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A proposal for cooling the translational motion of optically levitated magnetic nanoparticles is presented. The theoretical cooling scheme involves the sympathetic cooling of a ferromagnetic YIG nanosphere with a spin-polarized atomic gas. Particle-atom cloud coupling is mediated through the magnetic dipole-dipole interaction. When the particle and atom oscillations are small compared to their separation, the interaction potential becomes dominantly linear which allows the particle to exchange energy with the $N$ atoms. While the atoms are continuously Doppler cooled, energy is able to be removed from the nanoparticle's motion as it exchanges energy with the atoms. The rate at which energy is removed from the nanoparticle's motion was studied for three species of atoms (Dy, Cr, Rb) by simulating the full $N+1$ equations of motion and was found to depend on system parameters with scalings that are consistent with a simplified model. The nanoparticle's damping rate due to sympathetic cooling is competitive with and has the potential to exceed commonly employed cooling methods., Comment: 8 pages, 2 figures

We show that a single photon pulse (SPP) incident on two interacting two-level atoms induces a transient entanglement force between them. After absorption of a multi-mode Fock state pulse, the time-dependent atomic interaction mediated by the vacuum fluctuations changes from the van der Waals interaction to the resonant dipole-dipole interaction (RDDI). We explicitly show that the RDDI force induced by the SPP fundamentally arises from the two-body transient entanglement between the atoms. This SPP induced entanglement force can be continuously tuned from being repulsive to attractive by varying the polarization of the pulse. We further demonstrate that the entanglement force can be enhanced by more than three orders of magnitude if the atomic interactions are mediated by graphene plasmons. These results demonstrate the potential of shaped SPPs as a powerful tool to manipulate this entanglement force and also provides a new approach to witness transient atom-atom entanglement., Comment: We corrected errors related to the Green's function in the manuscript

Spontaneous symmetry breaking is a universal concept throughout science. For instance, the Landau-Ginzburg paradigm of translational symmetry breaking underlies the classification of nearly all quantum phases of matter and explains the emergence of crystals, insulators, and superconductors. Usually, the consequences of translational invariance are studied in large systems to suppress edge effects which cause undesired symmetry breaking. While this approach works for investigating global properties, studies of local observables and their correlations require access and control of the individual constituents. Periodic boundary conditions, on the other hand, could allow for translational symmetry in small systems where single particle control is achievable. Here, we crystallize up to fifteen 40Ca+ ions in a microscopic ring with inherent periodic boundary conditions. We show the ring's translational symmetry is preserved at millikelvin temperatures by delocalizing the Doppler laser cooled ions. This establishes an upper bound for undesired symmetry breaking at a level where quantum control becomes feasible. These findings pave the way towards studying quantum many-body physics with translational symmetry at the single particle level in a variety of disciplines from simulation of Hawking radiation to exploration of quantum phase transitions., Comment: 15 pages, 4 figures

We present a design of an r.f. trap using planar electrodes with the goal to trap on the order of 100 ions in a small ring structure of diameters ranging between 100 $\mu$m and 200 $\mu$m. In order to minimize the influence of trap electrode imperfections due to the fabrication, we aim at trapping the ions around 400 $\mu$m above the trap electrodes. In view of experiments to create freely rotating crystals near the ground state, we numerically study factors breaking the rotational symmetry such as external stray electric fields, local charging of the trap electrodes, and fabrication imperfections. We conclude that these imperfections can be controlled sufficiently well under state-of-the-art experimental conditions to allow for freely rotating ion rings even at energies comparable to the ground state energy of the rotational degree-of-freedom., Comment: 8 pages, 11 figures; submitted to Physical Review A

This is a reply to the comment from Patrick Bruno (arXiv:1211.4792) on our paper (Phys. Rev. Lett. 109, 163001 (2012)).

Spontaneous symmetry breaking can lead to the formation of time crystals, as well as spatial crystals. Here we propose a space-time crystal of trapped ions and a method to realize it experimentally by confining ions in a ring-shaped trapping potential with a static magnetic field. The ions spontaneously form a spatial ring crystal due to Coulomb repulsion. This ion crystal can rotate persistently at the lowest quantum energy state in magnetic fields with fractional fluxes. The persistent rotation of trapped ions produces the temporal order, leading to the formation of a space-time crystal. We show that these space-time crystals are robust for direct experimental observation. We also study the effects of finite temperatures on the persistent rotation. The proposed space-time crystals of trapped ions provide a new dimension for exploring many-body physics and emerging properties of matter., Comment: updated to the version published in PRL