Crystalline Silicate Feature of the Vega-like star HD145263

We have observed the 8-13 $\mu$m spectrum (R$\sim$250) of the Vega-like star candidate HD145263 using Subaru/COMICS. The spectrum of HD145263 shows the broad trapezoidal silicate feature with the shoulders at 9.3 $\mu$m and 11.44 $\mu$m, indicating the presence of crystalline silicate grains. This detection implies that crystalline silicate may also be commonly present around Vega-like stars. The 11.44 $\mu$m feature is slightly shifted to a longer wavelength compared to the usual 11.2-3 $\mu$m crystalline forsterite feature detected toward Herbig Ae/Be stars and T Tauri stars. Although the peak shift due to the effects of the grain size can not be ruled out, we suggest that Fe-bearing crystalline olivine explains the observed peak wavelength fairly well. Fe-bearing silicates are commonly found in meteorites and most interplanetary dust particles, which originate from planetesimal-like asteroids. According to studies of meteorites, Fe-bearing silicate must have been formed in asteroidal planetesimals, supporting the scenario that dust grains around Vega-like stars are of planetesimal origin, if the observed 11.44 $\mu$m peak is due to Fe-bearing silicates.Comment: accepted for Publication in ApJ

Structural study on Pr0.55(Ca[1-y]Sr[y])0.45MnO3 thin films on perovskite (011) substrate

Structural study on the photo-switching system Pr{0.55}(Ca{1-y}Sr y){0.45}MnO3 thin films on perovskite (011) substrate has been made with synchrotron radiation diffraction experiment. The insulating phase of y=0.20 sample was found to be an antiferro-orbital ordered phase with large lattice distortion and the ferromagnetic metallic phase of y=0.40 film show no distinct lattice distortion from the paramagnetic phase, which are very similar with (Nd,Pr)0.5Sr0.5MnO3 films. A striking contrast of the orbital ordered phase of y=0.20 film to (Nd,Pr)0.5Sr0.5MnO3 films was its untwinned structure.Comment: 8 pages, 4 figures. To be published in European Journal of Physics Special Topic

In-gap state and effect of light illumination in CuIr2_2S4_4 probed by photoemission spectroscopy

We have studied disorder-induced in-gap states and effect of light illumination in the insulating phase of spinel-type CuIr$_2$S$_4$ using ultra-violet photoemission spectroscopy (UPS). The Ir$^{3+}$/Ir$^{4+}$ charge-ordered gap appears below the metal-insulator transition temperature. However, in the insulating phase, in-gap spectral features with $softgap$ are observed in UPS just below the Fermi level ($E_F$), corresponding to the variable range hopping transport observed in resistivity. The spectral weight at $E_F$ is not increased by light illumination, indicating that the Ir$^{4+}$-Ir$^{4+}$ dimer is very robust although the long-range octamer order would be destructed by the photo-excitation. Present results suggest that the Ir$^{4+}$-Ir$^{4+}$ bipolaronic hopping and disorder effects are responsible for the conductivity of CuIr$_2$S$_4$.Comment: 14 pages, 5 figure

Absence of magnetic ordering in NiGa_2S_4

Triangular-layered NiGa2S4, contrary to intuitive expectation, does not form a noncollinear antiferromagnetic structure, as do isoelectronic NaCrO2 and LiCrO2. Instead, the local magnetic moments remain disordered down to the lowest measured temperature. To get more insight into this phenomenon, we have performed first principles calculations of the first, second end third neighbors exchange interactions, and found that the second neighbor exchange is negligible, while the first and the third neighbor exchanges are comparable and antiferromagnetic. Both are rapidly suppressed by the on-site Hubbard repulsion.Comment: 4 pages, 4 figure

Correlation effects in CaCu3Ru4O12

We have investigated the electronic structure of CaCu3Ru4O12 and LaCu3Ru4O12 using soft x-ray photoelectron and absorption spectroscopy together with band structure and cluster configuration interaction calculations. We found the Cu to be in a robust divalent ionic state while the Ru is more itinerant in character and stabilizes the metallic state. Substitution of Ca by La predominantly affects the Ru states. We observed strong correlation effects in the Cu 3d states affecting the valence band line shape considerably. Using resonant photoelectron spectroscopy at the Cu L3 edge we were able to unveil the position of the Zhang-Rice singlet states in the one-electron removal spectrum of the Cu with respect to the Ru-derived metallic bands in the vicinity of the chemical potential

Epitaxial-strain effect on charge/orbital order in Pr0.5Ca0.5MnO3 films

Effect of growth orientation on charge- and orbital-ordering (CO-OO) phenomena has been studied for Pr0.5Ca0.5MnO3 epitaxial thin films fabricated on (LaAlO3)0.3-(SrAl0.5Ta0.5O3)0.7 (LSAT) substrates by means of resistivity, synchrotron x-ray diffraction, and polarized optical microscopy measurements. CO-OO transition is observed around 220 K for a film grown on an LSAT (011) substrate ((011)-film), similarly to a bulk sample, while a film grown on a (001) plane of LSAT ((001)-film) shows much higher transition temperature around 300 K. The domain size of OO is approximately 3 times as large in the (011)-film as in the (001)-film. These results demonstrate that various properties of CO-OO phenomena can be controlled with the growth orientation via the epitaxial strain from the substrate.Comment: 4 pages, 4 figure

Effect of Pt substitution on the electronic structure of AuTe2

We report a photoemission and x-ray absorption study on Au1-xPtxTe2 (x = 0 and 0.35) triangular lattice in which superconductivity is induced by Pt substitution for Au. Au 4f and Te 3d core-level spectra of AuTe2 suggests a valence state of Au2+(Te2)2-, which is consistent with its distorted crystal structure with Te-Te dimers and compressed AuTe6 otahedra. On the other hand, valence-band photoemission spectra and pre-edge peaks of Te 3d absorption edge indicate that Au 5d bands are almost fully occupied and that Te 5p holes govern the transport properties and the lattice distortion. The two apparently conflicting pictures can be reconciled by strong Au 5d/Au 6s-Te 5p hybridization. Absence of a core-level energy shift with Pt substitution is inconsistent with the simple rigid band picture for hole doping. The Au 4f core-level spectrum gets slightly narrow with Pt substitution, indicating that the small Au 5d charge modulation in distorted AuTe2 is partially suppressed.Comment: 13 pages, 4 figures, accepted by Physical Review