Polariton-assisted incoherent to coherent excitation energy transfer between colloidal nanocrystal quantum dots

We explore the dynamics of energy transfer between two nanocrystal quantum dots placed within an optical microcavity. By adjusting the coupling strength between the cavity photon mode and the quantum dots, we have the capacity to fine-tune the effective coupling between the donor and acceptor. Introducing a non-adiabatic parameter, γ, governed by the coupling to the cavity mode, we demonstrate the system's capability to shift from the overdamped Förster regime (γ ≪ 1) to an underdamped coherent regime (γ ≫ 1). In the latter regime, characterized by swift energy transfer rates, the dynamics are influenced by decoherence time. To illustrate this, we study the exciton energy transfer dynamics between two closely positioned CdSe/CdS core/shell quantum dots with sizes and separations relevant to experimental conditions. Employing an atomistic approach, we calculate the excitonic level arrangement, exciton-phonon interactions, and transition dipole moments of the quantum dots within the microcavity. These parameters are then utilized to define a model Hamiltonian. Subsequently, we apply a generalized non-Markovian quantum Redfield equation to delineate the dynamics within the polaritonic framework.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2024-10-17
DOI
https://doi.org/10.1063/5.0223369
Citations
6
Primary Topic
Strong Light-Matter Interactions
Type
article
Field-Weighted Citation Impact
2.03

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article

Polariton-assisted incoherent to coherent excitation energy transfer between colloidal nanocrystal quantum dots

Eran Rabani, Kaiyue Peng
6 citations
The Journal of Chemical Physics
Strong Light-Matter Interactions
2.03
article

Polariton-assisted incoherent to coherent excitation energy transfer between colloidal nanocrystal quantum dots

Eran Rabani, Kaiyue Peng
article en
6 citations

Abstract

We explore the dynamics of energy transfer between two nanocrystal quantum dots placed within an optical microcavity. By adjusting the coupling strength between the cavity photon mode and the quantum dots, we have the capacity to fine-tune the effective coupling between the donor and acceptor. Introducing a non-adiabatic parameter, γ, governed by the coupling to the cavity mode, we demonstrate the system's capability to shift from the overdamped Förster regime (γ ≪ 1) to an underdamped coherent regime (γ ≫ 1). In the latter regime, characterized by swift energy transfer rates, the dynamics are influenced by decoherence time. To illustrate this, we study the exciton energy transfer dynamics between two closely positioned CdSe/CdS core/shell quantum dots with sizes and separations relevant to experimental conditions. Employing an atomistic approach, we calculate the excitonic level arrangement, exciton-phonon interactions, and transition dipole moments of the quantum dots within the microcavity. These parameters are then utilized to define a model Hamiltonian. Subsequently, we apply a generalized non-Markovian quantum Redfield equation to delineate the dynamics within the polaritonic framework.

The Journal of Chemical PhysicsVol. 161(15)
Lawrence Berkeley National Laboratory (US), Tel Aviv University (IL), University of California, Berkeley (US)
U.S. Department of Energy, National Energy Research Scientific Computing Center, Office of Science, Basic Energy Sciences
Affordable and clean energy
Openalex Percentile: Top 13%
Strong Light-Matter Interactions
2.03
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Polariton-assisted incoherent to coherent excitation energy transfer between colloidal nanocrystal quantum dots — Eran Rabani, Kaiyue Peng · The Journal of Chemical Physics (2024) | TGRS Research Map | TGRS