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ChemPhysChem

Highly Coherent Spectroscopy of Ultracold Atoms and Molecules in Optical Lattices

Tanya Zelevinsky, Sebastian Blatt, Martin M. Boyd, Gretchen K. Campbell, Andrew D. Ludlow, Jun Ye

Published Feb 14, 2008• 15 citations
Publisher

Abstract

Cooling and trapping of neutral atoms using laser techniques has enabled extensive progress in precise, coherent spectroscopy. In particular, trapping ultracold atoms in optical lattices in a tight confinement regime allows us to perform high-resolution spectroscopy unaffected by atomic motion. We report on the recent developments of optical lattice atomic clocks that have led to optical spectroscopy coherent at the one second timescale. The lattice clock techniques also open a promising pathway toward trapped ultracold molecules and the possible precision measurement opportunities such molecules offer.

DOI
10.1002/cphc.200700713

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Cooling and trapping of neutral atoms using laser techniques has enabled extensive progress in precise, coherent spectroscopy. In particular, trapping ultracold atoms in optical lattices in a tight confinement regime allows us to perform high-resolution spectroscopy unaffected by atomic motion. We report on the recent developments of optical lattice atomic clocks that have led to optical spectroscopy coherent at the one second timescale. The lattice clock techniques also open a promising pathway toward trapped ultracold molecules and the possible precision measurement opportunities such molecules offer.
The study of ultracold molecules tightly trapped in an optical lattice can expand the frontier of precision measurement and spectroscopy, and provide a deeper insight into molecular and fundamental physics. Here we create, probe, and image microkelvin 88 Sr 2 molecules in a lattice, and demonstrate precise measurements of molecular parameters as well as coherent control of molecular quantum states using optical fields. We discuss the sensitivity of the system to dimensional effects, a new bound-to-continuum spectroscopy technique for highly accurate binding energy measurements, and prospects for new physics with this rich experimental system.
— Modern capabilities in quantum state engineering of ultracold matter and precise control of light fields now permit accurate control of interactions between matter and field to suit applications for precision tests of fundamental physics. We report on our recent development of a highly stable and accurate optical atomic clock based on ultracold neutral Sr atoms confined in an optical lattice. We discuss precision tools for the lattice clock, including stabilized lasers with sub-Hz linewidth, femtosecond-comb based technology allowing accurate clock comparison in both microwave and optical domains, and clock transfer over optical fibers. With microkelvin Sr atoms confined in an optical lattice that provide a zero differential a.c. Stark shift between two clock states, we achieve a resonance quality factor >2×10 on the S0 − P0 doubly forbidden Sr clock transition at 698 nm. High resolution spectroscopy of spin-polarized atoms is used for both high-performance clock operations and accurate atomic structure measurement. The overall systematic uncertainty of the clock has been evaluated at the 10−16 level, while the stability approaches low 10−15 at 1 s. These developments in precise engineering of lightatom interactions can be extended to the field of ultracold molecules, bringing new prospects for precision measurements, quantum control, and determinations of the constancy of the fundamental constants.
Highest-resolution laser spectroscopy has generally been limited to single trapped ion systems because of the rapid decoherence that plagues neutral atom ensembles. Precision spectroscopy of ultracold neutral atoms confined in a trapping potential now shows superior optical coherence without any deleterious effects from motional degrees of freedom, revealing optical resonance linewidths at the hertz level with a good signal-to-noise ratio. The resonance quality factor of 2.4 x 10(14) is the highest ever recovered in any form of coherent spectroscopy. The spectral resolution permits direct observation of the breaking of nuclear spin degeneracy for the 1S0 and 3P0 optical clock states of 87Sr under a small magnetic bias field. This optical approach for excitation of nuclear spin states allows an accurate measurement of the differential Landé g factor between 1S0 and 3P0. The optical atomic coherence demonstrated for collective excitation of a large number of atoms will have a strong impact on quantum measurement and precision frequency metrology.
Over the past few decades, rapid development of laser cooling techniques and narrow-linewidth lasers have allowed atom-based quantum clocks to achieve unprecedented precision. Techniques originally developed for atomic clocks can be extended to ultracold molecules, with applications ranging from quantum-state-controlled ultracold chemistry to searches for new physics. Because of the richness of molecular structure, quantum metrology based on molecules provides possibilities for testing physics that is beyond the scope of traditional atomic clocks. This thesis presents the work performed to establish a state-of-the-art quantum clock based on ultracold molecules. The molecular clock is based on a frequency difference between two vibrational levels in the electronic ground state of 88Sr2 diatomic molecules. Such a clock allows us test molecular QED, improve constraints on nanometer-scale gravity, and potentially provide a model-independent test of temporal variations of the proton-electron mass ratio. Trap-insensitive spectroscopy is crucial for extending coherent molecule-light interactions and achieving a high quality factor Q. We have demonstrated a magic wavelength technique for molecules by manipulating the optical lattice frequency near narrow polarizability resonances. This general technique allows us to increase the coherence time to tens of ms, an improvement of a factor of several thousand, and to narrow the linewidth of a 25 THz vibrational transition initially to 30 Hz. This width corresponds to the quality factor Q=8x10^11. Besides the molecular quantum metrology, investigations of novel phenomena in state-selected photodissociation are also described in this thesis, including magnetic-field control of photodissociation and observation of the crossover from ultracold to quasiclassical chemistry.
We review the current research on precision spectroscopy and quantum optics applications of laser-cooled lanthanides. We discuss the specific electronic structure of hollow atoms, which determine prospects for application in optical frequency standards and in quantum simulators based on spin interactions in optical lattices. Using the example of the thulium atom, we describe the specifics of laser cooling, optical lattice trapping techniques, and clock transition spectroscopy using spectrally narrow lasers.
Clocks based on optical transitions in ions and atoms are quickly moving to the forefront of the frequency standards field mainly because of the high spec-tral resolution, and therefore the potential stability and accuracy, which can be achieved. In this thesis a new optical clock based on neutral atoms trapped in an optical lattice is presented, demonstrating spectroscopy of the clock transition free of any lineshape or accuracy degradation due to atomic motion. The system simu-lates a single trapped ion clock, but allows use of thousands of atoms for improved signal to noise ratio, and clock stability. High accuracy can also be achieved as the lattice can be designed to shift the energy of the two atomic clock states equally, such that the transition frequency is unchanged. Strontium is a natural candidate for such a clock as it offers an extremely narrow optical transition (∼1 mHz) based on atomic states which are very insensitive to external fields. The strontium level structure allows efficient laser cooling to 1 µK with diode laser sources, and a con-venient wavelength of 813 nm for the zero-differential Stark shift optical lattice. The strontium lattice clock system has allowed observation of high signal-to-noise