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Autore principale: Zhang, Chao
Natura: Preprint
Pubblicazione: 2026
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Accesso online:https://arxiv.org/abs/2605.25019
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author Zhang, Chao
author_facet Zhang, Chao
contents Microwave-dressed polar molecules offer a route to lattice quantum simulators in which the angular form of long-range dipolar interactions, not only their overall strength, can be engineered. We study this setting in a minimal hard-core Bose lattice model on a square optical lattice, with particles interacting through a sign-changing non-axisymmetric dipolar tail \mathcal V(\mathbf r)\propto (x^2-y^2)/(x^2+y^2)^{5/2} that is repulsive along one lattice axis and attractive along the other. Using worm-algorithm path-integral quantum Monte Carlo simulations, supported by a hard-core spin mapping and a Gutzwiller soft-mode diagnostic, we find two regimes controlled by t/V: at larger t/V the system remains superfluid but develops a pronounced directional stiffness anisotropy, while at smaller t/V it forms a stripe solid selected in the (q,0) axial family, corresponding to real-space stripes parallel to y. The leading ordering wave vector remains in this axial family but reorganizes with filling, showing that the robust ordered object is a family of stripe states rather than one fixed commensurate Bragg peak. Near the closure of the stripe lobe, averaged observables can mimic a narrow supersolid signal; measurement-resolved stripe structure-factor histograms instead reveal first-order switching between superfluid and stripe-solid sectors. NaCs lattice estimates place the relevant V/t window within reach of modest effective dressed dipole moments, linking the predicted stripe-family order and its experimental diagnostics to accessible molecular quantum-simulation scales.
format Preprint
id arxiv_https___arxiv_org_abs_2605_25019
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Programmable dipolar interaction geometry selects stripe-family order in a molecular lattice quantum simulator
Zhang, Chao
Quantum Gases
Microwave-dressed polar molecules offer a route to lattice quantum simulators in which the angular form of long-range dipolar interactions, not only their overall strength, can be engineered. We study this setting in a minimal hard-core Bose lattice model on a square optical lattice, with particles interacting through a sign-changing non-axisymmetric dipolar tail \mathcal V(\mathbf r)\propto (x^2-y^2)/(x^2+y^2)^{5/2} that is repulsive along one lattice axis and attractive along the other. Using worm-algorithm path-integral quantum Monte Carlo simulations, supported by a hard-core spin mapping and a Gutzwiller soft-mode diagnostic, we find two regimes controlled by t/V: at larger t/V the system remains superfluid but develops a pronounced directional stiffness anisotropy, while at smaller t/V it forms a stripe solid selected in the (q,0) axial family, corresponding to real-space stripes parallel to y. The leading ordering wave vector remains in this axial family but reorganizes with filling, showing that the robust ordered object is a family of stripe states rather than one fixed commensurate Bragg peak. Near the closure of the stripe lobe, averaged observables can mimic a narrow supersolid signal; measurement-resolved stripe structure-factor histograms instead reveal first-order switching between superfluid and stripe-solid sectors. NaCs lattice estimates place the relevant V/t window within reach of modest effective dressed dipole moments, linking the predicted stripe-family order and its experimental diagnostics to accessible molecular quantum-simulation scales.
title Programmable dipolar interaction geometry selects stripe-family order in a molecular lattice quantum simulator
topic Quantum Gases
url https://arxiv.org/abs/2605.25019