Nonlinear elastic and electronic properties of Mo_6S_3I_6 nanowires

The properties of Mo_6S_3I_6 nanowires were investigated with ab initio calculations based on the density-functional theory. The molecules build weakly coupled one-dimensional chains with three sulfur atoms in the bridging planes between the Mo octahedra, each dressed with six iodines. Upon uniaxial strain along the wires, each bridging plane shows two energy minima, one in the ground state with the calculated Young modulus Y=82 GPa, and one in the stretched state with Y=94 GPa. Both values are at least four times smaller than the experimental values and the origin of the discrepancy remains a puzzle. The ideal tensile strength is about 8.4 GPa, the chains break in the Mo-Mo bonds within the octahedra and not in the S bridges. The charge-carrier conductivity is strongly anisotropic and the Mo_6S_3I_6 nanowires behave as quasi-one-dimensional conductors in the whole range of investigated strains. The conductivity is extremely sensitive to strain, making this material very suitable for stain gauges. Very clean nanowires with good contacts may be expected to behave as ballistic quantum wires over lengths of several $\mu$m. On the other hand, with high-impedance contacts they are good candidates for the observation of Luttinger liquid behaviour. The pronounced 1D nature of the Mo_6S_3I_6 nanowires makes them a uniquely versatile and user-friendly system for the investigation of 1D physics.Comment: 7 pages, 8 figures include

Single particle and collective excitations in the one-dimensional charge density wave solid K0.3MoO3 probed in real time by femtosecond spectroscopy

Ultrafast transient reflectivity changes caused by collective and single particle excitations in the quasi one-dimensional charge-density wave (CDW) semiconductor K0.3MoO3 are investigated with optical pump-probe spectroscopy. The temperature-dependence of non-equilibrium single particle excitations across the CDW gap and their recombination dynamics are reported for the first time. In addition, amplitude mode reflectivity oscillations are observed in real time. A T-dependent overdamped response is also observed which is attributed to relaxation of the phason mode.Comment: 5 pages, 4 figures, accepted for publication in Phys.Rev.Let

Femtosecond "snapshots "of gap-forming charge-density-wave correlations in quasi-two-dimensional dichalcogenides 1T-TaS2 and 2H-TaSe2

Time-resolved optical spectroscopy of collective and single-particle excitations of 1T-TaS2 and 2H-TaSe2 reveals the presence of a large gap in the excitation spectrum on the femtosecond timescale, associated with the formation of various degrees of CDW order. In common with superconducting cuprates, excitations with energies less than the full gap show much slower relaxation. This separation of timescales cannot be explained in a quasi-2D Fermi-Liquid picture with an anisotropic gap but rather suggests the formation of a fluctuating spatially inhomogeneous state eventually forming a long-range ordered state at low temperatures.Comment: to appear in Phys. Rev.B Rapid Com

The attainable superconducting Tc in a model of phase coherence by percolation

The onset of macroscopic phase coherence in superconducting cuprates is considered to be determined by random percolation between mesoscopic Jahn-Teller pairs, stripes or clusters. The model is found to predict the onset of superconductivity near 6% doping, maximum Tc near 15% doping and Tc= T* at optimum doping, and accounts for the destruction of superconductivity by Zn doping near 7%. The model also predicts a relation between the pairing (pseudogap) energy and Tc in terms of experimentally measurable quantities.Comment: 3 pages + 3 postscript figure

Low-energy electronic structure in Y1-xCaxBa2Cu3O7-y comparison of t ime-resolved optical spectroscopy, NMR, neutron and tunneling data

Time-resolved optical measurements give information on the quasiparticle relaxation dynamics in YBCO, from which the evolution of the gap with doping and temperature can be systematically deduced. In this paper these optical charge-channel `pseudogap' data are compared with the `pseudogap' obtained from the NMR Knight shift Ks, spin polarized neutron scattering (SPNS) and single particle tunneling measurements. A simple energy level diagram is proposed to explain the different `gap' magnitudes observed by different spectroscopies in Y1-xCaxBa2Cu3O7-y, whereby the spin gap Delta_s in NMR and SPNS corresponds to a triplet local pair state, while Delta_p in the charge excitation spectrum corresponds to the pair dissociation energy. At optimum doping and in the overdoped state, an additional T-dependent gap becomes evident, which closes at T_c, suggesting a cross-over to a more conventional BCS-like superconductivity scenario.Comment: 9 pages, 4 figures. Presented in HTS99, Miami, January 9