A model for electrical conductivity in (TMTSF)2ClO4, (TMTSF)2ReO4 and related materials

To describe quantitatively the diverse variations of the temperature-dependent electrical conductivities of tetramethyltetraselenafulvenium (TMTSF) salts, a model based on small Fermi (E_f) and small gap (E_g − E_f) energies and T⁻ⁿ dependence of scattering is presented. The difference between the conductivities of quenched and slowly cooled (TMTSF)₂ClO₄ is described by different values of E_f and E_g − E_f in the two cases. The model illustrates, in terms of variables E_f and E_g − E_f, the effect of pressure on the metal-insulator transition in (TMTSF)₂ReO₄, for example, and indicates a relation between E_f and E_g − E_f at the onset of superconductivity.     

Superconducting state of the organic conductor (TMTSF)2ClO4

(TMTSF)2ClO4 is a quasi-one-dimensional organic conductor and superconductor with Tc=1.4 K, and one of at least two Bechgaard salts observed to have upper critical fields far exceeding the paramagnetic limit. Nevertheless, the 77Se NMR Knight shift at low fields reveals a decrease in spin susceptibility chi(s) consistent with singlet spin pairing. The field dependence of the spin-lattice relaxation rate at 100 mK exhibits a sharp crossover (or phase transition) at a field Hs approximately 15 kOe, to a regime where chi(s) is close to the normal state value, even though Hc2> Hs.     

Magnetic determination of H(c2) under accurate alignment in (TMTSF)2ClO4

Cantilever magnetometry has been used to measure the upper critical magnetic field H(c2) of the quasi-one-dimensional molecular organic superconductor (TMTSF)2ClO4. From simultaneous resistivity and torque magnetization experiments conducted under precise field alignment, H(c2) at low temperature is shown to reach 5 T, nearly twice the Pauli paramagnetic limit imposed on spin singlet superconductors. These results constitute the first thermodynamic evidence for a large H(c2) in this system and provide support for spin triplet pairing in this unconventional superconductor.     

Field-induced confinement in (TMTSF)2ClO4 under accurately aligned magnetic fields

We present transport measurements along the least conducting c direction of the organic superconductor (TMTSF)₂ClO₄  performed under an accurately aligned magnetic field in the low temperature regime. The experimental results reveal a two-dimensional confinement of the carriers in the (a, b) planes which is governed by the magnetic field component along the b^′ direction. This 2-D confinement is accompanied by a metal-insulator transition for the c axis resistivity. These data are supported by a quantum mechanical calculation of the transverse transport taking into account in self consistent treatment the effect of the field on the interplane Green function and on the intraplane scattering time.     

Oscillatory magnetoresistance in the field-induced SDW state in (TMTSF)2 ClO4

The transverse magnetoresistance of (TMTSF)₂ ClO₄ was measured in pulsed high magnetic fields up to 35 T at T = 1.8−-4.2K for studying the field-induced spin density wave (FISDW) phase. In addition to a structure corresponding to the threshold field B_th (_T) of the FISDW phase, we found two temperature dependent structures in higher field range at 15–17 and 22–25 T, respectively. Moreover, Shubnikov-de Haas type oscillations with smaller period were also observed superposing on the structures. It was found that the peak positions of the oscillation are independent of temperature, whereas their amplitude changes discontinuously at the structures.     

Competing phases in the high field phase diagram of (TMTSF)(2)ClO(4)

A model is presented for the high field phase diagram of (TMTSF)(2)ClO(4), taking into account the anion ordering, which splits the Fermi surface into two bands. For strong enough field, the largest metal spin density wave critical temperature corresponds to the N=0 phase, which originates from two intraband nesting processes. At lower temperature, the competition between these processes puts at disadvantage the N=0 phase vs the N=1 phase, which is due to interband nesting. A first order transition then takes place from the N=0 to N=1 phase. We ascribe to this effect the experimentally observed phase diagrams.     

Subterahertz electrodynamics of (TMTSF)2X (X = ClO4, PF6) salts

The terahertz-subterahertz spectra of the complex permittivity and dynamic conductivity of polycrystalline (TMTSF)₂ClO₄ and (TMTSF)₂PF₆ samples are measured quantitatively. The spectra of (TMTSF)₂ClO₄ have absorption lines at frequencies of 7 and 30 cm^?1. The obtained temperature dependences of the line parameters in the range 5–300 K cast some doubt on the earlier concept of their phonon origin. An excitation is detected at temperatures below 20 K in the frequency range near 30 cm^?1, and its nature is related to the activation of a transverse acoustic phonon caused by the folding of the Brillouin zone due to the ordering of noncentrosymmetrical anions below 20 K. An increase in the carrier relaxation rate is found in this temperature range, which indicates a close relation between the electron and phonon subsystems in (TMTSF)₂ClO₄. Sings of additional low-energy excitations that should manifest themselves at frequencies below 1–2 cm^?1 are detected. (TMTSF)₂PF₆ containing centrosymmetrical anions has no absorption lines in the frequency range 3–20 cm^?1 and the temperature range 5–300 K.     

Anomalous in-plane anisotropy of the onset of superconductivity in (TMTSF)2ClO4

We report the magnetic-field amplitude and field-angle dependence of the superconducting onset temperature Tconset of the organic superconductor (TMTSF)2ClO4 in magnetic fields H accurately aligned to the conductive ab' plane. We revealed that the rapid increase of the onset fields at low temperatures occurs both for H || b' and H || a, irrespective of the carrier confinement. Moreover, in the vicinity of the Pauli-limiting field, we report a shift of a principal axis of the in-plane field-angle dependence of Tconset. This feature may be related to an occurrence of Fulde-Ferrell-Larkin-Ovchinnikov phases.