On-chain electrodynamics of metallic (TMTSF)_2 X salts: Observation of Tomonaga-Luttinger liquid response
A. Schwartz (1), M. Dressel (1), G. Gruner (1), V. Vescoli (2), L., Degiorgi (2), and T. Giamarchi (3) ((1) UCLA, (2) ETH-Zurich, (3) UPS-Orsay)

TL;DR
This study investigates the electrodynamic response of (TMTSF)_2 X salts, revealing features consistent with Tomonaga-Luttinger liquid behavior and Coulomb correlations in a nearly one-dimensional metallic state.
Contribution
The paper provides experimental evidence of Tomonaga-Luttinger liquid response in (TMTSF)_2 X salts, highlighting deviations from Drude behavior and identifying characteristic optical conductivity features.
Findings
Optical conductivity shows a narrow zero-frequency mode with small spectral weight.
A mode around 200 cm^{-1} carries most of the spectral weight.
High-frequency response aligns with interacting Tomonaga-Luttinger liquid calculations.
Abstract
We have measured the electrodynamic response in the metallic state of three highly anisotropic conductors, (TMTSF)_2 X, where X=PF_6, AsF_6, or ClO_4, and TMTSF is the organic molecule tetramethyltetraselenofulvalene. In all three cases we find dramatic deviations from a simple Drude response. The optical conductivity has two features: a narrow mode at zero frequency, with a small spectral weight, and a mode centered around 200 cm^{-1}, with nearly all of the spectral weight expected for the relevant number of carriers and single particle bandmass. We argue that these features are characteristic of a nearly one-dimensional half- or quarter-filled band with Coulomb correlations, and evaluate the finite energy mode in terms of a one-dimensional Mott insulator. At high frequencies (\hbar\omega > t_\perp, the transfer integral perpendicular to the chains), the frequency dependence of the…
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