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arXiv:1110.1359 · Physical Review A

Raman-laser spectroscopy of Wannier-Stark states

Gunnar Tackmann, Bruno Pelle, Adèle Hilico, Quentin Beaufils, Franck Pereira dos Santos

Published Dec 22, 2011• 20 citations
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Abstract

Raman lasers are used as a spectroscopic probe of the state of atoms confined in a shallow one-dimensional (1D) vertical lattice. For sufficiently long laser pulses, resolved transitions in the bottom band of the lattice between Wannier Stark states corresponding to neighboring wells are observed. Couplings between such states are measured as a function of the lattice laser intensity and compared to theoretical predictions, from which the lattice depth can be extracted. Limits to the linewidth of these transitions are investigated. Transitions to higher bands can also be induced, as well as between transverse states for tilted Raman beams. All these features allow for a precise characterization of the trapping potential and for an efficient control of the atomic external degrees of freedom.

DOI
10.1103/physreva.84.063422

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Raman lasers are used as a spectroscopic probe of the state of atoms confined in a shallow one-dimensional (1D) vertical lattice. For sufficiently long laser pulses, resolved transitions in the bottom band of the lattice between Wannier Stark states corresponding to neighboring wells are observed. Couplings between such states are measured as a function of the lattice laser intensity and compared to theoretical predictions, from which the lattice depth can be extracted. Limits to the linewidth of these transitions are investigated. Transitions to higher bands can also be induced, as well as between transverse states for tilted Raman beams. All these features allow for a precise characterization of the trapping potential and for an efficient control of the atomic external degrees of freedom.
Raman laser pulses are used to induce coherent tunneling between neighboring sites of a vertical 1D optical lattice. Such tunneling occurs when the detuning of a probe laser from the atomic transition frequency matches multiples of the Bloch frequency, allowing for a spectroscopic control of the coupling between Wannier-Stark (WS) states. In particular, we prepare coherent superpositions of WS states of adjacent sites, and investigate the coherence time of these superpositions by realizing a spatial interferometer. This scheme provides a powerful tool for coherent manipulation of external degrees of freedom of cold atoms, which is a key issue for quantum information processing.
We present details on the ultraviolet lattice spectroscopy of the (6sss2{}^{2}2) 1{}^{1}1SSS${}_{0}\ensuremath{\leftrightarrow}$ (6$s666p$) 3{}^{3}3PPP0{}_{0}0​ transition in neutral mercury, specifically 199{}^{199}199Hg. Mercury atoms are loaded into a one-dimensional vertically aligned optical lattice from a magneto-optical trap with an rms temperature of $\ensuremath{\sim}$60 $\ensuremath{\mu}$K. We describe aspects of the magneto-optical trapping, the lattice cavity design, and the techniques employed to trap and detect mercury in an optical lattice. The clock-line frequency dependence on lattice depth is measured at a range of lattice wavelengths. We confirm the magic wavelength to be 362.51(0.16) nm. Further observations to those reported by Yi et al. [Phys. Rev. Lett. 106, 073005 (2011)] are presented regarding the laser excitation of a Wannier-Stark ladder of states.
In two recent experiments Verkerk et al. and our group have observed quantization of the center-of-mass motion of laser cooled atoms in sub-wavelength sized potential wells formed by the light field of a 1-dimensional optical molasses. Our 1-dimensional optical molasses consists of a pair of counterpropagating laser beams of orthogonal, linear polarization, creating a series of potential wells separated by {lambda}/4. Polarization gradient laser cooling reduces the thermal energy of the atoms until they are trapped in well resolved vibrational levels near the bottom of the wells. Transitions between these vibrational levels are seen in a high resolution spectrum of fluorescence, where they give rise to a Rayleigh peak centered at the laser frequency, and well resolved Raman sidebands shifted by a frequency {plus_minus}{omega}, typically on the order of 100 kHz. We find quantitative agreement between the measured level separation h{omega} and the results of a calculation of the bandstructure in the periodic optical potential. Based on the observed ratio of the strength of the blue to the red sideband we determine the temperature of the atoms, and find agreement with theoretical predictions. Based on the level spacing and temperature we find the atoms to be localized to {approx}/15, withmore » up to 50-60% of the population of the trapped atoms in the vibrational ground state. We observe intriguing differences between fluorescence radiated by localized atoms, and the fluorescence radiated by non-localized atoms in a 1-dimensional optical molasses composed of a pair of counterpropagating laser beams of opposite circular polarization. The prospect of observing quantum motion and spatial order in 2 and 3 dimensions, and the consequences for the spectrum of fluorescence, will be discussed.« less
We report on the Lamb-Dicke spectroscopy of the doubly forbidden (6s(2))(1)S(0)↔(6s6p)(3)P(0) transition in (199)Hg atoms confined to a vertical 1D optical lattice. With lattice trapping of ≲10(3) atoms and a 265.6 nm probe laser linked to the LNE-SYRTE primary frequency reference we have determined the center frequency of the transition for a range of lattice wavelengths and at two lattice trap depths. We find the Stark-free (magic) wavelength to be 362.53(0.21) nm-essential knowledge for future use of this line in a clock with anticipated 10(-18) range accuracy. We also present evidence of the laser excitation of a Wannier-Stark ladder of states in a lattice of well depth 10E(R).