Ionization potentials of tantalum-carbide clusters: An experimental and density functional theory study
Date
2005
Authors
Dryza, V.
Addicoat, M.
Gascooke, J.
Buntine, M.
Metha, G.
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Journal article
Citation
Journal of Physical Chemistry A, 2005; 109(49):11180-11190
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Viktoras Dryza, M. A. Addicoat, Jason R. Gascooke, Mark A. Buntine, and Gregory F. Metha
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Abstract
We have used photoionization efficiency spectroscopy to determine the ionization potentials (IP) of the tantalum-carbide clusters, Ta₃Cn(n = 1-3) and Ta₄Cn (n = 1-4). The ionization potentials follow an overall reduction as the number of carbon atoms increases; however, the trend is not steady as expected from a simple electrostatic argument. Instead, an oscillatory behavior is observed such that clusters with an odd number of carbon atoms have higher IPs and clusters with an even number of carbon atoms have lower IPs, with the Ta₄C₄ cluster exhibiting the lowest IP. Excellent agreement is found with relative IPs calculated using density functional theory for the lowest energy structures, which are consistent with the development of a 2 × 2 × 2 face-centered nanocrystal. This work shows that IPs may be used as a reliable validation for the geometries of metal-carbide clusters calculated by theory. The variation in IP can also be interpreted qualitatively with application of a simple model based upon isolobal frontier orbitals.
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Copyright © 2005 American Chemical Society