IP Library Granted Patent US 12,279,519
Granted Patent B2
US 12,279,519 · App. 16/997,715 · Granted Apr 15, 2025

Organic electroluminescence device

Inventors: Hyejin Jung (Hwaseong-si, KR); Minje Kim (Suwon-si, KR); Eung Do Kim (Seoul, KR); Hyunyoung Kim (Yongin-si, KR); Hyojeong Kim (Hwaseong-si, KR); Hyosup Shin (Hwaseong-si, KR); Seokgyu Yoon (Hwaseong-si, KR); Youngki Lee (Asan-si, KR); Jungsub Lee (Hwaseong-si, KR); Jiyoung Lee (Hwaseong-si, KR); Kunwook Cho (Seoul, KR); Hyeon Gu Cho (Yongin-si, KR); Minsoo Choi (Hwaseong-si, KR); Youngeun Choi (Jeonju-si, KR); Hyein Jeong (Suwon-si, KR)
Assignee: Samsung Display Co., Ltd.
H10K85/40H10K85/322H10K85/342H10K85/346H10K85/654H10K85/6572H10K85/6574H10K85/6576H10K50/11H10K50/12H10K2101/10
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 12,279,519
App. No.
16/997,715
Granted
Apr 15, 2025
Kind
B2
Abstract

An organic electroluminescence device of an embodiment includes a first electrode, a second electrode on the first electrode, and an emission layer between the first electrode and the second electrode, wherein the emission layer includes a first host and a second host which are different from each other, a first dopant including an organic metal complex containing Ir, Ru, Rh, Pt, Pd, Cu, or Os as a central metal atom, and a second dopant represented by Formula D-2 below, and thereby the organic electroluminescence device may exhibit high luminous efficiency and long service life characteristics.

Claims (137)

1. An organic electroluminescence device comprising:

a first electrode;

a second electrode on the first electrode; and

an emission layer between the first electrode and the second electrode,

wherein the emission layer comprises:

a first host;

a second host different from the first host;

a first dopant represented by Formula D-1a or Formula D-1b; and

a second dopant represented by Formula D-2:

wherein, in Formula D-1a,

M1 is Pt, Pd, Cu, or Os,

Q 1 to Q 4 are each independently C or N,

C1 to C4 are each independently a substituted or unsubstituted hydrocarbon ring having 5 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heterocyclic ring having 2 to 30 carbon atoms for forming a ring,

L 21 to L 24 are each independently a direct linkage, *—O— *, * —S—* ,

a substituted or unsubstituted divalent alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted arylene group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroarylene group having 2 to 30 carbon atoms for forming a ring,

e1 to e4 are each independently 0 or 1,

R 31 to R 36 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a cyano group, a substituted or unsubstituted amine group, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 1 to 30 carbon atoms for forming a ring, and any of R 31 to R 36 are optionally combined with an adjacent group to form a ring, and

d1 to d4 are each independently an integer of 0 to 4,

in Formula D-lb,

M2 is Ir, Ru, or Rh,

n is 1 or 2,

X 1 to X 4 , Y 1 to Y 4 and Z 1 to Z 4 are each independently CR n or N, and R p , R q , and R n are each independently a hydrogen atom, a deuterium atom, a halogen atom, a cyano group, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted hydrocarbon ring having 5 to 30 carbon atoms for forming a ring, a substituted or unsubstituted heterocyclic ring having 2 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted amine group, and any of R p , R q , and R n are optionally combined with an adjacent group to form a ring,

and

wherein in Formula D-2,

A 1 and A 2 are each independently NR m or O,

R m is a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group of 2 to 30 carbon atoms for forming a ring, and

R 1 to R 11 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a cyano group, a substituted or unsubstituted amine group, a substituted or unsubstituted boryl group, a substituted or unsubstituted oxy group, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring, and any of R 1 to R 11 are optionally combined with an adjacent group to form a ring.

2. The organic electroluminescence device of claim 1 , wherein the first host is represented by Formula H-1:

and

wherein in Formula H-1,

L 1 is a direct linkage, a substituted or unsubstituted arylene group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroarylene group having 2 to 30 carbon atoms for forming a ring,

Ar 1 is a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring,

a and b are each independently an integer of 0 to 4, and

R a and R b are each independently a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring.

3. The organic electroluminescence device of claim 1 ,

wherein the second host is represented by Formula H-2:

and

wherein in Formula H-2,

Z 1 to Z 3 are each independently CR y or N, and

R y and R 21 to R 23 are each independently a hydrogen atom, a deuterium atom, a cyano group, a substituted or unsubstituted silyl group, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring.

4. The organic electroluminescence device of claim 3 ,

wherein Formula H-2 is represented by Formula H-2a:

and

wherein, in Formula H-2a, R 21 to R 23 are the same as those defined in Formula H-2.

5. The organic electroluminescence device of claim 3 ,

wherein Formula H-2 is represented by Formula H-2b:

and

wherein in Formula H-2b,

R 21 to R 23 and R y1 to R y3 are each independently a hydrogen atom, a deuterium atom, a cyano group, a substituted or unsubstituted silyl group, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring, and

at least one selected from R 21 to R 23 and R y1 to R y3 is a cyano group, an aryl group having 6 to 30 carbon atoms for forming a ring and comprising at least one cyano group as a substituent, or a heteroaryl group having 2 to 30 carbon atoms for forming a ring and comprising at least one cyano group as a substituent.

6. The organic electroluminescence device of claim 1 ,

wherein Formula D-2 is represented by any one of Formulae D-2a to D-2d:

and

wherein in Formula D-2a to Formula D-2d,

R m1 to R m4 are each independently a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring, and

R 1 to R 18 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a cyano group, a substituted or unsubstituted amine group, a substituted or unsubstituted boryl group, a substituted or unsubstituted oxy group, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring, and any of R 1 to R 18 are optionally combined with an adjacent group to form a ring.

7. The organic electroluminescence device of claim 1 ,

wherein the weight ratio of the first host and the second host is 7:3 to 3:7.

8. The organic electroluminescence device of claim 1 ,

wherein the content of the first dopant is about 10 wt % to about 15 wt %, and the content of the second dopant is about 1 wt % to about 5 wt %, with respect to the total compound weight of the first host, the second host, the first dopant, and the second dopant.

9. The organic electroluminescence device of claim 1 , wherein the first host comprises at least one compound selected from Compound Group 1:

10. The organic electroluminescence device of claim 1 ,

wherein the second host comprises at least one compound selected from Compound Group 2-1 and Compound Group 2-2:

11. The organic electroluminescence device of claim 1 ,

wherein the first dopant comprises at least one compound selected from Compound Group 3-1 and Compound Group 3-2:

and

wherein in each of Compound Group 3-2, in AD2-1 to AD2-4, AD2-13 to AD2-16, and AD2-25 to AD2-28, R is independently a hydrogen atom, a methyl group, an isopropyl group, a tert-butyl group, or a dimethylamine group.

12. The organic electroluminescence device of claim 1 ,

wherein the second dopant comprises at least one compound selected from Compound Group 4:

13. The organic electroluminescence device of claim 1 ,

wherein the emission layer is to emit blue fluorescence.

14. The organic electroluminescence device of claim 1 ,

wherein the lowest triplet exciton energy level of the first dopant is higher than the lowest triplet exciton energy level of the second dopant.

15. An organic electroluminescence device comprising:

a first electrode;

a second electrode on the first electrode; and

an emission layer between the first electrode and the second electrode,

wherein the emission layer comprises:

a first host represented by Formula H-1;

a second host represented by Formula H-2;

a first dopant represented by Formula D-1a or Formula D-1b; and

a second dopant as a delayed fluorescence emitter,

wherein the lowest triplet exciton energy level of the first dopant is higher than the lowest triplet exciton energy level of the second dopant:

wherein in Formula H-1,

L 1 is a direct linkage, a substituted or unsubstituted arylene group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroarylene group having 2 to 30 carbon atoms for forming a ring,

Ar 1 is a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring,

a and b are each independently an integer of 0 to 4, and

R a and R b are each independently a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring,

in Formula H-2,

Z 1 to Z 3 are each independently CR y or N, and

R y and R 21 to R 23 are each independently a hydrogen atom, a deuterium atom, a cyano group, a substituted or unsubstituted silyl group, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring,

and

wherein in Formula D-1a,

M1 is Pt, Pd, Cu, or Os,

Q 1 to Q 4 are each independently C or N,

C1 to C4 are each independently a substituted or unsubstituted hydrocarbon ring having 5 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heterocyclic ring having 2 to 30 carbon atoms for forming a ring,

L 21 to L 24 are each independently a direct linkage, *—O—*, *—S—

a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted arylene group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroarylene group having 2 to 30 carbon atoms for forming a ring,

e1 to e4 are each independently 0 or 1,

R 31 to R 36 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a cyano group, a substituted or unsubstituted amine group, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 1 to 30 carbon atoms for forming a ring, and any of R 31 to R 36 are optionally combined with an adjacent group to form a ring, and

d1 to d4 are each independently an integer of 0 to 4,

in Formula D-1b,

M2 is Ir, Ru, or Rh,

n is 1 or 2,

X 1 to X 4 , Y 1 to Y 4 , and Z 1 to Z 4 are each independently CRn or N, and

R p , R q , and R n are each independently a hydrogen atom, a deuterium atom, a halogen atom, a cyano group, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted hydrocarbon ring having 5 to 30 carbon atoms for forming a ring, a substituted or unsubstituted heterocyclic ring having 2 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted amine group, and any of R p , R q , and R n are optionally combined with an adjacent group to form a ring.

16. The organic electroluminescence device of claim 15 ,

wherein the second dopant is represented by Formula D-2:

and

wherein in Formula D-2,

A 1 and A 2 are each independently NR m or O,

R m is a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group of 2 to 30 carbon atoms for forming a ring, and

R 1 to R 11 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a cyano group, a substituted or unsubstituted amine group, a substituted or unsubstituted boryl group, a substituted or unsubstituted oxy group, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring, and any of R 1 to R 11 are optionally combined with an adjacent group to form a ring.

17. The organic electroluminescence device of claim 16 ,

wherein the second host is represented by Formula H-2a, and the first dopant is represented by Formula D-1a-1 or Formula D-1b-1:

and

wherein in Formula H-2a, R 21 to R 23 are the same as those defined in Formula H-2,

in Formula D-1a-1, C1 to C4, Q 1 to Q 4 , R 31 to R 34 , d1 to d4, L 22 , and e2 are the same as those defined in Formula D-1a, and

in Formula D-1 b-1, X 1 to X 4 , Y 1 to Y 4 , Z 1 to Z 4 , R p , and R q are the same as those defined in Formula D-1b.

18. The organic electroluminescence device of claim 16 ,

wherein the second host is represented by Formula H-2b, and the first dopant is represented by the following Formula D-1a-1 or Formula D-1b-1:

and

wherein, in Formula H-2b,

R 21 to R 23 and R y1 to R y3 are each independently a hydrogen atom, a deuterium atom, a cyano group, a substituted or unsubstituted silyl group, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, or a substituted or unsubstituted heteroaryl group having 2 to 30 carbon atoms for forming a ring, and

at least one selected from R 21 to R 23 and R y1 to R y3 is a cyano group, an aryl group having 6 to 30 carbon atoms for forming a ring and comprising at least one cyano group as a substituent, or a heteroaryl group having 2 to 30 carbon atoms for forming a ring and comprising at least one cyano group as a substituent,

in Formula D-1a-1, C1 to C4, Q 1 to Q 4 , R 31 to R 34 , and d1 to d4 are the same as those defined in Formula D-1a, and

in Formula D-1b-1, X 1 to X 4 , Y 1 to Y 4 , Z 1 to Z 4 , R p , and R q are the same as those defined in Formula D-1b.

19. The organic electroluminescence device of claim 15 ,

wherein the first host comprises at least one compound selected from Compound Group 1:

20. The organic electroluminescence device of claim 15 ,

wherein the second host comprises at least one compound selected from Compound Group 2-1 and Compound Group 2-2:

21. The organic electroluminescence device of claim 16 ,

wherein the first dopant comprises at least one compound selected from Compound Group 3-1 and Compound Group 3-2:

and

wherein, in each of Compound Group 3-2, in AD2-1 to AD2-4, AD2-13 to AD2-16, and AD2-25 to AD2-28, R is independently a hydrogen atom, a methyl group, an isopropyl group, a tert-butyl group, or a dimethylamine group.

22. The organic electroluminescence device of claim 15 ,

wherein the second dopant comprises at least one compound selected from Compound Group 4:

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 19, 2020
From: JUNG, HYEJIN; KIM, MINJE; KIM, EUNG DO; KIM, HYUNYOUNG; KIM, HYOJEONG; SHIN, HYOSUP; YOON, SEOKGYU; LEE, YOUNGKI; LEE, JUNGSUB; LEE, JIYOUNG; CHO, KUNWOOK; CHO, HYEON GU; CHOI, MINSOO; CHOI, YOUNGEUN; JEONG, HYEIN
To: SAMSUNG DISPLAY CO., LTD.
Reel/Frame 053555/0517 →
Priority Claims (1)
KR 10-2019-0121388 · Oct 1, 2019 · national
Continuity (1)
Related Publication 20210098721A1 · Apr 1, 2021
References Cited (136)
US 9604928B2 · Shitagaki et al. · 2017 [cited by applicant]
US 9666817B2 · Kim et al. · 2017 [cited by applicant]
US 9741939B2 · Kim et al. · 2017 [cited by applicant]
US 9923155B2 · Li et al. · 2018 [cited by applicant]
US 9980358B2 · Kim · 2018 [cited by applicant]
US 9985233B2 · Hashimoto · 2018 [cited by examiner]
US 10008676B2 · Han et al. · 2018 [cited by applicant]
US 10062850B2 · Jung et al. · 2018 [cited by applicant]
US 10090483B2 · Kim et al. · 2018 [cited by applicant]
US 10374166B2 · Hatakeyama et al. · 2019 [cited by applicant]
US 10418573B2 · Kim et al. · 2019 [cited by applicant]
US 10431766B2 · Ito et al. · 2019 [cited by applicant]
US 10886478B2 · Li et al. · 2021 [cited by applicant]
US 10916715B2 · Ko et al. · 2021 [cited by applicant]
US 11316124B2 · Ito et al. · 2022 [cited by applicant]
US 11482680B2 · Kim et al. · 2022 [cited by applicant]
US 20130264560A1 · Dobbs et al. · 2013 [cited by applicant]
US 20140077172A1 · So et al. · 2014 [cited by applicant]
US 20150001502A1 · Seo · 2015 [cited by examiner]
US 20150105556A1 · Li et al. · 2015 [cited by applicant]
US 20150207079A1 · Cho et al. · 2015 [cited by applicant]
US 20150295197A1 · Adamovich et al. · 2015 [cited by applicant]
US 20160028028A1 · Li et al. · 2016 [cited by applicant]
US 20160087227A1 · Kim et al. · 2016 [cited by applicant]
US 20160164020A1 · Kim et al. · 2016 [cited by applicant]
US 20160233442A1 · Yen et al. · 2016 [cited by applicant]
US 20160301014A1 · Kawamura et al. · 2016 [cited by applicant]
US 20170179395A1 · Kim et al. · 2017 [cited by applicant]
US 20170294613A1 · Cho et al. · 2017 [cited by applicant]
US 20170346029A1 · Kim · 2017 [cited by examiner]
US 20180033987A1 · Kim · 2018 [cited by examiner]
US 20180108857A1 · Adachi et al. · 2018 [cited by applicant]
US 20180151821A1 · Peng · 2018 [cited by examiner]
US 20180312533A1 · Ahn et al. · 2018 [cited by applicant]
US 20180323394A1 · Haldi et al. · 2018 [cited by applicant]
US 20180337361A1 · Lee et al. · 2018 [cited by applicant]
US 20180375036A1 · Chen et al. · 2018 [cited by applicant]
US 20190013478A1 · Iijima · 2019 [cited by examiner]
US 20190019964A1 · Jeon et al. · 2019 [cited by applicant]
US 20190019971A1 · Xie · 2019 [cited by examiner]
US 20190036055A1 · Lin et al. · 2019 [cited by applicant]
US 20190058124A1 · Hatakeyama et al. · 2019 [cited by applicant]
US 20190058137A1 · Ko · 2019 [cited by examiner]
US 20190062312A1 · Zink · 2019 [cited by applicant]
US 20190067616A1 · Jeon et al. · 2019 [cited by applicant]
US 20190093009A1 · Yen et al. · 2019 [cited by applicant]
US 20190097155A1 · Kim et al. · 2019 [cited by applicant]
US 20190148640A1 · Lim et al. · 2019 [cited by applicant]
US 20190157351A1 · Kim et al. · 2019 [cited by applicant]
US 20190203114A1 · Ihn et al. · 2019 [cited by applicant]
US 20190207112A1 · Hatakeyama et al. · 2019 [cited by applicant]
US 20190296254A1 · Ko et al. · 2019 [cited by applicant]
US 20190393422A1 · Sakamoto · 2019 [cited by applicant]
US 20200083461A1 · Duan et al. · 2020 [cited by applicant]
US 20200136046A1 · Béalle et al. · 2020 [cited by applicant]
US 20200203651A1 · Duan · 2020 [cited by examiner]
US 20200321539A1 · Zhao · 2020 [cited by examiner]
US 20210098713A1 · Choi et al. · 2021 [cited by applicant]
US 20210098714A1 · Choi et al. · 2021 [cited by applicant]
US 20210098716A1 · Lee et al. · 2021 [cited by applicant]
US 20210098721A1 · Jung et al. · 2021 [cited by applicant]
US 20210104681A1 · Kim et al. · 2021 [cited by applicant]
US 20210292342A1 · Suzuki et al. · 2021 [cited by applicant]
US 20220024958A1 · Ko et al. · 2022 [cited by applicant]
US 20220131086A1 · Lee et al. · 2022 [cited by applicant]
US 20230127039A1 · Naijo et al. · 2023 [cited by applicant]
US 20230138754A1 · Lee et al. · 2023 [cited by applicant]
CN 106910831A · 2017 [cited by applicant]
CN 107275496A · 2017 [cited by applicant]
CN 109192874A · 2019 [cited by applicant]
CN 109786569A · 2019 [cited by applicant]
EP 3109253A1 · 2016 [cited by applicant]
EP 3435438A2 · 2019 [cited by applicant]
EP 3800683A1 · 2021 [cited by applicant]
JP 2004273190A · 2004 [cited by applicant]
JP 2011153276A · 2011 [cited by applicant]
JP 2016130231A · 2016 [cited by applicant]
JP 2019169710A · 2019 [cited by applicant]
KR 101219668B1 · 2013 [cited by applicant]
KR 101419810B1 · 2014 [cited by applicant]
KR 1020160012941A · 2016 [cited by applicant]
KR 1020160034528A · 2016 [cited by applicant]
KR 1020160039974A · 2016 [cited by applicant]
KR 101617877B1 · 2016 [cited by applicant]
KR 1020160067629A · 2016 [cited by applicant]
KR 1020160101519A · 2016 [cited by applicant]
KR 101646732B1 · 2016 [cited by applicant]
KR 1020160119683A · 2016 [cited by applicant]
KR 101680934B1 · 2016 [cited by applicant]
KR 1020170014797A · 2017 [cited by applicant]
KR 101706752B1 · 2017 [cited by applicant]
KR 1020170026075A · 2017 [cited by applicant]
KR 1020170078573A · 2017 [cited by applicant]
KR 1020170083960A · 2017 [cited by applicant]
KR 20180013380A · 2018 [cited by applicant]
KR 1020180033094A · 2018 [cited by applicant]
KR 20180043886A · 2018 [cited by applicant]
KR 20180108604A · 2018 [cited by applicant]
KR 1020180120865A · 2018 [cited by applicant]
KR 20180134850A · 2018 [cited by applicant]
KR 1020190000812A · 2019 [cited by applicant]
KR 1020190008481A · 2019 [cited by applicant]
KR 1020190034126A · 2019 [cited by applicant]
WO WO2011081286A2 · 2011 [cited by applicant]
WO WO2016152605A1 · 2016 [cited by applicant]
WO 2019128105A1 · 2019 [cited by applicant]
Liang, Xiao, et al. “Peripheral amplification of multi-resonance induced thermally activated delayed fluorescence for highly efficient OLEDs.” Angewandte Chemie 130.35 (2018): 11486-11490. (Year: 2018). [cited by examiner]
Martin C. E. Huber, et al., “The measurement of oscillator strengths,” Reports on Progress in Physics, Institute of Physics Publishing, Bristol, GB, Vo. 49, No. 4, Apr. 1, 1986, pp. 397-490, XP020024846, DOI: 10.1088/00… [cited by applicant]
Translation—JP-2004273190-A (Year: 2004). [cited by applicant]
Translation—WO-2011081286-A2 (Year: 2011). [cited by applicant]
U.S. Office Action dated Jan. 24, 2023, issued in U.S. Appl. No. 16/919,858 (25 pages). [cited by applicant]
US Notice of Allowance dated Jun. 1, 2023, issued in U.S. Appl. No. 18/064,787 (8 pages). [cited by applicant]
JP-2011153276-A—translation (Year: 2011). [cited by applicant]
US Final Office Action dated Aug. 2, 2023, issued in U.S. Appl. No. 16/919,858 (26 pages). [cited by applicant]
Chiu, et al., “High-Efficiency Blue Phosphorescence Organic Light-Emitting Diode with Ambipolar Carbozole-Triazole Host,” J. Phys. Chem. C (2015), vol. 119, pp. 16846-16852. [cited by applicant]
Choi, et al., “Simultaneous achievement of High Efficiency and Long Lifetime in Deep Blue Phosphorescent Organic Light-Emitting Diodes,” Advanced Optical Materials (2019), vol. 7, No. 23, pp. 1901374-1901374. [cited by applicant]
Finkenzeller, et al., “Emission of Ir(ppy) [cited by applicant]
Hatakeyama, et al., “Ultrapure Blue Thermally Activated Delayed Fluorescence Molecules: Efficient HOMO-LUMO Separation by the Multiple Resonance Effect,” Adv. Mater. (2016), vol. 28, pp. 2777-2781. [cited by applicant]
Hedley, et al., “Ultrafast Luminescence in Ir(ppy) [cited by applicant]
Huang, et al., “Investigation of Exciton Recombination Zone in Quantum Dot Light-Emitting Diodes Using a Fluorescent Probe”, ACS Appl. Mater. Interfaces (2017), vol. 9, pp. 27809-27816. [cited by applicant]
Joo, et al., “Development of Solution-Processable Blue/Hybrid-White OLEDs Based on Thermally Activated Delayed Fluorescence”, Journal of Industrial and Engineering Chemistry (2018), vol. 65, pp. 35-39. [cited by applicant]
Lee, et al., “Phosphor Sensitized Thermally Activated Delayed Fluorescence Organic Light-Emitting Diodes with Ideal Deep Blue Device Performances”, Journal of Materials Chemistry C (2019), vol. 7, pp. 8562-8568. [cited by applicant]
Li, et al. “Efficient and Stable White Organic Light-Emitting Diodes Employing a Single Emitter,” Adv. Mater. (2014), vol. 26, pp. 2931-2936. [cited by applicant]
Li, et al., “Efficient Solution-Processed Blue and White OLEDs Based on a High-Triplet Bipolar Host and a Blue TADF Emitter”, Organic Electronics (2018), vol. 58, pp. 276-282. [cited by applicant]
Office Action for U.S. Appl. No. 17/131,555 dated Oct. 18, 2023, 20 pages. [cited by applicant]
Park, et al., “High Efficiency of Over 25% and Long Device Lifetime of Over 500 h at 1000 nit in Blue Fluorescent Organic Light-Emitting Diodes” Adv. Mater. (2022), vol. 34, 7 pages. [cited by applicant]
Saghaei, et al., “Effect of PEDOT:PSS on the Performance of Solution-Processed Blue Phosphorescent Organic Light-emitting Diodes with an Exciplex Host,” Mater. Adv. (2022), vol. 3, pp. 1055-1063. [cited by applicant]
Zhao, et al., “Highly Efficient Red OLEDs Using DCJTB as the Dopant and Delayed Fluorescent Exciplex as the Host,” Scientific Reports (2015), vol. 5, 8 pages. [cited by applicant]
US Office Action dated Feb. 12, 2024, issued in U.S. Appl. No. 16/919,858 (19 pages). [cited by applicant]
US Final Office Action dated Mar. 8, 2024, issued in U.S. Appl. No. 17/131,555 (19 pages). [cited by applicant]
US Final Office Action dated Jun. 12, 2024, issued in U.S. Appl. No. 16/919,858 (20 pages). [cited by applicant]
Wong, Michael Y. and Eli Zysman-Colman. “Purely organic thermally activated delayed fluorescence materials for organic light-emitting diodes.” Advanced Materials 29.22 (2017): 1605444. (Year: 2017). [cited by applicant]
US Office Action dated Oct. 10, 2024, issued in U.S. Appl. No. 18/528,604 (8 pages). [cited by applicant]
US Office Action dated Oct. 10, 2024, issued in U.S. Appl. No. 17/131,555 (25 pages). [cited by applicant]
US Office Action dated Dec. 18, 2024, issued in U.S. Appl. No. 16/919,858 (20 pages). [cited by applicant]
US Notice of Allowance dated Feb. 12, 2025, issued in U.S. Appl. No. 18/528,604 (6 pages). [cited by applicant]