Hostname: page-component-8448b6f56d-c47g7 Total loading time: 0 Render date: 2024-04-24T19:00:33.860Z Has data issue: false hasContentIssue false
  • English
  • Français

Self – Assembling of Nanoparticles in the form of Double Linear Chains and Superlattices on Their Basis

Published online by Cambridge University Press:  17 March 2011

R.T. Malkhasyan ,
R.K. Karakhanyan ,
M.N. Nazaryan  and
C. Sung
R.T. Malkhasyan
Affiliation:
Scientific – Production Enterprise “Atom”, Tevosyan str. 3/1, Yerevan 375076, Armenia. rmalkhas@aua.am
R.K. Karakhanyan
Affiliation:
Scientific – Production Enterprise “Atom”, Tevosyan str. 3/1, Yerevan 375076, Armenia. rmalkhas@aua.am
M.N. Nazaryan
Affiliation:
Scientific – Production Enterprise “Atom”, Tevosyan str. 3/1, Yerevan 375076, Armenia. rmalkhas@aua.am
C. Sung
Affiliation:
University of Massachusetts, Lowell M.A.
Get access

Abstract

The self-assembling systems in nanoscale powders of crystalline MoO3 are disclosed. For the first time, the double linear chain aggregates of the MoO3 nanoparticles were revealed in nanoscale powders of MoO3, treated by vibrationally excited molecules of hydrogen. Double linear chain aggregates form a linear and an orthogonal supperlattices. Both the double linear chain aggregates and the supperlattices formed are being considered as self-assembling systems. The treatment of the powders by the molecules of hydrogen is a method of obtaining long self-assembling chains of inorganic materials and supperlattices on their basis.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 704: Symposium W – Nanoparticulate Materials , 2001 , W4.9.1/AA4.9.1
Copyright
Copyright © Materials Research Society 2002

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. Tolles, W.M., MRS Bulletin. 25, 36 (2000).Google Scholar
2. Lehn, J.-M., Angew. Chem. Int. Ed. Engl. 29, 1304 (1990).Google Scholar
3. Whitesides, G.M., Mathias, J.P. and Seto, C.T., Science. 254, 1312 (1991).Google Scholar
4. Lindsey, I.S., New J. Chem. 15, 153 (1991).Google Scholar
5. Malkhasyan, R.T. and Movsesyan, G.H., Review Scientific Instruments USSR. 4, 127 (1991).Google Scholar
6. Malkhasyan, R.T. and Movsesyan, G.L. and Potapov, V.K., High Energy Chemistry. 26, 3 (1992).Google Scholar
7. Malkhasyan, R.T. in Metastable Phases and Microstructures, edited by Bormann, R., Mazzone, G., Shull, R.D., Averbakh, R.S. and Ziolo, R.F. (Mater. Res. Soc. Proc. 400, Pittsburgh PA, 1995)pp. 77–82.Google Scholar
8. Malkhasyan, R.T., Agababyan, E. and Karakhanyan, R.K.. Chemical Physic. 30, 57 (1996).Google Scholar
9. Tholen, A.R., in Nanophase Materials, edited by Haadjipanayis, G.S. and Siegel, R.W.(Kluwer Academic Publishers, Dordrecht/ Boston/ London, 1994), p.57.Google Scholar
10. Friedlander, S.K., Journal of Nanoparticles Research. 1, 9 (1999).Google Scholar
11. Pierre, T.G.St., Sipos, P., Chan, P., Chua-Anusorn, W., Bauchspiess, K.R. and Webb, J., in Nanophase Materials, edited by Haadjipanayis, G.S. and Siegel, R.W. (Kluwer Academic Publishers, Dordrecht/ Boston/ London, 1994), p.49.Google Scholar