journal article·2013-04-10

p-Channel Field-Effect Transistors Based on C60 Doped with Molybdenum Trioxide

Tae Hoon Lee, Björn Lüssem, Kwanpyo Kim, Gaurav Giri, Yoshio Nishi, Zhenan Bao

Publisher page

Abstract

Fullerene (C60) is a well-known n-channel organic semiconductor. We demonstrate that p-channel C60 field-effect transistors are possible by doping with molybdenum trioxide (MoO3). The device performance of the p-channel C60 field-effect transistors, such as mobility, threshold voltage, and on/off ratio is varied in a controlled manner by changing doping concentration. This work demonstrates the utility of charge transfer doping to obtain both n- and p-channel field-effect transistors with a single organic semiconductor.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Semiconductor materials and devices · Advanced Memory and Neural Computing

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

Affiliations

Institut für Angewandte Photophysik, Technische Universität Dresden, George-Bähr-Str. 1, 01062 Dresden, Germany

References (30)

Show source-provided references
1. Arias A. C. · Chem. Rev. · 2010 · 110 · 310.1021/cr900150b ↗
2. Klauk H. · Chem. Soc. Rev. · 2010 · 39 · 264310.1039/b909902f ↗
3. Someya T. · Proc. Natl. Acad. Sci. U. S. A. · 2004 · 101 · 996610.1073/pnas.0401918101 ↗
4. Rogers J. A. · Science · 2010 · 327 · 160310.1126/science.1182383 ↗
5. Sokolov A. N. · Acc. Chem. Res. · 2012 · 45 · 36110.1021/ar2001233 ↗
6. Weste N. H. E. · 1985 · 854
7. Dodabalapur A. · Appl. Phys. Lett. · 1996 · 69 · 422710.1063/1.116953 ↗
8. Klauk H. · Nature · 2007 · 445 · 74510.1038/nature05533 ↗
9. Yan H. · Nature · 2009 · 457 · 67910.1038/nature07727 ↗
10. Li H. · Adv. Mater. · 2012 · 24 · 258810.1002/adma.201200151 ↗
11. Zaumseil J. · Chem. Rev. · 2007 · 107 · 129610.1021/cr0501543 ↗
12. Meijer E. J. · Nat. Mater. · 2003 · 2 · 67810.1038/nmat978 ↗
13. Ahles M. · Appl. Phys. Lett. · 2004 · 85 · 449910.1063/1.1818737 ↗
14. Schmechel R. · J. Appl. Phys. · 2005 · 98 · 08451110.1063/1.2106009 ↗
15. Wei P. · J. Am. Chem. Soc. · 2010 · 132 · 885210.1021/ja103173m ↗
16. Wei P. · J. Am. Chem. Soc. · 2012 · 134 · 399910.1021/ja211382x ↗
17. Kubo M. · Appl. Phys. Lett. · 2011 · 98 · 07331110.1063/1.3556312 ↗
18. Kröger M. · Appl. Phys. Lett. · 2009 · 95 · 12330110.1063/1.3231928 ↗
19. Kröger M. · Org. Electron. · 2009 · 10 · 93210.1016/j.orgel.2009.05.007 ↗
20. Irfan · Appl. Phys. Lett. · 2010 · 96 · 07330410.1063/1.3309600 ↗
21. Irfan · Appl. Phys. Lett. · 2010 · 96 · 24330710.1063/1.3454779 ↗
22. Gwinner M. C. · Adv. Funct. Mater. · 2011 · 21 · 143210.1002/adfm.201002696 ↗
23. Reynolds K. J. · J. Appl. Phys. · 2002 · 92 · 755610.1063/1.1522812 ↗
24. Chu C.-W. · Appl. Phys. Lett. · 2005 · 87 · 19350810.1063/1.2126140 ↗
25. Kubo M. · AIP Advances · 2011 · 1 · 03217710.1063/1.3647994 ↗
26. Ito Y. · J. Am. Chem. Soc. · 2009 · 131 · 939610.1021/ja9029957 ↗
27. Virkar A. · Adv. Funct. Mater. · 2009 · 19 · 196210.1002/adfm.200801727 ↗
28. Smilgies D. · J. Appl. Crystallogr. · 2009 · 42 · 103010.1107/S0021889809040126 ↗
29. Singh T. B. · Appl. Phys. Lett. · 2007 · 90 · 21351210.1063/1.2743386 ↗
30. Walzer K. · Chem. Rev. · 2007 · 107 · 123310.1021/cr050156n ↗