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Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE

Atom-trapping in the Lamb-Dicke regime in a far-off-resonance optical lattice

D. L. Haycock, S. E. Hamann, Gerd Klose, Poul Jessen

Published May 1, 1997• 1 citation
Publisher

Abstract

We form a 1D optical lattices for Cs atoms using light tuned a few thousand linewidths below the 6S1/2(F equals 4) yields 6P3/2(F' equals 5) transition at 852 nm. In this far-off- resonance lattice the time scale for damping of motional coherences and kinetic energy can be orders of magnitude longer than the vibrational oscillation period for atoms trapped in the lattice potential wells. Atoms are loaded directly into deeply bound states, by adiabatic transfer from a superimposed, near-resonance optical lattice. This yields a mean vibrational excitation n approximately equals 0.3, and localization (Delta) z approximately (lambda) /20 deep in the Lamb-Dicke regime. Light scattering subsequently heats the atoms, but the initial rate is only of order 10-3 vibrational quanta per oscillation period. Low vibrational excitation, localization in the Lamb-Dicke regime and low heating rates make these atoms good candidates for resolved- sideband Raman cooling, and for the generation and study of non-classical states of center-of-mass motion. We propose a scheme for resolved-sideband Raman cooling and quantum state preparation; the scheme employs Raman coupling between magnetic sublevels induced by the lattice light field itself.

DOI
10.1117/12.273754

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We form a 1D optical lattices for Cs atoms using light tuned a few thousand linewidths below the 6S1/2(F equals 4) yields 6P3/2(F' equals 5) transition at 852 nm. In this far-off- resonance lattice the time scale for damping of motional coherences and kinetic energy can be orders of magnitude longer than the vibrational oscillation period for atoms trapped in the lattice potential wells. Atoms are loaded directly into deeply bound states, by adiabatic transfer from a superimposed, near-resonance optical lattice. This yields a mean vibrational excitation n approximately equals 0.3, and localization (Delta) z approximately (lambda) /20 deep in the Lamb-Dicke regime. Light scattering subsequently heats the atoms, but the initial rate is only of order 10-3 vibrational quanta per oscillation period. Low vibrational excitation, localization in the Lamb-Dicke regime and low heating rates make these atoms good candidates for resolved- sideband Raman cooling, and for the generation and study of non-classical states of center-of-mass motion. We propose a scheme for resolved-sideband Raman cooling and quantum state preparation; the scheme employs Raman coupling between magnetic sublevels induced by the lattice light field itself.
We form a one-dimensional optical lattice for Cs atoms using light tuned a few thousand linewidths below atomic resonance. Atoms are selectively loaded into deeply bound states by adiabatic transfer from a superimposed, near-resonance optical lattice. This yields a mean vibrational excitation n-bar\ensuremath{\approx}0.3 and localization \ensuremath{\Delta}z\ensuremath{\approx}\ensuremath{\lambda}/20. Light scattering subsequently heats the atoms, but the initial rate is only of order ${10}^{\mathrm{\ensuremath{-}}3}$ vibrational quanta per oscillation period. Low vibrational excitation, strong localization, and low heating rates make these atoms good candidates for resolved-sideband Raman cooling.
Summary form only given.Dissipation from photon scattering can be virtually eliminated if the lattice is formed by light detuned a few thousand linewidths from atomic resonance, in which case the frequency of oscillation in the optical potential wells can be several orders of magnitude larger than the rate of vibrational excitation. The atoms are then good candidates for resolved-sideband Raman cooling. We believe we have demonstrated for the first time resolved-sideband Raman laser cooling of neutral Cs atoms close to the zero-point of motion in a two-dimensional optical lattice.
This dissertation reports on quantum state preparation of cesium atoms in a two-dimensional optical lattice, by resolved-sideband Raman cooling. An optical lattice is a periodic potential produced by the light shift interaction between an atom and light field. Laser cooled atoms can become strongly localized about the bottom of potential wells in an optical lattice, where they occupy a discrete spectrum of bound vibrational energy levels. The distribution over vibrational levels of atoms in the lattice is characterized by the mean vibrational excitation, n . In an optical lattice, absorption and emission of photons from lattice beams causes n to increase in time. This source of heating is always present, but its rate can be greatly reduced in a lattice detuned far from the atomic resonance. Sideband cooling is an efficient means of transferring atoms from higher into lower-lying vibrational levels and, thus, it reduces n for the ensemble. If the sideband cooling rate is much greater than the heating rate, then n approaches zero and virtually all atoms are in the lowest vibrational level in their potential wells. Our sideband cooling scheme involves stimulated Raman transitions between bound states in the potential wells of a pair of magnetic sublevels, followed by optical pumping, for a net loss of one quantum of vibration per cooling cycle. The process accumulates 98% of atoms in the ground vibrational level of a potential well associated with a single Zeeman substate. Each atom in the lattice is then very close to a pure state. For two-dimensional lattice with sideband cooling we find nx≈ny≈0.008 &parl0;16&parr0; . Various issues related to state preparation and sideband cooling are also discussed in the context of a one dimensional lin ⊥ lin optical lattice. These include improvement of laser cooling in a near resonance lattice by application of weak magnetic fields, transfer of atoms from near into far off-resonance lattices, and heating rates in far off-resonance lattices.
Optical lattices induced by light detuned far from the frequency of any atomic resonance transition are ideal systems in which to develop techniques for the coherent control of atomic motional and internal states. Decoherence arising from spontaneous emission can be eliminated to an arbitrary degree by varying the detuning of the optical field. The atoms trapped in these lattices are to a large extent isolated from environmental disturbances and from each other. The first step towards the coherent control of atoms in a far-detuned lattice is their preparation in a single motional state. In this thesis the preparation of atoms in the ground vibrational state of a two-dimensional far-detuned optical lattice via resolved-sideband Raman cooling is presented. This sideband-cooling scheme involves stimulated Raman transitions between bound vibrational states of a pair of magnetic ground state sublevels, followed by an irreversible step due to optical pumping, resulting in a net loss of one quantum of vibrational energy per cooling cycle. This process provides efficient cooling in two-dimensions and leads to the accumulation of a large fraction of atoms in the 2-D ground vibrational state of a potential well associated with a single Zeeman substate. Experiments aimed at improving and monitoring the characteristics of the lar-detuned lattice and the sideband-Raman cooling efficiency are also described. Parametric excitation experiments and modelling are employed to investigate the degree of anharmonicity of the optical potential and the importance of heating induced by laser intensity noise, whilst Zeeman-state analysis of the sample is performed for monitoring the distribution of atoms over different magnetic sub- states. Finally, spin-polarization experiments are carried out in order to study the paramagnetic properties of the lattice and lead to an evaluation of a spin-temperature for the sample.
We trap neutral Cs atoms in a two-dimensional optical lattice and cool them close to the zero point of motion by resolved-sideband Raman cooling. Sideband cooling occurs via transitions between the vibrational manifolds associated with a pair of magnetic sublevels, and the required Raman coupling is provided by the lattice potential itself. We obtain mean vibrational excitations ${\overline{n}}_{x}\ensuremath{\approx}{\overline{n}}_{y}<0.024$, corresponding to a population >95>95%>95 in the vibrational ground state. Atoms in the ground state of an optical lattice provide a new system in which to explore quantum state control and subrecoil laser cooling.
We propose a scheme that combines velocity-selective coherent population trapping (CPT) and Raman sideband cooling (RSC) for subrecoil cooling of optically trapped atoms outside the Lamb-Dicke regime. This scheme is based on an inverted Y\mathsf{Y}Y configuration in an alkali-metal atom. It consists of a $\mathrm{\ensuremath{\Lambda}}$ formed by two Raman transitions between the ground hyperfine levels and the DDD transition, allowing RSC along two paths and formation of a CPT dark state. Using the state-dependent difference in vibration frequency of the atom in a circularly polarized trap, we can tune the $\mathrm{\ensuremath{\Lambda}}$ to make only the motional ground state a CPT dark state. We call this scheme motion-selective coherent population trapping (MSCPT). We write the master equations for RSC and MSCPT and solve them numerically for a 87Rb^{87}\mathrm{Rb}87Rb atom in a one-dimensional optical lattice when the Lamb-Dicke parameter is 1. Although MSCPT reaches the steady state slowly compared with RSC, the former consistently produces colder atoms than the latter. The numerical results also show that subrecoil cooling by MSCPT outside the Lamb-Dicke regime is possible under a favorable, yet experimentally feasible, condition. We explain this performance quantitatively by calculating the relative darkness of each motional state. Finally, we discuss the application of the MSCPT scheme to an optically trapped diatomic polar molecule whose Stark shift and vibration frequency exhibit large variations depending on the rotational quantum number.