Bipolar Phenanthroimidazole Derivatives Containing Bulky Polyaromatic Hydrocarbons for Nondoped Blue Electroluminescence Devices with High Efficiency and Low Efficiency Roll-Off
Source abstract
Abstract
A series of bipolar phenanthroimidazole derivatives, TTP-TPI, DPT-TPI, and DPF-TPI, were designed and synthesized by incorporating polyaromatic hydrocarbon groups to phenanthroimidazole through a phenyl bridge. The bulky polyaromatic hydrocarbon units endow the molecules with high glass-transition temperatures, nonplanar twisty structures which reduce molecular aggregations. The bipolar transporting natures of these materials are demonstrated by single-carrier devices with supported of theoretical calculations. Nondoped organic light-emitting devices (OLEDs) using these phenanthroimidazole derivatives as emitters show blue-violet to sky-blue emissions with Commission Internationale de l’Eclairage (CIE) coordinates of (0.16, 0.05) for TTP-TPI, (0.16, 0.07) for DPT-TPI, and (0.17, 0.24) for DPF-TPI. The TTP-TPI-, DPT-TPI-, and DPF-TPI-based nondoped devices show impressive external quantum efficiencies (EQE) of 5.02, 5.25, 4.85%, respectively (corresponding current efficiencies: 2.10, 3.13, and 8.41 cd/A). These values are the best or among the best comparing to those of the reported nondoped OLEDs with the corresponding color gamuts. These devices also show small efficiency roll-off at high brightness (1000 cd/m 2 ) with EQEs drop by 20.7, 12, and 0%. Moreover, with well-balanced carrier transport, DPF-TPI based device can achieve a higher brightness of 10000 cd/m 2 with EQE maintaining at 4.49% (only drop by 7.4%).
Source: openalex_inverted_index · Quality: baseline
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.
Affiliations
Department of Chemistry, Shantou University, Guangdong 515063, China
Nano-organic Photoelectronic Laboratory and Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, , Chinese Academy of Sciences, Beijing 100190, China
References (70)
Show source-provided references
1. Wen S. W. · J. Disp. Int. Symp. · 2004 · 35 · 48
2. Sun Y. · Nature · 2006 · 440 · 90810.1038/nature04645 ↗
3. Schwartz G. · Appl. Phys. Lett. · 2008 · 92 · 05331110.1063/1.2836772 ↗
4. Luo J. · Adv. Mater. · 2007 · 19 · 111310.1002/adma.200601241 ↗
5. Tung Y. J. · Dig. Tech. Pap.–Soc. Inf. Disp. Int. Symp · 2004 · 35 · 4810.1889/1.1811453 ↗
6. Lee M. T. · Adv. Mater. · 2005 · 17 · 249310.1002/adma.200501169 ↗
7. Lee S. J. · Adv. Funct. Mater. · 2008 · 18 · 392210.1002/adfm.200800697 ↗
8. Lai M. Y. · Angew. Chem., Int. Ed. · 2008 · 47 · 58110.1002/anie.200704113 ↗
9. Chen C. H. · Adv. Funct. Mater. · 2009 · 19 · 266110.1002/adfm.200900561 ↗
10. Zheng C. J. · Adv. Mater. · 2013 · 25 · 220510.1002/adma.201204724 ↗
11. Baldo M. A. · Nature · 1998 · 395 · 15110.1038/25954 ↗
12. Baldo M. A. · Appl. Phys. Lett. · 1999 · 75 · 410.1063/1.124258 ↗
13. Adachi C. · J. Appl. Phys. · 2001 · 90 · 504810.1063/1.1409582 ↗
14. Sasabe H. · Chem. Commun. · 2008 · 582110.1039/b812270a ↗
15. Tao Y. T. · Adv. Funct. Mater. · 2010 · 20 · 30410.1002/adfm.200901615 ↗
16. Cai M. · Adv. Mater. · 2012 · 24 · 433710.1002/adma.201202035 ↗
17. Jankus V. · Adv. Mater. · 2013 · 25 · 145510.1002/adma.201203615 ↗
18. Chang C. H. · J. Mater. Chem. · 2012 · 22 · 383210.1039/c2jm14686j ↗
19. Benor A. · Appl. Phys. Lett. · 2010 · 96 · 24331010.1063/1.3452344 ↗
20. Lee S. · Adv. Funct. Mater. · 2013 · 23 · 410510.1002/adfm.201300187 ↗
21. Gong S. L. · Adv. Funct. Mater. · 2011 · 21 · 116810.1002/adfm.201002066 ↗
22. Huang J. H. · J. Mater. Chem. · 2011 · 21 · 295710.1039/c0jm03300f ↗
23. Lin S. L. · Adv. Mater. · 2008 · 20 · 394710.1002/adma.200801023 ↗
24. Thomas K. R. J. · Chem. Mater. · 2005 · 17 · 186010.1021/cm047705a ↗
25. Chou H. H. · Adv. Mater. · 2010 · 22 · 246810.1002/adma.201000061 ↗
26. Gong S. L. · Adv. Mater. · 2010 · 22 · 537010.1002/adma.201002732 ↗
27. Gong S. L. · Chem. Mater. · 2012 · 24 · 312010.1021/cm301032p ↗
28. Uoyama H. · Nature · 2012 · 492 · 23410.1038/nature11687 ↗
29. Zhang Q. S. · J. Am. Chem. Soc. · 2012 · 134 · 1470610.1021/ja306538w ↗
30. Lin W. Y. · Org. Lett. · 2008 · 10 · 557710.1021/ol802436j ↗
31. Yuan Y. · New J. Chem. · 2011 · 35 · 153410.1039/c1nj20072k ↗
32. Zhang Y. · Chem. Mater. · 2012 · 24 · 6110.1021/cm201789u ↗
33. Li W. J. · Adv. Funt. Mater. · 2012 · 22 · 279710.1002/adfm.201200116 ↗
34. Huang H. · J. Phys. Chem. C · 2012 · 116 · 1945810.1021/jp305764b ↗
35. Xu X. J. · Adv. Mater. · 2007 · 19 · 128110.1002/adma.200601919 ↗
36. Qin T. S. · Angew. Chem., Int. Ed. · 2008 · 47 · 829210.1002/anie.200802854 ↗
37. Qin T. S. · J. Am. Chem. Soc. · 2011 · 133 · 130110.1021/ja109734e ↗
38. Thomas K. R. J. · Chem. Commun. · 2004 · 232810.1039/b409800e ↗
39. Kapoor N. · New J. Chem. · 2010 · 34 · 273910.1039/c0nj00415d ↗
40. Lambert C. · J. Org. Chem. · 2012 · 77 · 614710.1021/jo300924x ↗
41. Yang X. · Langmuir · 2010 · 26 · 1124410.1021/la1005727 ↗
42. Wehmeier M. · Chem.—Eur. J. · 2001 · 7 · 219710.1002/1521-3765(20010518)7:10<2197::AID-CHEM2197>3.0.CO;2-G ↗
43. Chiechi R. C. · Adv. Mater. · 2006 · 18 · 32510.1002/adma.200501682 ↗
44. Kuo C. J. · J. Mater. Chem. · 2009 · 19 · 186510.1039/b816327h ↗
45. Wang Z. M. · J. Mater. Chem. · 2011 · 21 · 545110.1039/c1jm10321k ↗
46. Zhang Y. · J. Mater. Chem. · 2011 · 21 · 820610.1039/c1jm10326a ↗
47. Tyagi P. · J. Org. Chem. · 2011 · 76 · 457110.1021/jo2004764 ↗
48. Eaton D. F. · Pure Appl. Chem. · 1988 · 60 · 110710.1351/pac198860071107 ↗
49. Jiang W. · Org. lett · 2011 · 13 · 314610.1021/ol201039n ↗
50. Wang K. · Adv. Funct. Mater. · 2013 · 23 · 267210.1002/adfm.201202981 ↗
51. Pointer M. R. · Color Res. Appl. · 1980 · 5 · 14510.1002/col.5080050308 ↗
52. Tonzola C. J. · Adv. Funct. Mater. · 2007 · 17 · 86310.1002/adfm.200600542 ↗
53. Huang J. · J. Mater. Chem. · 2012 · 22 · 1200110.1039/c2jm31855e ↗
54. Tong Q. X. · J. Phys. Chem. C · 2009 · 113 · 622710.1021/jp810305b ↗
55. Zhuang S. Q. · Org. Electron. · 2012 · 13 · 305010.1016/j.orgel.2012.08.032 ↗
56. Chi C. C. · J. Mater. Chem. · 2009 · 19 · 556110.1039/b902910a ↗
57. Tao S. L. · J. Phys. Chem. C · 2008 · 112 · 1460310.1021/jp803957p ↗
58. Zhang Y. · Dyes Pigm. · 2013 · 98 · 19010.1016/j.dyepig.2013.01.022 ↗
59. Wu C. C. · Adv. Mater. · 2004 · 16 · 6110.1002/adma.200305619 ↗
60. Hung W. Y. · J. Mater. Chem. · 2010 · 20 · 1011310.1039/c0jm02143a ↗
61. Li Z. F. · J. Phys. Chem. C · 2012 · 116 · 2050410.1021/jp3028929 ↗
62. Gao Z. · Chem.—Eur. J. · 2013 · 19 · 260210.1002/chem.201203335 ↗
63. Kim R. · Chem. Commun. · 2013 · 49 · 466410.1039/c3cc41441h ↗
64. Chien C. H. · Adv. Funct. Mater. · 2009 · 19 · 56010.1002/adfm.200801240 ↗
65. Yu D. H. · Chem. Commun. · 2012 · 48 · 615710.1039/c2cc31066j ↗
66. Tang T. · J. Mater. Chem. · 2011 · 21 · 1296910.1039/c1jm11438g ↗
67. Zheng C. J. · J. Mater. Chem. · 2010 · 20 · 156010.1039/b918739a ↗
68. Jiang Z. Q. · Adv. Funct. Mater. · 2009 · 19 · 398710.1002/adfm.200901534 ↗
69. Gong S. L. · Chem. Asian J. · 2010 · 5 · 209310.1002/asia.201000206 ↗
70. Wan J. · J. Mater. Chem. · 2012 · 22 · 450210.1039/c2jm14904d ↗