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arXiv:2602.14323

Dirac Spin Liquid Candidate in a Rydberg Quantum Simulator

Guillaume Bornet, Marcus Bintz, Cheng Chen, Gabriel Emperauger, Mu Qiao, Romain Martin, Daniel Barredo, Shubhayu Chatterjee, Vincent S. Liu, Thierry Lahaye, Michael P. Zaletel, Norman Y. Yao, Antoine Browaeys

cond-mat.quant-gascond-mat.str-elphysics.atom-phquant-phSubmitted Feb 15, 2026• Announced Feb 17, 2026• 0 citations• Revised Jul 7, 2026 (v3)
v1 · Feb 15, 2026v2 · Apr 12, 2026v3 · Jul 7, 2026
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Abstract

We experimentally investigate a frustrated spin-exchange antiferromagnet in a quantum simulator, composed of N = 114 dipolar Rydberg atoms arranged into a kagome array. Motivated by a recent theoretical proposal of a gapless U(1) Dirac spin liquid ground state, we use local addressing to adiabatically prepare low-energy states. We measure the local polarization and spin-spin correlations over this adiabatic protocol, and observe our system move from a staggered product state, through an intermediate magnetic crystal, and finally into a disordered, correlated liquid. We estimate the entropy density of this atomic liquid to be similar to that of frustrated magnetic insulators at liquid nitrogen temperatures. We compare the correlations in our liquid to those of a simple, parameter-free ansatz for the Dirac spin liquid, and find good agreement in the sign structure and spatial decay. Finally, we probe the static susceptibility of our system to a local field perturbation and to a geometrical distortion. Our results establish Rydberg atom arrays as a promising platform for the preparation and microscopic characterization of quantum spin liquid candidates.

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We experimentally investigate a frustrated spin-exchange antiferromagnet in a quantum simulator, composed of N = 114 dipolar Rydberg atoms arranged into a kagome array. Motivated by a recent theoretical proposal of a gapless U(1) Dirac spin liquid ground state, we use local addressing to adiabatically prepare low-energy states. We measure the local polarization and spin-spin correlations over this adiabatic protocol, and observe our system move from a staggered product state, through an intermediate magnetic crystal, and finally into a disordered, correlated liquid. We estimate the entropy density of this atomic liquid to be similar to that of frustrated magnetic insulators at liquid nitrogen temperatures. We compare the correlations in our liquid to those of a simple, parameter-free ansatz for the Dirac spin liquid, and find good agreement in the sign structure and spatial decay. Finally, we probe the static susceptibility of our system to a local field perturbation and to a geometrical distortion. Our results establish Rydberg atom arrays as a promising platform for the preparation and microscopic characterization of quantum spin liquid candidates.
We predict that the gapless U(1)U(1)U(1) Dirac spin liquid naturally emerges in a two-dimensional array of quantum dipoles. In particular, we demonstrate that the dipolar XY model$\unicode{x2014}$realized in both Rydberg atom arrays and ultracold polar molecules$\unicode{x2014}$hosts a quantum spin liquid ground state on the kagome lattice. Large-scale density matrix renormalization group calculations indicate that this spin liquid exhibits signatures of gapless, linearly-dispersing spinons, consistent with the U(1)U(1)U(1) Dirac spin liquid. We identify a route to adiabatic preparation via staggered on-site fields and demonstrate that this approach can prepare cold spin liquids within experimentally realistic time-scales. Finally, we propose a number of novel signatures of the Dirac spin liquid tailored to near-term quantum simulators, including termination-dependent edge modes and the Friedel response to a local perturbation.
This thesis demonstrates that arrays of electric dipoles are good analogs for quantum magnets. We center our investigation on a recently developed experiment, in which rubidium-87 atoms are trapped in optical tweezers and then excited into two distinct electronic Rydberg states. The electric dipole-dipole interaction between these Rydberg atoms is mathematically modeled by a spin Hamiltonian with easy-plane anisotropy, and coupling strength decaying as the inverse cube of the distance. We approximately solve for the ground state of this model Hamiltonian on each of the eleven Archimedean lattices, through large-scale density matrix renormalization group calculations. For the kagome lattice, we gather extensive numerical evidence for an emergent quantum spin liquid, similar to that occurring in the canonical Heisenberg model of quantum magnetism. We predict this spin liquid to be of 𝑈(1) Dirac type, and propose new protocols for experimentally preparing and characterizing it. Our theoretical calculations support the collaborative design and analysis of experiments studying dipolar Rydberg atoms in square, circular, and kagome arrays. These respectively result in observations of continuous symmetry breaking, Tomonaga-Luttinger liquid behavior, and an atomic spin liquid candidate.
Dual-species arrays of ultracold neutral atoms have recently attracted increased interest due to the ability to independently control different atomic species and tune the interatomic interactions. This capability provides additional flexibility essential for both quantum computing and quantum simulation. In this work we theoretically investigate a quantum spin liquid (QSL) state to be simulated on a programmable quantum simulator based on a dual-species atomic array, arranged on a Kagome lattice. The Kagome lattice is formed by corner sharing triangles. This specific spatial arrangement enhances the competing interactions between atoms and is often considered as a model for realizing QSL states. When the atoms are excited into Rydberg states, long-range interactions result in Rydberg blockade. The geometric frustration of the Kagome lattice, combined with the Rydberg blockade, drives the system into exotic phases with topological order and long-range entanglement. To drive an array into the QSL state, we use a sweep-hold-sweep protocol, when the atoms are quasi-adiabatically excited into Rydberg state with individually controlled detuning from the resonance for each atomic species. The filling fraction, indicating emergence of a QSL state, is represented by a density of Rydberg excitations. We identified the conditions required for QSL state in a dual-species array with non-uniform interaction energies. We calculated the correlation length and studied the mutual information as a function of the size of the subset of the system. The existence of a topological order was proved by estimating the Kitaev-Preskill topological quantum entanglement entropy, and further confirmed by evaluating diagonal and off-diagonal topological string operators, which respectively probe the classical dimer-covering structure and the quantum coherence between distinct dimer configurations.
Despite long-standing theoretical interest, the chiral spin liquid, a topologically ordered phase, has yet to be observed experimentally. Here we surprisingly find its emergence in an experimentally realized dipolar XY\text{XY}XY model when Rydberg atoms are arranged in a breathing kagome lattice. Using the infinite density matrix renormalization group, we numerically calculate the ground state's chiral order parameter, spin-spin correlations, Chern number, and entanglement spectrum. Our numerical results provide strong evidence for the chiral spin liquid phase. Furthermore, we identify a quantum phase transition from a Dirac spin liquid to a chiral spin liquid as the lattice geometry is tuned from the isotropic kagome to the breathing kagome lattice.
Continuous control over lattice geometry, when combined with long-range interactions, offers a powerful yet underexplored tool to generate highly frustrated quantum spin systems. By considering long-range dipolar antiferromagnetic interactions on a breathed Kagome lattice, we demonstrate how these tools can be leveraged to stabilize a chiral spin liquid. We support this prediction with large-scale density-matrix renormalization group calculations and explore the surrounding phase diagram, identifying a route to adiabatic preparation via a locally varying magnetic field. At the same time, we identify the relevant low-energy degrees of freedom in each unit cell, providing a complementary language to study the chiral spin liquid. Finally, we carefully analyze its stability and signatures in finite-sized clusters, proposing direct, experimentally viable measurements of the chiral edge mode in both Rydberg atom and ultracold polar molecule arrays.
A complicating factor in the realization and observation of quantum spin liquids in materials is the ubiquitous presence of other degrees of freedom, in particular lattice distortion modes (phonons). These provide additional routes for relieving magnetic frustration, thereby possibly destabilizing spin-liquid ground states. In this work, we focus on triangular-lattice Heisenberg antiferromagnets, where recent numerical evidence suggests the presence of an extended U(1) Dirac spin liquid phase which is described by compact quantum electrodynamics in 2+1 dimensions (QED3_33​), featuring gapless spinons and monopoles as gauge excitations, and believed to flow to a strongly-coupled fixed point with conformal symmetry. Using complementary perturbation theory and scaling arguments, we show that a symmetry-allowed coupling between (classical) finite-wavevector lattice distortions and monopole operators of the U(1) Dirac spin liquid generally induces a spin-Peierls instability towards a (confining) 12-site valence-bond solid state. We support our theoretical analysis with state-of-the-art density matrix renormalization group simulations. Away from the limit of static distortions, we demonstrate that the phonon energy gap establishes a parameter regime where the spin liquid is expected to be stable, and show that the monopole-lattice coupling leads to softening of the phonon in analogy to the Kohn anomaly. We discuss the applicability of our results to similar systems, in particular the Dirac spin liquid on the Kagome lattice.