We perform narrowline cooling of single dysprosium atoms trapped in a 1D optical tweezers array, employing the narrow single-photon transition at 741 nm. At the trapping wavelength of 532 nm, the excited state is less trapped than the ground state. To obtain efficient cooling performances, we chirp the frequency of the cooling beam to subsequently address the red sidebands of different motional states. We demonstrate the effectiveness of the cooling protocol through Raman thermometry, which we characterize for our experimental conditions. We obtain an array of 75 atoms close to the motional ground state in the radial direction of the tweezers. Our results demonstrate the possibility to manipulate the motional degree of freedom of dysprosium in optical tweezers arrays, a key ingredient to exploit the potential of lanthanide-based tweezers platforms for quantum science.
We perform narrowline cooling of single dysprosium atoms trapped in a 1D optical tweezers array, employing the narrow single-photon transition at 741 nm. At the trapping wavelength of 532 nm, the excited state is less trapped than the ground state. To obtain efficient cooling performances, we chirp the frequency of the cooling beam to subsequently address the red sidebands of different motional states. We demonstrate the effectiveness of the cooling protocol through Raman thermometry, which we characterize for our experimental conditions. We obtain an array of 75 atoms close to the motional ground state in the radial direction of the tweezers. Our results demonstrate the possibility to manipulate the motional degree of freedom of dysprosium in optical tweezers arrays, a key ingredient to exploit the potential of lanthanide-based tweezers platforms for quantum science.
We report the preparation and observation of single atoms of dysprosium in arrays of optical tweezers with a wavelength of 532 nm, imaged on the intercombination line at 626 nm. We use the anisotropic light shift specific to lanthanides and in particular a large difference in tensor and vector polarizabilities between the ground and excited states to tune the differential light shift and produce tweezers in near-magic or magic polarization. This allows us to find a regime where single atoms can be trapped and imaged. Using the tweezer array toolbox to manipulate lanthanides will open new research directions for quantum physics studies by taking advantage of their rich spectrum, large spin, and magnetic dipole moment.
Laser cooling of single atoms in optical tweezers is a prerequisite for neutral atom quantum computing and simulation. Resolved sideband cooling comprises a well-established method for efficient motional ground-state preparation, but typically requires careful cancellation of light shifts in so-called magic traps. Here, we study a novel laser cooling scheme which overcomes such constraints, and applies when the ground state of a narrow cooling transition is trapped stronger than the excited state. We demonstrate our scheme, which exploits sequential addressing of red sideband transitions via frequency chirping of the cooling light, at the example of 88Sr atoms and report ground-state populations compatible with recent experiments in magic tweezers. The scheme also induces light-assisted collisions, which are key to the assembly of large atom arrays. Our work enriches the toolbox for tweezer-based quantum technology, also enabling applications for tweezer-trapped molecules and ions that are incompatible with resolved sideband cooling conditions.
This dissertation advances optical tweezer platforms for neutral-atom quantum processors by addressing three interconnected bottlenecks: imaging survival, motional ground-state preparation, and narrow-line cooling, through experimental and theoretical work on single lithium and cesium atoms.For Li, the lightest stable alkali atom, this work demonstrates a per-image survival probability of 99.950(2)% and a state-detection fidelity of 99.97(2)% across 2000 consecutive 15 ms images, a record for any trapped neutral atom at the time of publication. This was achieved by applying Λ-enhanced gray-molasses (Λ-GM) cooling continuously on the D1 line while simultaneously imaging with the same beam, and represents the first demonstration of loading lithium into a tweezer directly from a MOT. To explain this performance, the dissertation develops a unified Lindblad master-equation formalism for laser cooling in a tightly confined harmonic trap, encompassing polarization-gradient, gray-molasses, EIT, Λ-GM, and single-photon sideband cooling within a single theoretical framework, with 1D simulations that correctly predict steady-state temperature, excited-state fraction, and cooling efficiency across these techniques.For133133Cs, the work exploits the forbidden electric-quadrupole transition 6S1/2→5D5/26S1/2→5D5/2 at 685 nm (Γ ≈ 2π × 117.6 kHz) to demonstrate background-free imaging and narrow-line sideband cooling for the first time in an alkali atom. By positioning the atom at the intensity node of a Laguerre-Gaussian vortex beam, the drive is enhanced while cascade fluorescence at 852 nm is optically isolated from the excitation light, enabling both high-fidelity background-free detection and single-photon sideband cooling to near the motional ground state.Beyond the core cooling and imaging results, the dissertation includes a comprehensive experimental techniques chapter (fiber coupling, AOM design, polarimetry, laser locking, optical pumping, and a Gaussian-process optimization framework), a chapter on quadrupole transition theory and orbital-angular-momentum selection rules, and a concluding survey of the competitive quantum computing landscape across neutral-atom, superconducting, trapped-ion, photonic, spin, and topological qubit platforms. Together, this work establishes the Cs and Li cooling/imaging toolbox as a foundation for future assembly of ultracold LiCs polar molecules in optical tweezer arrays.
We report cooling of a single neutral atom to its three-dimensional vibrational ground state in an optical tweezer.After employing Raman sideband cooling for tens of milliseconds, we measure via sideband spectroscopy a three-dimensional ground-state occupation of about 90%.We further observe coherent control of the spin and motional state of the trapped atom.Our demonstration shows that an optical tweezer, formed simply by a tightly focused beam of light, creates sufficient confinement for efficient sideband cooling.This source of ground-state neutral atoms will be instrumental in numerous quantum simulation and logic applications that require a versatile platform for storing and manipulating ultracold single neutral atoms.For example, these results will improve current optical-tweezer experiments studying atom-photon coupling and Rydberg quantum logic gates, and could provide new opportunities such as rapid production of single dipolar molecules or quantum simulation in tweezer arrays.
Abstract We report simultaneous Raman sideband cooling of a single 87Rb atom and a single 133Cs atom held in separate optical tweezers at 814 nm and 938 nm, respectively. Starting from outside the Lamb-Dicke regime, after 45 ms of cooling we measure probabilities to occupy the three-dimensional motional ground state of 0.8 6 − 0.04 + 0.03 for Rb and 0.9 5 − 0.04 + 0.03 for Cs. Our setup overlaps the Raman laser beams used to cool Rb and Cs, reducing hardware requirements by sharing equipment along the same beam path. The cooling protocol is scalable, and we demonstrate cooling of single Rb atoms in an array of four tweezers. After motional ground-state cooling, a 938 nm tweezer is translated to overlap with a 814 nm tweezer so that a single Rb and a single Cs atom can be transferred into a common 1064 nm trap. By minimising the heating during the merging and transfer, we prepare the atoms in the relative motional ground state with an efficiency of 0.8 1 − 0.08 + 0.08 . This is a crucial step towards the formation of single RbCs molecules confined in optical tweezer 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 atoms, we homogenize differential light shifts imparted by the 813-nm tweezers to the narrow 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.