Gabriele De Chiara

Quantum thermodynamics of boundary time-crystals

Federico Carollo [1], Igor Lesanovsky [1,2], Mauro Antezza [3,4], Gabriele De Chiara [5,4]

Abstract

Time-translation symmetry breaking is a mechanism for the emergence of non-stationary many-body phases, so-called time-crystals, in Markovian open quantum systems. Dynamical aspects of time-crystals have been extensively explored over the recent years. However, much less is known about their thermodynamic properties, also due to the intrinsic nonequilibrium nature of these phases. Here, we consider the paradigmatic boundary time-crystal system, in a finite-temperature environment, and demonstrate the persistence of the time-crystalline phase at any temperature. Furthermore, we analyze thermodynamic aspects of the model investigating, in particular, heat currents, power exchange and irreversible entropy production. Our work sheds light on the thermodynamic cost of sustaining nonequilibrium time-crystalline phases and provides a framework for characterizing time-crystals as possible resources for, e.g., quantum sensing. Our results may be verified in experiments, for example with trapped ions or superconducting circuits, since we connect thermodynamic quantities with mean value and covariance of collective (magnetization) operators.

Thermodynamics of trajectories of a quantum harmonic oscillator coupled to $N$ baths

Simon Pigeon [1], Lorenzo Fusco [1,2], André Xuereb, Gabriele De Chiara [1], Mauro Paternostro [1]

Abstract

We undertake a thorough analysis of the thermodynamics of the trajectories followed by a quantum harmonic oscillator coupled to $N$ dissipative baths by using a new approach to large-deviation theory inspired by phase-space quantum optics. As an illustrative example, we study the archetypal case of a harmonic oscillator coupled to two thermal baths, allowing for a comparison with the analogous classical result. In the low-temperature limit, we find a significant quantum suppression in the rate of work exchanged between the system and each bath. We further show how the presented method is capable of giving analytical results even for the case of a driven harmonic oscillator. Based on that result, we analyse the laser cooling of the motion of a trapped ion or optomechanical system, illustrating how the emission statistics can be controllably altered by the driving force.

Formation of helical ion chains

Ramil Nigmatullin, Adolfo del Campo, Gabriele De Chiara, Giovanna Morigi, Martin B. Plenio, Alex Retzker

Abstract

We study the nonequilibrium dynamics of the linear to zigzag structural phase transition exhibited by an ion chain confined in a trap with periodic boundary conditions. The transition is driven by reducing the transverse confinement at a finite quench rate, which can be accurately controlled. This results in the formation of zigzag domains oriented along different transverse planes. The twists between different domains can be stabilized by the topology of the trap and under laser cooling the system has a chance to relax to a helical chain with nonzero winding number. Molecular dynamics simulations are used to obtain a large sample of possible trajectories for different quench rates. The scaling of the average winding number with different quench rates is compared to the prediction of the Kibble-Zurek theory, and a good quantitative agreement is found.

Entangling two distant oscillators with a quantum reservoir

Alexander Wolf [1], Gabriele De Chiara [2,3], Endre Kajari [1,4], Eric Lutz [5], Giovanna Morigi [2,4]

Abstract

The generation of entanglement between two oscillators that interact via a common reservoir is theoretically studied. The reservoir is modeled by a one-dimensional harmonic crystal initially in thermal equilibrium. Starting from a separable state, the oscillators can become entangled after a transient time, that is of the order of the thermalization time scale. This behavior is observed at finite temperature even when the oscillators are at a distance significantly larger than the crystal's interparticle spacing. The underlying physical mechanisms can be explained by the dynamical properties of the collective variables of the two oscillators which may decouple from or be squeezed by the reservoir. Our predictions can be tested with an ion chain in a linear Paul trap.

Spontaneous nucleation of structural defects in inhomogeneous ion chains

Gabriele De Chiara [1,2], Adolfo del Campo [3,4], Giovanna Morigi [1,5], Martin B. Plenio [3,4], Alex Retzker [3,4]

Abstract

Structural defects in ion crystals can be formed during a linear quench of the transverse trapping frequency across the mechanical instability from a linear chain to the zigzag structure. The density of defects after the sweep can be conveniently described by the Kibble-Zurek mechanism. In particular, the number of kinks in the zigzag ordering can be derived from a time-dependent Ginzburg-Landau equation for the order parameter, here the zigzag transverse size, under the assumption that the ions are continuously laser cooled. In a linear Paul trap the transition becomes inhomogeneous, being the charge density larger in the center and more rarefied at the edges. During the linear quench the mechanical instability is first crossed in the center of the chain, and a front, at which the mechanical instability is crossed during the quench, is identified which propagates along the chain from the center to the edges. If the velocity of this front is smaller than the sound velocity, the dynamics becomes adiabatic even in the thermodynamic limit and no defect is produced. Otherwise, the nucleation of kinks is reduced with respect to the case in which the charges are homogeneously distributed, leading to a new scaling of the density of kinks with the quenching rate. The analytical predictions are verified numerically by integrating the Langevin equations of motion of the ions, in presence of a time-dependent transverse confinement. We argue that the non-equilibrium dynamics of an ion chain in a Paul trap constitutes an ideal scenario to test the inhomogeneous extension of the Kibble-Zurek mechanism, which lacks experimental evidence to date.

Thermal and quantum fluctuations in chains of ultracold polar molecules

G. E. Astrakharchik [1], Gabriele De Chiara [2], Giovanna Morigi [2], Jordi Boronat [1]

Abstract

Ultracold polar molecules, in highly anisotropic traps and interacting via a repulsive dipolar potential, may form one-dimensional chains at high densities. According to classical theory, at low temperatures there exists a critical value of the density at which a second order phase transition from a linear to a zigzag chain occurs. We study the effect of thermal and quantum fluctuations on these self-organized structures using classical and quantum Monte Carlo methods, by means of which we evaluate the pair correlation function and the static structure factor. Depending on the parameters, these functions exhibit properties typical of a crystalline or of a liquid system. We compare the thermal and the quantum results, identifying analogies and differences. Finally, we discuss experimental parameter regimes where the effects of quantum fluctuations on the linear - zigzag transition can be observed.