Light-emitting device and electronic apparatus including the same

US2024284697A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2024284697-A1
Application numberUS-202318482327-A
CountryUS
Kind codeA1
Filing dateOct 6, 2023
Priority dateFeb 2, 2023
Publication dateAug 22, 2024
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A light-emitting device including an anode, a cathode, a first emission layer arranged on the anode and including a first phosphorescent emitter, and a second emission layer arranged on the first emission layer and including a first fluorescent emitter and a second phosphorescent emitter.

First claim

Opening claim text (preview).

What is claimed is: 1 . A light-emitting device comprising: an anode; a cathode facing the anode; a first emission layer arranged on the anode and comprising a first phosphorescent emitter; and a second emission layer arranged on the first emission layer and comprising a first fluorescent emitter and a second phosphorescent emitter, wherein a decay time T decay (1) of the first emission layer is shorter than a decay time T decay (2) of the second emission layer. 2 . The light-emitting device of claim 1 , wherein the first emission layer and the second emission layer each independently comprise at least one of a first host or a second host. 3 . The light-emitting device of claim 2 , wherein the first host is a hole-transporting host, and the second host is an electron-transporting host. 4 . The light-emitting device of claim 2 , wherein the first host comprises at least one carbazole moiety, and the second host comprises at least one azine moiety. 5 . The light-emitting device of claim 2 , wherein the first host comprises a compound represented by Formula 1: wherein, in Formulae 1 and 1A, CY 11 to CY 14 are each independently an unsubstituted or substituted C 5 -C 30 carbocyclic group or an unsubstituted or substituted C 1 -C 30 heterocyclic group, E 1 is a group represented by Formula 1A, k 1 is an integer from 0 to 5, n11 is an integer from 0 to 3, n12 is an integer from 0 to 3, R 11 to R 17 are each independently 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 substituted or unsubstituted C 1 -C 60 alkyl group, a substituted or unsubstituted C 2 -C 60 alkenyl group, a substituted or unsubstituted C 2 -C 60 alkynyl group, a substituted or unsubstituted C 1 -C 60 alkoxy group, 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 2 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 6 -C 60 aryloxy group, a substituted or unsubstituted C 6 -C 60 arylthio group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, a substituted or unsubstituted C 1 -C 60 heteroaryloxy group, a substituted or unsubstituted C 1 -C 60 heteroarylthio group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q 1 )(Q 2 )(Q 3 ), —Ge(Q 1 )(Q 2 )(Q 3 ), —N(Q 4 )(Q 5 ), —B(Q 6 )(Q 7 ), or —P(═O)(Q 8 )(Q 9 ), b15 and b16 are each independently an integer from 0 to 4, b17 is an integer from 0 to 5, b11 to b14 are each independently an integer from 0 to 10, * indicates a binding site to a neighboring atom, wherein Q 1 to Q 9 , are each independently hydrogen, 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 substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 alkoxy group, 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 30 aryl group, a substituted or unsubstituted C 6 -C 30 aryloxy group, a substituted or unsubstituted C 6 -C 30 arylthio group, a substituted or unsubstituted C 1 -C 30 heteroaryl group, a substituted or unsubstituted C 1 -C 30 heteroaryloxy group, a substituted or unsubstituted C 1 -C 30 heteroarylthio group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, or a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group. 6 . The light-emitting device of claim 2 , wherein the second host comprises a compound represented by Formula 2: wherein, in Formula 2, CY 23 and CY 24 are each independently a C 5 -C 30 carbocyclic group or a C 1 -C 30 heterocyclic group, X 21 is N or C(R 21a ), X 22 is N or C(R 22a ), X 23 is N or C(R 23a ), and at least one of X 21 to X 23 is N, L 21 and L 22 are each independently a single bond, a substituted or unsubstituted C 3 -C 60 carbocyclic group, or a substituted or unsubstituted C 1 -C 60 heterocyclic group, n21 and n22 are each independently an integer from 1 to 5, R 21 to R 24 , R 21a , R 22a , and R 23a are each independently 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 substituted or unsubstituted C 1 -C 60 alkyl group, a substituted or unsubstituted C 2 -C 60 alkenyl group, a substituted or unsubstituted C 2 -C 60 alkynyl group, a substituted or unsubstituted C 1 -C 60 alkoxy group, 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 2 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 6 -C 60 aryloxy group, a substituted or unsubstituted C 6 -C 60 arylthio group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, a substituted or unsubstituted C 1 -C 60 heteroaryloxy group, a substituted or unsubstituted C 1 -C 60 heteroarylthio group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q 1 )(Q 2 )(Q 3 ), —Ge(Q 1 )(Q 2 )(Q 3 ), —N(Q 4 )(Q 5 ), —B(Q 6 )(Q 7 ), or —P(═O)(Q 8 )(Q 9 ), b21 to b24 are each independently an integer from 1 to 10, wherein Q 1 to Q 9 , are each independently hydrogen, 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 substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 alkoxy group, 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 30 aryl group, a substituted or unsubstituted C 6 -C 30 aryloxy group, a substituted or unsubstituted C 6 -C 30 arylthi

Assignees

Inventors

Classifications

  • Metal complexes comprising a group IB metal element, e.g. comprising copper, gold or silver · CPC title

  • Transition metal complexes, e.g. Ru(II)polypyridine complexes (H10K85/331 takes precedence) · CPC title

  • comprising platinum · CPC title

  • Coordination compounds · CPC title

  • H10K50/12Primary

    comprising dopants · CPC title

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What does patent US2024284697A1 cover?
A light-emitting device including an anode, a cathode, a first emission layer arranged on the anode and including a first phosphorescent emitter, and a second emission layer arranged on the first emission layer and including a first fluorescent emitter and a second phosphorescent emitter.
Who is the assignee on this patent?
Samsung Electronics Co Ltd
What technology area does this patent fall under?
Primary CPC classification H10K50/12. Mapped technology areas include Electricity.
When was this patent published?
Publication date Thu Aug 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).