We review the field of cavity optomechanics, which explores the interaction between electromagnetic radiation and nano- or micromechanical motion This review covers the basics of optical cavities and mechanical resonators, their mutual optomechanical interaction mediated by the radiation pressure force, the large variety of experimental systems which exhibit this interaction, optical measurements of mechanical motion, dynamical backaction amplification and cooling, nonlinear dynamics, multimode optomechanics, and proposals for future cavity quantum optomechanics experiments In addition, we describe the perspectives for fundamental quantum physics and for possible applications of optomechanical devices

Cavity Optomechanics

Feshbach resonances are the essential tool to control the interaction between atoms in ultracold quantum gases. They have found numerous experimental applications, opening up the way to important breakthroughs. This review broadly covers the phenomenon of Feshbach resonances in ultracold gases and their main applications. This includes the theoretical background and models for the description of Feshbach resonances, the experimental methods to find and characterize the resonances, a discussion of the main properties of resonances in various atomic species and mixed atomic species systems, and an overview of key experiments with atomic Bose-Einstein condensates, degenerate Fermi gases, and ultracold molecules.

Feshbach resonances in ultracold gases

Feshbach Resonances in Ultracold Gases

A quantum gas of ultracold polar molecules, with long-range and anisotropic interactions, not only would enable explorations of a large class of many-body physics phenomena but also could be used for quantum information processing We report on the creation of an ultracold dense gas of potassium-rubidium (40K87Rb) polar molecules Using a single step of STIRAP (stimulated Raman adiabatic passage) with two-frequency laser irradiation, we coherently transfer extremely weakly bound KRb molecules to the rovibrational ground state of either the triplet or the singlet electronic ground molecular potential The polar molecular gas has a peak density of 1012 per cubic centimeter and an expansion-determined translational temperature of 350 nanokelvin The polar molecules have a permanent electric dipole moment, which we measure with Stark spectroscopy to be 0052(2) Debye (1 Debye = 3336 × 10–30 coulomb-meters) for the triplet rovibrational ground state and 0566(17) Debye for the singlet rovibrational ground state

A High Phase-Space-Density Gas of Polar Molecules

This paper reviews the recent theoretical and experimental advances in the study of ultra-cold gases made of bosonic particles interacting via the long-range, anisotropic dipole–dipole interaction, in addition to the short-range and isotropic contact interaction usually at work in ultra-cold gases. The specific properties emerging from the dipolar interaction are emphasized, from the mean-field regime valid for dilute Bose–Einstein condensates, to the strongly correlated regimes reached for dipolar bosons in optical lattices. (Some figures in this article are in colour only in the electronic version)

https://iopscience.iop.org/article/10.1088/0034-4885/72/12/126401/pdf

The physics of dipolar bosonic quantum gases

We report Raman sideband cooling of a single sodium atom to its three-dimensional motional ground state in an optical tweezer. Despite a large Lamb-Dicke parameter, high initial temperature, and large differential light shifts between the excited state and the ground state, we achieve a ground state population of 81(4)% after 100 ms of cooling, for the 85% of atoms that survive cooling and re-imaging. Our technique includes addressing high-order sidebands, where several motional quanta are removed by a single laser pulse, and fast modulation of the optical tweezer intensity. We demonstrate that Raman sideband cooling to the 3D motional ground state is possible, even without tight confinement and low initial temperature.

Motional-ground-state cooling outside the Lamb-Dicke regime

Microscopically controlled neutral atoms in optical tweezers and lattices have led to exciting advances in the study of quantum information and quantum many-body systems. The light shifts of atomic levels from the trapping potential in these systems can result in detrimental effects such as fluctuating dipole force heating, inhomogeneous detunings, and inhibition of laser cooling, which limits the atomic species that can be manipulated. In particular, these light shifts can be large enough to prevent loading into optical tweezers directly from a magneto-optical trap. We present a general solution to these limitations by loading, cooling, and imaging single atoms with temporally alternating beams. Because this technique does not depend on any specific spectral properties, we expect it to enable the optical tweezer method to control nearly any atomic or molecular species that can be laser cooled and optically trapped. Furthermore, we present an analysis of the role of heating and required cooling for single atom tweezer loading.

Eliminating light shifts in single-atom optical traps

State-specific detection of trapped HfF+ by photodissociation

Qubit coherence times are critical to the performance of any robust quantum computing platform. For quantum information processing using arrays of polar molecules, a key performance parameter is the molecular rotational coherence time. We report a 93(7) ms coherence time for rotational state qubits of laser cooled CaF molecules in optical tweezer traps, over an order of magnitude longer than previous systems. Inhomogeneous broadening due to the differential polarizability between the qubit states is suppressed by tuning the tweezer polarization and applied magnetic field to a ``magic'' angle. The coherence time is limited by the residual differential polarizability, implying improvement with further cooling. A single spin-echo pulse is able to extend the coherence time to nearly half a second. The measured coherence times demonstrate the potential of polar molecules as high fidelity qubits.

Rotational Coherence Times of Polar Molecules in Optical Tweezers.

Microscopically controlled neutral atoms in optical tweezers and lattices have led to exciting advances in the study of quantum information and quantum many-body systems. The light shifts of atomic levels from the trapping potential in these systems can result in detrimental effects such as fluctuating dipole force heating, inhomogeneous detunings, and inhibition of laser cooling, which limits the atomic species that can be manipulated. In particular, these light shifts can be large enough to prevent loading into optical tweezers directly from a magneto-optical trap. We implement a general solution to these limitations by loading, as well as cooling and imaging the atoms with temporally alternating beams, and present an analysis of the role of heating and required cooling for single atom tweezer loading. Because this technique does not depend on any specific spectral properties, it should enable the optical tweezer platform to be extended to nearly any atomic or molecular species that can be laser cooled and optically trapped.

/pdf/eliminating-light-shifts-for-single-atom-trapping-3omxe29bdb.pdf

Kang-Kuen Ni

Papers

Motional-ground-state cooling outside the Lamb-Dicke regime

Eliminating light shifts in single-atom optical traps

State-specific detection of trapped HfF+ by photodissociation

Rotational Coherence Times of Polar Molecules in Optical Tweezers.

Eliminating light shifts for single atom trapping