Amine-based compound and organic light-emitting device including the same
US-2015364705-A1 · Dec 17, 2015 · US
US10050212B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10050212-B2 |
| Application number | US-201414302464-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 12, 2014 |
| Priority date | Oct 11, 2013 |
| Publication date | Aug 14, 2018 |
| Grant date | Aug 14, 2018 |
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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.
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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:
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