IP Library Granted Patent US 7,084,425
Granted Patent B2
US 7,084,425 · App. 10/729,208 · Granted Aug 1, 2006

Organic electroluminescent devices

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Quick Facts
Patent No.
US 7,084,425
App. No.
10/729,208
Granted
Aug 1, 2006
Kind
B2
Abstract

Disclosed is an electroluminescent device comprising a cathode and an anode; and, located therebetween, a light-emitting layer (LEL) comprising a phosphorescent green-light-emitting material and a host material for the light-emitting material, and in a layer adjacent to the LEL on the anode side, an exciton-blocking layer containing a compound having a hole mobility of at least 1×10 −3 cm 2 V −1 s −1 and a triplet energy exceeding that of the green-light-emitting material of the LEL. Such a device provides useful light emission.

Claims (90)

1. An electroluminescent device comprising a cathode and an anode; and, located therebetween, a light-emitting layer (LEL) comprising a phosphorescent green-light-emitting material and a host material for the light-emitting material, and in a layer adjacent to the LEL on the anode side, an exciton-blocking layer containing a compound having a hole mobility of at least 1×10 −3 cm 2 V −1 s −1 and a triplet energy exceeding that of the green-light-emitting material of the LEL.

2. The device of claim 1 wherein the exciton-blocking layer contains a compound having a hole mobility of at least 5×10 −3 cm 2 V −1 s −1 .

3. The device of claim 1 wherein the phosphorescent green-light-emitting material is an organometallic compound comprising a 5th-row Periodic Table transition metal.

4. The device of claim 2 wherein the metal is iridium or platinum.

5. The device of claim 2 wherein the organometallic compound includes a ligand that can be coordinated to a metal through an sp 2 carbon and a heteroatom.

6. The device of claim 4 wherein the ligand is a phenylpyridine group.

7. The device of claim 5 wherein the organometallic compound is chosen from tris(2-phenylpyridinato-N,C 2′ )iridium(III), bis(2-phenylpyridinato-N,C 2′ )iridium(III)(acetylacetonate), and bis(2-phenylpyridinato-N,C 2′ )platinum(II) group containing compounds.

8. The device of claim 1 wherein the compound in the exciton-blocking layer is a triarylamine compound.

9. The device of claim 7 wherein the compound includes two or more distinct triarylamine groups and wherein no multiple-ring or fused-ring systems are attached simultaneously to the nitrogen atoms of the two or more triarylamine groups.

10. The device of claim 1 wherein the compound in the exciton-blocking layer is a represented by Formula (2):

wherein:

R 1 and R 2 represent hydrogen or substituents, provided that R 1 and R 2 can join to form a ring;

Ar 1 –Ar 4 represent independently selected aromatic groups;

each R a independently represents hydrogen or an independently selected substituent;

with the provision that R 1 , R 2 , R a , and Ar 1 –Ar 4 do not contain fused aromatic rings; and

each n is independently selected as 0–4.

11. The device of claim 10 wherein R 1 and R 2 , independently represents hydrogen or an independently selected hydrocarbon substituent, provided that R 1 and R 2 can join to form a hydrocarbon ring, and each R a represents an independently selected hydrocarbon substituent.

12. The device of claim 8 wherein the compound is chosen from among:

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)cyclohexane (TAPC);

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)-4-phenylcyclohexane;

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)-4-methylcyclohexane; or

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)-3-phenylpropane.

13. An electroluminescent device comprising a cathode and an anode, and, located therebetween, a light-emitting layer (LEL) comprising a phosphorescent light-emitting material and a host for the light-emitting material, a hole-injecting layer, and, in a layer adjacent to the LEL on the anode side, an exciton-blocking layer containing a compound having a hole mobility of at least 1×10 −3 cm 2 V −1 s −1 and a triplet energy exceeding that of the phosphorescent light-emitting material of the LEL.

14. The device of claim 13 wherein the phosphorescent light-emitting material is an organometallic compound comprising a 5th-row Periodic Table transition metal.

15. The device of claim 14 wherein the transition metal is iridium or platinum.

16. The device of claim 14 wherein the organometallic compound includes a ligand that can be coordinated to a metal through an sp 2 carbon and a heteroatom.

17. The device of claim 16 wherein the ligand is a phenylpyridine group containing compound.

18. The device of claim 14 wherein the organometallic compound is chosen from tris(2-phenylpyridinato-N,C 2′ )iridium(III), bis(2-phenylpyridinato-N,C 2′ )iridium(III)(acetylacetonate), and bis(2-phenylpyridinato-N,C 2′ )platinum(II) group containing compounds.

19. The device of claim 13 wherein the compound having hole mobility in the exciton-blocking layer is a triarylamine compound.

20. The device of claim 19 wherein the c compound having hole mobility in the exciton-blocking layer includes two or more triarylamine groups and wherein no multiple-ring or fused-ring systems are attached to the nitrogen atoms of two or more triarylamine groups.

21. The device of claim 13 wherein the compound having hole mobility in the exciton-blocking layer is a represented by Formula (2):

wherein:

R 1 and R 2 represent substituents, provided that R 1 and R 2 can join to form a ring;

Ar 1 –Ar 4 represent independently selected aromatic groups;

each R a independently represents hydrogen or an independently selected substituent;

with the provision that R 1 , R 2 , R a , and Ar 1 –Ar 4 do not contain fused aromatic rings; and

each n is independently selected as 0–4.

22. The device of claim 21 wherein R 1 and R 2 , independently represent hydrogen or an independently selected hydrocarbon substituent, provided that R 1 and R 2 can join to form a hydrocarbon ring, and each R a independently represents a selected hydrocarbon substituent.

23. The device of claim 19 wherein the compound is chosen from:

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)cyclohexane (TAPC);

1,1-Bis(4-(N,N-(di-p-tolylamino)phenyl)-4-phenylcyclohexane;

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)-4-methylcyclohexane; and 1,1-Bis(4-(N,N′di-p-tolylamino)phenyl)-3-phenylpropane.

24. The device of claim 13 wherein the hole-injecting layer comprises a plasma-deposited fluorocarbon polymer.

25. An electroluminescent device comprising a cathode and an anode, and, located therebetween, a light-emitting layer (LEL) comprising a phosphorescent light-emitting material and a host for the light-emitting material, and, in a layer adjacent to the LEL on the anode side, an exciton-blocking layer containing a compound having a hole mobility of at least 1×10 −1 cm 2 V −1 s −1 and a triplet energy exceeding that of the phosphorescent light-emitting material, and, on the cathode side of the LEL, a hole-blocking layer.

26. The device of claim 25 wherein the phosphorescent light-emitting material is an organometallic compound comprising a 5th-row Periodic Table transition metal.

27. The device of claim 26 wherein the metal is iridium or platinum.

28. The device of claim 25 wherein the organometallic compound includes a ligand that can be coordinated to a metal through an sp 2 carbon and a heteroatom.

29. The device of claim 25 wherein the ligand is a phenylpyridine grop containing compound.

30. The device of claim 25 wherein the organometallic compound is chosen from tris(2-phenylpyridinato-N,C 2′ )iridium(III), bis(2-phenylpyridinato-N,C 2′ )iridium(III)(acetylacetonate), and bis(2-phenylpyridinato-N,C 2 )platinum(II) group containing comounds.

31. The device of claim 25 wherein the compound in the exciton-blocking layer is a triarylamine compound.

32. The device of claim 31 wherein the compound includes two or more triarylamine groups and wherein no multiple-ring or fused-ring systems are attached to the nitrogen atoms of two or more triarylamine groups.

33. The device of claim 25 wherein the compound in the exciton-blocking layer is a represented by Formula (2):

wherein:

R 1 and R 2 represent hydrogen or substituents, provided that R 1 and R 2 can join to form a ring;

Ar 1 –Ar 4 represent independently selected aromatic groups;

each R a independently represents hydrogen or an independently selected substituent;

with the provision that R 1 , R 2 , R a , and Ar 1 –Ar 4 do not contain fused aromatic rings and;

each n is independently selected as 0–4.

34. The device of claim 33 wherein R 1 and R 2 independently represent hydrogen or an independently selected hydrocarbon substituent, provided that R 1 and R 2 can join to form a hydrocarbon ring and each R a represents a hydrocarbon substituent.

35. The device of claim 31 wherein the compound is chosen from:

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)cyclohexane (TAPC);

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)-4-phenylcyclohexane;

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)-4-methylcyclohexane; and

1,1-Bis(4-(N,N-di-p-tolylamino)phenyl)-3-phenylpropane.

36. The device of claim 25 wherein the hole-blocking layer comprises an aluminum complex that emits blue light when it luminesces.

37. The device of claim 36 wherein the aluminum complex is bis(2-methyl-8-quinolinolato)(4-phenylphenylato)aluminum(III).

38. The device of claim 1 wherein there is hole-transporting layer adjacent to the exciton-blocking layer on the anode side, comprising a material of Formula A:

wherein:

Q 1 and Q 2 are independently selected aromatic tertiary amine moieties provided at least one of Q 1 or Q 2 contains a polycyclic fused ring; and

G is an aryl group.

39. The device of claim 13 wherein there is a hole-transporting layer adjacent to the exciton-blocking layer on the anode side, comprising a material of Formula A,

wherein:

Q 1 and Q 2 are independently selected aromatic tertiary amine moieties provided at least one of Q 1 or Q 2 contains a polycyclic fused ring; and

G is an aryl group.

40. The device of claim 25 wherein there is hole-transporting layer adjacent to the exciton-blocking layer on the anode side, comprises a material of Formula A:

wherein:

Q 1 and Q 2 are independently selected aromatic tertiary amine moieties provided at least one of Q 1 or Q 2 contains a polycyclic fused ring; and

G is an aryl group.

41. The device of claim 1 including a means for emitting white light.

42. The device of claim 41 including two or more compounds capable of emitting complimentary colors.

43. The device of claim 41 including a compound capable of emitting white light.

44. The device of claim 41 including a filtering means.

45. A display comprising the electroluminescent device of claim 1 .

46. An area lighting device comprising the electroluminescent device of claim 1 .

47. The device of claim 1 wherein the host in the LEL layer comprises a carbazole represented by Formula 1:

wherein:

W independently represents hydrogen or an independently selected substituent;

each p independently is 0–4, and

L A represents a linking group.

48. A process for emitting light comprising applying a potential across the device of claim 1 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2010
From: EASTMAN KODAK COMPANY
To: GLOBAL OLED TECHNOLOGY LLC
Reel/Frame 023998/0368 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 3, 2004
From: KONDAKOVA, MARINA E.; YOUNG, RALPH H.
To: EASTMAN KODAK COMPANY
Reel/Frame 015038/0850 →