Angular dependence of the magnetization of isotropic superconductors: which is the vortex direction?

We present studies of the dc magnetization of thin platelike samples of the isotropic type II superconductor PbTl(10%), as a function of the angle between the normal to the sample and the applied magnetic field ${\bf H}$. We determine the magnetization vector ${\bf M}$ by measuring the components both parallel and normal to ${\bf H}$ in a SQUID magnetometer, and we further decompose it in its reversible and irreversible contributions. The behavior of the reversible magnetization is well understood in terms of minimization of the free energy taking into account geometrical effects. In the mixed state at low fields, the dominant effect is the line energy gained by shortening the vortices, thus the flux lines are almost normal to the sample surface. Due to the geometrical constrain, the irreversible magnetization ${\bf M}_{irr}$ remains locked to the sample normal over a wide range of fields and orientations, as already known. We show that in order to undestand the angle and field dependence of the modulus of ${\bf M}_{irr}$, which is a measure of the vortex pinning, and to correctly extract the field dependent critical current density, the knowledge of the modulus and orientation of the induction field ${\bf B}$ is required.Comment: 11 pages, 6 figure

Magnetic field dependence of charge stripe order in La2-xBaxCuO4 (x~1/8)

We have carried out a detailed investigation of the magnetic field dependence of charge ordering in La2-xBaxCuO4 (x~1/8) utilizing high-resolution x-ray scattering. We find that the charge order correlation length increases as the magnetic field greater than ~5T is applied in the superconducting phase (T=2K). The observed unusual field dependence of the charge order correlation length suggests that the static charge stripe order competes with the superconducting ground state in this sample.Comment: 4 pages, 4 figure

Charge-transfer exciton in La2CuO4 probed with resonant inelastic x-ray scattering

We report a high-resolution resonant inelastic x-ray scattering study of La2CuO4. A number of spectral features are identified that were not clearly visible in earlier lower-resolution data. The momentum dependence of the spectral weight and the dispersion of the lowest energy excitation across the insulating gap have been measured in detail. The temperature dependence of the spectral features was also examined. The observed charge transfer edge shift, along with the low dispersion of the first charge transfer excitation are attributed to the lattice motion being coupled to the electronic system. In addition, we observe a dispersionless feature at 1.8 eV, which is associated with a d-d crystal field excitation.Comment: 5 pages, 4 figure

Persistent X-Ray Photoconductivity and Percolation of Metallic Clusters in Charge-Ordered Manganites

Charge-ordered manganites of composition $\rm Pr_{1-x}(Ca_{1-y}Sr_{y})_{x}MnO_3$ exhibit persistent photoconductivity upon exposure to x-rays. This is not always accompanied by a significant increase in the {\it number} of conduction electrons as predicted by conventional models of persistent photoconductivity. An analysis of the x-ray diffraction patterns and current-voltage characteristics shows that x-ray illumination results in a microscopically phase separated state in which charge-ordered insulating regions provide barriers against charge transport between metallic clusters. The dominant effect of x-ray illumination is to enhance the electron {\it mobility} by lowering or removing these barriers. A mechanism based on magnetic degrees of freedom is proposed.Comment: 8 pages, 4 figure

Quartz-based flat-crystal resonant inelastic x-ray scattering spectrometer with sub-10 meV energy resolution

Continued improvement of the energy resolution of resonant inelastic x-ray scattering (RIXS) spectrometers is crucial for fulfilling the potential of this technique in the study of electron dynamics in materials of fundamental and technological importance. In particular, RIXS is the only alternative tool to inelastic neutron scattering capable of providing fully momentum resolved information on dynamic spin structures of magnetic materials, but is limited to systems whose magnetic excitation energy scales are comparable to the energy resolution. The state-of-the-art spherical diced crystal analyzer optics provides energy resolution as good as 25 meV but has already reached its theoretical limit. Here, we demonstrate a novel sub-10meV RIXS spectrometer based on flat-crystal optics at the Ir-L$_3$ absorption edge (11.215$\sim$ keV) that achieves an analyzer energy resolution of 3.9$\sim$meV, very close to the theoretical value of 3.7$\sim$meV. In addition, the new spectrometer allows efficient polarization analysis without loss of energy resolution. The performance of the instrument is demonstrated using longitudinal acoustical and optical phonons in diamond, and magnon in Sr$_3$Ir$_2$O$_7$. The novel sub-10$\sim$meV RIXS spectrometer thus provides a window into magnetic materials with small energy scales

X-ray induced electronic structure change in CuIr2_2S4_4

The electronic structure of CuIr$_2$S$_4$ has been investigated using various bulk-sensitive x-ray spectroscopic methods near the Ir $L_3$-edge: resonant inelastic x-ray scattering (RIXS), x-ray absorption spectroscopy in the partial fluorescence yield (PFY-XAS) mode, and resonant x-ray emission spectroscopy (RXES). A strong RIXS signal (0.75 eV) resulting from a charge-density-wave gap opening is observed below the metal-insulator transition temperature of 230 K. The resultant modification of electronic structure is consistent with the density functional theory prediction. In the spin- and charge- dimer disordered phase induced by x-ray irradiation below 50 K, we find that a broad peak around 0.4 eV appears in the RIXS spectrum.Comment: 4 pages and 4 figure

Doping Evolution of Magnetic Order and Magnetic Excitations in (Sr1−x_{1-x}Lax_x)3_3Ir2_2O7_7

We use resonant elastic and inelastic X-ray scattering at the Ir-$L_3$ edge to study the doping-dependent magnetic order, magnetic excitations and spin-orbit excitons in the electron-doped bilayer iridate (Sr$_{1-x}$La$_{x}$)$_3$Ir$_2$O$_7$ ($0 \leq x \leq 0.065$). With increasing doping $x$, the three-dimensional long range antiferromagnetic order is gradually suppressed and evolves into a three-dimensional short range order from $x = 0$ to $0.05$, followed by a transition to two-dimensional short range order between $x = 0.05$ and $0.065$. Following the evolution of the antiferromagnetic order, the magnetic excitations undergo damping, anisotropic softening and gap collapse, accompanied by weakly doping-dependent spin-orbit excitons. Therefore, we conclude that electron doping suppresses the magnetic anisotropy and interlayer couplings and drives (Sr$_{1-x}$La$_x$)$_3$Ir$_2$O$_7$ into a correlated metallic state hosting two-dimensional short range antiferromagnetic order and strong antiferromagnetic fluctuations of $J_{\text{eff}} = \frac{1}{2}$ moments, with the magnon gap strongly suppressed.Comment: 6 Pages, 3 Figures, with supplementary in Sourc

Equilibrium tuned by a magnetic field in phase separated manganite

We present magnetic and transport measurements on La5/8-yPryCa3/8MnO3 with y = 0.3, a manganite compound exhibiting intrinsic multiphase coexistence of sub-micrometric ferromagnetic and antiferromagnetic charge ordered regions. Time relaxation effects between 60 and 120K, and the obtained magnetic and resistive viscosities, unveils the dynamic nature of the phase separated state. An experimental procedure based on the derivative of the time relaxation after the application and removal of a magnetic field enables the determination of the otherwise unreachable equilibrium state of the phase separated system. With this procedure the equilibrium phase fraction for zero field as a function of temperature is obtained. The presented results allow a correlation between the distance of the system to the equilibrium state and its relaxation behavior.Comment: 13 pages, 5 figures. Submited to Journal of Physics: Condensed Matte