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

IF 3.1 2区 化学 Q3 CHEMISTRY, PHYSICAL
Kaiyue Peng, Eran Rabani
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引用次数: 0

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.

胶体纳米晶体量子点之间的极化子辅助非相干到相干激发能量转移。
我们探索了置于光学微腔内的两个纳米晶体量子点之间的能量传递动力学。通过调整空腔光子模式与量子点之间的耦合强度,我们可以微调供体与受体之间的有效耦合。我们引入了一个非绝热参数γ,该参数受与腔模间耦合的影响,从而证明了该系统能够从过阻尼佛斯特机制(γ ≪ 1)转变为欠阻尼相干机制(γ ≫ 1)。在以快速能量传输速率为特征的后一机制中,动力学受到退相干时间的影响。为了说明这一点,我们研究了两个紧密定位的镉硒/镉硒核/壳量子点之间的激子能量转移动力学,其尺寸和间隔与实验条件相关。我们采用原子论方法计算了微腔内量子点的激子水平排列、激子-声子相互作用和过渡偶极矩。然后利用这些参数定义模型哈密顿。随后,我们应用广义的非马尔可夫量子雷德菲尔德方程来描述极子框架内的动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Chemical Physics
Journal of Chemical Physics 物理-物理:原子、分子和化学物理
CiteScore
7.40
自引率
15.90%
发文量
1615
审稿时长
2 months
期刊介绍: The Journal of Chemical Physics publishes quantitative and rigorous science of long-lasting value in methods and applications of chemical physics. The Journal also publishes brief Communications of significant new findings, Perspectives on the latest advances in the field, and Special Topic issues. The Journal focuses on innovative research in experimental and theoretical areas of chemical physics, including spectroscopy, dynamics, kinetics, statistical mechanics, and quantum mechanics. In addition, topical areas such as polymers, soft matter, materials, surfaces/interfaces, and systems of biological relevance are of increasing importance. Topical coverage includes: Theoretical Methods and Algorithms Advanced Experimental Techniques Atoms, Molecules, and Clusters Liquids, Glasses, and Crystals Surfaces, Interfaces, and Materials Polymers and Soft Matter Biological Molecules and Networks.
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