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Tunable Optical Absorption of Composites of Nanocrystalline Copper Prepared by in situ Chemical Reduction within a Cu2+-Polymer Complex

Published online by Cambridge University Press:  01 February 2011

Cheng Huang ,
Gang Huang  and
C. Z. Yang
Cheng Huang
Affiliation:
Materials Research Institute and Electrical Engineering Department, The Pennsylvania State University, University Park, PA 16802, cxh57@psu.edu
Gang Huang
Affiliation:
Electronic Materials & Thin Film Devices Division, Physics Dept., Suzhou University, 215006, China
C. Z. Yang
Affiliation:
Department of Polymer Science and Engineering, Nanjing University, Nanjing 210093, China
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Abstract

Research on nanocrystalline materials and the physics behind their properties have attracted considerable attention. A number of physical and chemical techniques have been used to synthesize different nanomaterials and nanocomposites. Optical absorption characteristics of composites containing nanosized metals or semiconductors have been investigated for potential applications in nonlinear optics and photonic crystals and also to understand the effect of particle size on the band gap of the material concerned. These materials show a large third-order nonlinear susceptibility. A polymer-matrix nanocomposite containing copper particles has been prepared by in situ chemical reduction within a polymer-metal complex solid film. The copper particle size in the order of 10 nm is controlled by the initial content of the metal ions in the complex. Their fractal pattern and the value of the fractal dimension indicate that there exists a cluster-cluster aggregation (CCA) process in the present system. Optical absorption spectra of copper-polymer nanocomposites show distinct plasma absorption bands and quantum size effect in the samples. More studies on optical properties of composites containing nanosized metals are within the Drudeframe on the basis of Mie theory, but the electrons behave in a wavelike rather than a particlelike way as the particle size decreases to below 10 nm, and the classical Drude model should be modified considering the quantum confinement effect. In this paper, the calculated blueshift of the resonance peak based on a quantum-sphere model (QSM) proposed by Huang and Lue, gives remarkable agreement with the experimental data as the size of copper particles embedded in the polymer becomes smaller.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 789 , 2003 , N3.30
Copyright
Copyright © Materials Research Society 2004

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References

REFERENCES

1. Lee, K. and Asher, S.A., J. Am. Chem. Soc. 122, 9534 (2000).Google Scholar
2. Xu, S., Zhang, J., Paquet, C., Lin, Y. and Kumacheva, E., Adv. Funct. Mater. 13, 468 (2003).Google Scholar
3. Roy, S. and Chakravorty, D., Appl. Phys. Lett. 59, 1415 (1991).Google Scholar
4. Witten, T.A. and Sander, L.M., Phys. Rev. Lett. 47, 1400 (1981)Google Scholar
5. Weitz, D.A. and Oliveria, M., Phys. Rev. Lett. 52, 1433 (1984).Google Scholar
6. Meakin, P., Phys. Rev. Lett. 51, 1119 (1983).Google Scholar
7. Wang, H.Z., Zhao, F.L., He, Y.J., Zheng, X.G., Huang, X.G. and Wu, M.M., Opt. Lett. 23, 777 (1998).Google Scholar
8. Banerjee, S. and Chakravorty, D., Appl. Phys. Lett. 72, 1027 (1998).Google Scholar
9. Mie, G., Ann. Phys. 25, 377(1908).Google Scholar
10. Huang, W.C. and Lue, J.T., Phys. Rev. B 49, 17279 (1994).Google Scholar
11. Huang, C. and Yang, C.Z., Appl. Phys. Lett. 74, 1692 (1999).Google Scholar
12. Forrest, S.R. and Witten, T.A. Jr, J. Phys. A 12, L109 (1979).Google Scholar
13. Klug, H.P. and Alexander, L.E., X-ray diffraction procedures (John Wiley, NY, 1954).Google Scholar
14. Huang, C., Chen, L. and Yang, C.Z., Polym. Bull. 41, 585 (1998).Google Scholar
15. Lisiecki, I. and Pileni, M.P., J. Am. Chem. Soc. 115, 3887 (1993).Google Scholar
16. Kreibig, U., J. Phys. F: Metal Phys. 4, 999 (1974).Google Scholar
17. Su, K.H., Wei, Q.-H., Zhang, X., Mock, J.J., Smith, D.R., and Schultz, S., Nano Letters 3(8), 1087 (2003).Google Scholar