Exploring the Charge-Ordering Transition in (TMTTF)X via Thermal Expansion Measurements
arXiv:0909.4153 · doi:10.1016/j.physb.2009.12.022
Abstract
We report results of high-resolution measurements of the \emph{c}-axis expansivity () at the charge-ordering (CO) transition for the quasi-1D (TMTTF)X compounds with X = SbF and Br and make a comparison with previous results for the X = PF and AsF salts. For X = SbF, due to the screening of the long-range Coulomb forces, a sharp -type anomaly is observed at , which contrasts with the step-like mean-field anomaly at for PF and AsF, where CO occurs in the Mott-Hubbard charge-localized regime. For the latter two salts, a negative contribution to is observed above . This feature is assigned to the anions' rigid-unit modes, which become inactive for . Our results for the X = Br salt, where such rigid-unit modes are absent, reveal no traces of such negative contribution, confirming the model based on the anions' rigid-unit modes for the X = PF and AsF salts.
Submitted to Special Issue - ISCOM 2009 - Physica B Condensed Matter
References in corpus (6)
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Cited by in corpus (6)
- Electronic crystals: an experimental overview
- Comprehensive transport studies of anisotropy and ordering phenomena in quasi-one-dimensional (TMTTF)2X salts (X = PF6, AsF6, SbF6; BF4, ClO4, ReO4)
- Charge-Ordering Transition in (TMTTF)X Explored via Dilatometry
- Probing the Mott Physics in -(BEDT-TTF)X Salts via Thermal Expansion
- Low temperature structural effects in the (TMTSF)PF and AsF Bechgaard salts
- Superlattice Induced by Charge Order in the Organic Spin Chain (TMTTF) ( SbF, AsF and PF) Revealed by High Field EPR