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Register a new userMicroscopic control and detection of ultracold strontium in optical-tweezer arrays
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We demonstrate a set of tools for microscopic control of neutral strontium atoms. We report single-atom loading into an array of sub-wavelength scale optical tweezers, light-shift free control of a narrow-linewidth optical transition, three-dimensional ground-state cooling, and high-fidelity nondestructive imaging of single atoms on sub-wavelength spatial scales. Extending the microscopic control currently achievable in single-valence-electron atoms to species with more complex internal structure, like strontium, unlocks a wealth of opportunities in quantum information science, including tweezer-based metrology, new quantum computing architectures, and new paths to low-entropy many-body physics.
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We present programmable two-dimensional arrays of microscopic atomic ensembles consisting of more than 400 sites with nearly uniform filling and small atom number fluctuations. Our approach involves direct projection of light patterns from a digital micromirror device with high spatial resolution onto an optical pancake trap acting as a reservoir. This makes it possible to load large arrays of tweezers in a single step with high occupation numbers and low power requirements per tweezer. Each atomic ensemble is confined to $sim 1,mu$m$^3$ with a controllable occupation from 20 to 200 atoms and with (sub)-Poissonian atom number fluctuations. Thus they are ideally suited for quantum simulation and for realizing large arrays of collectively encoded Rydberg-atom qubits for quantum information processing.
We report on the trapping of single Rb atoms in tunable arrays of optical tweezers in a cryogenic environment at $sim 4$ K. We describe the design and construction of the experimental apparatus, based on a custom-made, UHV compatible, closed-cycle cryostat with optical access. We demonstrate the trapping of single atoms in cryogenic arrays of optical tweezers, with lifetimes in excess of $sim6000$ s, despite the fact that the vacuum system has not been baked out. These results open the way to large arrays of single atoms with extended coherence, for applications in large-scale quantum simulation of many-body systems, and more generally in quantum science and technology.
We present a combined experimental and theoretical study of the effects of Rydberg interactions on Autler-Townes spectra of ultracold gases of atomic strontium. Realizing two-photon Rydberg excitation via a long-lived triplet state allows us to probe the thus far unexplored regime where Rydberg state decay presents the dominant decoherence mechanism. The effects of Rydberg interactions are observed in shifts, asymmetries, and broadening of the measured atom-loss spectra. The experiment is analyzed within a one-body density matrix approach, accounting for interaction-induced level shifts and dephasing through nonlinear terms that approximately incorporate correlations due to the Rydberg blockade. This description yields good agreement with our experimental observations for short excitation times. For longer excitation times, the loss spectrum is altered qualitatively, suggesting additional dephasing mechanisms beyond the standard blockade mechanism based on pure van der Waals interactions.
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.
The preparation of large, low-entropy, highly coherent ensembles of identical quantum systems is foundational for many studies in quantum metrology, simulation, and information. Here, we realize these features by leveraging the favorable properties of tweezer-trapped alkaline-earth atoms while introducing a new, hybrid approach to tailoring optical potentials that balances scalability, high-fidelity state preparation, site-resolved readout, and preservation of atomic coherence. With this approach, we achieve trapping and optical clock excited-state lifetimes exceeding $ 40 $ seconds in ensembles of approximately $ 150 $ atoms. This leads to half-minute-scale atomic coherence on an optical clock transition, corresponding to quality factors well in excess of $10^{16}$. These coherence times and atom numbers reduce the effect of quantum projection noise to a level that is on par with leading atomic systems, yielding a relative fractional frequency stability of $5.2(3)times10^{-17}~(tau/s)^{-1/2}$ for synchronous clock comparisons between sub-ensembles within the tweezer array. When further combined with the microscopic control and readout available in this system, these results pave the way towards long-lived engineered entanglement on an optical clock transition in tailored atom arrays.
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