Organic electroluminescence device and electronic apparatus

US12514115B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12514115-B2
Application numberUS-202017766213-A
CountryUS
Kind codeB2
Filing dateSep 28, 2020
Priority dateOct 4, 2019
Publication dateDec 30, 2025
Grant dateDec 30, 2025

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

An organic electroluminescence device containing a cathode, an anode, and an organic layer disposed between the cathode and the anode, wherein the organic layer contains an emitting layer, a first layer, and a second layer, the first layer is disposed between the anode and the emitting layer, the second layer is disposed between the anode and the first layer, the first layer contains a first hole-transporting material and a second hole-transporting material, and the second layer contains an acceptor material having an affinity value in the range of 3.8 to 6.0 eV and at least one hole-transporting material.

First claim

Opening claim text (preview).

The invention claimed is: 1 . An organic electroluminescence device comprising a cathode, an anode, and an organic layer disposed between the cathode and the anode, wherein the organic layer comprises an emitting layer, a first layer, and a second layer, the first layer is disposed between the anode and the emitting layer, the second layer is disposed between the anode and the first layer, the first layer comprises a first hole-transporting material, and a second hole-transporting material, and the second layer comprises an acceptor material having an affinity value in the range of 3.8 to 6.0 eV, one or more compounds selected from compounds represented by one of the following formulas (11-3B) and (11-3D), and one or more compounds represented by the following formula (11) other than the compound represented by the following formula (11-3B) or (11-3D): wherein in the formula (11-3B), L 11B is a single bond, or a substituted or unsubstituted arylene group including 6 to 50 ring carbon atoms; Ar 11B is a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms; R 11B to R 18B are independently a hydrogen atom, a substituted or unsubstituted alkyl group including 1 to 50 carbon atoms, a substituted or unsubstituted alkenyl group including 2 to 50 carbon atoms, a substituted or unsubstituted alkynyl group including 2 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group including 3 to 50 ring carbon atoms, —Si(R 901 )(R 902 )(R 903 ), —O—(R 904 ), —S—(R 905 ), —N(R 906 )(R 907 ), a halogen atom, a cyano group, a nitro group, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms; R 901 to R 907 are independently a hydrogen atom, a substituted or unsubstituted alkyl group including 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group including 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms; when two or more of each of R 901 to R 907 are present, the two or more of each of R 901 to R 907 may be the same as or different from each other; substituents when L 11B , Ar 11B , and R 11B to R 18B have substituents are independently a substituted or unsubstituted alkyl group including 1 to 50 carbon atoms, a substituted or unsubstituted alkenyl group including 2 to 50 carbon atoms, a substituted or unsubstituted alkynyl group including 2 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group including 3 to 50 ring carbon atoms, —Si(R 901 )(R 902 )(R 903 ), —O—(R 904 ), —S—(R 905 ), a halogen atom, a cyano group, a nitro group, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms; and R 901 to R 905 are as defined above; wherein in the formula (11-3D), L 11D and L 12D are independently a single bond, or a substituted or unsubstituted arylene group including 6 to 50 ring carbon atoms; Ar 11D to Ar 13D are independently a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms; R 11D , R 12D , and R 14D to R 18D are independently a hydrogen atom, a substituted or unsubstituted alkyl group including 1 to 50 carbon atoms, a substituted or unsubstituted alkenyl group including 2 to 50 carbon atoms, a substituted or unsubstituted alkynyl group including 2 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group including 3 to 50 ring carbon atoms, —Si(R 901 )(R 902 )(R 903 ), —O—(R 904 ), —S—(R 905 ), a halogen atom, a cyano group, a nitro group, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms; R 901 to R 907 are independently a hydrogen atom, a substituted or unsubstituted alkyl group including 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group including 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms; when two or more of each of R 901 to R 907 are present, the two or more of each of R 901 to R 907 may be the same as or different from each other; substituents when L 11D , L 12D , Ar 11D to Ar 13D , R 11D , R 12D , and R 14D to R 18D have substituents are independently a substituted or unsubstituted alkyl group including 1 to 50 carbon atoms, a substituted or unsubstituted alkenyl group including 2 to 50 carbon atoms, a substituted or unsubstituted alkynyl group including 2 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group including 3 to 50 ring carbon atoms, —Si(R 901 )(R 902 )(R 903 ), —O—(R 904 ), —S—(R 905 ), a halogen atom, a cyano group, a nitro group, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms; and R 901 to R 905 are as defined above; wherein in the formula (11), two of -L 11 -Ar 11 , -L 12 -Ar 12 , and -L 13 -Ar 13 form a substituted or unsubstituted N-carbazolyl group by bonding with each other, or do not form the N-carbazolyl group; L 11 to L 13 which are not involved in formation of the N-carbazolyl group are independently a single bond or a linking group; Ar 11 to Ar 13 which are not involved in formation of the N-carbazolyl group are independently a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, a substituted or unsubstituted monovalent heterocyclic group including 5 to 60 ring atoms, or —N(R 906 )(R 907 ); R 906 and R 907 are independently a hydrogen atom, a substituted or unsubstituted alkyl group including 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group including 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, or a substituted or unsubstituted monovalent heterocyclic group including 5 to 50 ring atoms; when two or more of each of R 906 and R 907 are present, the two or more of each of R 906 and R 907 may be the same as or different from each other. 2 . The organic electroluminescence device according to claim 1 , wherein the acceptor material is one or more compounds selected from the group con

Assignees

Inventors

Classifications

  • Organic light-emitting devices (integrated devices or assemblies of multiple devices H10K59/00, H10K65/00; organic semiconductor lasers H01S5/36) · CPC title

  • comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole · CPC title

  • containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene · CPC title

  • comprising a multilayered structure · CPC title

  • Polycyclic condensed aromatic hydrocarbons, e.g. anthracene · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US12514115B2 cover?
An organic electroluminescence device containing a cathode, an anode, and an organic layer disposed between the cathode and the anode, wherein the organic layer contains an emitting layer, a first layer, and a second layer, the first layer is disposed between the anode and the emitting layer, the second layer is disposed between the anode and the first layer, the first layer contains a first ho…
Who is the assignee on this patent?
Idemitsu Kosan Co
What technology area does this patent fall under?
Primary CPC classification H10K85/636. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Dec 30 2025 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 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).