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We report on the quasi-linear in field intrachain magnetoresistance in the normal state of a quasi-one-dimensional superconductor Ta$_4$Pd$_3$Te$_{16}$ ($T_c$$sim$4.6 K). Both the longitudinal and transverse in-chain magnetoresistance shows a power-l aw dependence, $Delta rho$$propto$B$^alpha$, with the exponent $alpha$ close to 1 over a wide temperature and field range. The magnetoresistance shows no sign of saturation up to 50 tesla studied. The linear magnetoresistance observed in Ta$_4$Pd$_3$Te$_{16}$ is found to be overall inconsistent with the interpretations based on the Dirac fermions in the quantum limit, charge conductivity fluctuations as well as quantum electron-electron interference. Moreover, it is observed that the Kohlers rule, regardless of the field orientations, is violated in its normal state. This result suggests the loss of charge carriers in the normal state of this chain-containing compound, due presumably to the charge-density-wave fluctuations.
The hyperkagome antiferromagnet Na$_{4}$Ir$_3$O$_8$ represents the first genuine candidate for the realisation of a three-dimensional quantum spin-liquid. It can also be doped towards a metallic state, thus offering a rare opportunity to explore the nature of the metal-insulator transition in correlated, frustrated magnets. Here we report thermodynamic and transport measurements in both metallic and weakly insulating single crystals down to 150 mK. While in the metallic sample the phonon thermal conductivity ($kappa^{ph}$) is almost in the boundary scattering regime, in the insulating sample we find a large reduction $kappa^{ph}$ over a very wide temperature range. This result can be ascribed to the scattering of phonons off nanoscale disorder or off the gapless magnetic excitations that are seen in the low-temperature specific heat. This works highlights the peculiarity of the metal-insulator transition in Na$_{3+x}$Ir$_3$O$_8$ and demonstrates the importance of the coupling between lattice and spin degrees of freedom in the presence of strong spin-orbit coupling.
We report a comparative study of the specific heat, electrical resistivity and thermal conductivity of the quasi-two-dimensional purple bronzes Na$_{0.9}$Mo$_6$O$_{17}$ and K$_{0.9}$Mo$_6$O$_{17}$, with special emphasis on the behavior near their res pective charge-density-wave transition temperatures $T_P$. The contrasting behavior of both the transport and the thermodynamic properties near $T_P$ is argued to arise predominantly from the different levels of intrinsic disorder in the two systems. A significant proportion of the enhancement of the thermal conductivity above $T_P$ in Na$_{0.9}$Mo$_6$O$_{17}$, and to a lesser extent in K$_{0.9}$Mo$_6$O$_{17}$, is attributed to the emergence of phason excitations.
The upper critical field $H_{c2}$ of purple bronze Li$_{0.9}$Mo$_6$O$_{17}$ is found to exhibit a large anisotropy, in quantitative agreement with that expected from the observed electrical resistivity anisotropy. With the field aligned along the mos t conducting axis, $H_{c2}$ increases monotonically with decreasing temperature to a value five times larger than the estimated paramagnetic pair-breaking field. Theories for the enhancement of $H_{c2}$ invoking spin-orbit scattering or strong-coupling superconductivity are shown to be inadequate in explaining the observed behavior, suggesting that the pairing state in Li$_{0.9}$Mo$_6$O$_{17}$ is unconventional and possibly spin-triplet.
In the quasi-one-dimensional cuprate PrBa$_2$Cu$_4$O$_8$, the Pr cations order antiferromagnetically at 17 K in zero field. Through a combination of magnetic susceptibility, torque magnetometry, specific heat and interchain transport measurements, th e anisotropic temperature-magnetic field phase diagram associated with this ordering has been mapped out. A low-temperature spin-flop transition in the Pr sub-lattice is found to occur at the same magnetic field strength and orientation as a dimensional crossover in the ground state of the metallic CuO chains. This coincidence suggests that the spin reorientation is driven by a change in the anisotropic Rudermann-Kittel-Kasuya-Yosida (RKKY) interaction induced by a corresponding change in effective dimensionality of the conduction electrons.
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