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arXiv:2606.02560

A Mid-Infrared Platform Based on Strontium Tweezer Arrays

Aaron Holman, Ximo Sun, Bojeong Seo, Joshua Corn, Zezheng Zhu, Yuan Xu, Jiahao Wu, Nanfang Yu, Dmytro Filin, Marianna Safronova, Sebastian Will

physics.atom-phcond-mat.quant-gasphysics.app-phphysics.opticsquant-phSubmitted Jun 1, 2026• Announced Jun 2, 2026• 0 citations
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Abstract

Subwavelength atomic tweezer arrays, in which atoms can be positioned at distances smaller than their emission wavelength, have been proposed as a versatile platform to study collective emission phenomena, such as superradiance and subradiance. Experimentally, the realization of such arrays has been a challenge as typical emission wavelengths in the visible or near-infrared are short compared to typical tweezer spacings in the micrometer range. Here, we use $^{88}$Sr atoms in optical tweezer arrays to access a mid-infrared transition at 2,923 nm ($5s5p\:^{3}P_{2} \rightarrow\, 5s4d\:^{3}D_{3}$). We identify a magic trapping wavelength at 597.14(3) nm and demonstrate single-atom preparation and imaging with high fidelity. In addition, using 2,923 nm light, we demonstrate resolved-sideband cooling of tweezer-trapped strontium. Beyond enabling studies of collective emission phenomena in flexible arrangements of atoms, our platform opens novel opportunities for dipolar many-body physics and enhanced control over Rydberg dynamics and the strontium fine-structure qubit.

Comments
10 pages, 7 main figures, 3 appendix figures

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SciPost Physics Core•Aug 12, 2026•0 citations
Subwavelength atomic tweezer arrays, in which atoms can be positioned at distances smaller than their emission wavelength, have been proposed as a versatile platform to study collective emission phenomena, such as superradiance and subradiance. Experimentally, the realization of such arrays has been a challenge as typical emission wavelengths in the visible or near-infrared are short compared to typical tweezer spacings in the micrometer range. Here, we use 88^{88}88Sr atoms in optical tweezer arrays to access a mid-infrared transition at 2,923 nm (5s5p 3P2→ 5s4d 3D35s5p\:^{3}P_{2} \rightarrow\, 5s4d\:^{3}D_{3}5s5p3P2​→5s4d3D3​). We identify a magic trapping wavelength at 597.14(3) nm and demonstrate single-atom preparation and imaging with high fidelity. In addition, using 2,923 nm light, we demonstrate resolved-sideband cooling of tweezer-trapped strontium. Beyond enabling studies of collective emission phenomena in flexible arrangements of atoms, our platform opens novel opportunities for dipolar many-body physics and enhanced control over Rydberg dynamics and the strontium fine-structure qubit.
Optical tweezers provide a versatile platform for the manipulation and detection of single atoms.Here, we use optical tweezers to demonstrate a set of tools for the microscopic control of atomic strontium, which has two valence electrons.Compared to the single-valence-electron atoms typically used with tweezers, strontium has a more complex internal state structure with a variety of transition wavelengths and linewidths.We report single-atom loading into an array of subwavelength scale optical tweezers and lightshift-free control of a narrow-linewidth optical transition.We use this transition to perform threedimensional ground-state cooling and to enable high-fidelity nondestructive imaging of single atoms on subwavelength spatial scales.These capabilities, combined with the rich internal structure of strontium, open new possibilities including tweezer-based metrology, new quantum computing architectures, and new paths to low-entropy many-body physics.
Optical tweezer arrays of neutral atoms have emerged as a versatile and powerful platform for quantum simulation and quantum information processing. In this thesis, I present the realization of an experimental platform for quantum simulation based on individually trapped strontium atoms in optical tweezer arrays. The experiment combines precise laser cooling, optical control, and high-resolution imaging to enable the manipulation and high fidelity detection of single atoms. I developed and optimized a two-stage three-dimensional magneto-optical trap (3D-MOT) that produces cold and dense samples of strontium atoms from a thermal beam. In the f irst stage, atoms are captured and precooled using the dipole-allowed 1S0 → 1P1 transition at 461nm (which has a linewidth of !=2ω ↑ 32MHz). The second stage employs the 1S0 → 3P1 narrow intercombination transition at 689nm (with a linewidth of !=2ω ↑7.5kHz) to further cool and compress the atomic cloud. By optimizing the trapping parameters, I achieved clouds with temperatures around 5μK and densities above 1010cm→3, providing ideal initial conditions for e!cient loading into optical tweezers. A 3↑3 array of 360μK deep optical tweezers is generated by spatially modulating an 813.4nm laser beam using two crossed acousto-optic deflectors. The deflected beams are relayed and focused into the science chamber using a high–numericalaperture objective, which simultaneously serves as the collection optics for atomic f luorescence. The fluorescence light emitted by the atoms is imaged onto a scientific qCMOS camera, enabling site-resolved detection of individual atoms. I implemented and optimized the in-trap cooling dynamics to prevent atom loss during imaging and to minimize residual thermal motion. In addition, by precisely tuning lightassisted collisions, multiple atoms occupancies are removed from the traps and a single-atom regime is reached in the array, with a filling fraction of about 50%. I have demonstrated a single-atom detection fidelity of 99,986(1)% and a survival probability of 97(2)% between subsequent image acquisition, comparable to other current state-of-the-art experiments. To characterize the platform, I carried out release-and-recapture experiments, from which it is possible to measure a temperature for the individually trapped atoms of 12.95(5)μK. These results demonstrate the successful implementation of a robust and high-fidelity platform for optical trapping and imaging of single strontium atoms. The apparatus provides the foundation for future quantum simulation experiments with alkalineearth atoms excited to the Rydberg state, o"ering precise control over individual particles and the ability to scale towards larger, programmable atomic arrays.
Single strontium atoms held in optical tweezers have so far only been imaged using the broad ${}^{1}{S}_{0}{\text{\ensuremath{-}}}^{1}{P}_{1}\phantom{\rule{0.16em}{0ex}}$transition. For Yb, use of the narrow (183-kHz wide) ${}^{1}{S}_{0}{\text{\ensuremath{-}}}^{3}{P}_{1}\phantom{\rule{0.16em}{0ex}}$transition for simultaneous imaging and cooling has been demonstrated in tweezers with a magic wavelength for the imaging transition. We demonstrate high-fidelity imaging of single Sr atoms using its even narrower (7.4-kHz wide) ${}^{1}{S}_{0}{\text{\ensuremath{-}}}^{3}{P}_{1}\phantom{\rule{0.16em}{0ex}}$transition. The atoms are trapped in nonmagic-wavelength tweezers. We detect the photons scattered during Sisyphus cooling, thus keeping the atoms near the motional ground state of the tweezer throughout imaging. The fidelity of detection is 0.9991(4) with a survival probability of 0.97(2). An atom in a tweezer can be held under imaging conditions for 79(3) seconds allowing for hundreds of images to be taken, limited mainly by background gas collisions. The use of a fully closed (cycling) transition for imaging will provide a useful tool for state specific detection. We detect atoms in an array of 36 tweezers with 813.4-nm light and trap depths of 135(20) $\ensuremath{\mu}$K. This trap depth is three times shallower than typically used for imaging on the broad ${}^{1}{S}_{0}{\text{\ensuremath{-}}}^{1}{P}_{1}\phantom{\rule{0.16em}{0ex}}$transition. Narrow-line imaging opens the possibility to even further reduce this trap depth, as long as all trap frequencies are kept larger than the imaging transition linewidth. Imaging using a narrow-linewidth transition in a nonmagic-wavelength tweezer also allows for selective imaging of a given tweezer. As a demonstration, we selectively image (hide) a single tweezer from the array. This provides a useful tool for quantum error correction protocols.
Efficient trapping and detection of single atoms in optical tweezers are important for realizing atom arrays, a promising platform for quantum simulation and quantum information processing. However, the scaling up of atom arrays can be impeded by detrimental light shifts induced by the tweezer trap, making it challenging to cool and image single atoms. Here, we report an order-of-magnitude increase in the scalability of 23Na^{23}\mathrm{Na}23Na atom arrays by using D1{D}_{1}D1​ magic wavelength tweezers to reduce the required tweezer power per trap. D1{D}_{1}D1​ magic wavelengths have been previously predicted to exist for all the alkali atoms but are not yet observed to date. We first experimentally confirm a D1{D}_{1}D1​ magic wavelength that is predicted to lie at 615.87 nm, which we then use to trap and image single atoms without having to modulate the trapping and imaging light intensities. We further demonstrate that the mean loading efficiency remains as high as 80.0(6)% for a single trap and 74.2(7)% for a one-dimensional array of eight atoms. The methods reported here are applicable to all the alkalis, including those that are attractive candidates for dipolar molecule assembly, Rydberg dressing, or are fermionic in nature.
When quantum emitters couple indistinguishably to light, they can synchronize into a collective light matter system with radiative properties profoundly different from those of independent particles. To date, the resulting collective effects have largely been confined to point like or homogeneous ensembles. Here, we open access to a qualitatively new collective regime by realizing geometrically ordered, spatially extended atom arrays with subwavelength spacing. This establishes a fundamentally new platform in which collective emission is no longer confined to a single Dicke mode but instead emerges from an ordered network of photon mediated interactions. We find that 2D atom arrays undergo strong super and subradiant emission. Despite subwavelength spacing, we achieve site resolved imaging and directly observe the buildup of spatial correlations, demonstrating the transformation of cooperative decay into a strongly correlated many-body process. We observe extensive scaling of superradiance, uncover superradiant revivals, and reveal the ferromagnetic nature of superradiance and the antiferromagnetic nature of subradiance. Our results realize a novel programmable platform for exploring and utilizing dissipative many-body quantum physics, opening new possibilities for photon capture, storage, and atom photon entanglement.