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Intercalation Compounds: Covalent and Ionic Approach

Published online by Cambridge University Press:  21 February 2011

Paul Hagenmuller*
Affiliation:
Laboratoire de Chimie du Solide du CNRS, Université de BORDEAUX I, 351 cours de la Libération, 33405 TALENCE Cedex, France
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Abstract

In contrast with amphoteric graphite layer type oxides or chalcogenides play generally the role of acceptors in intercalation reactions. Due to the more ionic character of the M-0 bonds the structural evolution of the oxides may usually be explained on hand of electrostatic considerations, or in terms of cation oxido-reduction. On contrary for the more covalent chalcogenides occupancy of energy levels in the band structure by the transferred electrons constitute a determining factor, influencing strongly not only the structural changes but also the physical properties. Similar bonding considerations account for the strong tendency of the oxides to undergo 2D → 3D transformations.

Type
Research Article
Copyright
Copyright © Materials Research Society 1989

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References

[1] DAUMAS, N. and HEROLD, A., C.R. Acad. Sc. 268, 373 (1971).Google Scholar
[2] DRESSELHAUS, M.S., Physics Today 37, 60 (1984).Google Scholar
[3] SILBERNAGEL, B.G., Sol. St. Comm. 17, 361 (1975).Google Scholar
[4] ROUXEL, J., Chemica Scripta 28, 33 (1988).Google Scholar
[5] DELMAS, C., BRACONNIER, J.J., FOUASSIER, C. and HAGENMULLER, P., Mat. Res. Bull. 3/4, 165 (1981).Google Scholar
[6] ROUXEL, J., DANOT, M. and PICHON, J., Bull. Soc. Chim. Fr. 3390 (1971).Google Scholar
[7] ROUXEL, J., Intercalated Layered Materials, Levy, F.A. ed. (Reidel Publ., 1979).Google Scholar
[8] FOUASSIER, C., DELMAS, C. and HAGENMULLER, P., Mat. Res. Bull. 10, 443 (1975).Google Scholar
[9] BLANC, A. LE, DANOT, M., TRICHET, L. and ROUXEL, J., Mat. Res. Bull. 9, 191 (1974).Google Scholar
[10] ROUXEL, J., J. Sol. St. Chem. 17, 223 (1976).Google Scholar
[11] FATSEAS, G.A., PALVADEAU, P. and VENIEN, J.P., J. Sol. St. Chem. 51, 17 (1984).Google Scholar
[12] LIANG, W.Y., Physics and Chemistry of Electrons and Ions in Condensed Matter, NATO ASI 130 (1984).Google Scholar
[13] NADIRI, A., Thèse de Doctorat ès sciences physiques, BORDEAUX I University, 1985.Google Scholar
[14] THOMPSON, A.H., Phys. Rev. Lett. 40, 1511 (1978).Google Scholar
[15] SCHOLLHORN, R., Angew. Chem. English ed. 19, 983 (1980).Google Scholar
[16] FOUASSIER, C., MATEJKA, G., REAU, J.M. and HAGENMULLER, P., J. Sol. St. Chem. 6, 532 (1973).Google Scholar
[17] DELMAS, C., FOUASSIER, C. and HAGENMULLER, P., Mat. Res. Bull. 11, 1483 (1976).Google Scholar
[18] MAAZAZ, A., DELMAS, C., FOUASSIER, C., REAU, J.M. and HAGENMULLER, P., Mat. Res. Bull. 14, 329 (1979).Google Scholar
[19] THOMAS, M.G., W.I. DAVID, GOODENOUGH, J.B. and GROVES, P., Mat. Res. Bull. 20, 1137 (1985).Google Scholar
[20] PICCIOTTO, L.A. DE and THACKERAY, m.M., Mat. Res. Bull. 20, 187 (1985), Sol. St. Ionics 18/19, 773 (1986).Google Scholar
[21] MAAZAZ, A., DELMAS, C. and HAGENMULLER, P., J. Incl. Phenom. 1, 45 (1983).Google Scholar
[22] MAAZAZ, A. and DELMAS, C., C.R. Acad. Sc. 295, 759 (1982).Google Scholar
[23] BRUCE, W.I., M.M. THACKERAY, BRUCE, P.G. and GOODENOUGH, J.B., Mater. Res. Bull. 19, 99 (1984).Google Scholar
[24] DOUMERC, J.P., AMMAR, A., WICHAINCHAI, A., POUCHARD, M. et HAGENMULLER, P., J. Phys. Chem. Solids 48, 37 (1987).Google Scholar