Organic electroluminescent device
US-10862047-B2 · Dec 8, 2020 · US
US12439821B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12439821-B2 |
| Application number | US-202217937762-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 3, 2022 |
| Priority date | Jul 8, 2019 |
| Publication date | Oct 7, 2025 |
| Grant date | Oct 7, 2025 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
An light emitting device of the present embodiments includes oppositely disposed first electrode and second electrode, and a plurality of organic layers disposed between the first electrode and the second electrode, wherein at least one among the plurality of organic layers includes a fused polycyclic compound represented by Formula 1 below, thereby showing improved emission efficiency:
Opening claim text (preview).
What is claimed is: 1. A light emitting device, comprising: a first electrode; a second electrode facing the first electrode; and a plurality of organic layers between the first electrode and the second electrode, wherein at least one organic layer among the plurality of organic layers comprises a fused polycyclic compound represented by Formula 1: wherein, in Formula 1, M is B, Al, Ga, or In, X 1 and X 2 are each independently NR 1 , O, S, P(═O)R 2 , or P(═S)R 3 , R 1 to R 3 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a substituted or unsubstituted alkyl group of 1 to 20 carbon atoms, a substituted or unsubstituted aryl group of 6 to 60 carbon atoms to form a ring, or a substituted or unsubstituted heteroaryl group of 2 to 60 carbon atoms to form a ring, and any of R 1 to R 3 are optionally combined with an adjacent group to form a ring, Cy 1 to Cy 3 are each independently a substituted or unsubstituted aromatic hydrocarbon ring, or a substituted or unsubstituted aromatic heterocycle, and any of Cy 1 to Cy 3 are optionally combined with an adjacent group to form a ring, and at least one among Cy 1 to Cy 3 is substituted with a substituent represented by Formula 2: wherein, in Formula 2, R 4 and R 5 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a substituted or unsubstituted amine group, a substituted or unsubstituted alkyl group of 1 to 20 carbon atoms, a substituted or unsubstituted aryl group of 6 to 60 carbon atoms to form a ring, or a substituted or unsubstituted heteroaryl group of 2 to 60 carbon atoms to form a ring, and any of R 4 and R 5 are optionally combined with an adjacent group to form a ring, “n 1 ” and “n 2 ” are each independently an integer of 0 to 5, at least one among R 4 and R 5 is a substituted or unsubstituted amine group, or a substituted or unsubstituted carbazole group, if R 4 is the substituted or unsubstituted amine group, or the substituted or unsubstituted carbazole group, n 1 is an integer of 1 to 5, if R 5 is the substituted or unsubstituted amine group, or the substituted or unsubstituted carbazole group, n 2 is an integer of 1 to 5, Y is a direct linkage, a is 0 or 1, a sum of “a” and “n1” is an integer of 5 or less, and a sum of “a” and “n 2 ” is an integer of 5 or less. 2. The light emitting device of claim 1 , wherein the plurality of organic layers comprise: a hole transport region on the first electrode; an emission layer on the hole transport region; and an electron transport region on the emission layer, and the emission layer comprises the fused polycyclic compound represented by Formula 1. 3. The light emitting device of claim 2 , wherein the emission layer is to emit delayed fluorescence. 4. The light emitting device of claim 2 , wherein the emission layer is a delayed fluorescence emission layer comprising a first compound and a second compound, and the second compound comprises the fused polycyclic compound represented by Formula 1. 5. The light emitting device of claim 2 , wherein the emission layer comprises: a first compound having a first lowest triplet excitation energy level; a second compound having a second lowest triplet excitation energy level which is lower than the first lowest triplet excitation energy level; and a third compound having a third lowest triplet excitation energy level which is lower than the second lowest triplet excitation energy level, and the second compound comprises the fused polycyclic compound represented by Formula 1. 6. The light emitting device of claim 5 , wherein the second compound is a delayed fluorescence material, and the third compound is a phosphorescence material or a fluorescence material. 7. The light emitting device of claim 1 , wherein the fused polycyclic compound represented by Formula 1 is represented by Formula 3: wherein, in Formula 3, R 11 to R 21 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a substituted or unsubstituted amine group, a substituted or unsubstituted alkyl group of 1 to 20 carbon atoms, a substituted or unsubstituted aryl group of 6 to 60 carbon atoms to form a ring, or a substituted or unsubstituted heteroaryl group of 2 to 60 carbon atoms to form a ring, and any of R 11 to R 21 are optionally combined with an adjacent group to form a ring, at least one among R 11 to R 21 is represented by Formula 2, and M, X 1 , and X 2 are the same as defined in Formula 1. 8. The light emitting device of claim 7 , wherein the fused polycyclic compound represented by Formula 3 is represented by Formula 4: wherein, in Formula 4, R 31 to R 33 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a substituted or unsubstituted amine group, a substituted or unsubstituted alkyl group of 1 to 20 carbon atoms, a substituted or unsubstituted aryl group of 6 to 60 carbon atoms to form a ring, or a substituted or unsubstituted heteroaryl group of 2 to 60 carbon atoms to form a ring, and any of R 31 to R 33 are optionally combined with an adjacent group to form a ring, at least one among R 31 to R 33 is represented by Formula 2, and M, X 1 , and X 2 are the same as defined in Formula 1. 9. The light emitting device of claim 1 , wherein the substituent represented by Formula 2 is represented by Formula 5-1 or Formula 5-2: wherein, in Formulae 5-1 and 5-2, R 4 , R 5 , n 1 , and n 2 are the same as defined in Formula 2. 10. The light emitting device of claim 9 , wherein the substituent represented by Formula 2 is represented by any one among Formula 6-1 to Formula 6-4: wherein, in Formulae 6-1 to 6-4, R 41 to R 46 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a substituted or unsubstituted alkyl group of 1 to 20 carbon atoms, a substituted or unsubstituted aryl group of 6 to 60 carbon atoms to form a ring, or a substituted or unsubstituted heteroaryl group of 2 to 60 carbon atoms to form a ring, and any of R 41 to R 46 are optionally combined with an adjacent group to form a ring, n 3 and n 4 are each independently an integer of 0 to 3, n 5 to n 8 are each independently an integer of 0 to 4, m 1 and m 2 are each independently 0 or 1, and at least one of m 1 and m 2 is 1. 11. The light emitting device of claim 1 , wherein the substituent represented by Formula 2 is represented by Formula 7-1 to Formula 7-4: wherein, in Formulae 7-1 to 7-4, R 4 , and R 5 are the same as defined in Formula 2. 12. The light emitting device of claim 1 , wherein X 1 and X 2 are each independently NR 1 , or O, and R 1 is a substituted or unsubstituted aryl group of 6 t
comprising boron · CPC title
Combination of fluorescent and phosphorescent emission · CPC title
Triplet emission · CPC title
comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole · CPC title
comprising heteroaromatic hydrocarbons as substituents on the nitrogen atom · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.