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arXiv:2410.03241 · Nature Communications

Atom camera: super-resolution scanning microscope of a light pattern with a single ultracold atom

Takafumi Tomita, Yuki Torii Chew, René A. Villela, Tirumalasetty Panduranga Mahesh, Hiroto Sakai, Keisuke Nishimura, Taro Ando, Sylvain de Léséleuc, Kenji Ohmori

Published May 29, 2026• 0 citations
arXivHTMLPDF

Abstract

Sub-micrometer light patterns play a pivotal role in biology, biophysics, and AMO physics, yet their in situ characterization is limited in spatial resolution and sensitivity. Here, we present an atom camera with a single ultracold atom in an optical tweezer as a scanning probe. Measuring the energy shift on the spin states with the long coherence time and polarization-sensitive transitions yields highly sensitive, high-resolution 2D imaging of both intensity and polarization ellipticity. We characterize the polarization of a tightly-focused beam, observing its non-trivial profile. The spatial resolution is fundamentally limited by the atom’s position uncertainty, suppressed down to quantum fluctuations (~25 nm) in the motional ground state of the tweezer, with an experimentally obtained upper bound of σ ≤ 96(4) nm. This method enables imaging beyond the diffraction limit, surpassing previous approaches limited by thermal fluctuations of the atom, and provides a powerful tool for designing and analyzing submicron-scale light patterns. In situ super-resolution imaging of light has inherent limitations when applied to the polarization profile. Here, the authors introduce an “atom camera” approach by means of a single tweezer-trapped 87Rb atom measuring the field-induced shifts at sub-micrometer steps, achieving resolution beyond the optical diffraction limit.

DOI
10.1038/s41467-026-73348-x

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Sub-micrometer light patterns play a pivotal role in biology, biophysics, and AMO physics, yet their in situ characterization is limited in spatial resolution and sensitivity. Here, we present an atom camera with a single ultracold atom in an optical tweezer as a scanning probe. Measuring the energy shift on the spin states with the long coherence time and polarization-sensitive transitions yields highly sensitive, high-resolution 2D imaging of both intensity and polarization ellipticity. We characterize the polarization of a tightly-focused beam, observing its non-trivial profile. The spatial resolution is fundamentally limited by the atom’s position uncertainty, suppressed down to quantum fluctuations (~25 nm) in the motional ground state of the tweezer, with an experimentally obtained upper bound of σ ≤ 96(4) nm. This method enables imaging beyond the diffraction limit, surpassing previous approaches limited by thermal fluctuations of the atom, and provides a powerful tool for designing and analyzing submicron-scale light patterns. In situ super-resolution imaging of light has inherent limitations when applied to the polarization profile. Here, the authors introduce an “atom camera” approach by means of a single tweezer-trapped 87Rb atom measuring the field-induced shifts at sub-micrometer steps, achieving resolution beyond the optical diffraction limit.
The mapping of the potential landscape with high spatial resolution is crucial for quantum technologies based on ultracold atoms. However, the imaging of optical dipole traps is challenging because purely optical methods, commonly used to profile laser beams in free space, are not applicable in a vacuum. In this work, we demonstrate precise in situ imaging of optical dipole traps by probing a hyperfine transition with Ramsey interferometry. Thereby, we obtain an absolute map of the potential landscape with micrometer resolution and shot-noise-limited spectral precision. The idea of the technique is to control the polarization ellipticity of the trap laser beam to induce a differential light shift proportional to the trap potential. By studying the response to polarization ellipticity, we uncover a small but significant nonlinearity in addition to a dominant linear behavior, which is explained by the geometric distribution of the atomic ensemble. Our technique for imaging of optical traps can find wide application in quantum technologies based on ultracold atoms, as it applies to multiple atomic species and is not limited to a particular wavelength or trap geometry.
We realize a scanning probe microscope using single trapped ^{87}Rb atoms to measure optical fields with subwavelength spatial resolution. Our microscope operates by detecting fluorescence from a single atom driven by near-resonant light and determining the ac Stark shift of an atomic transition from other local optical fields via the change in the fluorescence rate. We benchmark the microscope by measuring two standing-wave Gaussian modes of a Fabry-Pérot resonator with optical wavelengths of 1560 and 781 nm. We attain a spatial resolution of 300 nm, which is superresolving compared to the limit set by the 780 nm wavelength of the detected light. Sensitivity to short length scale features is enhanced by adapting the sensor to characterize an optical field via the force it exerts on the atom.
Our knowledge on ultracold quantum gases is strongly influenced by our ability to probe these objects. In situ imaging combined with single atom sensitivity is an especially appealing scenario as it can provide direct information on the structure and the correlations of such systems. For a precise characterization a high spatial resolution is mandatory. In particular, the perspective to study quantum gases in optical lattices makes a resolution well below one micrometer highly desirable. Here, we report on a novel microscopy technique which is based on scanning electron microscopy and allows for the detection of single atoms inside a quantum gas with a spatial resolution of better than 150 nm. Imaging a Bose-Einstein condensate in a one-dimensional optical lattice with 600 nm period we demonstrate single site addressability in a sub-um optical lattice. The technique offers exciting possibilities for the preparation, manipulation and analysis of quantum gases.
As one of the most critical methods for optical super-resolved microscopy, stimulated emission depletion (STED) microscopy has been widely applied in biological and chemical fields, leading to the Nobel prize of 2014 in chemistry. In cold atomic systems, fast and high-resolution microscopy of individual atoms is crucial since it can provide direct information on the dynamics and correlations of the system. Here, we demonstrate nanosecond two-dimensional snapshots of a single trapped ion beyond the optical diffraction limit, by combining the main idea of STED with the quantum state transition control in cold atoms. We achieve a spatial resolution up to 175 nm and a time resolution up to 50 ns simultaneously using a NA=0.1 objective in the experiment, which is improved over ten times compared to direct fluorescence imaging. To show the potential of this method, we applied it to record the motion of the trapped ion and observe one cycle of the secular motion of the ion with a displacement detection sensitivity of 10 nm. Our method provides a powerful tool for probing particles' positions, momenta and correlations, as well as their dynamics in cold atomic systems.
Quantum simulations with ultracold atoms typically create atomic wavefunctions with structures at optical length scales, where direct imaging suffers from the diffraction limit. In analogy to advances in optical microscopy for biological applications, we use a non-linear atomic response to surpass the diffraction limit. Exploiting quantum interference, we demonstrate imaging with super-resolution of λ/50 and excellent temporal resolution of 500 ns. We characterize our microscope's performance by measuring the ensemble averaged probability density of atoms within the unit cells of an optical lattice, and observe the dynamics of atoms excited into motion. This approach can be readily applied to image any atomic or molecular system, as long as it hosts a three-level system.
This thesis reports on new experimental techniques for the study of strongly correlated states of ultracold atoms in optical lattices. We used a high numerical aperture imaging system to probe 87Rb atoms in a two-dimensional lattice with single-site resolution. Fluorescence imaging allows to detect single atoms with a large signal to noise ratio and to reconstruct the atom distribution on the lattice. We applied this new technique to a two-dimensional Mott insulator and directly observed number squeezing and the emerging shell structure. A comparison of the radial density and variance distributions to theory provides a precise in situ temperature and entropy measurement from single images. We find entropies around the critical value for quantum magnetism. In a second series of experiments, we demonstrated two-dimensional single-site spin control in the optical lattice. The differential light shift of a tightly focused laser beam shifts selected atoms into resonance with a microwave field driving a spin flip. In this way, we reach sub-diffraction limited spatial resolution well below the lattice spacing. Starting from a Mott insulator with unity filling we were able to create arbitrary spin patterns. We used this ability to prepare atom distributions to study one-dimensional single-particle tunneling dynamics in a lattice. By discriminating the dynamics of the ground state and of the first excited band, we find that our addressing scheme leaves most atoms in the vibrational ground state. Moreover, we studied coherent light scattering from the atoms in the optical lattice and found diffraction maxima in the far-field. We showed that an antiferromagnetic order leads to additional diffraction peaks which can be used to detect this order also when single-site resolution is not available. The new techniques described in this thesis open the path to a wide range of novel applications from quantum dynamics of spin impurities, entropy transport, implementation of novel cooling schemes, and engineering of quantum many-body phases to quantum information processing.