Organic optoelectric device and display device

US10050212B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10050212-B2
Application numberUS-201414302464-A
CountryUS
Kind codeB2
Filing dateJun 12, 2014
Priority dateOct 11, 2013
Publication dateAug 14, 2018
Grant dateAug 14, 2018

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.

Disclosed is an organic optoelectric device, including an anode and a cathode facing each other, an emission layer interposed between the anode and the cathode, a hole transport layer interposed between the anode and the emission layer, and a hole transport auxiliary layer interposed between the hole transport layer and the emission layer. The emission layer includes at least one first compound represented by Chemical Formula 1: The emission layer further includes at least one second compound represented by Chemical Formula 2: The hole transport auxiliary layer includes a third compound represented by Chemical Formula 2, the third compound being the same as or different from the second compound.

First claim

Opening claim text (preview).

What is claimed is: 1. An organic optoelectric device, comprising: an anode and a cathode facing each other, an emission layer interposed between the anode and the cathode, a hole transport layer interposed between the anode and the emission layer, and a hole transport auxiliary layer interposed between the hole transport layer and the emission layer, the emission layer including at least one first compound represented by Chemical Formula 1: wherein, in Chemical Formula 1, Z is independently N or CR a , at least one of Z is N, R 1 to R 10 and R a are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted biphenyl group, or a combination thereof, the total number of 6-membered rings substituted on the triphenylenyl group is less than or equal to 6, L is a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group or a substituted or unsubstituted terphenylene group, wherein a substituent of the substituted phenylene group, the substituted biphenylene group, and the substituted terphenylene group is a C1 to C30 alkyl group, a C6 to C30 aryl group, or a cyano group, n1 to n3 are independently 0 or 1, and n1+n2+n3≥1; the emission layer further including at least one second compound represented by Chemical Formula 2: wherein, in Chemical Formula 2, Y 1 is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C2 to C20 alkenylene group, a substituted or unsubstituted C6 to C30 arylene group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof, Ar 1 is a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof, R 11 to R 14 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C50 aryl group, a substituted or unsubstituted C2 to C50 heterocyclic group, or a combination thereof, and at least one of R 11 to R 14 and Ar 1 includes a substituted or unsubstituted triphenylenyl group or a substituted or unsubstituted carbazolyl group; and the hole transport auxiliary layer including a third compound represented by Chemical Formula 2, the third compound being the same as or different from the second compound. 2. The organic optoelectric device as claimed in claim 1 , wherein the first compound is represented by Chemical Formula 1-I or Chemical Formula 1-II: wherein, in Chemical Formula 1-I or 1-II, Z is independently N or CR a , at least one of Z is N, R 1 to R 10 and R a are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted biphenyl group, or a combination thereof, the total number of 6-membered rings substituted on the triphenylenyl group is less than or equal to 6, L is a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group or a substituted or unsubstituted terphenylene group, a substituent of the substituted phenylene group, the substituted biphenylene group, and the substituted terphenylene group is a C1 to C30 alkyl group, a C6 to C30 aryl group, or a cyano group, n1 to n3 are independently 0 or 1, and n1+n2+n3≥1. 3. The organic optoelectric device as claimed in claim 1 , wherein L of Chemical Formula 1 is a single bond, a substituted or unsubstituted phenylene having a kink structure, a substituted or unsubstituted biphenylene group having a kink structure, or a substituted or unsubstituted terphenylene group having a kink structure, and a substituent of the substituted phenylene group, the substituted biphenylene group, and the substituted terphenylene group is a C1 to C30 alkyl group, a C6 to C30 aryl group or a cyano group. 4. The organic optoelectric device as claimed in claim 3 , wherein L of Chemical Formula 1 is a single bond or a substituted or unsubstituted group selected from Group 1: wherein, in the Group 1, R 15 to R 42 are independently hydrogen, C1 to C10 alkyl group, C6 to C30 aryl group, a cyano group. 5. The organic optoelectric device as claimed in claim 1 , wherein the first compound has at least two kink structures. 6. The organic optoelectric device as claimed in claim 1 , wherein the first compound is a compound selected from Group 2:

Assignees

Inventors

Classifications

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 US10050212B2 cover?
Disclosed is an organic optoelectric device, including an anode and a cathode facing each other, an emission layer interposed between the anode and the cathode, a hole transport layer interposed between the anode and the emission layer, and a hole transport auxiliary layer interposed between the hole transport layer and the emission layer. The emission layer includes at least one first compound…
Who is the assignee on this patent?
Cho Pyeong Seok, Kang Gi Wook, Kang Eui Su, and 9 more
What technology area does this patent fall under?
Primary CPC classification C09B57/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 14 2018 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).