OLED display apparatus of claim 1 , wherein the first material is represented by Chemical Formula 201: wherein, L 201 , L 202 , and L 203 are each independently selected from a substituted or unsubstituted C 3 -C 10 cycloalkylene, a substituted or unsubstituted C 1 -C 10 heterocycloalkylene, a substituted or unsubstituted C 3 -C 10 cycloalkenylene, a substituted or unsubstituted C 1 -C 10 hetetocycloalkenylene, a substituted or unsubstituted C 6 -C 60 arylene, a substituted or unsubstituted C 1 -C 60 heteroarylene, a substituted or unsubstituted divalent non-aromatic condensed polycyclic group, and a substituted or unsubstituted divalent non-aromatic condensed heteropolycyclic group; xa1, xa2, and xa3 are each independently selected from 0, 1, 2, and 3; R 201 , R 202 , and R 203 are each independently selected from a substituted or unsubstituted C 3 -C 10 cycloalkyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkyl group, a substituted or unsubstituted C 3 -C 10 cycloalkenyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, and a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group; at least one substituent of the substituted C 3 -C 10 cycloalkylene group, substituted C 1 -C 10 heterocycloalkylene group, substituted C 3 -C 10 cycloalkenylene group, substituted C 1 -C 10 heterocycloalkenylene group, substituted C 6 -C 60 arylene group, substituted C 1 -C 60 heteroarylene group, substituted divalent non-aromatic condensed polycyclic group, substituted divalent non-aromatic condensed heteropolycyclic group, substituted C 3 -C 10 cycloalkyl group, substituted C 1 -C 10 heterocycloalkyl group, substituted C 3 -C 10 cycloalkenyl group, substituted C 1 -C 10 heterocycloalkenyl group, substituted C 6 -C 60 aryl group, substituted C 1 -C 60 heteroaryl group, substituted monovalent non-aromatic condensed polycyclic group, and substituted monovalent non-aromatic condensed heteropolycyclic group is selected from: a deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C 1 -C 60 alkyl group, a C 2 -C 60 alkenyl group, a C 2 -C 60 alkynyl group, and a C 1 -C 60 alkoxy group; a C 1 -C 60 alkyl group, a C 2 -C 60 alkenyl group, a C 2 -C 60 alkynyl group, and a C 1 -C 60 alkoxy group, each substituted with at least one selected from a deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C 3 -C 10 cycloalkyl group, a C 1 -C 10 heterocycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 1 -C 10 heterocycloalkenyl group, a C 6 -C 60 aryl group, a C 6 -C 60 aryloxy group, a C 6 -C 60 arylthio group, a C 1 -C 60 heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group; a C 3 -C 10 cycloalkyl group, a C 1 -C 10 heterocycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 1 -C 10 heterocycloalkenyl group, a C 6 -C 60 aryl group, a C 6 -C 60 aryloxy group, a C 6 -C 60 arylthio group, a C 1 -C 60 heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group; and a C 3 -C 10 cycloalkyl group, a C 1 -C 10 heterocycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 1 -C 10 heterocycloalkenyl group, a C 6 -C 60 aryl group, a C 6 -C 60 aryloxy group, a C 6 -C 60 arylthio group, a C 1 -C 60 heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group, each substituted with at least one selected from a deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, 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 10 cycloalkyl group, a C 1 -C 10 heterocycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 1 -C 10 heterocycloalkenyl group, a C 6 -C 60 aryl group, a C 6 -C 60 aryloxy group, a C 6 -C 60 arylthio group, a C 1 -C 60 heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group. 4. The OLED display apparatus of claim 1 , wherein the first material is selected from Chemical Compounds HT1, HT2, HT3, HT4, HT5, HT6, HT7, HT8, HT9, HT10, HT11, and HT12: 5. The OLED display apparatus of claim 1 , wherein the first material is selected from an acrylic resin, a polyimide, and a polyamide. 6. The OLED display apparatus of claim 1 , wherein the second material is represented by one of Chemical Formulas 1-1, 1-2, 1-3, 1-4, and 1-5: wherein R 11 R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , R 20 , R 21 , R 22 , R 23 , R 24 , R 25 , and R 26 are each independently selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a cyano group, and a nitro group; wherein X 11 is N or C(Q 11 ); X 12 is N or C(Q 12 ); X 13 is N or C(Q 13 ); X 14 is N or C(Q 14 ); X 15 is N or C(Q 15 ); X 16 is N or C(Q 16 ); X 17 is N or C(Q 17 ); X 18 is N or C(Q 18 ); X 19 is N or C(Q 19 ), X 20 is N or C(Q 20 ); X 21 is N or C(Q 21 ); and X 22 is N or C(Q 22 ); and wherein Q 11 Q 12 , Q 13 , Q 14 , Q 15 , Q 16 , Q 17 , Q 18 , Q 19 , Q 20 , Q 21 , and Q 22 are each independently selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a cyano group, and a nitro group. 7. The OLED display apparatus of

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What does patent US10326111B2 cover?
Provided are an organic light-emitting diode display apparatus and a method of manufacturing the same. In an exemplary embodiment, an organic light-emitting diode (OLED) display apparatus includes a substrate, an OLED device on the substrate, and a capping layer on the organic light-emitting device. The capping layer includes a first capping layer and a second capping layer. The second capping …
Who is the assignee on this patent?
Samsung Display Co Ltd
What technology area does this patent fall under?
Primary CPC classification H01L51/5275. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Jun 18 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).