771 research outputs found

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

    Full text link
    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

    Properties of charge density waves in La2−x_{2-x}Bax_{x}CuO4_4

    Full text link
    We report a comprehensive x-ray scattering study of charge density wave (stripe) ordering in La2−xBaxCuO4(x≈1/8)\rm La_{2-x}Ba_xCuO_4 (x \approx 1/8), for which the superconducting TcT_c is greatly suppressed. Strong superlattice reflections corresponding to static ordering of charge stripes were observed in this sample. The structural modulation at the lowest temperature was deduced based on the intensity of over 70 unique superlattice positions surveyed. We found that the charge order in this sample is described with one-dimensional charge density waves, which have incommensurate wave-vectors (0.23, 0, 0.5) and (0, 0.23, 0.5) respectively on neighboring CuO2\rm CuO_2 planes. The structural modulation due to the charge density wave order is simply sinusoidal, and no higher harmonics were observed. Just below the structural transition temperature, short-range charge density wave correlation appears, which develops into a large scale charge ordering around 40 K, close to the spin density wave ordering temperature. However, this charge ordering fails to grow into a true long range order, and its correlation length saturates at ∼230A˚\sim 230\AA, and slightly decreases below about 15 K, which may be due to the onset of two-dimensional superconductivity.Comment: 11 pages, 9 figure

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

    Full text link
    Charge-ordered manganites of composition Pr1−x(Ca1−ySry)xMnO3\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

    Get PDF
    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-L3_3 absorption edge (11.215∼\sim keV) that achieves an analyzer energy resolution of 3.9∼\simmeV, very close to the theoretical value of 3.7∼\simmeV. 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 Sr3_3Ir2_2O7_7. The novel sub-10∼\simmeV RIXS spectrometer thus provides a window into magnetic materials with small energy scales

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

    Get PDF
    We use resonant elastic and inelastic X-ray scattering at the Ir-L3L_3 edge to study the doping-dependent magnetic order, magnetic excitations and spin-orbit excitons in the electron-doped bilayer iridate (Sr1−x_{1-x}Lax_{x})3_3Ir2_2O7_7 (0≤x≤0.0650 \leq x \leq 0.065). With increasing doping xx, the three-dimensional long range antiferromagnetic order is gradually suppressed and evolves into a three-dimensional short range order from x=0x = 0 to 0.050.05, followed by a transition to two-dimensional short range order between x=0.05x = 0.05 and 0.0650.065. 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 (Sr1−x_{1-x}Lax_x)3_3Ir2_2O7_7 into a correlated metallic state hosting two-dimensional short range antiferromagnetic order and strong antiferromagnetic fluctuations of Jeff=12J_{\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

    Full text link
    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

    Doping dependence of charge-transfer excitations in La_{2-x}Sr_xCuO_4

    Full text link
    We report a resonant inelastic x-ray scattering (RIXS) study of the doping dependence of charge-transfer excitations in La2−xSrxCuO4\rm La_{2-x}Sr_xCuO_4. The mome ntum dependence of these charge excitations are studied over the whole Brillouin zone in underdoped (x=0.05) and optimally doped (x=0.17) samples, and compared with that of the undoped (x=0) sample. We observe a large change in the RIXS spectra between the x=0 and x=0.17 sample, while the RIXS spectra of the x=0.05 sample are similar to that of the x=0 sample. The most prominent effect of doped-holes on the charge excitation spectra is the appearance of a continuum of intensity, which exhibits a strong momentum-dependence below 2 eV. For the x=0.17 sample, some of the spectral weight from the lowest-lying charge-transfer excitation of the undoped compound is transferred to the continuum intensity below the gap, in agreement with earlier optical studies. However, the higher energy charge-transfer excitation carries significant spectral weight even for the x=0.17 sample. The doping dependence of the dispersion of this charge-transfer excitation is also discussed and compared with recent theoretical calculations.Comment: 7 pages, 6 figures, to appear in Phys. Rev.
    • …
    corecore