journal article·2006-10-01

Efficient High Area OFETs by Solution Based Processing of a π-Electron Rich Donor

Pawel Miskiewicz, Marta Mas-Torrent, Jaroslaw Jung, Sylwia Kotarba, Ireneusz Glowacki, Elba Gomar-Nadal, David B. Amabilino, Jaume Veciana, Bärbel Krause, Dina Carbone, Concepció Rovira, Jacek Ulanski

Chemistry of Materials· Volume 18· Issue 20
Publisher page

Abstract

We report on the preparation of high performance field-effect transistors (FETs) based on large areas of aligned films of a TTF derivative, namely, tetrakis-(octadecylthio)-tetrathiafulvalene (TTF-4SC18). TTF-4SC18 assembles into one-dimensional stacks in which the long alkyl chains promote intermolecular π−π overlapping due to their extremely closely packed nature. The films were prepared from solution by zone-casting, a simple technique that does not require the use of preoriented substrates. The films were characterized by AFM and X-ray, indicating an extremely high crystalline quality. The TTF molecules are tilted with respect to the substrate surface and are well-aligned in the casting direction. More than 40 FETs were measured, showing a remarkable reproducibility of their performance. The average charge carrier mobility value measured along the casting direction was about 0.006 cm 2 /V s for a channel length L = 100 μm and about 0.01 cm 2 /V s for L = 80 μm and L = 50 μm. The FET mobilities determined in the direction perpendicular to the orientation were ca. 1 order of magnitude lower. We found that all the devices after annealing exhibited an enhanced performance with FETs mobilities about 1 order of magnitude higher. The best devices revealed a charge carrier mobility close to 0.1 cm 2 /V s with an on/off ratio of the order of 10 4 .
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic and Molecular Conductors Research · Organic Electronics and Photovoltaics · Perovskite Materials and Applications

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

Affiliations

Department of Molecular Physics, Technical University of Lodz, 90-924 Lodz, Poland, Institut de Ciència de Materials de Barcelona (CSIC), Campus Universitari de Bellaterra, 08193 Cerdanyola del Vallès, Spain, and European Synchrotron Radiation Facility, ESRF BP 220 F-38043, Grenoble Cedex, France

References (38)

Show source-provided references
1. Sun Y. M. · J. Mater. Chem. · 2005 · 15 · 5310.1039/b411245h ↗
2. Dimitrakopoulos C. D. · Adv. Mater. · 2002 · 14 · 9910.1002/1521-4095(20020116)14:2<99::AID-ADMA99>3.0.CO;2-9 ↗
3. Dimitrakopoulos C. D. · Science · 1999 · 283 · 82210.1126/science.283.5403.822 ↗
4. Afzali A. · J. Am. Chem. Soc. · 2002 · 124 · 881210.1021/ja0266621 ↗
5. Murphy A. R. · J. Am. Chem. Soc. · 2004 · 126 · 159610.1021/ja039529x ↗
6. Herwig P. T. · Adv. Mater. · 1999 · 11 · 48010.1002/(SICI)1521-4095(199904)11:6<480::AID-ADMA480>3.0.CO;2-U ↗
7. Gelink G. H. · Nat. Mater. · 2004 · 3 · 10610.1038/nmat1061 ↗
8. Nagamatsu S. · Macromolecules · 2003 · 36 · 525210.1021/ma025887t ↗
9. Chem. Rev. · 2004 · 104
10. Mas-Torrent M. · J. Mater. Chem. · 2006 · 16 · 43310.1039/B510121B ↗
11. Noda B. · Chem. Lett. · 2005 · 34 · 39210.1246/cl.2005.392 ↗
12. Katsuhara M. · Synth. Met. · 2005 · 149 · 21910.1016/j.synthmet.2005.01.005 ↗
13. Naraso · J. Am. Chem. Soc. · 2005 · 127 · 1014210.1021/ja051755e ↗
14. Dimitrakopoulos C. D. · IBM J. Res. Dev. · 2001 · 45 · 1110.1147/rd.451.0011 ↗
15. Locklin J. · Chem. Mater. · 2005 · 17 · 336610.1021/cm047851g ↗
16. Curtis M. D. · J. Am. Chem. Soc. · 2004 · 126 · 431810.1021/ja0397916 ↗
17. Halik M. · Adv. Mater. · 2003 · 15 · 91710.1002/adma.200304654 ↗
18. Li Y. · Adv. Mater. · 2005 · 17 · 84910.1002/adma.200401290 ↗
19. Van de Craats A. M. · Adv. Mater. · 2003 · 15 · 49510.1002/adma.200390114 ↗
20. Yamada J. · 200410.1007/978-3-662-10630-3 ↗
21. Mas-Torrent M. · J. Am. Chem. Soc. · 2004 · 126 · 854610.1021/ja048342i ↗
22. Bromley S. T. · J. Am. Chem. Soc. · 2004 · 126 · 654410.1021/ja049762a ↗
23. Mas-Torrent M. · J. Am. Chem. Soc. · 2004 · 126 · 98410.1021/ja0393933 ↗
24. Mas-Torrent M. · Appl. Phys. Lett. · 2005 · 86 · 01211010.1063/1.1848179 ↗
25. Wu P. · Chem. Lett. · 1986 · 44110.1246/cl.1986.441 ↗
26. Inokuchi H. · Chem. Lett. · 1986 · 126310.1246/cl.1986.1263 ↗
27. Burda, L.; Tracz, A.; Pakula, T.; Ulanski, J.; Kryszewski, M.J. Phys.D: Appl. Phys.1983,16, 1737. (b) Ulanski, J.; Tracz, A.; El Shafee, E.; Debrue, G.; Deltour, R.Synth. Met.1990,35, 221. (c) Tracz, A.; El Shafee, E.; Ulanski, J.; Jeszka, J. K.; Kryszewski, M.Synth. Met.1990,37, 175.10.1088/0022-3727/16/9/019 ↗
28. Miskiewicz P. · Synth. Met. · 2003 · 137 · 90510.1016/S0379-6779(02)01023-8 ↗
29. Miskiewicz P. · 2003
30. Pisula W. · Adv. Mater. · 2005 · 17 · 68410.1002/adma.200401171 ↗
31. Rodriguez-Navarro A. · Eur. J. Mineral. · 2000 · 12 · 60910.1127/ejm/12/3/0609 ↗
32. Nitz V. · Phys. Rev. B · 1996 · 54 · 503810.1103/PhysRevB.54.5038 ↗
33. Salditt T. · J. Phys. Condens. Matter · 2005 · 17 · R28710.1088/0953-8984/17/6/R02 ↗
34. Gibaud A. · Phys. Rev. Lett. · 1995 · 74 · 320510.1103/PhysRevLett.74.3205 ↗
35. Linda Chen, X.; Lovinger, A. J.; Bao, Z.; Sapjeta, J.Chem. Mater.2001,13, 134110.1021/cm0008563 ↗
36. Li S. P. · Appl. Phys. Lett. · 2005 · 87 · 06210110.1063/1.2009063 ↗
37. Shi Z. · J. Phys. Chem. · 1988 · 92 · 504410.1021/j100328a042 ↗
38. Newman C. R. · Chem. Mater. · 2004 · 16 · 443610.1021/cm049391x ↗