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arXiv:2603.21147

Chiral Spin Liquid in Rydberg Atom Arrays

Yu-Feng Mao, Shicheng Ma, Yong Xu

Published Mar 22, 2026• 0 citations
arXivHTMLPDF

Abstract

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 $\text{XY}$ 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.

DOI
10.48550/arxiv.2603.21147

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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.
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.
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.
Motivated by experimental studies that have found signatures of a quantum spin liquid phase in organic crystals whose structure is well described by the two-dimensional triangular lattice, we study the Hubbard model on this lattice at half filling using the infinite-system density matrix renormalization group (iDMRG) method. On infinite cylinders with finite circumference, we identify an intermediate phase between observed metallic behavior at low interaction strength and Mott insulating spin-ordered behavior at strong interactions. Chiral ordering from spontaneous breaking of time-reversal symmetry, a fractionally quantized spin Hall response, and characteristic level statistics in the entanglement spectrum in the intermediate phase provide strong evidence for the existence of a chiral spin liquid in the full two-dimensional limit of the model.
Abstract Quantum spin liquids are elusive but paradigmatic examples of strongly correlated quantum states that are characterized by long-range quantum entanglement. Recently, signatures of a gapped topological Z2{{\mathbb{Z}}}_{2}Z2​ Z 2 spin liquid have been observed in a system of Rydberg atoms; however, the full capability of these platforms to realize quantum spin liquids extends far beyond this state alone. Here, we propose the realization of a different class of spin liquids in a honeycomb array of Rydberg atoms. Exploring the system’s quantum phase diagram using density-matrix renormalization group and exact diagonalization calculations, we identify several density-wave-ordered phases and a trimer spin liquid ground state with an emergent U(1) × U(1) local symmetry. This liquid state originates from superpositions of classical trimer configurations on the dual triangular lattice in the regime where third-nearest-neighbor atoms lie within the Rydberg blockade radius. Finally, we discuss the conditions to enhance the preparation fidelity of this state by a general Rydberg-blockade-based projection mechanism, test the robustness of the trimer spin liquid phase in a range of realistic parameters, and outline methods for its experimental detection.