Quenches in an ion chain can create coherent superpositions of motional states across the linear-zigzag structural transition. The procedure has been described in Baltrusch et al. [Phys. Rev. A 84, 063821 (2011)] and makes use of spin-dependent forces, so that a coherent superposition of the electronic states of one ion evolves into an entangled state between the chain's internal and external degrees of freedom. The properties of the crystalline state so generated are theoretically studied by means of Ramsey interferometry on one ion of the chain. An analytical expression for the visibility of the interferometric measurement is obtained for a chain of an arbitrary number of ions and as a function of the time elapsed after the quench. Sufficiently close to the linear-zigzag instability the visibility decays very fast, but exhibits revivals at the period of oscillation of the mode that drives the structural instability. These revivals have a periodicity that is independent of the crystal size, and they signal the creation of entanglement by the quantum quench.
Quenches in an ion chain can create coherent superpositions of motional states across the linear-zigzag structural transition. The procedure has been described in Baltrusch et al. [Phys. Rev. A 84, 063821 (2011)] and makes use of spin-dependent forces, so that a coherent superposition of the electronic states of one ion evolves into an entangled state between the chain's internal and external degrees of freedom. The properties of the crystalline state so generated are theoretically studied by means of Ramsey interferometry on one ion of the chain. An analytical expression for the visibility of the interferometric measurement is obtained for a chain of an arbitrary number of ions and as a function of the time elapsed after the quench. Sufficiently close to the linear-zigzag instability the visibility decays very fast, but exhibits revivals at the period of oscillation of the mode that drives the structural instability. These revivals have a periodicity that is independent of the crystal size, and they signal the creation of entanglement by the quantum quench.
We theoretically analyze the efficiency of a protocol for creating mesoscopic superpositions of ion chains, described in Baltrusch et al. [Phys. Rev. A 84, 063821 (2011)], as a function of the temperature of the crystal. The protocol makes use of state-dependent forces, so that a coherent superposition of the electronic states of one ion evolves into an entangled state between the chain's internal and external degrees of freedom. Ion Coulomb crystals are well isolated from the external environment and should therefore experience a coherent, unitary evolution, which follows the quench and generates structural Schr\"odinger-cat-like states. The temperature of the chain, however, introduces a statistical uncertainty in the final state. We characterize the quantum state of the crystal by means of the visibility of Ramsey interferometry performed on one ion of the chain and determine its decay as a function of the crystal's initial temperature. This analysis allows one to determine the conditions on the chain's initial state in order to efficiently perform the protocol.
A procedure is discussed for creating coherent superpositions of motional states of ion strings. The motional states are across the structural transition linear-zigzag, and their coherent superposition is achieved by means of spin-dependent forces, such that a coherent superposition of the electronic states of one ion evolves into an entangled state between the chain's internal and external degrees of freedom. It is shown that the creation of such an entangled state can be revealed by performing Ramsey interferometry with one ion of the chain.
We show that the statistical properties of a Coulomb crystal can be measured by means of a standard interferometric procedure performed on the spin of one ion in the chain. The ion spin, constituted by two internal levels of the ion, couples to the crystal modes via spatial displacement induced by photon absorption. The loss of contrast in the interferometric signal allows one to measure the autocorrelation function of the crystal observables. Close to the critical point, where the chain undergoes a second-order phase transition to a zigzag structure, the signal gives the behavior of the correlation function at the critical point.
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 a zigzag structure. The density of defects after the sweep can be conveniently described by the Kibble–Zurek mechanism (KZM). 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, since the charge density is 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 that propagates along the chain from the center to the edges. If the velocity of this front is smaller than the sound velocity, the dynamics become 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 the 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 KZM, which lacks experimental evidence to date.
The electronic and motional degrees of freedom of trapped ions can be controlled and coherently coupled on the level of individual quanta.Assembling complex quantum systems ion by ion while keeping this unique level of control remains a challenging task.For many applications, linear chains of ions in conventional traps are ideally suited to address this problem.However, driven motion due to the magnetic or radio-frequency electric trapping fields sometimes limits the performance in one dimension and severely affects the extension to higher-dimensional systems.Here, we report on the trapping of multiple barium ions in a single-beam optical dipole trap without radio-frequency or additional magnetic fields.We study the persistence of order in ensembles of up to six ions within the optical trap, measure their temperature, and conclude that the ions form a linear chain, commonly called a one-dimensional Coulomb crystal.As a proof-of-concept demonstration, we access the collective motion and perform spectrometry of the normal modes in the optical trap.Our system provides a platform that is free of driven motion and combines advantages of optical trapping, such as state-dependent confinement and nanoscale potentials, with the desirable properties of crystals of trapped ions, such as long-range interactions featuring collective motion.Starting with small numbers of ions, it has been proposed that these properties would allow the experimental study of many-body physics and the onset of structural quantum phase transitions between one-and two-dimensional crystals.
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 a zigzag structure. The density of defects after the sweep can be conveniently described by the Kibble–Zurek mechanism (KZM). 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, since the charge density is 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 that propagates along the chain from the center to the edges. If the velocity of this front is smaller than the sound velocity, the dynamics become 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 the 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 KZM, which lacks experimental evidence to date.