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This research presents a theoretical model demonstrating how chiral electrostatic potentials can selectively filter electrons based on their orbital angular momentum, offering new insights into electron transport mechanisms at the nanoscale. While grounded in condensed matter physics and quantum mechanics rather than standard machine learning or large-scale AI systems, it represents fundamental scientific inquiry relevant to future quantum materials and spintronic devices where precise control of particle states is essential.
Chirality-Induced Orbital Selectivity through Linear-Orbital Coupling
arXiv:2509.07675v2 Announce Type: replace-cross Abstract: We present a three-dimensional continuum model of electron transmission through a chiral electrostatic potential and show that it gives rise to chirality-induced orbital selectivity. In this model, electron transmittance depends strongly on the incident orbital angular momentum (OAM) associated with its transverse motion, and the selectivity reverses when the potential's handedness is inverted. The effect originates from a coupling between axial linear momentum and OAM mediated by the helical spatial dependence of the potential. For DNA-scale geometric parameters, this linear-orbital coupling produces sizable orbital selectivity, which remains robust to static and dynamic disorder, and increases with the length of chiral regions. Although bare spin-orbit coupling in the chiral potential considered here is too weak to generate considerable spin dynamics, spin-OAM correlations in the electrodes allow the same orbital selective mechanism to induce appreciable spin selectivity. These results identify orbital dynamics as an important contributor to electron transport in chiral systems.
Abstract:We present a three-dimensional continuum model of electron transmission through a chiral electrostatic potential and show that it gives rise to chirality-induced orbital selectivity. In this model, electron transmittance depends strongly on the incident orbital angular momentum (OAM) associated with its transverse motion, and the selectivity reverses when the potential's handedness is inverted. The effect originates from a coupling between axial linear momentum and OAM mediated by the helical spatial dependence of the potential. For DNA-scale geometric parameters, this linear-orbital coupling produces sizable orbital selectivity, which remains robust to static and dynamic disorder, and increases with the length of chiral regions. Although bare spin-orbit coupling in the chiral potential considered here is too weak to generate considerable spin dynamics, spin-OAM correlations in the electrodes allow the same orbital selective mechanism to induce appreciable spin selectivity. These results identify orbital dynamics as an important contributor to electron transport in chiral systems.
Mesoscale and Nanoscale Physics (cond-mat.mes-hall); Chemical Physics (physics.chem-ph); Quantum Physics (quant-ph)
arXiv:2509.07675 [cond-mat.mes-hall]
(or arXiv:2509.07675v2 [cond-mat.mes-hall] for this version)
https://doi.org/10.48550/arXiv.2509.07675 Focus to learn more arXiv-issued DOI via DataCite
https://doi.org/10.1021/acs.jpclett.6c01552 Focus to learn more DOI(s) linking to related resources
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