sigma and f_0(980) substructures from gamma-gamma to pi-pi, J/psi, phi radiative and D_s semi-leptonic decays

Using an improved "analytic K-matrix model", we reconsider the extraction of the sigma/f_0(600) and f_0(980) gamma-gamma widths from gamma-gamma to pi-pi scatterings data of Crystal Ball and Belle. Our main results are summarized in Tables 3 and 4. The averaged sigma "direct width" to gamma-gamma is 0.16(3) keV which confirms a previous result of [1] and which does neither favour a large four-quark (diquark-antidiquark) nor a molecule nor a pure \bar qq component. The "direct width" of the f_0(980) of 0.28(2) keV is much larger than the four-quark expectation but can be compatible with a \bar ss or gluonium component. We also found that the rescattering part of the amplitude is relatively large indicating an important contribution of the meson loops in the determination of the gamma-gamma total widths. This is mainly due to the large couplings of the sigma and f_0(980) to pi-pi and/or \bar KK, which can also be due to a light scalar gluonium with large OZI violating couplings but not necessary to a four-quark or molecule state. Our average results for the total (direct+rescattering) gamma-gamma widths: Gamma_sigma^{tot}= 3.08(82) keV, Gamma_{f_0}^{tot}= 0.16(1) keV} are comparable with the ones from dispersion relations and PDG values. Using the parameters from QCD spectral sum rules, we complete our analysis by showing that the production rates of unmixed scalar gluonia sigma_B(1) and G (1.5-1.6) agree with the data from J/\psi, phi radiative and D_s semi-leptonic decays.Comment: 11 pages, 6 figures (1 more figure added in Fig 6), 4 tables : version appeared on-line in doi:10.1016/j.physletb.2010.12.00

Oxygen Isotope Effect on the Spin State Transition in (Pr0.7_{0.7}Sm0.3_{0.3})0.7_{0.7}Ca0.3_{0.3}CoO3{_3}

Oxygen isotope substitution is performed in the perovskite cobalt oxide (Pr$_{0.7}$Sm$_{0.3}$)$_{0.7}$Ca$_{0.3}$CoO${_3}$ which shows a sharp spin state transition from the intermediate spin (IS) state to the low spin (LS) state at a certain temperature. The transition temperature of the spin state up-shifts with the substitution of $^{16}O$ by $^{18}$O from the resistivity and magnetic susceptibility measurements. The up-shift value is 6.8 K and an oxygen isotope exponent ($\alpha_S$) is about -0.8. The large oxygen isotope effect indicates strong electron-phonon coupling in this material. The substitution of $^{16}$O by $^{18}$O leads to a decrease in the frequency of phonon and an increase in the effective mass of electron ($m$$^\ast$), so that the bandwidth W is decreased and the energy difference between the different spin states is increased. This is the reason why the $T_s$ is shifted to high temperature with oxygen isotopic exchange.Comment: 4 pages, 3 figure

Hysteresis and Anisotropic Magnetoresistance in Antiferromagnetic Nd2−xCexCuO4Nd_{2-x}Ce_xCuO_{4}

The out-of-plane resistivity ($\rho_c$) and magnetoresistivity (MR) are studied in antiferromangetic (AF) $Nd_{2-x}Ce_xCuO_{4}$ single crystals, which have three types of noncollinear antiferromangetic spin structures. The apparent signatures are observed in $\rho_c(T)$ measured at the zero-field and 14 T at the spin structure transitions, giving a definite evidence for the itinerant electrons directly coupled to the localized spins. One of striking feature is an anisotropy of the MR with a fourfold symmetry upon rotating the external field (B) within ab plane in the different phases, while twofold symmetry at spin reorientation transition temperatures. The intriguing thermal hysteresis in $\rho_c(T,B)$ and magnetic hysteresis in MR are observed at spin reorientation transition temperatures.Comment: 4 pages, 4 figure

Infrared spectroscopy of the charge ordering transition in Na0.5_{0.5}CoO2_2

We report infrared spectra of a Na$_{0.5}$CoO$_2$ single crystal which exhibits a sharp metal-insulator transition near 50 K due to the formation of charge ordering. In comparison with x=0.7 and 0.85 compounds, we found that the spectral weight associated with the conducting carriers at high temperature increases systematically with decreasing Na contents. The charge ordering transition only affects the optical spectra below 1000 cm$^{-1}$. A hump near 800 cm$^{-1}$ develops below 100 K, which is accompanied by the appearance of new lattice modes as well as the strong anti-resonance feature of phonon spectra. At lower temperature $T_{co}$, an optical gap develops at the magnitude of 2$\Delta\approx3.5k_BT_{co}$, evidencing an insulating charge density wave ground state. Our experimental results and analysis unequivocally point towards the importance of charge ordering instability and strong electron-phonon interaction in Na$_x$CoO$_2$ system.Comment: 4 pages, 3 figure