journal article·2010-07-13

Synthesis and Application of 1,3,4,5,7,8-Hexafluorotetracyanonaphthoquinodimethane (F6-TNAP): A Conductivity Dopant for Organic Light-Emitting Devices

Phillip K. Koech, Asanga B. Padmaperuma, Liang Wang, James S. Swensen, Evgueni Polikarpov, Jens T. Darsell, James E. Rainbolt, Daniel J. Gaspar

Chemistry of Materials· Volume 22· Issue 13
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Abstract

Conductivity dopants are used in organic light-emitting devices (OLEDs) to reduce the operating voltage and consequently improve the power efficiency. Here, we report the synthesis, as well as photophysical and electroluminescent properties, of an organic molecular p- type conductivity dopant: 1,3,4,5,7,8-hexafluorotetracyanonaphthoquinodimethane (F6-TNAP). F6-TNAP was obtained in a three-step two-pot synthesis from commercially available octafluoronaphthalene. When 1%−5% of F6-TNAP was coevaporated with N, N′ -di-1-naphthyl- N, N′ -diphenyl-1,1′-biphenyl-4,4′diamine (α-NPD) an absorption band at 950 nm was formed, which is attributed to charge transfer and assigned to the F6-TNAP radical anion. Single-carrier (hole-only) devices fabricated with F6-TNAP doped into α-NPD as the hole transport layer (HTL) show a >2 V decrease in operating voltage, compared to the undoped device. A decrease in operating voltage was also demonstrated in blue OLED devices using a F6-TNAP-doped HTL, with only a slight decrease in external quantum efficiency, thus resulting in a net improvement in power efficiency. These results demonstrate that F6-TNAP may be useful in generating high-efficiency OLEDs.
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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

Energy and Environment Directorate, Pacific Northwest National Laboratory, Richland, Washington 99352

References (37)

Show source-provided references
1. Tang C. W. · Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
2. D’Andrade B. W. · Adv. Mater. · 2004 · 16 · 158510.1002/adma.200400684 ↗
3. Forrest S. R. · Chem. Rev. · 2007 · 107 · 92310.1021/cr0501590 ↗
4. Baldo M. A. · Nature · 1998 · 395 · 15110.1038/25954 ↗
5. Baldo M. A. · Appl. Phys. Lett. · 1999 · 75 · 410.1063/1.124258 ↗
6. Yersin H. · Top. Curr. Chem. · 2004 · 241 · 110.1007/b96858 ↗
7. Kawamura Y. · Appl. Phys. Lett. · 2005 · 86 · 07110410.1063/1.1862777 ↗
8. Hang J. · Appl. Phys. Lett. · 2002 · 80 · 13910.1063/1.1432110 ↗
9. Huang F. · Appl. Phys. Lett. · 1997 · 71 · 241510.1063/1.120078 ↗
10. Romero D. B. · Appl. Phys. Lett. · 1995 · 67 · 165910.1063/1.115048 ↗
11. Ganzorig C. · Appl. Phys. Lett. · 2000 · 77 · 421210.1063/1.1331640 ↗
12. Leem D.-S. · Appl. Phys. Lett. · 2007 · 91 · 01111310.1063/1.2754635 ↗
13. Chang C.-C. · Appl. Phys. Lett. · 2006 · 89 · 25350410.1063/1.2405856 ↗
14. Qi Y. · J. Am. Chem. Soc. · 2009 · 131 · 1253010.1021/ja904939g ↗
15. Qi Y. · Chem. Mater. · 2009 · 22 · 52410.1021/cm9031623 ↗
16. Matsushima T. · Appl. Phys. Lett. · 2006 · 89 · 25350610.1063/1.2410236 ↗
17. Blochwitz J. · Appl. Phys. Lett. · 1998 · 73 · 72910.1063/1.121982 ↗
18. Zhou X. · Appl. Phys. Lett. · 2001 · 73 · 3202
19. Gao Z. Q. · Chem. Commun. · 2008 · 11710.1039/B713566A ↗
20. Mi B. X. · Appl. Phys. Lett. · 2009 · 94 · 07350710.1063/1.3073719 ↗
21. Diekmann J. · J. Org. Chem. · 1963 · 28 · 271910.1021/jo01045a054 ↗
22. Sandman D. J. · J. Org. Chem. · 1974 · 39 · 116510.1021/jo00922a035 ↗
23. Yamaguchi S. · Synth. Met. · 1996 · 78 · 11710.1016/0379-6779(96)80111-1 ↗
24. Ostapenko N. I. · Synth. Met. · 2002 · 129 · 1910.1016/S0379-6779(02)00041-3 ↗
25. Wheland R. C. · J. Am. Chem. Soc. · 1976 · 98 · 391610.1021/ja00429a030 ↗
26. aZeika, O.; Birnstock, J.; Limmert, M.; Vehse, M.(Novaled AG, Germany).Eur. Patent ApplicationEP1912268 A1 20080416, 2008.
27. bHofmann, M.; Birnstock, J.; Blochwitz, N. J.; Werner, A.; Pfeiffer, M.; Harada, K.(Novaled AG, Germany).Eur. Patent ApplicationEP19122681713136 A1 20061018, 2006; 26 pp.
28. Bylaska, E. J.; de Jong, W. A.; Govind, N.; Kowalski, K.; Straatsma, T. P.; Valiev, M.; Wang, D.; Apra, E.; Windus, T. L.; Hammond, J.; Nichols, P.; Hirata, S.; Hackler, M. T.; Zhao, Y.; Fan, P.D.; Harrison, R. J.; Dupuis, M.; Smith, D. M. A.; Nieplocha, J.; Tipparaju, V.; Krishnan, M.; Wu, Q.; T. Van Voorhis; Auer, A. A.; Nooijen, M. Crosby, L. D.; Brown, E.; Cisneros, G.; Fann, G. I.; Fruchtl, H.; Garza, J.; Hirao, K.; Kendall, R.; Nichols, J. A.; Tsemekhman, K.; Wolinski, K.; Anchell, J.; Bernholdt, D.; Borowski, P.; Clark, T.; Clerc, D.; Dachsel, H.; Deegan, M.; Dyall, K.; Elwood, D.; Glendening, E.; Gutowski, M.; Hess, A.; Jaffe, J.; Johnson, B.; Ju, J.; Kobayashi, R.; Kutteh, R.; Lin, Z.; Littlefield, R.; Long, X.; Meng, B.; Nakajima, T.; Niu, S.; Pollack, L.; Rosing, M.; Sandrone, G.; Stave, M.; Taylor, H.; Thomas, G.; van Lenthe, J.; Wong, A. Zhang, Z.NWChem, A Computational Chemistry Package for Parallel Computer, Version 5.1;Pacific Northwest National Laboratory,Richland, WA, 2007.
29. Black, G.; Daily, J.; Didier, B.; Elsethagen, T.; Feller, D.; Gracio, D.; Hackler, M.; Havre, S.; Jones, D.; Jurrus, E.; Keller, T.; Lansing, C.; Matsumoto, S.; Palmer, B.; Peterson, M.; Schuchardt, K.; Stephan, E.; Sun, L.; Swanson, K.; Taylor, H.; Thomas, G.; Vorpagel, E.; Windus, T.; Winters, C.ECCE, A Problem Solving Environment for Computational Chemistry, Software Version 4.5.1;Pacific Northwest National Laboratory,Richland, WA, 2007.
30. McGhie A. R. · J. Cryst. Growth · 1974 · 22 · 29510.1016/0022-0248(74)90173-0 ↗
31. Andersson M. R. · Macromolecules · 1995 · 28 · 752510.1021/ma00126a033 ↗
32. Agrawal A. K · Chem. Mater. · 1996 · 8 · 57910.1021/cm9504753 ↗
33. Seguy I. · J. Appl. Phys. · 2001 · 89 · 544210.1063/1.1365059 ↗
34. D’Andrade B. W. · Org. Electron. · 2005 · 6 · 1110.1016/j.orgel.2005.01.002 ↗
35. Gao W. · Appl. Phys. Lett. · 2001 · 79 · 404010.1063/1.1424067 ↗
36. Gao W. · J. Appl. Phys. · 2003 · 94 · 35910.1063/1.1577400 ↗
37. Gao W. · J. Phys.: Condens. Matter · 2003 · 15 · S2757