Emergence of a Luttinger Liquid Phase in an Array of Chiral Molecules

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Main Authors: Akbar, Muhammad Arsalan Ali, Friedrich, Bretislav, Kais, Sabre
Format: Preprint
Published: 2026
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author Akbar, Muhammad Arsalan Ali
Friedrich, Bretislav
Kais, Sabre
author_facet Akbar, Muhammad Arsalan Ali
Friedrich, Bretislav
Kais, Sabre
contents We propose a robust platform for simulating chiral quantum magnetism using linear arrays of trapped asymmetric top molecules, specifically 1,2-propanediol ($\mathrm{C_{3}H_{8}O_{2}}$). By mapping the Stark-dressed rotational states onto an effective spin-$1/2$ subspace, we rigorously derive a generalized $XXZ$ Heisenberg Hamiltonian governing the underlying many-body dynamics. Unlike standard solid-state models where the topological Dzyaloshinskii-Moriya Interaction (DMI) is introduced phenomenologically, we demonstrate that DMI emerges \textit{ab initio} from the molecular stereochemistry. Specifically, the interference between the transition dipole moments of heterochiral enantiomer pairs (L-R), which breaks inversion symmetry, generates a tunable DMI that stabilizes a Chiral Luttinger Liquid phase. Through a comprehensive phase-diagram analysis, we identify an optimal experimental regime characterized by intermolecular separations of \( r \approx 1.5~\mathrm{nm} \) and intermediate electric-field strengths \( d\varepsilon/B \approx 2.5 \). In this window, the system is protected from trivial field-polarized phases and exhibits a robust gapless spin-spiral texture. Our results establish 1,2-propanediol arrays as a versatile quantum simulator, providing a direct microscopic link between molecular chirality and topological many-body phases.
format Preprint
id arxiv_https___arxiv_org_abs_2602_10002
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Emergence of a Luttinger Liquid Phase in an Array of Chiral Molecules
Akbar, Muhammad Arsalan Ali
Friedrich, Bretislav
Kais, Sabre
Quantum Physics
We propose a robust platform for simulating chiral quantum magnetism using linear arrays of trapped asymmetric top molecules, specifically 1,2-propanediol ($\mathrm{C_{3}H_{8}O_{2}}$). By mapping the Stark-dressed rotational states onto an effective spin-$1/2$ subspace, we rigorously derive a generalized $XXZ$ Heisenberg Hamiltonian governing the underlying many-body dynamics. Unlike standard solid-state models where the topological Dzyaloshinskii-Moriya Interaction (DMI) is introduced phenomenologically, we demonstrate that DMI emerges \textit{ab initio} from the molecular stereochemistry. Specifically, the interference between the transition dipole moments of heterochiral enantiomer pairs (L-R), which breaks inversion symmetry, generates a tunable DMI that stabilizes a Chiral Luttinger Liquid phase. Through a comprehensive phase-diagram analysis, we identify an optimal experimental regime characterized by intermolecular separations of \( r \approx 1.5~\mathrm{nm} \) and intermediate electric-field strengths \( d\varepsilon/B \approx 2.5 \). In this window, the system is protected from trivial field-polarized phases and exhibits a robust gapless spin-spiral texture. Our results establish 1,2-propanediol arrays as a versatile quantum simulator, providing a direct microscopic link between molecular chirality and topological many-body phases.
title Emergence of a Luttinger Liquid Phase in an Array of Chiral Molecules
topic Quantum Physics
url https://arxiv.org/abs/2602.10002