IP Library Granted Patent US 11,107,997
Granted Patent B2
US 11,107,997 · App. 16/327,955 · Granted Aug 31, 2021

Organic electroluminescent device comprising an electron buffer layer and an electron transport layer

Inventors: Sang-Hee Cho (Gyeonggi-do, KR); Doo-Hyeon Moon (Gyeonggi-do, KR)
H01L51/0072H01L51/0052H01L51/0058H01L51/0067H01L51/0073H01L51/0074H01L51/5004H01L51/5012H01L51/5092H01L51/50H01L51/508H01L51/5056H01L51/5072H01L51/5096
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,107,997
App. No.
16/327,955
Granted
Aug 31, 2021
Kind
B2
Abstract

The present disclosure relates to an organic electroluminescent device. The organic electroluminescent device of the present disclosure comprises a specific combination of an electron buffer material and an electron transport material which can provide high efficiency and/or long lifespan.

Claims (30)

1. An organic electroluminescent device comprising a first electrode, a second electrode facing the first electrode, a light-emitting layer between the first electrode and the second electrode, and an electron transport layer and an electron buffer layer between the light-emitting layer and the second electrode, wherein the electron buffer layer comprises a compound represented by the following formula 1, and the electron transport layer comprises a compound represented by the following formula 2:

wherein

X 1 to X 5 each independently represent CR 1 or N;

R 1 represents hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted mono- or di-(C1-C30)alkylamino, or a substituted or unsubstituted mono- or di-(C6-C30)arylamino; or may be linked to an adjacent substituent to form a substituted or unsubstituted, mono- or polycyclic, (C3-C30) alicyclic, aromatic, or a combination of alicyclic and aromatic ring, whose carbon atom(s) may be replaced with at least one heteroatom selected from nitrogen, oxygen, and sulfur;

L represents a single bond, a substituted or unsubstituted (C6-C50)arylene, or a substituted or unsubstituted (5- to 50-membered)heteroarylene;

Ar represents a substituted or unsubstituted (C6-C50)aryl, or a substituted or unsubstituted (5- to 50-membered)heteroaryl;

Ar 1 and Ar 2 each independently represent a substituted or unsubstituted (C6-C30)aryl;

L 1 represents a naphthylene;

ring A and ring B each independently represent a benzene, a phenylbenzene, or a naphthalene, with a proviso that at least one of ring A and ring B represent naphthalene;

n represents an integer of 1 to 3; and

the heteroaryl(ene) contains at least one heteroatom selected from B, N, O, S, Si, and P.

2. The organic electroluminescent device according to claim 1 , wherein formula 1 is represented by the following formula 3 or 4:

wherein

Ar 3 and Ar 4 are identical to the definition of R 1 ; and

L, Ar, and n are as defined in claim 1 .

3. The organic electroluminescent device according to claim 1 , wherein formula 2 is represented by the following formula 5 or 6:

wherein

X 1 , L 1 , Ar 1 , and Ar 2 are as defined in claim 1 ; and

m represents 0 or 1.

4. The organic electroluminescent device according to claim 1 , wherein in formula 2, L 1 is represented by any one of the following formulae 8 to 10:

wherein

represents a bonding site.

5. The organic electroluminescent device according to claim 1 , wherein the compound represented by formula 1 is selected from the group consisting of:

6. The organic electroluminescent device according to claim 1 , wherein the compound represented by formula 2 is selected from the group consisting of:

7. The organic electroluminescent device according to claim 1 , wherein the light-emitting layer comprises a host compound and a dopant compound, the LUMO (lowest unoccupied molecular orbital) energy level of the electron buffer layer is higher than the LUMO energy level of the host compound, and the LUMO energy level of the electron transport layer is higher than the LUMO energy level of the electron buffer layer.

8. The organic electroluminescent device according to claim 1 , wherein the LUMO energy level of the electron transport layer (Ae) and the LUMO energy level of the light-emitting layer (Ah) satisfy the following equation:

Ae≤Ah+ 0.5 eV.

9. The organic electroluminescent device according to claim 1 , wherein the LUMO energy level of the electron transport layer (Ae) and the LUMO energy level of the electron buffer layer (Ab) satisfy the following equation:

Ae≤Ab+ 0.2˜0.3 eV.

10. The organic electroluminescent device according to claim 1 , wherein the electron transport layer further comprises a reductive dopant.

Assignments (2)
CHANGE OF NAME Recorded Oct 17, 2024
From: ROHM & HAAS ELECTRONIC MATERIALS KOREA LTD
To: DUPONT SPECIALTY MATERIALS KOREA LTD
Reel/Frame 069185/0438 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 26, 2021
From: CHO, SANG-HEE; MOON, DOO-HYEON
To: ROHM AND HAAS ELECTRONIC MATERIALS KOREA LTD.
Reel/Frame 056974/0365 →
Priority Claims (2)
KR 10-2016-0121692 · Sep 22, 2016 · national
KR 10-2017-0114048 · Sep 6, 2017 · national
Continuity (1)
Related Publication 20190221751A1 · Jul 18, 2019