Topological Edge States from Molecular Chirality: A General Framework for Dimerized Dipolar Arrays
- URL: http://arxiv.org/abs/2606.00877v1
- Date: Sat, 30 May 2026 20:22:08 GMT
- Title: Topological Edge States from Molecular Chirality: A General Framework for Dimerized Dipolar Arrays
- Abstract summary: We show that molecular handedness provides a natural and tunable route to SSH-like topology in an interacting one-dimensional setting.<n>We also show that the chirality-induced Dzyaloshinskii--Moriya interaction amplifies the effective hopping amplitudes.<n>These findings establish dimerized chiral molecular arrays as a controllable and chirality-addressable platform.
- Score: 0.9685837672183748
- License: http://creativecommons.org/publicdomain/zero/1.0/
- Abstract: We establish a general theoretical framework for realizing topological edge states in dimerized arrays of chiral dipolar molecules and demonstrate that molecular handedness provides a natural and tunable route to SSH-like topology in an interacting one-dimensional setting. Starting from an effective spin-$\tfrac{1}{2}$ model generated by Stark-dressed chiral molecules, we introduce bond dimerization and show that the chirality-induced Dzyaloshinskii--Moriya interaction amplifies the effective hopping amplitudes and enlarges the bulk topological gap relative to an achiral chain of equivalent dipole strength. Using self-consistent mean-field theory with periodic- and open-boundary calculations, we map out the trivial, critical, and topological regimes through bulk spectra, complex-plane winding, and boundary-localized probability densities. A central result is that the two in-gap boundary modes carry \emph{opposite molecular chirality}: the left edge state localizes on a left-handed molecule and the right edge state on a right-handed molecule, a stereochemical labeling with no analogue in conventional SSH implementations. The two-leg ladder extension supports a richer four-band bulk structure and a rung-split edge sector whose robustness is characterized by a continuous sweep of the interchain coupling. All results are expressed in dimensionless units of the reference hopping scale $t_0$, making the framework directly applicable to any dipolar molecular platform -- from bialkali polar molecules at MHz coupling scales to future arrays of ultracold chiral polyatomic species. These findings establish dimerized chiral molecular arrays as a controllable and chirality-addressable platform for quasi-one-dimensional topological quantum matter.
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