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Optical Switching Devices Using Redox Polymer Nanosheet

Published online by Cambridge University Press:  01 February 2011

Jun Matsui
Affiliation:
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2–1–1, Katahira, Aoba-ku, Sendai 980–8577, Japan
Kenichi Abe
Affiliation:
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2–1–1, Katahira, Aoba-ku, Sendai 980–8577, Japan
Masaya Mitsuishi
Affiliation:
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2–1–1, Katahira, Aoba-ku, Sendai 980–8577, Japan
Atsushi Aoki
Affiliation:
Nagoya Institute of Technology Gokis-cho, Showa-ku, Nagoya, 466–8555, Japan.
Tokuji Miyashita
Affiliation:
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2–1–1, Katahira, Aoba-ku, Sendai 980–8577, Japan
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Abstract

Optical switching devices, which control the current direction by light stimuli, were constructed using redox polymer nanosheet assemblies. Two kind of nanosheet-photodiode, which can operate by different light irradiation wavelength were assembled in a series so that each current direction becomes opposite. In the nanosheet photodiodes, one photodiode contains ruthenium complex as a sensitizer and the other contains anthracene. When 460 nm light was irradiated to the nanosheet assemblies, only the photodiode containing the ruthenium complex becomes active and an anodic photocurrent was observed. On the other hand, when 390 nm light was irradiated to the photodiode assemblies, only the photodiode containing the anthracene chromophore becomes active and a cathodic photocurrent was observed. This means that we can control the photocurrent direction by 460 nm and 390 nm irradiation as input signals.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

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References

REFERENCES

1. de Silva, A. P., Gunaratne, H. Q. N., Gunnlaugsson, T., Huxley, A. J. M., Mccoy, C. P., Rademacher, J. T. and Rice, E. T., Chem Rev. 97, 15151566 (1997).Google Scholar
2. Raymo, F. M., Adv. Mater, 14, 401414 (2002)Google Scholar
3. Balzain, V., Credi, A. and Venturi, M., Molecular Devices and Machines (Wiley-VCH, 2003).Google Scholar
4. Caroll, L. R. and Gorman, C. B., Angew. Chem., Int. Ed. 41, 43784400 (2002).Google Scholar
5. Aoki, A., Abe, Y. and Miyashita, T., Langmuir, 15, 14631469 (1999).Google Scholar
6. Matsui, J., Mitsuishi, M., Aoki, A. and Miyashita, T., Angew. Chem., Int. Ed. 42, 22722275 (2003).Google Scholar
7. Matsui, J., Mitsuishi, M., Aoki, A. and Miyashita, T., J. Am. Chem. Soc. 126, 37083709 (2004)Google Scholar