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Andrew C. Hunt

Publications and source records attributed to Andrew C. Hunt.

4 recordsLinked to original sources

Exploiting the path-integral radius of gyration in open quantum dynamics

A major challenge in open quantum dynamics is the inclusion of Matsubara-decay terms in the memory kernel, which arise from the quantum-Boltzmann delocalisation of the bath modes. This delocalisation can be quantified by the radius of gyration squared ${\mathcal R}^2(\omega)$ of the imaginary-time Feynman paths of the bath modes as a function of the frequency $\omega$. In a Hierarchical Equations of Motion (HEOM) calculation with a Debye--Drude spectral density, ${\mathcal R}^2(\omega)$ is the only quantity that is treated approximately (assuming convergence with respect to hierarchy depth). Here, we show that the well-known Ishizaki--Tanimura correction is equivalent to separating smooth from `Brownian' contributions to ${\mathcal R}^2(\omega)$, and that modifying the correction leads to a more efficient HEOM in the case of fast baths. We also develop a simple `A4' adaptation of the `AAA' (Adaptive Antoulas--Anderson) algorithm in order to fit ${\mathcal R}^2(\omega)$ to a sum over poles, which results in an extremely efficient implementation of the standard HEOM method at low temperatures.

quant-ph

Out-of-time correlation functions in single-body systems

In the study of quantum chaos, `out of time ordered correlators' (OTOCs) are commonly used to quantify the rate at which quantum information is scrambled. This rate has been conjectured by Maldecena et al. to obey a universal, temperature dependent bound. Recent studies have shown that instantons, delocalised structures that dominate tunnelling statistics over barriers, reduce the growth rate of OTOCs. For the case of the symmetric double well, this reduction ensures the bound is maintained for OTOCs generated using ring polymer molecular dynamics (RPMD), a method with approximate dynamics but exact quantum statistics. In this report we set out to further understand the role of the instanton in the enforcement of the Maldacena bound and test whether RPMD is sufficient to satisfy the bound. We also investigate the impact of coherence on the flattening of of OTOCs by contrasting bounded with scattering systems. For the scattering system we observe a significantly smaller OTOC growth rate than that of the analogous bounded system, and a flattening in growth rate as time progresses. We attribute the first effect to influence of the Boltzmann operator, and the second to interference caused by anharmonicity of the potential. In our studies of RPMD, we find counterexamples showing that it is not sufficient to satisfy the bound. We develop a theory for OTOCs using (analytically-continued) Matsubara dynamics, revealing significantly different dynamical behaviour around the instanton compared to the predictions of RPMD. The instanton is found to be stationary in all coordinates but its collective angle $\Phi_0$, and fluctuations about it no longer resemble that of classical dynamics on a first order saddle as in RPMD.

quant-ph

Thermal quenching of classical and semiclassical scrambling

Quantum scrambling often gives rise to short-time exponential growth in out-of-time-ordered correlators (OTOCs). The scrambling rate over an isolated saddle point at finite temperature is shown here to be reduced by a hierarchy of quenching processes. Two of these appear in the classical limit, where escape from the neighbourhood of the saddle reduces the rate by a factor of two, and thermal fluctuations around the saddle reduce it further; a third process can be explained semiclassically as arising from quantum thermal fluctuations around the saddle, which are also responsible for imposing the Maldacena-Shenker-Stanford bound.

nlin.CD

Chemical Reaction Dynamics under Vibrational Strong Coupling

In this thesis, we use classical, semi-classical and quantum-mechanical methods to simulate chemical reaction dynamics inside of an optical cavity. Within such a cavity, by selectively coupling vibrational modes of the reactants to the vacuum state of light, recent experiments have observed significant changes in reaction rates and equilibrium constants - all without any external input of energy. We investigate the dynamics of both a single reaction and an ensemble of N identical reactions coupled to the cavity. In our single reactant studies, we find significant modification to the rate of reaction and to its quantum-mechanical equilibrium constant. All of the effects observed in our single molecule studies are however found to diminish as the number of reactants is increased. For any experimentally relevant number of molecules, the cavity effects on the reaction rate and the equilibrium constant are therefore shown to be negligible within all theories considered in this thesis. This thesis therefore does not offer any explanation for the experimental observations. It does however highlight issues with all current theoretical work on this topic, and provides suggestions - in light of the results presented here and in recent literature - as to what might be required to explain these effects.

physics.chem-ph