Novel Oxadiazole-Containing Polyfluorene with Efficient Blue Electroluminescence
Source abstract
Abstract
A novel oxdiazole-containing polyfluorene copolymer (PF−OXD) was synthesized by attaching two electron-deficient, 4- tert -butylphenyl-1,3,4-oxadiazole groups onto the C-9 position of the alternating fluorene unit to form a 3-D cardo-structure. This polymer possesses a very high glass transition temperature ( T g: 213 °C) and very good thermal stability due to its rigid cardo-linkage. The results from the photoluminescence measurements of the isothermally heated PF−OXD thin film (150 °C for 20 h) show that the commonly observed aggregate/excimer formation in polyfluorenes is very effectively suppressed in this polymer due to its 3-D structure and high T g . A double-layer LED device using this polymer as the emitting layer shows a bright blue emission with a low turn-on voltage at 5.3 V and a high brightness of 2770 cd/m 2 at a drive voltage of 10.8 V. The maximum external quantum efficiency is 0.52% at 537 cd/m 2 with a bias of 7.4 V. The improved device performance over that of poly(9,9-dioctylfluorene) (POF) may be due to better electron injection and transport in PF−OXD and the efficient energy transfer from the OXD side chain to the polyfluorene main chains.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (33)
Show source-provided references
1. Burroughes J. H. · Nature · 1990 · 347 · 53910.1038/347539a0 ↗
2. Kraft A. · Angew. Chem., Int. Ed. · 1998 · 37 · 40210.1002/(SICI)1521-3773(19980302)37:4<402::AID-ANIE402>3.0.CO;2-9 ↗
3. Friend R. H. · Nature · 1999 · 397 · 12110.1038/16393 ↗
4. Bernius M. T. · Adv. Mater. · 2000 · 12 · 173710.1002/1521-4095(200012)12:23<1737::AID-ADMA1737>3.0.CO;2-N ↗
5. Mitschke U. · J. Mater. Chem. · 2000 · 10 · 147110.1039/a908713c ↗
6. Kido J. · Appl. Phys. Lett. · 1994 · 64 · 81510.1063/1.111023 ↗
7. Pei Q. · J. Am. Chem. Soc. · 1996 · 118 · 741610.1021/ja9615233 ↗
8. Setayesh S. · J. Am. Chem. Soc. · 2001 · 123 · 94610.1021/ja0031220 ↗
9. Klärner G. · Chem. Mater. · 1999 · 11 · 180010.1021/cm990027l ↗
10. Huang W. · J. Adv. Mater. · 1998 · 10 · 59310.1002/(SICI)1521-4095(199805)10:8<593::AID-ADMA593>3.0.CO;2-9 ↗
11. Yu W.-L. · J. Macromolecules · 1998 · 31 · 483810.1021/ma9800212 ↗
12. Peng Z. · Chem. Mater. · 1998 · 10 · 208610.1021/cm970698o ↗
13. Huang W. · Macromolecules · 1999 · 32 · 11810.1021/ma9813237 ↗
14. Peng Z. · Chem. Mater. · 1999 · 11 · 113810.1021/cm981087e ↗
15. Lee Y.-Z. · J. Am. Chem. Soc. · 2001 · 123 · 229610.1021/ja003135d ↗
16. Zheng M. · Macromolecules · 2001 · 34 · 412410.1021/ma0019656 ↗
17. Zhan X. · Macromolecules · 2002 · 35 · 252910.1021/ma011593g ↗
18. Chiang C.-L. · Chem. Mater. · 2002 · 14 · 68210.1021/cm010665f ↗
19. Ranger M. · Macromolecules · 1997 · 30 · 768610.1021/ma970920a ↗
20. Greenhan N. C. · Adv. Mater. · 1994 · 6 · 49110.1002/adma.19940060612 ↗
21. Greczmiel M. · Macromolecules · 1997 · 30 · 604210.1021/ma970226v ↗
22. Bettenhausen J. · Adv Mater · 1996 · 8 · 50710.1002/adma.19960080612 ↗
23. Detert H. · Synthesis · 1999 · 99910.1055/s-1999-3511 ↗
24. Gallos J. · J. Chem. Res. Miniprint · 1982 · 1649
25. Miyaura N. · Chem. Rev. · 1995 · 95 · 245710.1021/cr00039a007 ↗
26. Ding J. · Macromolecules · 2002 · 35 · 347410.1021/ma011093n ↗
27. Tokito S. · Appl. Phys. Lett. · 1997 · 70 · 192910.1063/1.118782 ↗
28. Wu F.-I. · J. Mater. Chem. · 2002 · 12 · 289310.1039/b205334a ↗
29. Grice A. W. · Appl. Phys. Lett. · 1998 · 73 · 62910.1063/1.121878 ↗
30. Lee J. I. · Synth. Mater. · 1999 · 101 · 12610.1016/S0379-6779(98)01365-4 ↗
31. Pommerehne J. · Adv. Mater. · 1995 · 7 · 55110.1002/adma.19950070608 ↗
32. Janietz S. · Appl. Phys. Lett. · 1998 · 73 · 245310.1063/1.122479 ↗
33. Janietz S. · Adv. Mater. · 1997 · 9 · 40310.1002/adma.19970090508 ↗