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Quantum Sensing in Tweezer Arrays: Optical Magnetometry on an Individual-Atom Sensor Grid

Dominik Schäffner, Tobias Schreiber, Fabian Lenz, Malte Schlosser, G. Birkl

Published Jan 26, 2024• 32 citations
Publisher

Abstract

We implement a scalable platform for quantum sensing comprising hundreds of sites capable of holding individual laser-cooled atoms and demonstrate the applicability of this single-quantum-system sensor array to magnetic field mapping on a two-dimensional grid. With each atom being confined in an optical tweezer within an area of 0.5 μ m 2 at mutual separations of 7.0 ( 2 ) μ m , we obtain micrometer-scale spatial resolution and highly parallelized operation. An additional steerable optical tweezer allows rearrangement of atoms within the grid and enables single-atom scanning microscopy with submicron resolution. This individual-atom sensor platform finds an immediate application in mapping an externally applied dc gradient magnetic field. In a Ramsey-type measurement, we obtain a field resolution of 98(29) nT. We estimate the sensitivity to be 25 μ T / Hz . Published by the American Physical Society 2024

DOI
10.1103/prxquantum.5.010311

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We implement a scalable platform for quantum sensing comprising hundreds of sites capable of holding individual laser-cooled atoms and demonstrate the applicability of this single-quantum-system sensor array to magnetic-field mapping on a two-dimensional grid. With each atom being confined in an optical tweezer within an area of 0.5 micrometer^2 at mutual separations of 7.0(2) micrometer, we obtain micrometer-scale spatial resolution and highly parallelized operation. An additional steerable optical tweezer allows for a rearrangement of atoms within the grid and enables single-atom scanning microscopy with sub-micron resolution. This individual-atom sensor platform finds its immediate application in mapping an externally applied DC gradient magnetic field. In a Ramsey-type measurement, we obtain a field resolution of 98(29) nanotesla. We estimate the sensitivity to 25 microtesla/Hz^1/2.

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Control over the quantum states of individual molecules is crucial in the quest to harness their rich internal structure and dipolar interactions for applications in quantum science. In this paper, we develop a toolbox of techniques for the control and readout of individually trapped polar molecules in an array of optical tweezers. Starting with arrays of up to eight Rb and eight Cs atoms, we assemble arrays of RbCs molecules in their rovibrational and hyperfine ground state with an overall efficiency of 48(2)%. We demonstrate global microwave control of multiple rotational states of the molecules and use an auxiliary tweezer array to implement site-resolved addressing and state control. We show how the rotational state of the molecule can be mapped onto the position of Rb atoms and use this capability to readout multiple rotational states in a single experimental run. Further, using a scheme for the midsequence detection of molecule formation errors, we perform rearrangement of assembled molecules to prepare small defect-free arrays. Finally, we discuss a feasible route to scaling to larger arrays of molecules. Published by the American Physical Society 2024

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Single Strontium atoms trapped in optical tweezer arrays for quantum simulation

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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.

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Optical tweezer arrays trapping ultracold atoms and molecules are a versatile quantum science platform with broad impact in quantum simulation, quantum computation, and quantum metrology. The polarization dependence of anisotropic vector and tensor light shifts offers a degree of freedom for precise quantum state engineering of trapped particles. Similarly, state-selective operations depend on the polarization of the addressing light through the atom--light coupling strength. Yet, methods for controlling the polarization of individual tweezers or local addressing beams remain an experimental challenge. Here, we demonstrate independent, site-resolved linear polarization rotation across an optical tweezer array by exploiting the local birefringence tunability of a spatial light modulator. Applying this capability to an array of $^{88}\rm{Sr}$ atoms, we homogenize differential light shifts imparted by the 813-nm tweezers to the narrow ${^1{\rm S}_0}\leftrightarrow{^3{\rm P}_1}$ transition, enabling sideband cooling under a magic-angle condition. Furthermore, we show dynamic transport of trapped atoms across distinct polarization zones with high survival and preserved coherence. Finally, we characterize tweezer polarization noise and demonstrate closed-loop stabilization referenced to the atomic transition frequency, reaching mrad-level stability. Our work establishes a technique for manipulating polarization-sensitive atomic and molecular transitions in tweezer architectures, with immediate applications to optical tweezer clocks and multi-zone quantum processors.

physics.atom-phCross-listedarXiv:2610.12406•Oct 9, 2026•0 citations
We implement a scalable platform for quantum sensing comprising hundreds of sites capable of holding individual laser-cooled atoms and demonstrate the applicability of this single-quantum-system sensor array to magnetic field mapping on a two-dimensional grid. With each atom being confined in an optical tweezer within an area of 0.5 μ m 2 at mutual separations of 7.0 ( 2 ) μ m , we obtain micrometer-scale spatial resolution and highly parallelized operation. An additional steerable optical tweezer allows rearrangement of atoms within the grid and enables single-atom scanning microscopy with submicron resolution. This individual-atom sensor platform finds an immediate application in mapping an externally applied dc gradient magnetic field. In a Ramsey-type measurement, we obtain a field resolution of 98(29) nT. We estimate the sensitivity to be 25 μ T / Hz . Published by the American Physical Society 2024
We implement a scalable platform for quantum sensing comprising hundreds of sites capable of holding individual laser-cooled atoms and demonstrate the applicability of this single-quantum-system sensor array to magnetic-field mapping on a two-dimensional grid. With each atom being confined in an optical tweezer within an area of 0.5 micrometer^2 at mutual separations of 7.0(2) micrometer, we obtain micrometer-scale spatial resolution and highly parallelized operation. An additional steerable optical tweezer allows for a rearrangement of atoms within the grid and enables single-atom scanning microscopy with sub-micron resolution. This individual-atom sensor platform finds its immediate application in mapping an externally applied DC gradient magnetic field. In a Ramsey-type measurement, we obtain a field resolution of 98(29) nanotesla. We estimate the sensitivity to 25 microtesla/Hz^1/2.
Control over the quantum states of individual molecules is crucial in the quest to harness their rich internal structure and dipolar interactions for applications in quantum science. In this paper, we develop a toolbox of techniques for the control and readout of individually trapped polar molecules in an array of optical tweezers. Starting with arrays of up to eight Rb and eight Cs atoms, we assemble arrays of RbCs molecules in their rovibrational and hyperfine ground state with an overall efficiency of 48(2)%. We demonstrate global microwave control of multiple rotational states of the molecules and use an auxiliary tweezer array to implement site-resolved addressing and state control. We show how the rotational state of the molecule can be mapped onto the position of Rb atoms and use this capability to readout multiple rotational states in a single experimental run. Further, using a scheme for the midsequence detection of molecule formation errors, we perform rearrangement of assembled molecules to prepare small defect-free arrays. Finally, we discuss a feasible route to scaling to larger arrays of molecules. Published by the American Physical Society 2024
Microwave (MW) field sensing is foundational to modern technology, yet its evolution, reliant on classical antennas, is constrained by fundamental physical limits on field, temporal, and spatial resolutions. Here, we demonstrate an MW electrometry that simultaneously surpasses these constraints by using individual Rydberg atoms in an optical tweezer array as coherent sensors. This approach achieves a field sensitivity within 13% of the standard quantum limit, a response time that exceeds the Chu limit by more than 11 orders of magnitude, and in-situ near-field mapping with λ/3000 spatial resolution. This work establishes Rydberg-atom arrays as a powerful platform that unites quantum-limited sensitivity, nanosecond-scale response time, and sub-micrometer resolution, opening new avenues in quantum metrology and precision electromagnetic field imaging.
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.
Optical tweezer arrays trapping ultracold atoms and molecules are a versatile quantum science platform with broad impact in quantum simulation, quantum computation, and quantum metrology. The polarization dependence of anisotropic vector and tensor light shifts offers a degree of freedom for precise quantum state engineering of trapped particles. Similarly, state-selective operations depend on the polarization of the addressing light through the atom--light coupling strength. Yet, methods for controlling the polarization of individual tweezers or local addressing beams remain an experimental challenge. Here, we demonstrate independent, site-resolved linear polarization rotation across an optical tweezer array by exploiting the local birefringence tunability of a spatial light modulator. Applying this capability to an array of 88Sr^{88}\rm{Sr}88Sr atoms, we homogenize differential light shifts imparted by the 813-nm tweezers to the narrow 1S0↔3P1{^1{\rm S}_0}\leftrightarrow{^3{\rm P}_1}1S0​↔3P1​ transition, enabling sideband cooling under a magic-angle condition. Furthermore, we show dynamic transport of trapped atoms across distinct polarization zones with high survival and preserved coherence. Finally, we characterize tweezer polarization noise and demonstrate closed-loop stabilization referenced to the atomic transition frequency, reaching mrad-level stability. Our work establishes a technique for manipulating polarization-sensitive atomic and molecular transitions in tweezer architectures, with immediate applications to optical tweezer clocks and multi-zone quantum processors.