A Non-Lorentzian Model for Strong Exciton–Plasmon Coupling

We develop a non-Lorentzian analytical model for quantum emitters (QEs) resonantly coupled to localized surface plasmons (LSPs) in metal–dielectric structures. Using the explicit form of the LSP Green function, we derive non-Lorentzian version of semi-classical Maxwell–Bloch equations that describe LSPs directly in terms of metal complex dielectric function rather than via Lorentzian resonances. For a single QE resonantly coupled to an LSP, we obtain an analytical expression for effective optical polarizability of the hybrid system, which, in the Lorentzian approximation, recovers the results of the classical coupled oscillators model. We demonstrate that non-Lorentzian effects originating from temporal dispersion of the metal dielectric function affect significantly the optical spectra as the hybrid system transitions to the strong coupling regime. Specifically, in contrast to results of Lorentzian models, the main spectral weight in the system scattering spectra is shifted toward the lower energy polaritonic band, consistent with the experiment.

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Publication Details

Journal
The Journal of Physical Chemistry C
Published
2025-05-05
DOI
https://doi.org/10.1021/acs.jpcc.5c01891
Primary Topic
Quantum Information and Cryptography
Type
article
Field-Weighted Citation Impact
0.00

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article

A Non-Lorentzian Model for Strong Exciton–Plasmon Coupling

Tigran V. Shahbazyan
The Journal of Physical Chemistry C
Quantum Information and Cryptography
article

A Non-Lorentzian Model for Strong Exciton–Plasmon Coupling

Tigran V. Shahbazyan
article en

Abstract

We develop a non-Lorentzian analytical model for quantum emitters (QEs) resonantly coupled to localized surface plasmons (LSPs) in metal–dielectric structures. Using the explicit form of the LSP Green function, we derive non-Lorentzian version of semi-classical Maxwell–Bloch equations that describe LSPs directly in terms of metal complex dielectric function rather than via Lorentzian resonances. For a single QE resonantly coupled to an LSP, we obtain an analytical expression for effective optical polarizability of the hybrid system, which, in the Lorentzian approximation, recovers the results of the classical coupled oscillators model. We demonstrate that non-Lorentzian effects originating from temporal dispersion of the metal dielectric function affect significantly the optical spectra as the hybrid system transitions to the strong coupling regime. Specifically, in contrast to results of Lorentzian models, the main spectral weight in the system scattering spectra is shifted toward the lower energy polaritonic band, consistent with the experiment.

The Journal of Physical Chemistry CVol. 129(19)
Jackson State University (US)
National Science Foundation
Openalex Percentile: Top 96%
Quantum Information and Cryptography
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