Hostname: page-component-76fb5796d-vvkck Total loading time: 0 Render date: 2024-04-25T19:31:30.821Z Has data issue: false hasContentIssue false

The study of DNA nanofibers

Published online by Cambridge University Press:  01 February 2011

Mahi R. Singh*
Affiliation:
Department of Physics and Astronomy, University of Western Ontario, London, Canada N6G 3K7
Get access

Abstract

We study the acousto-optic effect on the polaritonic properties of DNA nanofibers which are fabricated by embedding a DNA wire into a polaritonic material. This is a new research area and can be called nanobiopolaritonics. Polaritonic materials have energy gaps in their dispersion relation due to the coupling between optical photons and photons. The bound states of DNA wire are calculated using transfer matrix method. It is found that some of the bound states of the DNA wire lie within the band gap of the polaritonic material. These states do not decay into the polaritonic material since there are not states available for decay process to occur. This means DNA nanofibers has an extremely high Q factor. We have also studied the acousto-optic effect on the photon absorption in DNA nanofibers doped with ensemble of quantum dots. The quantum dots interact with the DNA wire via electron bound polaritons interaction. We have discovered a switching mechanism in DNA nanofibers. When the resonance energy of the quantum dots lies near bound polaritons states, the system becomes transmitting for frequency of a probe field due to the strong electron bound polaritons interaction. This is can be assigned as ‘ON’ of the switch. However, when the strain field is applied the DNA fiber can now absorb the probe beam. This is can be assigned as ‘OFF’ of the switch.

Type
Research Article
Copyright
Copyright © Materials Research Society 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Feurer, T. et al., Annu. Rev. Mater. Res., 37, 317 (2007);Google Scholar
Kittel, C., Introduction to Solid State Physics, (John Wiley & Sons Inc., New York, 1986);Google Scholar
Rupasov, V. I. and Singh, Mahi R., Phys. Rev. Lett., 77, 338 (1996);Google Scholar
Rupasov, V. I. and Singh, Mahi R., Phys. Rev., A54, 3617 (1997).Google Scholar
2. Singh, Mahi R., Phys. Rev. (at press, 2009).Google Scholar
3. Endres, R. G. et al., Rev. Mod. Phys. 76, 195 (2004).Google Scholar
4. Singh, Mahi R., J. Biomater. Sc. 15, 1533 (2004).Google Scholar
5. Alenxandre, S. S. et al., Phys. Rev. Lett. 91, 108105 (2003).Google Scholar
6. Komineas, S. et al., Phys. Rev. B65, 061905 (2002).Google Scholar
7. Yoo, K.-H., et al, Phys. Rev. Lett. 87, 198102 (2001).Google Scholar
8. Tran, P. et al, Phys. Rev. Lett. 85, 1564 (2000).Google Scholar
9. Haakestad, M. W. and Engan, H. E.; Journal of Lightwave Technology 4, 38 (2006)Google Scholar
10. Dainese, P. et al., Nature Physics 2, 388 (2006.)Google Scholar
11. Edwards, G. S. et. al., Biophysics. J. 47, 799 (1985).Google Scholar
12. Fischer, B M et al., Phys. Med. Biol. 3807 47 (2002).Google Scholar
13. Storhoff, James J. et al., J. Am. Chem. Soc. 122, 4640 (2000).Google Scholar
14. Liu, X. and Tan, W., Anal. Chem. 71, 5054 (1999).Google Scholar
15. Ferguson, J. A. et al., Anal. Chem. 72, 5618 (2000).Google Scholar
16. Singh, Mahi R., J. Phys. B42, 065503 (2009).Google Scholar
17. Ariv, A. and Yeh, P., Photonics (Oxford University Press, Oxford, 2007).Google Scholar