Photocurrent generation by benzoporphyrin films prepared by a solution process

Journal of Porphyrins and Phthalocyanines

Volumn 11, Issue 5-6, 2007, Pages 383-389

  Yamada, Hiroko ^a,b   Kamio, Naoko ^a   Ohishi, Akihiro ^a   Kawano, Manami ^a   Okujima, Tetsuo ^a   Ono, Noboru ^a  

^a EHIME UNIVERSITY   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Benzoporphyrin; Organic semiconductors; Photocurrent; Retro Diels Alder reaction

Indexed keywords

EID: 34447338612     PISSN: 10884246     EISSN: None     Source Type: Journal    
DOI: 10.1142/s1088424607000436     Document Type: Article

References (34)

1. Brabec CJ, Sariciftci NS and Hummelen JC. Adv. Mater. Sci. 2001; 11: 15-26.
2. Nelson J. Curr. Opin. Solid. State Mater. Sci. 2002; 6: 87-95.
3. Goetzberger A, Hebling C and Schock HW. Mater. Sci. Eng. R 2003; 40: 1-46.
4. Forrest SR. Nature 2004; 428: 911-918.
5. Peumans P, Yakimov A and Forrest SR. J. Appl. Phys. 2003; 93: 3693-3723.
6. Tang CW. Appl. Phys. Lett. 1986; 48: 183-185.
7. Yu G, Gao J, Hummelen JC, Wudl F and Heeger AJ. Science 1995; 270: 1789-1791.
8. Organic Electronics Klauk H (Ed.) 2006, Wiley-VCH: Weinheim.
9. Ito S, Murashima T, Uno H and Ono N. Chem. Commun. 1998, 1661-1662.
10. Ito S, Ochi N, Murashima T, Uno H and Ono N. Heterocycles 2000; 52: 399-411.
11. Ito S, Uno H, Murashima T and Ono N. Tetrahedron Lett. 2001; 42: 45-47.
12. Shimizu Y, Shen Z, Okujima T, Uno H and Ono N. Chem. Commun. 2004; 374-375.
13. Okujima T, Komobuchi N, Shimizu Y, Uno H and Ono N. Tetrahedron Lett. 2004; 45: 5461-5464.
14. Yamada H, Kushibe K, Okujima T, Uno H and Ono N. Chem. Commun. 2006; 383-385.
15. Okujima T, Komobuchi N, Uno H and Ono N. Heterocycles 2006; 67: 255-267.
16. Okujima T, Kikuchi M, Yamada H, Uno H and Ono N. J. Porphyrins Phthalocyanines 2006; 10: 1197-1201.
17. Brown AR, Pomp A, de Leeuw DM, Klaassen DBM, Havinga EE, Herwig P and Müllen K. J. Appl. Phys. 1996; 79: 2136-2138.
18. Afzali A, Dimitrakopoulos CD and Breen TL. J. Am. Chem. Soc 2002; 124: 8812-8813.
19. Joung MJ, Ahn JH, Kang SY, Baek KH, Ahn SD, Do LM, Kim CA, Kim GH, You IK, Yoon SM and Suh KS. Bull. Korean Chem. Soc 2003; 24: 1862-1864.
20. Vets N, Smet M and Dehaen W. Tetrahedron. Lett. 2004; 45: 7287-7289.
21. Afzali A, Kagan CR and Traub GP. Synth. Met. 2005; 155: 490-494.
22. Tulevski GS, Miao Q, Afzali A, Graham TO, Kagan CR and Nuckolls C. J. Am. Chem. Soc. 2006; 128: 1788-1789.
23. Uno H, Yamashita Y, Kikuchi M, Watanabe H, Yamada H, Okujima T, Ogawa T and Ono N. Tetrahedron Lett. 2005; 46: 1981-1983.
24. Yamada H, Yamashita Y, Kikuchi M, Watanabe H, Okujima T, Uno H, Ogawa T, Ohara K and Ono N. Chem. Eur. J., 2005; 11: 6212-6220.
25. Yamada H, Kawamura E, Sakamoto S, Yamashita Y, Okujima T, Uno H and Ono N. Tetrahedron Lett. 2006; 47: 7501-7504.
26. Mondal R., Shah BK and Neckers DC. J. Am. Chem. Soc. 2006; 128: 9612-9613.
27. Aramaki S, Sakai Y and Ono N. Appl. Phys. Lett. 2004; 12: 2085-2087.
28. Shea PB, Johnson AR, Ono N and Kanicki J. IEEE Trans. Elect. Dev. 2005; 52: 1497-1503.
29. Shea P, Kanicki J and Ono N. J. Appl.Phys. 2005; 98: 014503-7.
30. Yamashita K Chem. Lett. 1982; 1085-1088.
31. Yamashita K, Harima Y, Kubota H and Suzuki H, Bull. Chem. Soc. Jpn 1987; 60: 803-805.
32. Hummelen JC, Knight BW, LePeg F and Wudl F. J. Org. Chem. 1995; 60: 532-538.
33. Yamada H, Imahori H, Nishimura Y, Yamazaki I, Ahn TK, Kim SK, Kim D and Fukuzumi S. J. Am. Chem. Soc. 2003; 125: 9129-9139.
34. In order to perform retro Diels-Alder reaction, ITO/CP was heated to 210°C under vacuum to remove oxygen and/or water. This thermal reaction can also be performed under nitrogen atmosphere without vacuum treatment. Compared to traditional vacuum deposition technique, the vacuum treatment in our method is simpler and our film-preparation method has the advantage of cost-effective, large-area, high-volume device formation.