Semiclassical Multistate Quantum Dynamics Using Thermalized Gaussian Wavepacket

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Yoosang Son, , , Yeseong Choi, , , Oleg V. Prezhdo*, , and , Hyungjun Kim*, 
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Abstract

Electronic dynamics in condensed-phase systems are predominantly influenced by thermal effects and decoherence arising from the quantum bath coupled to the system. A system–bath Hamiltonian, where the ″system″ interacts with a ″bath″ of many harmonic oscillators, provides a foundational framework for investigating quantum dynamics with environmental effects. Here, we introduce a novel wave function-based method that enables real-time propagation of a finite-temperature harmonic bath wave function using classical equations of motion. We begin by purifying the thermal density matrix of a harmonic oscillator through the introduction of an auxiliary function, which corrects the decoherence behavior of standard Gaussian wavepackets. Using the path-integral formalism, we show that the resulting wavepacket evolves along classical trajectories under a sequence of shifted harmonic potentials. We then derive an explicit analytical form of this state, termed the thermalized Gaussian wavepacket (TGW). To propagate the TGW, we develop two numerical schemes; a stochastic hopping method for the finite coupling regime and a perturbative method tailored for the weak-coupling limit. Our simulations demonstrate that the TGW not only recovers Marcus theory rates in the weak-coupling limit for two-state systems, but also accurately reproduces numerically exact time-dependent Schrödinger equation (TDSE) or multiconfiguration time-dependent Hartree (MCTDH) results for two- and three-state models. These findings demonstrate that the density matrix evolution can be accurately simulated only by forward-propagating the TGW based on the classical trajectories. We envision that the TGW framework offers an efficient and accurate route to simulate electronic transition dynamics in real time, while rigorously incorporating both decoherence and thermal effects, making it a promising tool for investigating quantum dynamics in more complex and realistic systems.

Abstract Image

利用热化高斯波包的半经典多态量子动力学。
凝聚相系统中的电子动力学主要受耦合于系统的量子浴产生的热效应和退相干的影响。系统浴哈密顿量,其中″系统″与许多谐振子的″浴″相互作用,为研究具有环境影响的量子动力学提供了基础框架。在这里,我们介绍了一种新的基于波函数的方法,该方法可以使用经典运动方程实时传播有限温度调和浴波函数。我们首先通过引入辅助函数来净化谐振子的热密度矩阵,该辅助函数校正了标准高斯波包的退相干行为。利用路径积分的形式,我们证明了所得到的波包在一系列移位的谐波势下沿经典轨迹演化。然后,我们推导出这种状态的显式解析形式,称为热化高斯波包(TGW)。为了传播TGW,我们开发了两种数值格式;有限耦合条件下的随机跳变方法和弱耦合条件下的微扰方法。我们的模拟表明,TGW不仅可以恢复两态系统在弱耦合极限下的Marcus理论速率,而且可以精确地再现两态和三态模型的数值精确时相关Schrödinger方程(TDSE)或多组态时相关Hartree (MCTDH)结果。这些结果表明,只有在经典轨迹的基础上,通过前向传播TGW才能准确地模拟密度矩阵的演化。我们设想TGW框架为实时模拟电子跃迁动力学提供了有效和准确的途径,同时严格结合退相干和热效应,使其成为研究更复杂和现实系统中的量子动力学的有前途的工具。
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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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