journal article·2015-06

High performance fluorescent and phosphorescent organic light-emitting diodes based on a charge-transfer-featured host material

Xu Wang, Jie Zhou, Juan Zhao, Zhiyun Lu, Junsheng Yu

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Abstract

Abstract Fluorescent and phosphorescent organic light-emitting diodes (OLEDs) were fabricated using a charge-transfer-featured compound, 6-{3,5-bis-[9-(4-t-butylphenyl)-9H-carbazol-3-yl]-phenoxy}-2-(4-t-butylphenyl)-benzo[de]isoquinoline-1,3-dione, as a host, and the electroluminescent (EL) characteristics of these two kinds of OLEDs were systematically studied. According to the photoluminescent quantum yields (ηpl), it was found that the external quantum efficiencies of both fluorescent and phosphorescent OLEDs were exceeding their theoretical limits. Based on the analysis of EL characteristics, the high device performance of fluorescent and phosphorescent OLEDs was attributed to both efficient energy transfer and triplet energy up-conversion, while direct exciton formation was also involved in phosphorescent OLEDs. In addition, the host film possessed high thermal and morphological stabilities due to the attachment of steric bulks on host molecule, resulting in the high doping concentration for both fluorescent and phosphorescent dyes. These results indicated that charge-transfer-featured material could be the promising host for both fluorescent and phosphorescent OLEDs.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (37)

Show source-provided references
1. Tang · Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
2. Baldo · Nature · 1998 · 395 · 15110.1038/25954 ↗
3. Liu · Chem. Commun. · 2009 · 369910.1039/b902807b ↗
4. Li · Tetrahedron · 2007 · 63 · 1016110.1016/j.tet.2007.07.104 ↗
5. Chew · Appl. Phys. Lett. · 2006 · 88 · 09351010.1063/1.2178468 ↗
6. Shih · Adv. Funct. Mater. · 2007 · 17 · 351410.1002/adfm.200700191 ↗
7. Jankus · Adv. Mater. · 2013 · 25 · 145510.1002/adma.201203615 ↗
8. Goushi · Nat. Photonics · 2012 · 6 · 25310.1038/nphoton.2012.31 ↗
10. Chao · Appl. Phys. Lett. · 1998 · 73 · 42610.1063/1.121888 ↗
11. Lee · Adv. Funct. Mater. · 2013 · 23 · 410510.1002/adfm.201300187 ↗
12. Park · Adv. Funct. Mater. · 2013 · 23 · 491410.1002/adfm.201300547 ↗
13. Lee · Org. Electron. · 2013 · 14 · 185610.1016/j.orgel.2013.04.020 ↗
14. Seino · Adv. Mater. · 2014 · 26 · 161210.1002/adma.201304253 ↗
15. Shin · Adv. Mater. · 2014 · 26 · 473010.1002/adma.201400955 ↗
16. Zhou · Chem. Commun. · 2014 · 50 · 758610.1039/C4CC00576G ↗
17. Li · J. Lumin. · 2007 · 122 · 62610.1016/j.jlumin.2006.01.243 ↗
18. Uchida · J. Appl. Phys. · 1999 · 86 · 168010.1063/1.370947 ↗
19. Holmes · Appl. Phys. Lett. · 2003 · 83 · 381810.1063/1.1624639 ↗
20. Wang · Adv. Funct. Mater. · 2009 · 19 · 8410.1002/adfm.200800918 ↗
21. Chen · Chem. Mater. · 2004 · 16 · 438910.1021/cm049679m ↗
22. Bulović · Chem. Phys. Lett. · 1998 · 287 · 45510.1016/S0009-2614(98)00168-7 ↗
23. Tsai · Adv. Mater. · 2006 · 18 · 121610.1002/adma.200502283 ↗
24. Luo · Adv. Funct. Mater. · 2010 · 20 · 128510.1002/adfm.200902329 ↗
25. Yokoyama · Appl. Phys. Lett. · 2011 · 99 · 12330310.1063/1.3637608 ↗
26. Wallikewitz · Phys. Rev. B · 2012 · 85 · 04520910.1103/PhysRevB.85.045209 ↗
27. Sun · Appl. Phys. Lett. · 2007 · 91 · 26350310.1063/1.2827178 ↗
28. Huang · Adv. Mater. · 2006 · 18 · 11410.1002/adma.200501105 ↗
29. Wang · Dyes Pigm. · 2014 · 100 · 8710.1016/j.dyepig.2013.08.021 ↗
30. Ren · Chem. Mater. · 2004 · 16 · 474310.1021/cm049402m ↗
31. Tsai · Adv. Mater. · 2007 · 19 · 86210.1002/adma.200600822 ↗
32. Wei · Adv. Funct. Mater. · 2007 · 17 · 331910.1002/adfm.200700359 ↗
33. Shinar · Appl. Surf. Sci. · 2007 · 254 · 74910.1016/j.apsusc.2007.04.090 ↗
34. Adamovich · New J. Chem. · 2002 · 26 · 117110.1039/b204301g ↗
35. Endo · Adv. Mater. · 2009 · 21 · 480210.1002/adma.200900983 ↗
36. Deaton · J. Am. Chem. Soc. · 2010 · 132 · 949910.1021/ja1004575 ↗
37. Uoyama · Nature · 2012 · 492 · 23410.1038/nature11687 ↗