journal article·2012-12

A promising phosphorescent heteroleptic iridium complex with carbazole-functionalized substituent: Synthesis, photophysical and electroluminescent performances

Xiao Li, Tienan Zang, Lianshui Yu, Dongyu Zhang, Gonghao Lu, Haijun Chi, Guoyong Xiao, Yan Dong, Zheng Cui, Zhiqiang Zhang, Zhizhi Hu

Optical Materials· Volume 35· Issue 2
Publisher page

Abstract

Abstract A promising heteroleptic iridium complex with carbazole-functionalized substituent, i.e., (cbbt)2Ir(acac), in which cbbt was 2-(4-(4-(9H-carbazol-9-yl)butoxy)phenyl)benzo[d]thiazole and acac acetylacetonate, was designed, synthesized and structurally characterized. The complex emitted intensely orange phosphorescence upon photoexcitation with high luminescent quantum efficiency (0.30), short triplet lifetime (0.15 μs) and high decomposition temperature (310 °C). The electronic properties of (cbbt)2Ir(acac) were also examined according to the density functional theory calculations. Organic light-emitting diodes using (cbbt)2Ir(acac) as doped emitter exhibited orange electrophosphorescence with prominent performances. An extremely high brightness of 17,910 cd m−2 at a high voltage (17 V) and a maximum luminance efficiency of 25.5 cd A−1 were achieved. More importantly, those devices exhibited low efficiency roll-off of 30–35% from 10 to 100 mA cm−2, which was probably attributed to the short triplet lifetime of (cbbt)2Ir(acac).
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Conducting polymers and applications

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

References (59)

Show source-provided references
1. Baldo · Nature · 1998 · 395 · 15110.1038/25954 ↗
2. Baldo · Nature · 2000 · 403 · 75010.1038/35001541 ↗
3. Paulose · Adv. Mater. · 2004 · 16 · 200310.1002/adma.200400149 ↗
4. Wong · Coord. Chem. Rev. · 2009 · 253 · 170910.1016/j.ccr.2009.01.013 ↗
5. Wong · J. Mater. Chem. · 2009 · 19 · 445710.1039/b819943d ↗
6. Zhou · Chem. Asian J. · 2011 · 6 · 170610.1002/asia.201000928 ↗
7. Xie · Adv. Mater. · 2001 · 13 · 124510.1002/1521-4095(200108)13:16<1245::AID-ADMA1245>3.0.CO;2-J ↗
8. You · J. Mater. Chem. · 2006 · 16 · 470610.1039/b611288a ↗
9. Zhou · Angew. Chem. Int. Ed. · 2007 · 46 · 114910.1002/anie.200604094 ↗
10. Zhou · Adv. Funct. Mater. · 2008 · 18 · 49910.1002/adfm.200700719 ↗
11. Zhang · Adv. Mater. · 2012 · 24 · 187310.1002/adma.201104758 ↗
12. Zou · Adv. Mater. · 2011 · 23 · 297610.1002/adma.201101130 ↗
13. Wu · Adv. Mater. · 2009 · 21 · 418110.1002/adma.200900638 ↗
14. Zhou · J. Organomet. Chem. · 2007 · 692 · 346110.1016/j.jorganchem.2007.04.013 ↗
15. Zhou · Chem. Commun. · 2009 · 357410.1039/b904382a ↗
16. He · Inorg. Chem. · 2006 · 45 · 1092210.1021/ic061566c ↗
17. Wong · Organometallics · 2005 · 24 · 407910.1021/om050343b ↗
18. Zhou · J. Mater. Chem. · 2010 · 20 · 747210.1039/c0jm01159b ↗
19. Li · Appl. Phys. Lett. · 2010 · 97 · 26330310.1063/1.3531576 ↗
20. Si · Inorg. Chem. · 2007 · 46 · 615510.1021/ic061645o ↗
21. Ho · Adv. Funct. Mater. · 2008 · 18 · 92810.1002/adfm.200701115 ↗
22. Chen · Appl. Phys. Lett. · 2007 · 91 · 02350510.1063/1.2757096 ↗
23. Schwartz · Appl. Phys. Lett. · 2006 · 89 · 08350910.1063/1.2338588 ↗
24. Shih · Appl. Phys. Lett. · 2006 · 88 · 25111010.1063/1.2214141 ↗
25. Yu · Chem. Mater. · 2006 · 18 · 509710.1021/cm061030p ↗
26. Zhou · ChemPhysChem · 2011 · 12 · 283610.1002/cphc.201100259 ↗
27. Ho · Appl. Phys. Lett. · 2008 · 92 · 08330110.1063/1.2883935 ↗
28. Zhou · J. Photochem. Photobio. C: Photochem. Rev. · 2010 · 11 · 13310.1016/j.jphotochemrev.2011.01.001 ↗
29. Yang · J. Mater. Chem. · 2012 · 22 · 713610.1039/c2jm14712b ↗
30. Al Attar · Appl. Phys. Lett. · 2005 · 86 · 12110110.1063/1.1873046 ↗
31. Lamansky · J. Am. Chem. Soc. · 2001 · 123 · 430410.1021/ja003693s ↗
32. Chen · Inorg. Chim. Acta · 2006 · 359 · 420710.1016/j.ica.2006.06.039 ↗
33. Wang · Adv. Mater. · 2011 · 23 · 282310.1002/adma.201100302 ↗
34. Zhang · Opt. Mater. · 2009 · 31 · 90510.1016/j.optmat.2008.10.037 ↗
35. Choi · Synth. Met. · 2009 · 159 · 151710.1016/j.synthmet.2009.04.021 ↗
36. Laskar · Chem. Mater. · 2004 · 16 · 11110.1021/cm030410x ↗
37. Ono · Eur. J. Inorg. Chem. · 2006 · 367610.1002/ejic.200600285 ↗
38. Liu · ChemPhysChem · 2008 · 9 · 63410.1002/cphc.200700648 ↗
39. Wong · Angew. Chem. Int. Ed. · 2006 · 45 · 780010.1002/anie.200602906 ↗
40. Ho · Chem. Asian J. · 2009 · 4 · 8910.1002/asia.200800226 ↗
41. Ding · Adv. Funct. Mater. · 2006 · 16 · 57510.1002/adfm.200500591 ↗
42. Ho · J. Organomet. Chem. · 2009 · 694 · 273510.1016/j.jorganchem.2009.03.002 ↗
43. Wang · Org. Electron. · 2010 · 11 · 23810.1016/j.orgel.2009.11.001 ↗
44. Ho · J. Mater. Chem. · 2012 · 22 · 21510.1039/C1JM13794H ↗
45. Ho · Adv. Funct. Mater. · 2007 · 17 · 292510.1002/adfm.200601205 ↗
46. Ho · Adv. Funct. Mater. · 2008 · 18 · 31910.1002/adfm.200700665 ↗
47. Al-Attar · Adv. Funct. Mater. · 2011 · 21 · 237610.1002/adfm.201100324 ↗
48. Tavasli · J. Mater. Chem. · 2012 · 22 · 641910.1039/c2jm15049b ↗
49. Shan · J. Organomet. Chem. · 2012 · 702 · 2710.1016/j.jorganchem.2011.12.020 ↗
50. Si · J. Lumin. · 2009 · 129 · 18110.1016/j.jlumin.2008.09.014 ↗
51. Xu · Inorg. Chim. Acta · 2009 · 362 · 51510.1016/j.ica.2008.04.047 ↗
52. Colombo · Inorg. Chem. · 1994 · 33 · 54510.1021/ic00081a024 ↗
53. Lamansky · Inorg. Chem. · 2001 · 40 · 170410.1021/ic0008969 ↗
54. Tamayo · J. Am. Chem. Soc. · 2003 · 125 · 737710.1021/ja034537z ↗
55. Hay · J. Phys. Chem. A · 2002 · 106 · 163410.1021/jp013949w ↗
56. Lowry · Chem. Eur. J. · 2006 · 12 · 797010.1002/chem.200600618 ↗
57. Lyu · J. Phys. Chem. B · 2006 · 110 · 1030310.1021/jp057446s ↗
58. Hwang · Inorg. Chem. · 2005 · 44 · 134410.1021/ic0489443 ↗
59. Zhou · J. Mater. Chem. · 2008 · 18 · 179910.1039/b718653c ↗