59Co-NMR Knight Shift of the Superconducting NaxCoO2.yH2O

Layered Co oxide NaxCoO2.yH2O with the superconducting transition temperature Tc =4.5 K has been studied by 59Co-NMR. The Knight shift K estimated from the observed spectra for powder sample exhibits almost temperature(T)-independent behavior above Tc and decreases with decreasing T below Tc. This result and the existence of the coherence peak in the spin-lattice-relaxation-rate versus T curve reported by the present authors indicate, naively speaking, that the singlet order parameter with s-wave symmetry is realized in NaxCoO2.yH2O. Differences of the observed behaviors between the spectra of the non-aligned sample and the one aligned in epoxy adhesive by applying the external magnetic field are discussed.Comment: 6 pages, 4 figures, submitted to J. Phys. Soc. Jp

Critical Behavior in Doping-Driven Metal−-Insulator Transition on Single-Crystalline Organic Mott-FET

We present the carrier transport properties in the vicinity of a doping-driven Mott transition observed at a field-effect transistor (FET) channel using a single crystal of the typical two-dimensional organic Mott insulator $\kappa$-(BEDT-TTF)$_2$CuN(CN)$_2$Cl ($\kappa$-Cl).The FET shows a continuous metal$-$insulator transition (MIT) as electrostatic doping proceeds. The phase transition appears to involve two-step crossovers, one in Hall measurement and the other in conductivity measurement. The crossover in conductivity occurs around the conductance quantum $e^2/h$ , and hence is not associated with "bad metal" behavior, which is in stark contrast to the MIT in half-filled organic Mott insulators or that in doped inorganic Mott insulators. Through in-depth scaling analysis of the conductivity, it is found that the above carrier transport properties in the vicinity of the MIT can be described by a high-temperature Mott quantum critical crossover, which is theoretically argued to be a ubiquitous feature of various types of Mott transitions. [This document is the unedited Authors' version of a Submitted Work that was subsequently accepted for publication in Nano Letters, copyright \copyright American Chemical Society after peer review. To access the final edited and published work see http://dx.doi.org/10.1021/acs.nanolett.6b03817]Comment: 40 pages, 16 figures in Nano Letters, ASAP (2017