Synthesis and characterization of anthracene derivative for organic field-effect transistor fabrication

Journal of Nanoscience and Nanotechnology

Volumn 12, Issue 5, 2012, Pages 4269-4273

  Madathil, Pramod Kandoth ^a   Lim, Jae Geon ^a   Kim, Tae Dong ^a   Beckmann, Dirk ^b   Mavrinskiy, Alexey ^b   Pisula, Wojciech ^b   Baumgarten, Martin ^b   Mullen, Klaus ^b   Lee, Kwang Sup ^a  

^a Hannam University   (South Korea)

^b MAX PLANCK INSTITUTE FOR POLYMER RESEARCH   (Germany)

Author keywords

Anthracene Derivative; Organic Field Effect Transistors; Supramolecular Organization

Indexed keywords

ANTHRACENE DERIVATIVES; BENZENE RING; BOTTOM-CONTACT; CHARGE MOBILITIES; FIELD-EFFECT MOBILITIES; LOW THRESHOLD VOLTAGE; ON/OFF RATIO; SOLUTION PROCESSABLE; STRUCTURAL INFORMATION; SUPRAMOLECULAR ORGANIZATIONS; WIDE ANGLE X-RAY SCATTERING;

BENZENE; ORGANIC FIELD EFFECT TRANSISTORS; THERMOANALYSIS;

ANTHRACENE;

EID: 84863955520     PISSN: 15334880     EISSN: 15334899     Source Type: Journal    
DOI: 10.1166/jnn.2012.5941     Document Type: Conference Paper

References (20)

1. J. Zaumseil and H. Sirringhaus, Chem. Rev. 107, 1296 (2007).
2. S. Allard, M. Forster, B. Souharce, H. Thiem, and U. Scherf, Angew. Chem. Int. Ed. 47, 4070 (2008).
3. H. Sirringhaus and M. Ando, MRS Bull. 33, 676 (2008).
4. D. Braga and G. Horowitz, Adv. Mater. 21, 1473 (2009).
5. D. Gundlach, J. Royer, S. Park, S. Subramanian, O. Jurchescu, B. Hamadani, A. Moad, R. Kline, L. Teague, and O. Kirillov, Nat. Mater. 7, 216 (2008).
6. Y. Wen and Y. Liu, Adv. Mater. 22, 1331 (2010).
7. A. B. Mallik, J. Locklin, S. C. B. Mannsfeld, C. Reese, M. E. Roberts, M. L. Senatore, and Z. Bao, Organic Field Effect Transistors, Boca Raton, Florida (2007), p. 160.
8. H. E. Katz, Z. Bao, and S. L. Gilat, Acc. Chem. Res. 34, 359 (2001).
9. F. Garnier, A. Hajlaoui, A. Yassar, and P. Srivastava, Science 265, 1684 (1994).
10. H. Sirringhaus, N. Tessler, and R. H. Friend, Science 280, 1741 (1998).
11. T. Mori, J. Phys. Condensed Matter 20, 184010 (2008).
12. R. Rotzoll, S. Mohapatra, V. Olariu, R. Wenz, M. Grigas, K. Dimmler, O. Shchekin, and A. Dodabalapur, App. Phys. Lett. 88, 123502 (2006).
13. A. R. Murphy and J. M. J. Frechet, Chem. Rev. 107, 1067 (2007).
14. B. S. Ong, Y. Wu, Y. Li, P. Liu, and H. Pan, Chem. Eur. J. 14, 4766 (2008).
15. M. Heeney, C. Bailey, M. Giles, M. Shkunov, D. Sparrowe, S. Tierney, W. Zhang, and I. McCulloch, Macromolecules 37, 5250 (2004).
16. S. Weng, P. Shukla, M. Kuo, Y. Chang, H. Sheu, I. Chao, and Y. Tao, ACS Appl. Mater. Interfaces. 1, 2071 (2009).
17. S. Ando, J. Nishida, E. Fujiwara, H. Tada, Y. Inoue, S. Tokito, and Y. Yamashita, Chem. Mater. 17, 1261 (2005).
18. M. A. M. Leenen, F. Cucinotta, L. Viani, A. Mavrinskiy, W. Pisula, J. Gierschner, J. Cornil, A. Prodi-Schwab, H. Thiem, K. Müllen, and L. D. Cola, J. Phys. Chem. B 114, 14614 (2010).
19. P. K. Madathil, B. Heinrich, B. Donnio, F. Mathevet, J. L. Fave, D. Guillon, A. J. Attias, C. Lee, T. D. Kim, and K.-S. Lee, J. Nanosci. Nanotechnol. 10, 6800 (2010).
20. K. Ito, T. Suzuki, Y. Sakamoto, D. Kubota, Y. Inoue, F. Sato, and S. Tokito, Angew. Chem. Int. Ed. 42, 1159 (2003).