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The Formation of Close-Packed Two-Dimensional CdSe Colloidal Films by Electric-Field-Induced Deposition

Published online by Cambridge University Press:  10 February 2011

L. Xu
Affiliation:
State key Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093, P. R.China
X.F. Huang
Affiliation:
State key Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093, P. R.China
H.M. Chen
Affiliation:
State key Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093, P. R.China
W. L. Chen
Affiliation:
State key Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093, P. R.China
Z.G. Liu
Affiliation:
State key Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093, P. R.China
K.J. Chen
Affiliation:
State key Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093, P. R.China
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Abstract

Monodispersed CdSe nanocrystals with average diameter of ∼5 nm were synthesized from SeSO32− and rich Cd2+ ionic reagents in aqueous solution. Two-dimensional (2D) close-packed colloidal CdSe films were formed on the electrode surface by electric-field induced deposition method. Transmission electron microscopy (TEM) images show that colloidal CdSe films exhibit different states, named “gas”, “liquid” and “solid” states, which can be transformed by adjusting applied field (E) or deposition time (T). The experimental results demonstrate that the average nearest-neighbor distance of clusters on the electrode surface is inversely proportional to the ET product.

Type
Research Article
Copyright
Copyright © Materials Research Society 2000

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References

REFERENCES

1. Alivisatos, A. P., Sci. 271, p.933 (1996)10.1126/science.271.5251.933Google Scholar
2. Vossmeyer, T., Katsikas, L., Glersig, M., Popovic, I. G., Diesuer, K., Chemseddine, A., Eychmuller, A. and Weller, H., J. Phys. Chem. 98, p.7665 (1994)10.1021/j100082a044Google Scholar
3. Steigerwald, M. L., Alivisatos, A. P., Gibson, J.M., Harris, T.D., Kortan, R., Muller, A. J., Thayer, A. M., Duncan, T. M., Douglass, D. C. and Brus, L. E., J. Am. Chem. Soc. 110, p.3046 (1988)10.1021/ja00218a008Google Scholar
4. Murray, C. B., Norris, D. J. and Bawendi, M. G., J. Am. Chem. Soc. 115, p. 8706 (1993).10.1021/ja00072a025Google Scholar
5. Giersig, M. and Mulvaney, P., J. Phys. Chem. 97, p.6334 (1993).10.1021/j100126a003Google Scholar
6. Trau, M., Saville, D. A. and Aksay, I. A., Sci. 272, p.706 (1996)10.1126/science.272.5262.706Google Scholar
7. Xu, L., Huang, X.F., Huang, H.B., Chen, H.M., Xu, J. and Chen, K.J., Jpn. J. Appl. Phys. 37, p. 3491 (1998).10.1143/JJAP.37.3491Google Scholar
8. Yeh, S.R., Seul, M., and Shralman, B. I., Nature 386, p.57 (1997)10.1038/386057a0Google Scholar