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Wannier function analysis of silicon–carbon alloys

P Fitzhenry, M M M Bilek, N A Marks, N C Cooper and D R McKenzie

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Maximally localized Wannier functions are the basis of a new technique for resolving ambiguous bonding issues for amorphous materials. Geometrical methods using the Wannier function representation provide an insightful chemical picture of local bonding and hybridization in disordered structures. Central to these methods is the notion of treating the Wannier function centres as a virtual atomic species with a well-defined degree of localization. Using Wannier function methods, we classify and quantify the types of bonding present in a sample of the ternary alloy hydrogenated amorphous silicon carbide, C22Si22H20. In addition to the bonding previously observed for this material, we see three-centre bonding and flipping bonds. We identify a cluster defect in our sample associated with these flipping bonds, and observe a temperature dependence of the bond flipping. This effect may be observable using temperature-dependent Raman spectroscopy.


PACS

71.15.Pd Molecular dynamics calculations (Car-Parrinello) and other numerical simulations

78.30.Ly Disordered solids

71.23.An Theories and models; localized states

Subjects

Condensed matter: electrical, magnetic and optical

Dates

Issue 2 (22 January 2003)

Received 2 July 2002

Published 20 December 2002



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