Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:2607.25783

Deterministic loading of molecular arrays by microwave-assisted collisions

Etienne F. Walraven, Kang Feng, Jonas Rodewald, Michael R. Tarbutt, Tijs Karman

physics.atom-phcond-mat.quant-gasphysics.chem-phquant-phSubmitted Jul 28, 2026• Announced Jul 29, 2026• 0 citations
v1 · Jul 28, 2026v2 · Jul 31, 2026v3 · Oct 20, 2026
arXivHTMLPDF

Abstract

Molecular tweezer arrays offer great prospects for quantum simulation, sensing, and computing, and would benefit from methods that enhance loading efficiency. Whereas light-assisted collisions underpin enhanced loading methods for atomic tweezer arrays, this approach cannot be directly extended to molecular arrays due to collisional loss. We show how this collisional loss can be suppressed by shelving molecules in rotationally or vibrationally excited states, so that a shelved molecule interacts with a newly loaded molecule through a repulsive van der Waals interaction. By introducing microwave assisted collisions, we show how to control the final states and the energy released in a collision between a pair of molecules. Following this controlled collision, one of the two molecules can be ejected, and we explore several strategies for ensuring deterministic ejection. Our schemes rely on currently available techniques for laser-coolable molecules, and we predict achievable filling fractions up to 96%, paving the way for scalable molecular arrays.

Related papers

Scheme for Deterministic Loading of Laser-Cooled Molecules into Optical Tweezers

Etienne F. Walraven, Michael R. Tarbutt, Tijs Karman

We propose to repeatedly load laser-cooled molecules into optical tweezers, and transfer them to storage states that are rotationally excited by two additional quanta. Collisional loss of molecules in these storage states is suppressed, and a dipolar blockade prevents the accumulation of more than one molecule. Applying three cycles loads tweezers with single molecules at an 80% success rate, limited by residual collisional loss. This improved loading efficiency reduces the time needed for rearrangement of tweezer arrays, which would otherwise limit the scalability of neutral molecule quantum computers.

arXiv:2401.06028•Physical Review Letters•May 3, 2024•6 citations

Dark-State Enhanced Loading of an Optical Tweezer Array

Adam L. Shaw, Pascal Scholl, Ran Finklestein +3 more

Neutral atoms and molecules trapped in optical tweezers have become a prevalent resource for quantum simulation, computation, and metrology. However, the maximum achievable system sizes of such arrays are often limited by the stochastic nature of loading into optical tweezers, with a typical loading probability of only 50%. Here we present a species-agnostic method for dark-state enhanced loading (DSEL) based on real-time feedback, long-lived shelving states, and iterated array reloading. We demonstrate this technique with a 95-tweezer array of ^{88}Sr atoms, achieving a maximum loading probability of 84.02(4)% and a maximum array size of 91 atoms in one dimension. Our protocol is complementary to, and compatible with, existing schemes for enhanced loading based on direct control over light-assisted collisions, and we predict it can enable close-to-unity filling for arrays of atoms or molecules.

arXiv:2302.10855•Physical Review Letters•May 12, 2023•20 citations

A Protocol for Shielding-Enhanced Loading of Single Polar Molecules into Optical Tweezers

Reuben R. W. Wang, Christian H. Nunez, Conner Williams +4 more

We propose the high-fidelity preparation of single bosonic molecules in optical tweezers starting from small tweezer-trapped molecular ensembles. Our scheme combines a static electric field and a microwave field to generate strong, tunable, anisotropic interactions that shield the molecules against two-body collisional loss. We show that this shielding eliminates all long-range bound states, preventing three-body recombination. This elimination persists for all microwave ellipticities, including the experimentally practical limit of linear polarization. Application of an additional electric field gradient can be used to induce controlled spilling of strongly interacting molecules out of the trap until one remains. With realistic experimental parameters, we estimate that single tweezer-trapped NaCs molecules can be isolated from a pair with fidelities exceeding 99\%, and $> 95\%$ per site across an array. These results establish collisional shielding with electric fields as an effective tool for preparing highly-filled tweezer arrays of polar molecules.

physics.atom-phCross-listedarXiv:2608.20332•Aug 21, 2026•0 citations

Low-entropy arrays of microwave-shielded molecules prepared by interaction blockade

Tijs Karman, Sebastian Will, Zoe Yan

Ultracold molecules are becoming an increasingly important technology for quantum simulation, computation, and sensing, but their state preparation in large, low-entropy arrays remains a key challenge. We propose to deterministically load single molecules into optical tweezer arrays or lattices from either thermal or degenerate gases, with a high probability of occupying the tweezer's motional ground state. Strong repulsion between microwave-shielded molecules prevents multiparticle occupancy. Our proposal represents a robust scheme for deterministic single molecule preparation directly in the motional ground state with expected fidelities exceeding 99 percent for small trap volumes and highly polar species. This method can be scaled to thousands of traps limited by the reservoir molecule number, opening the door to large, low-entropy polar molecule arrays for quantum computation, quantum simulation, and precision measurement.

quant-pharXiv:2603.00400•Mar 3, 2026•0 citations

Near-deterministic loading of optical tweezer arrays via repulsive barricade potentials

Archie C. Baldock, Alex J. Matthies, Luke Caldwell +1 more

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 $50\,\%$ for atoms and $35\,\%$ 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 $80\%$ 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.

arXiv:2604.22406•Apr 24, 2026•0 citations

Low-Entropy Arrays of Microwave-Shielded Molecules Prepared by Interaction Blockade

Tijs Karman, Sebastian Will, Zoe Z. Yan

Ultracold molecules are becoming an increasingly important technology for quantum simulation, computation, and sensing, but their state preparation in large, low-entropy arrays remains a key challenge. We propose to deterministically load single molecules into optical tweezer arrays or lattices from either thermal or degenerate gases, with a high probability of occupying the tweezer's motional ground state. Strong repulsion between microwave-shielded molecules prevents multiparticle occupancy. Our proposal represents a robust scheme for deterministic single molecule preparation directly in the motional ground state with expected fidelities exceeding 99% for small trap volumes and highly polar species. This method can be scaled to thousands of traps limited by the reservoir molecule number, opening the door to large, low-entropy polar molecule arrays for quantum computation, quantum simulation, and precision measurement.

Physical Review Letters•Aug 19, 2026•1 citation
Molecular tweezer arrays offer great prospects for quantum simulation, sensing, and computing, and would benefit from methods that enhance loading efficiency. Whereas light-assisted collisions underpin enhanced loading methods for atomic tweezer arrays, this approach cannot be directly extended to molecular arrays due to collisional loss. We show how this collisional loss can be suppressed by shelving molecules in rotationally or vibrationally excited states, so that a shelved molecule interacts with a newly loaded molecule through a repulsive van der Waals interaction. By introducing microwave assisted collisions, we show how to control the final states and the energy released in a collision between a pair of molecules. Following this controlled collision, one of the two molecules can be ejected, and we explore several strategies for ensuring deterministic ejection. Our schemes rely on currently available techniques for laser-coolable molecules, and we predict achievable filling fractions up to 96%, paving the way for scalable molecular arrays.
We propose to repeatedly load laser-cooled molecules into optical tweezers, and transfer them to storage states that are rotationally excited by two additional quanta. Collisional loss of molecules in these storage states is suppressed, and a dipolar blockade prevents the accumulation of more than one molecule. Applying three cycles loads tweezers with single molecules at an 80% success rate, limited by residual collisional loss. This improved loading efficiency reduces the time needed for rearrangement of tweezer arrays, which would otherwise limit the scalability of neutral molecule quantum computers.
Neutral atoms and molecules trapped in optical tweezers have become a prevalent resource for quantum simulation, computation, and metrology. However, the maximum achievable system sizes of such arrays are often limited by the stochastic nature of loading into optical tweezers, with a typical loading probability of only 50%. Here we present a species-agnostic method for dark-state enhanced loading (DSEL) based on real-time feedback, long-lived shelving states, and iterated array reloading. We demonstrate this technique with a 95-tweezer array of ^{88}Sr atoms, achieving a maximum loading probability of 84.02(4)% and a maximum array size of 91 atoms in one dimension. Our protocol is complementary to, and compatible with, existing schemes for enhanced loading based on direct control over light-assisted collisions, and we predict it can enable close-to-unity filling for arrays of atoms or molecules.
We propose the high-fidelity preparation of single bosonic molecules in optical tweezers starting from small tweezer-trapped molecular ensembles. Our scheme combines a static electric field and a microwave field to generate strong, tunable, anisotropic interactions that shield the molecules against two-body collisional loss. We show that this shielding eliminates all long-range bound states, preventing three-body recombination. This elimination persists for all microwave ellipticities, including the experimentally practical limit of linear polarization. Application of an additional electric field gradient can be used to induce controlled spilling of strongly interacting molecules out of the trap until one remains. With realistic experimental parameters, we estimate that single tweezer-trapped NaCs molecules can be isolated from a pair with fidelities exceeding 99\%, and >95%> 95\%>95% per site across an array. These results establish collisional shielding with electric fields as an effective tool for preparing highly-filled tweezer arrays of polar molecules.
Ultracold molecules are becoming an increasingly important technology for quantum simulation, computation, and sensing, but their state preparation in large, low-entropy arrays remains a key challenge. We propose to deterministically load single molecules into optical tweezer arrays or lattices from either thermal or degenerate gases, with a high probability of occupying the tweezer's motional ground state. Strong repulsion between microwave-shielded molecules prevents multiparticle occupancy. Our proposal represents a robust scheme for deterministic single molecule preparation directly in the motional ground state with expected fidelities exceeding 99 percent for small trap volumes and highly polar species. This method can be scaled to thousands of traps limited by the reservoir molecule number, opening the door to large, low-entropy polar molecule arrays for quantum computation, quantum simulation, and precision measurement.
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.
Ultracold molecules are becoming an increasingly important technology for quantum simulation, computation, and sensing, but their state preparation in large, low-entropy arrays remains a key challenge. We propose to deterministically load single molecules into optical tweezer arrays or lattices from either thermal or degenerate gases, with a high probability of occupying the tweezer's motional ground state. Strong repulsion between microwave-shielded molecules prevents multiparticle occupancy. Our proposal represents a robust scheme for deterministic single molecule preparation directly in the motional ground state with expected fidelities exceeding 99% for small trap volumes and highly polar species. This method can be scaled to thousands of traps limited by the reservoir molecule number, opening the door to large, low-entropy polar molecule arrays for quantum computation, quantum simulation, and precision measurement.