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arXiv:1506.04419 · Physical Review Letters

Rapid Production of Uniformly Filled Arrays of Neutral Atoms

Brian Lester, Niclas Luick, Adam M. Kaufman, Collin Reynolds, Cindy A. Regal

Published Aug 14, 2015• 149 citations
arXivHTMLPDF

Abstract

We demonstrate rapid loading of a small array of optical tweezers with a single ^{87}Rb atom per site. We find that loading efficiencies of up to 90% per tweezer are achievable in less than 170 ms for traps separated by more than 1.7 μm. Interestingly, we find the load efficiency is affected by nearby traps and present the efficiency as a function of the spacing between two optical tweezers. This enhanced loading, combined with subsequent rearranging of filled sites, will enable the study of quantum many-body systems via quantum gas assembly.

DOI
10.1103/physrevlett.115.073003

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physics.atom-phCross-listedarXiv:2610.21609•Oct 16, 2026•0 citations
We demonstrate rapid loading of a small array of optical tweezers with a single ^{87}Rb atom per site. We find that loading efficiencies of up to 90% per tweezer are achievable in less than 170 ms for traps separated by more than 1.7 μm. Interestingly, we find the load efficiency is affected by nearby traps and present the efficiency as a function of the spacing between two optical tweezers. This enhanced loading, combined with subsequent rearranging of filled sites, will enable the study of quantum many-body systems via quantum gas assembly.
Assembling and maintaining large arrays of individually addressable atoms is a key requirement for continued scaling of neutral-atom-based quantum computers and simulators. In this work, we demonstrate a new paradigm for assembly of atomic arrays, based on a synergistic combination of optical tweezers and cavity-enhanced optical lattices, and the incremental filling of a target array from a repetitively filled reservoir. In this protocol, the tweezers provide microscopic rearrangement of atoms, while the cavity-enhanced lattices enable the creation of large numbers of optical traps with sufficient depth for rapid low-loss imaging of atoms. We apply this protocol to demonstrate near-deterministic filling (99% per-site occupancy) of 1225-site arrays of optical traps. Because the reservoir is repeatedly filled with fresh atoms, the array can be maintained in a filled state indefinitely. We anticipate that this protocol will be compatible with mid-circuit reloading of atoms into a quantum processor, which will be a key capability for running large-scale error-corrected quantum computations whose durations exceed the lifetime of a single atom in the system. Published by the American Physical Society 2024
Low-entropy arrays of atomic quantum systems in optical tweezers offer unique prospects for fundamental research on few- and many-body systems as well as for extended applications in quantum technology. The significance of this approach relies on the achievable system size, its uniformity, and the rate of qubit allocation. We propel the neutral-atom quantum-technology platform by the rapid assembly of a regular two-dimensional quantum register of up to 1024 atomic qubits, enabled by a novel implementation of intensity-homogenized tweezer arrays and parallelized atom transport. Our highly efficient microoptical architecture modularizes intensity equalization and tweezer patterning in separate functional units, eliminating restrictions that arise for high-power, high-resolution, and large-scale light-field control within a single device. Arrays of precise grid structure, trap depth, and vibrational frequency with more than 3500 sites are demonstrated. Individual sites are interconnected by up to 50 parallelized transport tweezers with intensity and position control in real-time for swift qubit relocation. Multi-tweezer transport enables the operation of target patterns of up to 32 x 32 sites with sustained near-unity filling fraction. These results boost neutral-atom quantum information science above the kiloqubit level.
Large arrays of individually controlled atoms trapped in optical tweezers are a very promising platform for quantum engineering applications. However, deterministic loading of the traps is experimentally challenging. We demonstrate the preparation of fully loaded two-dimensional arrays of up to ~50 microtraps, each containing a single atom and arranged in arbitrary geometries. Starting from initially larger, half-filled matrices of randomly loaded traps, we obtain user-defined target arrays at unit filling. This is achieved with a real-time control system and a moving optical tweezers, which together enable a sequence of rapid atom moves depending on the initial distribution of the atoms in the arrays. These results open exciting prospects for quantum engineering with neutral atoms in tunable two-dimensional geometries.
Optical tweezers are a powerful tool for creating defect-free arrays of atoms and molecules, enabling advances in quantum simulation, computation, and precision metrology. However, the achievable array size is limited by the initial loading fraction, typically 50 %50\,\%50% for atoms and 35 %35\,\%35% for molecules. Here, we propose a general scheme for enabling multiple loading cycles by protecting trapped particles using a repulsive barrier. We show that collision-limited lifetimes of particles in protected tweezers can exceed one second, leading to filling fractions of over 80%80\%80% after four loading cycles. Combined with existing rearrangement techniques, this approach enables efficient unity filling of tweezer arrays and provides a scalable pathway towards larger quantum technology platforms.
Abstract Arrays of neutral atoms in optical tweezers are widely used in quantum simulation and computation, and precision frequency metrology. The capabilities of these arrays are enhanced by maximising the number of available sites. Here we increase the spatial extent of a two-dimensional array of 88 Sr atoms by sweeping the frequency of the cooling light to move the atomic reservoir across the array. We load arrays with vertical heights of > 100 µm, exceeding the height of an array loaded from a static reservoir by a factor of > 3. We investigate the site-to-site atom number distribution, tweezer lifetime, and temperature, achieving an average temperature across the array of 1.49 ( 3 ) µK. By controlling the frequency sweep we show it is possible to control the distribution of atoms across the array, including uniform and non-uniformly loaded arrays, and arrays with selectively loaded regions. We explain our results using a rate equation model which is in qualitative agreement with the data.
Assembling defect-free arrays of neutral atoms requires real-time rearrangement of stochastically loaded optical tweezers. Conventional rearrangement methods shuttle atoms sequentially, whereas high-speed spatial light modulators (SLMs) can move all atoms in parallel, which scales more favorably as the array size grows. For fast parallel rearrangement, the sequence of holograms displayed on the SLM should be computed more rapidly than the SLM refresh rate, and there should be phase continuity between successive holograms to minimize transient intensity fluctuations. We calculate holograms analytically by adding together the complex fields needed to produce each individual trap, and we ramp the phase of each trap linearly as it moves to its target location. Trap positions enter as continuous variables, rather than tied to points on a grid, so the method provides high positioning accuracy. Using a single GPU, we compute each intermediate hologram in 0.284 ms, considerably faster than the SLM refresh time of 0.696 ms, so the rearrangement speed is hardware-limited. In each step, we use the free processing time to iteratively optimize the holograms for equal intensity across the traps, decreasing trap non-uniformity to 1.24% during rearrangement at no cost in total time. Starting from an array of 256 sites loaded stochastically with 87^{87}87Rb atoms, we assemble a 100-atom array in under 20 ms with a rearrangement survival probability of 99.31(12)% per atom. This rearrangement increases the temperature of the atoms by 9(3) μμμK, which is small compared to the trap depth of 480 μμμK. Our method can also move individual atoms axially, enabling transport in different planes. We demonstrate this capability with a rearrangement protocol where one set of atoms leapfrogs over another.