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Register a new userNumber-resolved imaging of $^{88}$Sr atoms in a long working distance optical tweezer
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We demonstrate number-resolved detection of individual strontium atoms in a long working distance low numerical aperture (NA = 0.26) tweezer. Using a camera based on single-photon counting technology, we determine the presence of an atom in the tweezer with a fidelity of 0.989(6) (and loss of 0.13(5)) within a 200 $mu$s imaging time. Adding continuous narrow-line Sisyphus cooling yields similar fidelity, at the expense of much longer imaging times (30 ms). Under these conditions we determine whether the tweezer contains zero, one or two atoms, with a fidelity $>$0.8 in all cases with the high readout speed of the camera enabling real-time monitoring of the number of trapped atoms. Lastly we show that the fidelity can be further improved by using a pulsed cooling/imaging scheme that reduces the effect of camera dark noise.
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We report on a scanning microscopy technique for atom-number-resolved imaging of excited-state atoms. A tightly focused laser beam leads to local autoionization, and the resulting ions are counted electronically. Scanning the beam across the cloud builds up an image of the density distribution of excited atoms, with access to the full counting statistics at each spatial sampling point and an overall detection efficiency of 21 %. We apply this technique to the measurement of a spatially inhomogeneous electric field with a spatial resolution of 50 ?m and a sensitivity to electric field gradients of 0.04 V cm$^{-2}$.
The multichannel Na-Cs interactions are characterized by a series of measurements using two atoms in an optical tweezer, along with a multichannel quantum defect theory (MQDT). The triplet and singlet scattering lengths are measured by performing Raman spectroscopy of the Na-Cs motional states and least-bound molecular state in the tweezer. Magnetic Feshbach resonances are observed for only two atoms at fields which agree well with the MQDT. Our methodology, which promotes the idea of an effective theory of interaction, can be a key step towards the understanding and the description of more complex interactions. The tweezer-based measurements in particular will be an important tool for atom-molecule and molecule-molecule interactions, where high densities are experimentally challenging and where the interactions can be dominated by intra-species processes.
We have produced large samples of ultracold $^{88}$Sr$_2$ molecules in the electronic ground state in an optical lattice. The molecules are bound by 0.05 cm$^{-1}$ and are stable for several milliseconds. The fast, all-optical method of molecule creation via intercombination line photoassociation relies on a near-unity Franck-Condon factor. The detection uses a weakly bound vibrational level corresponding to a very large dimer. This is the first of two steps needed to create Sr$_2$ in the absolute ground quantum state. Lattice-trapped Sr$_2$ is of interest to frequency metrology and ultracold chemistry.
We describe a frequency stabilized diode laser at 698 nm used for high resolution spectroscopy of the 1S0-3P0 strontium clock transition. For the laser stabilization we use state-of-the-art symmetrically suspended optical cavities optimized for very low thermal noise at room temperature. Two-stage frequency stabilization to high finesse optical cavities results in measured laser frequency noise about a factor of three above the cavity thermal noise between 2 Hz and 11 Hz. With this system, we demonstrate high resolution remote spectroscopy on the 88Sr clock transition by transferring the laser output over a phase-noise-compensated 200 m-long fiber link between two separated laboratories. Our dedicated fiber link ensures a transfer of the optical carrier with frequency stability of 7 cdot 10^{-18} after 100 s integration time, which could enable the observation of the strontium clock transition with an atomic Q of 10^{14}. Furthermore, with an eye towards the development of transportable optical clocks, we investigate how the complete laser system (laser+optics+cavity) can be influenced by environmental disturbances in terms of both short- and long-term frequency stability.
We present results from two-photon photoassociative spectroscopy of the least-bound vibrational level of the X$^1Sigma_g^+$ state of the $^{88}$Sr$_2$ dimer. Measurement of the binding energy allows us to determine the s-wave scattering length, $a_{88}=-1.4(6) a_0$. For the intermediate state, we use a bound level on the metastable $^1S_0$-$^3P_1$ potential, which provides large Franck-Condon transition factors and narrow one-photon photoassociative lines that are advantageous for observing quantum-optical effects such as Autler-Townes resonance splittings.
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