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

被引:0
|
作者
Peng, Kaiyue [1 ]
Rabani, Eran [1 ,2 ,3 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
[3] Tel Aviv Univ, Sackler Ctr Computat Mol & Mat Sci, IL-69978 Tel Aviv, Israel
来源
JOURNAL OF CHEMICAL PHYSICS | 2024年 / 161卷 / 15期
关键词
ELECTRON-TRANSFER; FILTER-DIAGONALIZATION; ASSEMBLIES; DYNAMICS; SYSTEM; SHELL;
D O I
10.1063/5.0223369
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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, gamma, governed by the coupling to the cavity mode, we demonstrate the system's capability to shift from the overdamped F & ouml;rster regime (gamma << 1) to an underdamped coherent regime (gamma >> 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.
引用
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页数:8
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