复数子线性和非线性光谱的理论模型

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Chenghong Huang, Shuming Bai* and Qiang Shi*, 
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引用次数: 0

摘要

我们提出了一个理论模型来研究由一个分子激子耦合到一个短寿命等离子体模式组成的多激子系统的动力学和光谱特性。激子被描述为一个双能级系统(TLS),而等离子体模式被视为一个耗散谐振子。采用层次运动方程法模拟了系统在一定耦合强度范围内的能量传递动力学、吸收谱和二维电子谱(2DES)。结果表明,增加激子-等离子体耦合强度可使吸收光谱从不对称的法诺谱线形状转变为拉比谱线形状,而将TLS与分子内振动模式耦合可减小吸收光谱的中心倾角,使谱线形状更加对称。与耦合分子二聚体相比,模拟的2DES具有明显的特征,突出了多激子系统独特的非线性响应。此外,在强耦合状态下观察到的“呼吸模式”模式可以作为拉比振荡的直接证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Theoretical Model for Linear and Nonlinear Spectroscopy of Plexcitons

A Theoretical Model for Linear and Nonlinear Spectroscopy of Plexcitons

We present a theoretical model to investigate the dynamics and spectroscopic properties of a plexciton system consisting of a molecular exciton coupled to a single short-lived plasmonic mode. The exciton is described as a two-level system (TLS), while the plasmonic mode is treated as a dissipative harmonic oscillator. The hierarchical equations of motion method is employed to simulate energy transfer dynamics, absorption spectra, and two-dimensional electronic spectra (2DES) of the system across a range of coupling strengths. It is shown that increasing the exciton–plasmon coupling strength drives a transition in the absorption spectra from an asymmetric Fano line shape to a Rabi splitting pattern, while coupling the TLS to intramolecular vibrational modes reduces the central dip of the absorption spectra and makes the line shape more symmetric. The simulated 2DES exhibit distinct features compared to those of a coupled molecular dimer, highlighting the unique nonlinear response of plexciton systems. In addition, a “breathing mode” pattern observed in the strong coupling regime can serve as a direct evidence of Rabi oscillation.

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来源期刊
Journal of Chemical Theory and Computation
Journal of Chemical Theory and Computation 化学-物理:原子、分子和化学物理
CiteScore
9.90
自引率
16.40%
发文量
568
审稿时长
1 months
期刊介绍: The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.
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