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Fabrication of Polystyrene/CdS Hybrid Nanocomposites Embedded with CdS Nanowires by a Soft Solution-Processing Route

Published online by Cambridge University Press:  01 February 2011

Shu-Hong Yu
Affiliation:
Center for Materials Design, Materials and Structures Laboratory, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226, Japan
Masahiro Yoshimura
Affiliation:
Center for Materials Design, Materials and Structures Laboratory, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226, Japan
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Abstract

A novel one-step soft solution-processing (SSP) route called solvothermal-co-polymerization technique was successfully developed for in situ fabrication polystyrene (PS)/CdS nanocomposites embedded with CdS nanowires in ethylenediamine media at lower temperature (80–140°C). In this route, the polymerization of the styrene monomers and the formation of the CdS nanocrystallites occur simultaneously in a certain temperature range. The results show that the quantum-fined CdS nanowires with diameters 4–15 nm and lengths up to several micrometers via the present one-step route were embedded in the PS matrix and had [001] preferential orientation. Both temperature and solvent were found to play a key role in the synthesis of the nanocomposites. The produced novel hybrid nanocomposites display obvious quantum size effects and interesting fluorescence features.

Type
Research Article
Copyright
Copyright © Materials Research Society 2000

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References

REFERENCES

1. Antonietti, M. and Göltner, C., Angew. Chem. Int. Ed. Engl., 36, 910 (1997).Google Scholar
2. Beecroft, L. L., and Ober, C. K., Chem. Mater.,, 9, 1302 (1997).Google Scholar
3. Wozniak, M. E. and Sen, A., Chem. Mater.,, 4, 754 (1992).Google Scholar
4. Wang, Y. and Herron, N., Chem. Phys. Lett.,, 200, 71 (1992).Google Scholar
5. Sookal, K., Hanus, L. H., Ploehn, H. J. and Murphy, C. J., Adv. Mater.,, 10, 1083 (1998).Google Scholar
6. Lakowicz, J. R., Gryczynski, I., Gryczynski, Z. and Murphy, C. J., J. Phys. Chem. B,, 103, 7613 (1999).Google Scholar
7. Winiarz, J., Zhang, L. M., Lal, M., Friend, C. S. and Prasad, P. N., J. Am. Chem. Soc.,, 121, 5287 (1999).Google Scholar
8. Alivisatos, A. P., Science, 271, 933 (1996).Google Scholar
9. Colvin, V. L., Schlamp, M. C. and Alivisatos, A. P., Nature,, 370, 354 (1994).Google Scholar
10. Covin, V. L. and Alivisatos, A. P., J. Chem. Phys.,, 97, 730 (1992).Google Scholar
11. Dabbousi, B. O., Bawendi, M. G., Onitsuka, O. and Rubner, M. F., Appl. Phys. Lett.,, 66, 1316 (1995).Google Scholar
12. Greenham, N. C., Peng, X. G. and Alivisatos, A. P., Phys. Rew. B.,, 54, 17628 (1996).Google Scholar
13. Huynh, W., Peng, X. G. and Alivisatos, A. P., Adv. Mater.,, 11, 923 (1999).Google Scholar
14. Beddard, G. S. and Allen, N. S., Emission Spectroscopy, Comprehensive polymer science: The synthesis, characterization, reactions and applications of polymers, ed. Booth, C. and Price, C., (Pergamon Press, 1989), pp. 449516.Google Scholar
15. Klöpffer, W., Eur. Polym. J., 11, 203 (1975).Google Scholar
16. Modes, S. and Lianos, P., J. Phys. Chem.,, 93, 5834 (1989).Google Scholar
17. Brus, L. E., Rosetti, R. and Nakahara, S., J. Chem. Phys.,, 79, 1086 (1983).Google Scholar