Tongcang Li

Levitated optomechanics, a rapidly expanding field that employs light to monitor and manipulate the mechanical motion of levitated objects, is increasingly relevant across physics, engineering, and other fields. This technique, which involves levitating micro- and nano-scale objects in a vacuum where they exhibit high-quality motion, provides an essential platform for precision measurements. Noted for their ultra-high sensitivity, levitated particles hold potential for a wide range of real-world applications. This perspective article briefly introduces the principle of optical levitation and the dynamics of levitated particles. It then reviews the emerging applications of levitated particles in ultrasensitive force and torque measurements, acceleration and rotation sensing, electric and magnetic field detection, scanning probe microscopy, localized vacuum pressure gauging, acoustic transduction, and chemical and biological sensing. Moreover, we discuss the present challenges and explore opportunities to minimize and integrate levitation systems for broader applications. We also briefly review optomechanics with ion traps and magnetic traps which can levitate particles in high vacuum without laser heating.

Levitated diamond particles in high vacuum with internal spin qubits have been proposed for exploring macroscopic quantum mechanics, quantum gravity, and precision measurements. The coupling between spins and particle rotation can be utilized to study quantum geometric phase, create gyroscopes and rotational matter-wave interferometers. However, previous efforts in levitated diamonds struggled with vacuum level or spin state readouts. To address these gaps, we fabricate an integrated surface ion trap with multiple stabilization electrodes. This facilitates on-chip levitation and, for the first time, optically detected magnetic resonance measurements of a nanodiamond levitated in high vacuum. The internal temperature of our levitated nanodiamond remains moderate below $10^{-5}$ Torr. Impressively, we have driven a nanodiamond to rotate up to 20 MHz ($1.2 \times 10^{9}$ rpm), surpassing typical nitrogen-vacancy (NV) center electron spin dephasing rates. Using these NV spins, we observe the effect of the Berry phase arising from particle rotation. In addition, we demonstrate quantum control of spins in a rotating nanodiamond. These results mark an important development in interfacing mechanical rotation with spin qubits, expanding our capacity to study quantum phenomena.

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.

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 $μ$m and 200 $μ$m. In order to minimize the influence of trap electrode imperfections due to the fabrication, we aim at trapping the ions around 400 $μ$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.

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.