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Issue 24, 2020
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Plasmonic nano-shells: atomistic discrete interaction versus classic electrodynamics models

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Abstract

Using the extended discrete interaction model and Mie theory, we investigate the tunability of the optical polarizability of small metallic nano-shells. We show that the spectral positions of symmetric and antisymmetric dipolar plasmon resonances vary with the ratio of particle radius to hole radius in a manner similar to one predicted for uniform metallic nano-shells using a semiclassical approach of two coupled harmonic oscillators. We show that, according to the extended discrete interaction model, the dipolar plasmon resonances are also present for nano-shells in the 2–13 nm size region and show the same functional dependence seen for larger nano-shells. Using previously fitted data from experiment, we can predict the size-dependence of the plasma frequency for nano-shells in the 1–15 nm size region. We find that Mie theory, which utilizes the electron mean free path correction for the permittivity, is not able to reproduce the same functional form of the dipolar modes for the nano-shells of the same sizes.

Graphical abstract: Plasmonic nano-shells: atomistic discrete interaction versus classic electrodynamics models

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Article information


Submitted
27 Apr 2020
Accepted
02 Jun 2020
First published
02 Jun 2020

Phys. Chem. Chem. Phys., 2020,22, 13467-13473
Article type
Paper

Plasmonic nano-shells: atomistic discrete interaction versus classic electrodynamics models

V. I. Zakomirnyi, I. L. Rasskazov, L. K. Sørensen, P. S. Carney, Z. Rinkevicius and H. Ågren, Phys. Chem. Chem. Phys., 2020, 22, 13467
DOI: 10.1039/D0CP02248A

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