journal article·2017-10

New oligomers containing pendant 4-aryl-7-phenylfluorene units as efficient charge transporting materials for OLEDs

G. Krucaite, U. Baranauskyte, D. Tavgeniene, V. Andruleviciute, S. Sutkuviene, B. Yao, Z. Xie, B. Zhang, S. Grigalevicius

Optical Materials· Volume 72
Publisher page

Abstract

Abstract Monomers and oligomers containing electronically isolated 4-aryl-7-phenylfluorene fragments have been synthesized by the multi-step synthetic route. The materials were characterized by thermo-gravimetric analysis, differential scanning calorimetry and electron photoemission technique. The oligomers represent materials of very high thermal stability having initial thermal degradation temperatures in the range of 402–412 °C. The glass transition temperatures of the amorphous oligomers were in the rage of 97–129 °C. The electron photoemission spectra of thin layers of the oligomeric materials showed ionization potentials in the range of 5.7–6.1 eV. Hole injecting/transporting properties of the electroactive oligomers were tested in the structures of organic light emitting diodes with tris(quinolin-8-olato)aluminium as a green emitter. The device containing hole-transporting material with 4-biphenyl-7-phenylfluorene electrophores exhibited the best overall performance with low turn on voltage of 4.4 V, high current efficiency exceeding 3.6 cd/A and maximum brightness exceeding 3200 cd/m 2 .
Source: openaire · Quality: candidate unverified · Source record ↗

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 (30)

Show source-provided references
1. Xu · J. Mater. Chem. C · 2016 · 4 · 911610.1039/C6TC03230C ↗
2. AlSalhi · Int. J. Mol. Sci. · 2011 · 12 · 203610.3390/ijms12032036 ↗
3. Volz · J. Photonics Energy · 2016 · 6
4. Alexander · Chem. Soc. Rev. · 2010 · 39 · 269510.1039/b916787k ↗
5. Ho · J. Photonics Energy · 2015 · 5
6. Jou · Opt. Express · 2015 · 23 · A57610.1364/OE.23.00A576 ↗
7. Jou · Adv. Opt. Mater. · 2015 · 3 · 9510.1002/adom.201400366 ↗
8. Jou · J. Mater. Chem. C · 2015 · 3 · 297410.1039/C4TC02495H ↗
9. Baoxiu · Prog. Chem. · 2011 · 23 · 136
10. Grigalevicius · Org. Electron. · 2011 · 12 · 225310.1016/j.orgel.2011.08.018 ↗
11. Yin · Dyes Pigments · 2015 · 122 · 5910.1016/j.dyepig.2015.06.023 ↗
12. Chang · Dye Pigm. · 2015 · 122 · 25710.1016/j.dyepig.2015.06.038 ↗
13. Jou · Adv. Funct. Mater. · 2014 · 24 · 55510.1002/adfm.201302013 ↗
14. Kirkus · Eur. Polym. J. · 2009 · 45 · 41010.1016/j.eurpolymj.2008.10.014 ↗
15. Jou · J. Mater. Chem. C · 2015 · 3 · 1229710.1039/C5TC02889B ↗
16. Sek · Opt. Mater. · 2012 · 34 · 133310.1016/j.optmat.2012.02.014 ↗
17. Su · Prog. Chem. · 2015 · 27 · 1384
18. Karpicz · J. Chem. Phys. · 2011 · 134
19. Krucaite · Dyes Pigments · 2014 · 106 · 110.1016/j.dyepig.2014.02.008 ↗
20. Tao · Chem. Soc. Rev. · 2011 · 40 · 294310.1039/c0cs00160k ↗
21. Dumur · Org. Electron. · 2015 · 25 · 34510.1016/j.orgel.2015.07.007 ↗
22. Dumur · Org. Electron. · 2015 · 25 · 2110.1016/j.orgel.2015.06.013 ↗
23. Krucaite · Opt. Mater. · 2014 · 37 · 78810.1016/j.optmat.2014.09.008 ↗
24. Miyamoto · Electrophotography · 1989 · 28 · 364
25. Kukhta · Dyes Pigments · 2015 · 117 · 12210.1016/j.dyepig.2015.02.013 ↗
26. Kannan · Chem. Mater. · 2001 · 13 · 189610.1021/cm000747o ↗
27. Stanionyte · Polym. Int. · 2008 · 57 · 103610.1002/pi.2443 ↗
28. Saragi · Chem. Rev. · 2007 · 107 · 101110.1021/cr0501341 ↗
29. 2005
30. Lin · Org. Electron. · 2009 · 10 · 45910.1016/j.orgel.2009.01.013 ↗