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Sideband cooling is a popular method for cooling atoms to the ground state of an optical trap. Applying the same method to molecules requires a number of challenges to be overcome. Strong tensor Stark shifts in molecules cause the optical trapping potential, and corresponding trap frequency, to depend strongly on rotational, hyperfine and Zeeman state. Consequently, transition frequencies depend on the motional quantum number and there are additional heating mechanisms, either of which can be fatal for an effective sideband cooling scheme. We develop the theory of sideband cooling in state-dependent potentials, and derive an expression for the heating due to photon scattering. We calculate the ac Stark shifts of molecular states in the presence of a magnetic field, and for any polarization. We show that the complexity of sideband cooling can be greatly reduced by applying a large magnetic field to eliminate electron- and nuclear-spin degrees of freedom from the problem. We consider how large the magnetic field needs to be, show that heating can be managed sufficiently well, and present a simple recipe for cooling to the ground state of motion.
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We demonstrate rotational and vibrational cooling of cesium dimers by optical pumping techniques. We use two laser sources exciting all the populated rovibrational states, except a target state that thus behaves like a dark state where molecules pile up thanks to absorption-spontaneous emission cycles. We are able to accumulate photoassociated cold Cs2 molecules in their absolute ground state (v = 0, J = 0) with up to 40% efficiency. Given its simplicity, the method could be extended to other molecules and molecular beams. It also opens up general perspectives in laser cooling the external degrees of freedom of molecules.
We report enhanced three-dimensional degenerated Raman sideband cooling (3D DRSC) of caesium (Cs) atoms in a standard single-cell vapour-loading magneto-optical trap. Our improved scheme involves using a separate repumping laser and optimized lattice detuning. We load $1.5 times 10^7$ atoms into the Raman lattice with a detuning of -15.5 GHz (to the ground F = 3 state). Enhanced 3D DRSC is used to cool them from 60 $mu$K to 1.7 $mu$K within 12 ms and the number of obtained atoms is about $1.2 times 10^7$. A theoretical model is proposed to simulate the measured number of trapped atoms. The result shows good agreement with the experimental data. The technique paves the way for loading a large number of ultracold Cs atoms into a crossed dipole trap and efficient evaporative cooling in a single-cell system.
A method of sideband Raman cooling to the vibrational ground state of the $m=0$ Zeeman sublevel in a far-detuned two-dimensional optical lattice is proposed. In our scheme, the Raman coupling between vibrational manifolds of the adjacent Zeeman sublevels is shifted to the red sideband due to the ac Stark effect induced by a weak pump field. Thus, cooling and optical pumping to $m=0$ is achieved by purely optical means with coplanar cw laser beams. The optical lattice and cooling parameters are estimated in the framework of simple theoretical models. An application of the transverse sideband cooling method to frequency standards is discussed. Coherent population trapping for the sideband Raman transitions between the degenerate vibrational levels is predicted.
We utilize the dark state in a {Lambda}-type three-level system to cool an ensemble of 85Rb atoms in an optical lattice [Morigi et al., Phys. Rev. Lett. 85, 4458 (2000)]. The common suppression of the carrier transition of atoms with different vibrational frequencies allows them to reach a subrecoil temperature of 100 nK after being released from the optical lattice. A nearly zero vibrational quantum number is determined from the time-of-flight measurements and adiabatic expansion process. The features of sideband cooling are examined in various parameter spaces. Our results show that dark-state sideband cooling is a simple and compelling method for preparing a large ensemble of atoms into their vibrational ground state of a harmonic potential and can be generalized to different species of atoms and molecules for studying ultracold physics that demands recoil temperature and below.
We show how state-dependent optical potentials can be used to trap a pair of molecules in different internal states at a separation much smaller than the wavelength of the trapping light. This close spacing greatly enhances the dipole-dipole interaction and we show how it can be used to implement two-qubit gates between molecules that are 100 times faster than existing protocols and than rotational coherence times already demonstrated. We analyze complications due to hyperfine structure, tensor light shifts, photon scattering and collisional loss, and conclude that none is a barrier to implementing the scheme.
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