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Résumé
We present a chargedipole interaction model for the calculation of the frequencydependent polarizability of silver clusters. The model relies on the representation of silver atoms by both a net electric charge and a dipole. Time variations of the atomic charges are related to the currents that flow through the bonds of the structures considered and the atomic charges and dipoles are eventually determined from the application of a leastaction principle. After a generalization that enables the bonds of the bulk and surface atoms to have specific resistances, the model is parameterized on data obtained by the timedependent density functional theory for tetrahedral Ag , Ag and Ag clusters. We then study the polarization properties of dimers of silver clusters. We compare in particular the polarizability of the dimers with that of the isolated clusters, for a range of gap distances and frequencies. We also consider the field enhancements one can achieve with these systems. The results are in good agreement with reference data and enable an extension of these data to a wider range of situations. They show that significant field enhancements are achieved at frequencies associated with resonant polarization along the axis of the dimer.
langue originale  Anglais 

journal  Nanotechnology 
Volume  20 
Numéro de publication  19 
Les DOIs  
Etat de la publication  Publié  1 janv. 2009 
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Plateforme Technologique Calcul Intensif
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Modelling Nanostructures Symposium
Alexandre Mayer (Poster), Rachel Langlet (Poster), Per Olof Åstrand (Poster) & Philippe Lambin (Poster)
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