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We report thermoelectric (TE) properties of topological surface Dirac states (TSDS) in three-dimensional topological insulators (3D-TIs) purely isolated from the bulk by employing single crystal Bi$_{2-x}$Sb$_x$Te$_{3-y}$Se$_y$ films epitaxially grown in the ultrathin limit. Two intrinsic nontrivial topological surface states, a metallic TSDS (m-TSDS) and a gap-opened semiconducting topological state (g-TSDS), are successfully observed by electrical transport, and important TE parameters (electrical conductivity (${\sigma}$), thermal conductivity (${\kappa}$), and thermopower ($S$)) are accurately determined. Pure m-TSDS gives $S$=-44 {\mu}VK$^{-1}$, which is an order of magnitude higher than those of the conventional metals and the value is enhanced to -212 {\mu}VK$^{-1}$ for g-TSDS. It is clearly shown that the semi-classical Boltzmann transport equation (SBTE) in the framework of constant relaxation time (${\tau}$) most frequently used for conventional analysis cannot be valid in 3D-TIs and strong energy dependent relaxation time ${\tau}(E)$ beyond the Born approximation is essential for making intrinsic interpretations. Although ${\sigma}$ is protected on the m-TSDS, ${\kappa}$ is greatly influenced by the disorder on the topological surface, giving a dissimilar effect between topologically protected electronic conduction and phonon transport., Comment: 15 pages, 4 figures

We study the Seebeck effect in the $\tau$-type organic conductors, $\tau$-(EDO-$S$,$S$-DMEDT-TTF)$_{2}$(AuBr$_{2}$)$_{1+y}$ and $\tau$-(P-$S$,$S$-DMEDT-TTF)$_{2}$(AuBr$_{2}$)$_{1+y}$, where EDO-$S$,$S$-DMEDT-TTF and P-$S$,$S$-DMEDT-TTF are abbreviated as OOSS and NNSS, respectively, both experimentally and theoretically. Theoretically in particular, we perform first-principles band calculation for the two materials and construct a two-orbital model, on the basis of which we calculate the Seebeck coefficient. We show that the calculated temperature dependence of the Seebeck coefficient $S$ is semi-quantitatively consistent with the experimental observation. In both materials, the absolute value of the Seebeck coefficient is maximum at a certain temperature, and this temperature is lower for NNSS than for OOSS. From a band structure viewpoint, we find that this can be traced back to the narrowness of the band gap between the upper and the lower pudding-mold type bands. On the other hand, the Seebeck coefficient of NNSS in the low temperature regime steeply increases with increasing temperature, which is due to the narrowness of the upper band. These differences in thermoelectric properties demonstrate the effectiveness of controlling the band structure through molecular modification., Comment: 6 pages, 7 figures. To be published in J. Phys. Soc. Jpn

Extremely large magnetoresistance is realized in the nonmagnetic layered metal PdCoO2. In spite of a highly conducting metallic behavior with a simple quasi-two-dimensional hexagonal Fermi surface, the interlayer resistance reaches up to 35000% for the field along the [1-10] direction. Furthermore, the temperature dependence of the resistance becomes nonmetallic for this field direction, while it remains metallic for fields along the [110] direction. Such severe and anisotropic destruction of the interlayer coherence by a magnetic field on a simple Fermi surface is ascribable to orbital motion of carriers on the Fermi surface driven by the Lorentz force, but seems to have been largely overlooked until now., Comment: Phys. Rev. Lett. 111, 056601 (2013)

Angle dependent magnetoresistance experiments on organic conductors exhibit a wide range of angular oscillations associated with the dimensionality and symmetry of the crystal structure and electron energy dispersion. In particular, characteristics associated with 1, 2, and 3 dimensional electronic motion are separately revealed when a sample is rotated through different crystal planes in a magnetic field. Originally discovered in the TMTSF based conductors, these effects are particularly pronounced in the related system (DMET)2I3. Here, experimental and computational results for magnetoresistance oscillations in this material, over a wide range of magnetic field orientations, are presented in such a manner as to uniquely highlight this multidimensional behavior.The calculations employ the Boltzmann transport equation that incorporates the systems triclinic crystal structure, which allows for accurate estimates of the transfer integrals along the crystallographic axes, verifying the 1d, 2d and 3d nature of (DMET)2I3, as well as crossovers between dimensions in the electronic behavior.

We report the temperature dependence of the upper critical magnetic field in the quasi-onedimensional molecular organic superconductor (DMET)2I3, for magnetic field applied along the intrachain, interchain, and interplane directions. The upper critical field tends to saturation at low temperature for field in all directions and does not exceed the Pauli paramagnetic limit. Superconductivity in (DMET)2I3 thus appears to be conventional spin singlet, in contrast to the status of the isostructural Bechgaard salts. We also discuss a magnetic field-induced dimensional crossover effect in the normal metallic state which had previously appeared to be associated with superconductivity.

Measurements and calculations of magnetotransport in the molecular organic conductor (DMET)2I3 detect and simulate all known angular magnetoresistance oscillation (AMRO) phenomena for quasi-one dimensional (Q1D) systems. Employing the true triclinic crystal structure in the calculations, these results address the mystery of the putative vanishing of the primary AMRO phenomenon, the Lebed magic angle effect, for orientations in which it was expected to be strongest. They also show a common origin for Lebed and so-called "LN" oscillations, and confirm the generalized nature of AMRO in Q1D systems., Comment: Accepted for the publication in Phys. Rev. Lett

We study the origin of the large thermopower in quasi-two-dimensional a $\tau$-type organic conductor, $\tau-(EDO-S,S-DMEDT-TTF)_2(AuBr_2)_{1+y}$ ($y \le 0.875$), from the view point of a "pudding mold"-type band structure. We calculate the electronic band structure using an \textit{ab initio} band calculation package, and obtain a tight binding model fit to the \textit{ab initio} band structure. Using the model and the Boltzmann's equation approach, we calculate the temperature dependence of the Seebeck coefficient. We conclude that the peculiar band structure is the origin of the large Seebeck coefficient and the appearance of the maximum value at a certain temperature., Comment: proceedings of ISCOM 2009 (to be published in Physica B)