Decoherence dynamics in molecular qubits: Exponential, Gaussian and beyond.

IF 3.1 2区 化学 Q3 CHEMISTRY, PHYSICAL Journal of Chemical Physics Pub Date : 2025-02-14 DOI:10.1063/5.0246970
Ignacio Gustin, Xinxian Chen, Ignacio Franco
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Abstract

In this work, we examine how the structure of system-bath interactions can determine commonly encountered temporal decoherence patterns, such as Gaussian and exponential decay, in molecular and other qubits coupled to a thermal bosonic bath. The analysis, based on a pure dephasing picture that admits analytical treatment, shows that decoherence, in general, is neither purely Gaussian nor exponential but rather the exponential of oscillatory functions, with periods determined by the bath's frequencies. For initially unentangled qubit-bath states, Gaussian decay is always present at early times. It becomes increasingly dominant with increasing temperature, qubit-bath interaction strength, and bath correlation time. Initial system-bath entanglement that arises due to displacement in the position of the bath states preserves the Gaussian decay. By contrast, strict exponential decay arises only in very specific models that we isolate. However, it becomes dominant for times longer than the bath correlation time or for early times when there is initial entanglement due to momentum displacement of the bath states. For molecular electronic decoherence, the long-time exponential regime plays a limited role as it emerges after most coherence is lost. Thus, the Gaussian decay provides a more suitable (albeit imperfect) model of such decoherence. Furthermore, we discuss the connection between electronic decoherence dynamics and electronic spectroscopic line shape theory, where Gaussian spectral peaks correspond to Gaussian coherence decay and Lorentzian peaks correspond to exponential coherence decay. We find that Gaussian spectral peaks, usually associated with inhomogeneous broadening, can emerge from the entangling unitary system-bath dynamics even when there is no inhomogeneity in the initial conditions.

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分子量子位的退相干动力学:指数,高斯和超越。
在这项工作中,我们研究了系统浴相互作用的结构如何决定与热玻色子浴耦合的分子和其他量子比特中常见的时间退相干模式,如高斯和指数衰减。基于一个允许解析处理的纯消相图的分析表明,一般来说,退相干既不是纯高斯的,也不是指数的,而是振荡函数的指数,周期由槽的频率决定。对于初始未纠缠的量子位浴态,高斯衰减总是在早期存在。随着温度、量子比特-浴体相互作用强度和浴体相关时间的增加,它越来越占主导地位。初始系统浴纠缠由于浴态位置的位移而产生,保留了高斯衰减。相比之下,严格的指数衰减只出现在我们孤立的非常特定的模型中。然而,它成为主导的时间比浴相关时间长几倍,或者在早期由于浴态的动量位移而存在初始纠缠。对于分子电子退相干,长时间的指数谱在大部分相干性丧失后才出现,其作用有限。因此,高斯衰减为这种退相干提供了一个更合适(尽管不完美)的模型。进一步讨论了电子退相干动力学与电子能谱线形理论之间的联系,其中高斯谱峰对应高斯相干衰减,洛伦兹谱峰对应指数相干衰减。我们发现高斯谱峰通常与非均匀展宽有关,即使在初始条件没有非均匀性的情况下,也可以从纠缠酉系统动力学中出现。
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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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