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Lessons on electronic decoherence in molecules from exact modeling

机译:来自确切建模的分子中电子灭菌的课程

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Electronic decoherence processes in molecules and materials are usually thought and modeled via schemes for the system-bath evolution in which the bath is treated either implicitly or approximately. Here we present computations of the electronic decoherence dynamics of a model many-body molecular system described by the Su-Schrieffer-Heeger Hamiltonian with Hubbard electron-electron interactions using an exact method in which both electronic and nuclear degrees of freedom are taken into account explicitly and fully quantum mechanically. To represent the electron-nuclear Hamiltonian in matrix form and propagate the dynamics, the computations employ the Jordan-Wigner transformation for the fermionic creation/annihilation operators and the discrete variable representation for the nuclear operators. The simulations offer a standard for electronic decoherence that can be used to test approximations. They also provide a useful platform to answer fundamental questions about electronic decoherence that cannot be addressed through approximate or implicit schemes. Specifically, through simulations, we isolate basic mechanisms for electronic coherence loss and demonstrate that electronic decoherence is possible even for one-dimensional nuclear bath. Furthermore, we show that (i) decreasing the mass of the bath generally leads to faster electronic decoherence; (ii) electron-electron interactions strongly affect the electronic decoherence when the electron-nuclear dynamics is not pure-dephasing; (iii) classical bath models with initial conditions sampled from the Wigner distribution accurately capture the short-time electronic decoherence dynamics; (iv) model separable initial superpositions often used to understand decoherence after photoexcitation are only relevant in experiments that employ delta-like laser pulses to initiate the dynamics. These insights can be employed to interpret and properly model coherence phenomena in molecules. Published by AIP Publishing.
机译:分子和材料中的电子脱机过程通常是通过用于系统浴蒸馏的方案进行建模的,其中浴被含蓄地或大约进行浴。在这里,我们使用使用精确的方法,呈现由苏-Schrieffer-Heeger Hamiltonian的模型多体分子系统的型号多体分子系统的计算,其中通过精确的方法明确地考虑了电子和核自由度的精确方法并且机械地完全量子。为了代表矩阵形式的电子核汉密尔顿,并传播动态,计算采用了核算创建/湮灭运营商的约旦 - Wigner转换和核运营商的离散变量表示。模拟提供了可用于测试近似的电子脱机标准。他们还提供了一个有用的平台,以回答有关电子角色的基本问题,无法通过近似或隐含方案来解决。具体地,通过模拟,我们隔离电子相干损失的基本机制,并表明即使对于一维核浴,也可以进行电子干式。此外,我们表明(i)降低浴缸的质量通常导致更快的电子干式堵塞; (ii)当电子核动力学不是纯粹的相互作用时,电子 - 电子相互作用强烈影响电子干式; (iii)古典浴室模型,具有从Wigner分布采样的初始条件精确捕获短时间电子脱机动态; (iv)模型可分离的初始叠加通常用于理解运动后的消退仅在采用δ样激光脉冲以启动动力学的实验中才相关。这些见解可以用于解释和适当地模拟分子中的相干现象。通过AIP发布发布。

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