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Register a new userThe metallic transport of (TMTSF)_2X organic conductors close to the superconducting phase
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Pascale Auban-Senzier
Publication date
2011
fields
Physics
and research's language is
English
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Comparing resistivity data of quasi-one dimensional superconductors (TMTSF)_2PF_6 and (TMTSF)_2ClO_4 along the least conducting c*-axis and along the high conductivity a -axis as a function of temperature and pressure, a low temperature regime is observed in which a unique scattering time governs transport along both directions of these anisotropic conductors. However, the pressure dependence of the anisotropy implies a large pressure dependence of the interlayer coupling. This is in agreement with the results of first-principles DFT calculations implying methyl group hyperconjugation in the TMTSF molecule. In this low temperature regime, both materials exhibit for rc a temperature dependence aT + bT^2. Taking into account the strong pressure dependence of the anisotropy, the T-linear rc is found to correlate with the suppression of the superconducting Tc, in close analogy with ra data. This work is revealing the domain of existence of the 3D coherent regime in the generic (TMTSF)_2X phase diagram and provides further support for the correlation between T-linear resistivity and superconductivity in non-conventional superconductors.
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An exhaustive investigation of metallic electronic transport and superconductivity of organic superconductors (TMTSF)_2PF_6 and (TMTSF)_2ClO_4 in the Pressure-Temperature phase diagram between T=0 and 20 K and a theoretical description based on the weak coupling renormalization group method are reported. The analysis of the data reveals a high temperature domain (Tapprox 20 K) in which a regular T^2 electron-electron Umklapp scattering obeys a Kadowaki-Woods law and a low temperature regime (T< 8 K) where the resistivity is dominated by a linear-in temperature component. In both compounds a correlated behavior exists between the linear transport and the extra nuclear spin-lattice relaxation due to antiferromagnetic fluctuations. In addition, a tight connection is clearly established between linear transport and T_c. We propose a theoretical description of the anomalous resistivity based on a weak coupling renormalization group determination of electron-electron scattering rate. A linear resistivity is found and its origin lies in antiferromagnetic correlations sustained by Cooper pairing via constructive interference. The decay of the linear resistivity term under pressure is correlated with the strength of antiferromagnetic spin correlations and T_c, along with an unusual build-up of the Fermi liquid scattering. The results capture the key features of the low temperature electrical transport in the Bechgaard salts.
The critical cooling rate $R_{rm c}$ above which charge ordering is kinetically avoided upon cooling, which results in charge-glass formation, was investigated for the geometrically frustrated system $theta$-(BEDT-TTF)$_2X$. X-ray diffraction experiments revealed that $theta$-(BEDT-TTF)$_2$TlCo(SCN)$_4$ exhibits a horizontally charge-ordered state, and kinetic avoidance of this state requires rapid cooling of faster than 150 K/min. This value is markedly higher than that reported for two other isostructural $theta$-type compounds, thus demonstrating the lower charge-glass-forming ability of $X$ $=$ TlCo(SCN)$_4$. In accounting for the systematic variations of $R_{rm c}$ among the three $theta$-(BEDT-TTF)$_2X$, we found that stronger charge frustration leads to superior charge-glass former. Our results suggest that charge frustration tends to slow the kinetics of charge ordering.
Recently the ferroelectric anomaly (Nad, Monceau, et al) followed by the charge disproportionation (Brown, et al) have been discovered in (TMTTF)2X compounds. The corresponding theory of the combined Mott-Hubbard state describes both effects by interference of the build-in nonequivalence of bonds and the spontaneous one of sites. The state gives rise to three types of solitons: pi solitons (holons) are observed via the activation energy Delta in the conductivity $G$; noninteger alpha solitons (the FE domain walls) provide the frequency dispersion of the ferroelectric response; combined spin-charge solitons determine G(T) below subsequent structural transitions of the tetramerisation. The photoconductivity gap 2Delta is determined by creations of soliton - antisoliton pairs. The optical edge lies well below, given by the collective ferroelectric mode which coexists with the combined electron-phonon resonance and the phonon antiresonance. The charge disproportionation and the ferroelectricity can exist hiddenly even in the Se subfamily giving rise to the unexplained yet low frequency optical peak, the enhanced pseudogap and traces of phonons activation.
We report on dc and microwave experiments of the low-dimensional organic conductors (TMTSF)$_2$PF$_6$ and (TMTSF)$_2$ClO$_4$ along the $a$, $b^{prime}$, and $c^*$ directions. In the normal state of (TMTSF)$_2$PF$_6$ below T=70 K, the dc resistivity follows a power-law with $rho_a$ and $rho_{b^{prime}}$ proportional to $T^2$ while $rho_{c^*}propto T$. Above $T = 100$ K the exponents extracted from the data for the $a$ and $c^*$ axes are consiste1nt with what is to be expected for a system of coupled one-dimensional chains (Luttinger liquid) and a dimensional crossover at a temperature of about 100 K. The $b^prime$ axis shows anomalous exponents that could be attributed to a large crossover between these two regimes. The contactless microwave measurements of single crystals along the $b^{prime}$-axis reveal an anomaly between 25 and 55 K which is not understood yet. The organic superconductor (TMTSF)$_2$ClO$_4$ is more a two-dimensional metal with an anisotropy $rho_a/rho_{b^{prime}}$ of approximately 2 at all temperatures. Such a low anisotropy is unexpected in view of the transfer integrals. Slight indications to one-dimensionality are found in the temperature dependent transport only above 200 K. Even along the least conducting $c^*$ direction no region with semiconducting behavior is revealed up to room temperature.
We have investigated the magnetic field-induced metal-insulator transition in the tau-phase organic conductors, which occurs in fields above 35 T, and below 14 K, by magnetization, thermoelectric, and pressure dependent transport methods. Our results show that the transition is a bulk thermodynamic process where a magnetic field-dependent gap opens upon entry into the insulating state. We argue that the transition involves a magnetic field-induced change in the electronic structure.
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