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M@Si16, M = Ti, Zr, Hf: π conjugation, ionization potentials and electron affinities

Authors
Journal
Chemical Physics Letters
0009-2614
Publisher
Elsevier
Publication Date
Volume
363
Identifiers
DOI: 10.1016/s0009-2614(02)01184-3

Abstract

Abstract The bonding nature in the fullerene and Frank–Kasper (FK) polyhedral isomers of M@Si 16, M = Ti, Zr, and Hf clusters has been studied using ab initio calculations based on the G aussian 98 program as well as a ultrasoft pseudopotential plane wave method. The fullerene isomer is found to have double bonds between some Si atoms such that each silicon has two single bonds and a double bond on the cage of these endohedral clusters very similar to C 60. There is a mixed sp 2–sp 3 bonding character between Si atoms and only a small charge transfer from M to the Si cage. The sp 2 bonding gives rise to π conjugation. On the other hand in the FK isomer, about three electrons are transferred from M to the Si cage making the bonding nature in this isomer quite different. The ionization potentials of these clusters are large (≈7.5 eV) similar to C 60 and the electron affinities are small that make these clusters behave like superatoms.

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