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تسجيل مستخدم جديدQuantum Hall Transitions in (TMTSF)$_2$PF$_6$
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S. Valfells
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We have studied the temperature dependence of the integer quantum Hall transitions in the molecular crystal (TMTSF)$_2$PF$_6$. We find that the transition width between the quantum Hall plateaus does not exhibit the universal power-law scaling behavior of the integer quantum Hall effect observed in semiconducting devices. Instead, the slope of the $rho_{xy}$ risers, $drho_{xy}/dB$, and the (inverse) width of the $rho_{xx}$ peaks, $(Delta B)^{-1}$, show a BCS-like energy gap temperature dependence. We discuss these results in terms of the field-induced spin-density wave gap and order parameter of the system.
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We present a detailed low-temperature investigation of the statics and dynamics of the anions and methyl groups in the organic conductors (TMTSF)$_2$PF$_6$ and (TMTSF)$_2$AsF$_6$ (TMTSF : tetramethyl-tetraselenafulvalene). The 4 K neutron scattering
structure refinement of the fully deuterated (TMTSF)$_2$PF$_6$-D12 salt allows locating precisely the methyl groups at 4 K. This structure is compared to the one of the fully hydrogenated (TMTSF)$_2$PF$_6$-H12 salt previously determined at the same temperature. Surprisingly it is found that deuteration corresponds to the application of a negative pressure of 5 x 10$^2$ MPa to the H12 salt. Accurate measurements of the Bragg intensity show anomalous thermal variations at low temperature both in the deuterated PF$_6$ and AsF$_6$ salts. Two different thermal behaviors have been distinguished. Low-Bragg-angle measurements reflect the presence of low-frequency modes at characteristic energies {theta}$_E$ = 8.3 K and {theta}$_E$ = 6.7 K for the PF$_6$-D12 and AsF$_6$-D12 salts, respectively. These modes correspond to the low-temperature methyl group motion. Large-Bragg-angle measurements evidence an unexpected structural change around 55 K which probably corresponds to the linkage of the anions to the methyl groups via the formation of F...D-CD2 bonds observed in the 4 K structural refinement. Finally we show that the thermal expansion coefficient of (TMTSF)$_2$PF$_6$ is dominated by the librational motion of the PF$_6$ units. We quantitatively analyze the low-temperature variation of the lattice expansion via the contribution of Einstein oscillators, which allows us to determine for the first time the characteristic frequency of the PF6 librations: {theta}$_E$ = 50 K and {theta}$_E$ = 76 K for the PF$_6$-D12 and PF$_6$-H12 salts, respectively.
The layered quasi-one-dimensional molecular superconductor (TMTSF)$_2$PF$_6$ is a very exotic material with a superconducting order parameter whose ground state symmetry has remained ill-defined. Here we present a pulsed NMR Knight shift (K) study of
$^{77}$Se measured simultaneously with transport in pressurized (TMTSF)$_2$PF$_6$. The Knight shift is linearly dependent on the electron spin susceptibility $chi_s$, and is therefore a direct measure of the spin polarization in the superconducting state. For a singlet superconductor, the spin contribution to the Knight shift, K$_s$, falls rapidly on cooling through the transition. The present experiments indicate no observable change in K between the metallic and superconducting states, and thus strongly support the hypothesis of triplet p-wave superconductivity in (TMTSF)$_2$PF$_6$.
We report a study of the 16.5 GHz dielectric function of hydrogenated and deuterated organic salts (TMTTF)$_2$PF$_6$. The temperature behavior of the dielectric function is consistent with short-range polar order whose relaxation time decreases rapid
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