journal article·2015-06-09

Construction of Efficient Deep Blue Aggregation-Induced Emission Luminogen from Triphenylethene for Nondoped Organic Light-Emitting Diodes

Wei Qin, Zhiyong Yang, Yibin Jiang, Jacky W. Y. Lam, Guodong Liang, Hoi Sing Kwok, Ben Zhong Tang

Chemistry of Materials· Volume 27· Issue 11
Publisher page

Abstract

Deep blue emitters are crucial for full color displays and organic white lighting. Thanks to the research efforts by scientists, many efficient light emitters with aggregation-induced emission (AIE) characteristics have been synthesized and found promising applications in organic light-emitting diodes (OLEDs). However, few AIE emitters with deep blue emissions and excellent electroluminescence (EL) performance have been reported. The contribution here reports a simple but successful molecular design strategy for synthesizing efficient solid-state emitters for nondoped OLEDs with both deep blue and white emissions. This strategy utilizes triphenylethene, a weakly conjugated AIE luminogen, as building block for constructing deep blue emitter, involving no complicated control of emission color through adjustment of the steric hindrance of chromophores, and enables a wide selection of partnered functional units. The synthesized AIE luminogen, abbreviated as BTPE-PI, is thermally stable and exhibits high fluorescence quantum efficiency as well as good charge injection capability in the solid state. Nondoped deep blue OLED fabricated from BTPE-PI shows a very high external quantum efficiency of 4.4% with a small roll-off, whose performance is the best among deep blue AIE materials reported so far. An efficient white OLED with Commission Internationale de l’Eclairage (CIE) coordinates of (0.33, 0.33) at theoretical white point was first achieved by using AIE luminogen BTPE-PI as deep blue emitter. Such molecular design strategy opens a new avenue in the development of efficient solid-state deep blue emitters for nondoped OLED applications.
Source: openalex_inverted_index · Quality: baseline

Research context

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

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

Affiliations

HKUST-Shenzhen Research Institute, No. 9 Yuexing 1st RD, South Area, Hi-tech Park, Nanshan, Shenzhen, 518057, China

Department of Chemistry, Institute for Advanced Study, Division of Life Science, State Key Laboratory of Molecular Neuroscience, Institute of Molecular Functional Materials and Division of Biomedical Engineering, The Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong, China

Center for Display Research, The Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong, China

Guangdong Innovative Research Team, SCUT-HKUST Joint Research Laboratory, State Key Laboratory of Luminescent Materials and Device, South China University of Technology, Guangzhou 510640, China

Funding

Research Grants Council, University Grants Committee, Hong Kong · Ministry of Science and Technology of the People's Republic of China · University Grants Committee · Guangdong Province · Innovation and Technology Commission, Government of the Hong Kong Special Administrative Region

References (75)

Show source-provided references
1. Tang C. W. · Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
2. Huang H. · J. Phys. Chem. C · 2011 · 115 · 487210.1021/jp110652y ↗
3. Yang X. · J. Phys. Chem. C · 2011 · 115 · 1434710.1021/jp203115c ↗
4. Zhu M. R. · Chem. Soc. Rev. · 2013 · 42 · 496310.1039/c3cs35440g ↗
5. Hung L. S. · Mater. Sci. Eng. R · 2002 · 39 · 14310.1016/S0927-796X(02)00093-1 ↗
6. Xu H. · Chem. Soc. Rev. · 2014 · 43 · 325910.1039/C3CS60449G ↗
7. Jankus V. · Adv. Mater. · 2013 · 25 · 145510.1002/adma.201203615 ↗
8. Chi Y. · Chem. Soc. Rev. · 2010 · 39 · 63810.1039/B916237B ↗
9. Chien C. H. · Adv. Funct. Mater. · 2009 · 19 · 56010.1002/adfm.200801240 ↗
10. Hu J. Y. · Adv. Funct. Mater. · 2014 · 24 · 206410.1002/adfm.201302907 ↗
11. Figueira-Duarte T. M. · Adv. Mater. · 2010 · 22 · 99010.1002/adma.200902744 ↗
12. Hong Y. N. · Chem. Soc. Rev. · 2011 · 40 · 536110.1039/c1cs15113d ↗
13. Birks J. B. · 1970
14. Shimizu M. · Chem.—Asian J. · 2010 · 5 · 151610.1002/asia.200900727 ↗
15. Shirota Y. · J. Am. Chem. Soc. · 2000 · 122 · 1102110.1021/ja0023332 ↗
16. Doi H. · Chem. Mater. · 2003 · 15 · 108010.1021/cm020948n ↗
17. Lin S. L. · Adv. Mater. · 2008 · 20 · 394710.1002/adma.200801023 ↗
18. Xie Z. · J. Am. Chem. Soc. · 2005 · 127 · 1415210.1021/ja054661d ↗
19. Würthner F. · Angew. Chem., Int. Ed. · 2011 · 50 · 337610.1002/anie.201002307 ↗
20. Kaiser T. E. · Angew. Chem., Int. Ed. · 2007 · 46 · 554110.1002/anie.200701139 ↗
21. Deans R. · J. Am. Chem. Soc. · 2000 · 122 · 856510.1021/ja0007298 ↗
22. Chen Z. H. · Macromolecules · 2008 · 41 · 667210.1021/ma800486a ↗
23. Moorthy J. N. · J. Org. Chem. · 2010 · 75 · 259910.1021/jo1001565 ↗
24. Liu C. · Chem. Mater. · 2013 · 25 · 332010.1021/cm401640v ↗
25. Sato T. · J. Am. Chem. Soc. · 1999 · 121 · 1065810.1021/ja9922983 ↗
26. Langhals H. · Angew. Chem., Int. Ed. · 2005 · 44 · 242710.1002/anie.200461610 ↗
27. Wang J. · J. Phys. Chem. B · 2007 · 111 · 508210.1021/jp068646m ↗
28. Hong Y. N. · Chem. Commun. · 2009 · 433210.1039/b904665h ↗
29. Li K. · Sci. Rep. · 2013 · 3 · 115010.1038/srep01150 ↗
30. Mei J. · Adv. Mater. · 2014 · 26 · 542910.1002/adma.201401356 ↗
31. Huang J. · Chem. Commun. · 2012 · 48 · 958610.1039/c2cc34966c ↗
32. Du X. · Chem. Mater. · 2012 · 24 · 217810.1021/cm3008733 ↗
33. Dong Y. · Appl. Phys. Lett. · 2007 · 91 · 01111110.1063/1.2753723 ↗
34. Luo J. · Chem. Commun. · 2001 · 174010.1039/b105159h ↗
35. Huang J. · Adv. Funct. Mater. · 2013 · 23 · 232910.1002/adfm.201202639 ↗
36. Huang J. · J. Mater. Chem. C · 2014 · 2 · 202810.1039/c3tc32207f ↗
37. Yang Z. Y. · J. Mater. Chem. · 2009 · 19 · 554110.1039/b902802a ↗
38. Yang Z. Y. · Chem. Sci. · 2013 · 4 · 372510.1039/c3sc50648g ↗
39. Yuan Y. · New J. Chem. · 2011 · 35 · 153410.1039/c1nj20072k ↗
40. Gao Z. · Laser Photon. Rev. · 2014 · 8 · L610.1002/lpor.201300141 ↗
41. Xing X. · ACS Appl. Mater. Interfaces · 2012 · 4 · 287710.1021/am300685b ↗
42. Al-Riyami L. · J. Med. Chem. · 2013 · 56 · 998210.1021/jm401251p ↗
43. Jana D. · Dyes Pigm. · 2013 · 99 · 74010.1016/j.dyepig.2013.07.008 ↗
44. Wang S. J. · J. Am. Chem. Soc. · 2000 · 122 · 569510.1021/ja992924w ↗
45. Duan X. F. · J. Org. Chem. · 2006 · 71 · 987310.1021/jo061644d ↗
46. Zhang Y. · Chem. Mater. · 2012 · 24 · 6110.1021/cm201789u ↗
47. Grabowski Z. R. · Chem. Rev. · 2003 · 103 · 389910.1021/cr940745l ↗
48. Wei B. · Adv. Funct. Mater. · 2010 · 20 · 244810.1002/adfm.201000299 ↗
49. Wang Z. M. · J. Mater. Chem. · 2011 · 21 · 545110.1039/c1jm10321k ↗
50. Wu W. C. · Adv. Mater. · 2002 · 14 · 107210.1002/1521-4095(20020805)14:15<1072::AID-ADMA1072>3.0.CO;2-Z ↗
51. Yeh H. C. · Chem. Commun. · 2003 · 263210.1039/b309780c ↗
52. Chang S. C. · Appl. Phys. Lett. · 2001 · 79 · 208810.1063/1.1404995 ↗
53. Zhong G. Y. · Appl. Phys. Lett. · 2002 · 81 · 112210.1063/1.1497438 ↗
54. Gong J. R. · J. Phys. Chem. B · 2005 · 109 · 167510.1021/jp046509o ↗
55. Lee M. T. · Adv. Mater. · 2005 · 17 · 249310.1002/adma.200501169 ↗
56. Wu K. C. · Adv. Funct. Mater. · 2008 · 18 · 6710.1002/adfm.200700803 ↗
57. Lee S. J. · Adv. Funct. Mater. · 2008 · 18 · 392210.1002/adfm.200800697 ↗
58. Chang H. W. · Org. Electron. · 2014 · 15 · 102810.1016/j.orgel.2014.02.017 ↗
59. Shim Y. S. · Adv. Funct. Mater. · 2014 · 24 · 641410.1002/adfm.201401253 ↗
60. Sun J. W. · Adv. Mater. · 2014 · 26 · 568410.1002/adma.201401407 ↗
61. Wang Z. · Phys. Chem. Chem. Phys. · 2014 · 16 · 2077210.1039/C4CP03284E ↗
62. Yuan Y. · Chem. Mater. · 2013 · 25 · 495710.1021/cm4030414 ↗
63. Li W. · Adv. Funct. Mater. · 2012 · 22 · 279710.1002/adfm.201200116 ↗
64. Liu C. · Chem.—Eur. J. · 2012 · 18 · 1382810.1002/chem.201201512 ↗
65. Thangthong A. M. · Eur. J. Org. Chem. · 2012 · 2012 · 526310.1002/ejoc.201200641 ↗
66. Thangthong A. M. · Chem. Commun. · 2011 · 47 · 712210.1039/c1cc11624j ↗
67. Zhang T. · J. Mater. Chem. · 2011 · 21 · 1296910.1039/c1jm11438g ↗
68. Zhu M. · J. Mater. Chem. · 2011 · 21 · 640910.1039/c1jm10465a ↗
69. Tao S. · Chem. Mater. · 2010 · 22 · 213810.1021/cm100100w ↗
70. Liao S. H. · J. Am. Chem. Soc. · 2009 · 131 · 76310.1021/ja807284e ↗
71. Chen W. C. · Adv. Opt. Mater. · 2014 · 2 · 62610.1002/adom.201400078 ↗
72. Chen W. C. · Org. Electron. · 2015 · 17 · 15910.1016/j.orgel.2014.11.024 ↗
73. Lee B. M. · J. Lumin. · 2014 · 148 · 7210.1016/j.jlumin.2013.11.065 ↗
74. Ying L. · Adv. Mater. · 2014 · 26 · 245910.1002/adma.201304784 ↗
75. Schwartz G. · Adv. Funct. Mater. · 2009 · 19 · 131910.1002/adfm.200801503 ↗