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Hauptverfasser: Raghavan-Chitra, Sricharan, Koner, Arghadip, Yuen-Zhou, Joel
Format: Preprint
Veröffentlicht: 2026
Schlagworte:
Online-Zugang:https://arxiv.org/abs/2604.12395
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author Raghavan-Chitra, Sricharan
Koner, Arghadip
Yuen-Zhou, Joel
author_facet Raghavan-Chitra, Sricharan
Koner, Arghadip
Yuen-Zhou, Joel
contents Linear optical spectra of molecular aggregates are often approximated by classical optics methods such as the discrete-dipole approximation (DDA), coherent exciton scattering (CES), and coherent potential approximation (CPA), where the only quantum-mechanical input to the calculation is the linear susceptibility of the monomers. However, the limits of validity of these classical optics methods remain opaque. Here, starting from a quantum mechanical Hamiltonian for the aggregate, we identify a limit where DDA/CPA/CES is exact: all-to-all coupled permutationally symmetric aggregates of $N \to \infty$ monomers. The permutational symmetry of this molecular version of the Lipkin-Meshkov-Glick model, which is closely related to that of the molecular polariton problem of many identical molecules coupled to a single-cavity mode, allows us to borrow recent techniques developed for the latter. In particular, we identify a $1/N$ expansion that corrects the classical optics limit with finite $N$ corrections to the linear response of the aggregate. These corrections feature as Raman-like transitions of a single monomer. We illustrate these findings with calculations on the very physically-relevant setup of a homodimer. Our findings clarify how quantum optical features that go beyond classical optics can already be present in simple arrays of quantum emitters such as molecular aggregates.
format Preprint
id arxiv_https___arxiv_org_abs_2604_12395
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Permutationally symmetric molecular aggregates
Raghavan-Chitra, Sricharan
Koner, Arghadip
Yuen-Zhou, Joel
Quantum Physics
Optics
Linear optical spectra of molecular aggregates are often approximated by classical optics methods such as the discrete-dipole approximation (DDA), coherent exciton scattering (CES), and coherent potential approximation (CPA), where the only quantum-mechanical input to the calculation is the linear susceptibility of the monomers. However, the limits of validity of these classical optics methods remain opaque. Here, starting from a quantum mechanical Hamiltonian for the aggregate, we identify a limit where DDA/CPA/CES is exact: all-to-all coupled permutationally symmetric aggregates of $N \to \infty$ monomers. The permutational symmetry of this molecular version of the Lipkin-Meshkov-Glick model, which is closely related to that of the molecular polariton problem of many identical molecules coupled to a single-cavity mode, allows us to borrow recent techniques developed for the latter. In particular, we identify a $1/N$ expansion that corrects the classical optics limit with finite $N$ corrections to the linear response of the aggregate. These corrections feature as Raman-like transitions of a single monomer. We illustrate these findings with calculations on the very physically-relevant setup of a homodimer. Our findings clarify how quantum optical features that go beyond classical optics can already be present in simple arrays of quantum emitters such as molecular aggregates.
title Permutationally symmetric molecular aggregates
topic Quantum Physics
Optics
url https://arxiv.org/abs/2604.12395