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.
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.
Neutral atom optical standards require the highest levels of laser precision to operate near the limit set by quantum fluctuations. We develop state-of-the-art ultra-stable laser systems to achieve a factor of 10 enhancement in clock measurement precision and additionally demonstrate optical linewidths below 50 mHz. The most stable of these lasers reaches its thermal noise floor of 1 × 10-16 fractional frequency instability, allowing the attainment of near quantum-noise-limited clock operation with single-clock instabilities of 3×10-16 at 1 s. We utilize this high level of spectral resolution to operate a 87Sr optical lattice clock in a regime in which quantum collisions play a dominant role in the dynamics, enabling the study of quantum many-body physics. With a fractional level of precision of near 1 × 10-16 at 1 s, we clearly resolve the signatures of many-body interactions. We find that the complicated interplay between the p wave-dominated elastic and inelastic interaction processes between lattice-trapped atoms leads to severe lineshape distortion, shifts, and loss of Ramsey fringe contrast. We additionally explore the theoretical prediction that these many-body interactions will modify the quantum fluctuations of the system and we find that in certain parameter regimes the quantum noise distribution exhibits a quadrature dependence. We further present technological advancements that will permit ultra-stable lasers to operate with reduced thermal noise, leading to a potential gain of an additional factor of 10 in stability. This indicates that laser fractional frequency instabilities of 1 × 10-17 are within experimental reach, as is a fully-quantum-limited regime of optical clock operation.
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
Recent results from the JILA 87Sr optical lattice clock are presented. Using the tight confinement of an optical lattice in combination wit a sub-Hz linewidth diode laser we have achieved a pulse-length limited linewidth of 1.8 Hz for the 1S0- 3P0 clock transition. This corresponds to a quality factor of Q ≈ 2.4 x 1014, and is a record for coherent spectroscopy. With the addition of a small magnetic bias field, the high line Q of the clock transition has also allowed us to resolve the nuclear-spin sublevels, and make a precision measurement of the differential Landé g-factor between the 1S0 and 3P0. We present the current accuracy and stability of the lattice clock, and in addition, we report on our development of precision tools for the lattice clock, including a stabilized clock laser, fs-comb based technology allowing accurate clock comparison in both the microwave and optical domains, and clock transfer over an optical fiber in an urban environment.
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.
Ultracold atoms and molecules provide ideal stages for precision tests of fundamental physics. With microkelvin neutral strontium atoms confined in an optical lattice, we have achieved a fractional resolution of 4 × 10-15 on the 1S0–3P0 doubly forbidden 87 Sr clock transition at 698 nm. Measurements of the clock line shifts as a function of experimental parameters indicate systematic errors below the 10-15 level. The ultrahigh spectral resolution permits resolving the nuclear spin states of the clock transition at small magnetic fields, leading to measurements of the 3P0 magnetic moment and metastable lifetime. In addition, photoassociation spectroscopy performed on the narrow 1S0–3P1 transition of 88 Sr shows promise for efficient optical tuning of the ground state scattering length and production of ultracold ground state molecules. Lattice-confined Sr 2 molecules are suitable for constraining the time variation of the proton–electron mass ratio. In a separate experiment, cold, stable, ground state polar molecules are produced from Stark decelerators. These cold samples have enabled an order-of-magnitude improvement in the measurement precision of ground state, Λ doublet microwave transitions in the OH molecule. Comparing the laboratory results to those from OH megamasers in interstellar space will allow a sensitivity of 10-6 for measuring the potential time variation of the fundamental fine structure constant Δα/α over 1010 years. These results have also led to improved understandings of the molecular structure. The study of the low magnetic field behavior of OH in its 2Π3/2 ro-vibronic ground state precisely determines a differential Landé g factor between opposite parity components of the Λ doublet.
— 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.