arXiv subjects

M. v. Zimmermann

Publications and source records attributed to M. v. Zimmermann.

63 records · Page 4Linked to original sources

arXiv2003

Effect of a magnetic field on the spin- and charge-density wave order in La1.45Nd0.4Sr0.15CuO4

The spin-density wave (SDW) and charge-density wave (CDW) order in superconducting La1.45Nd0.4Sr0.15CuO4 were studied under an applied magnetic field using neutron and X-ray diffraction techniques. In zero field, incommensurate (IC) SDW order appears below ~ 40 K, which is characterized by neutron diffraction peaks at (1/2 +/- 0.134, 1/2 +/- 0.134, 0). The intensity of these IC peaks increases rapidly below T_Nd ~ 8 K due to an ordering of the Nd^3+ spins. The application of a 1 T magnetic field parallel to the c-axis markedly diminishes the intensity below T_Nd, while only a slight decrease in intensity is observed at higher temperatures for fields up to 7 T. Our interpretation is that the c-axis field suppresses the parasitic Nd^3+ spin order at the incommensurate wave vector without disturbing the stripe order of Cu^2+ spins. Consistent with this picture, the CDW order, which appears below 60 K, shows no change for magnetic fields up to 4 T. These results stand in contrast to the significant field-induced enhancement of the SDW order observed in superconducting La2-xSrxCuO4 with x ~ 0.12 and stage-4 La2CuO4+y. The differences can be understood in terms of the relative volume fraction exhibiting stripe order in zero field, and the collective results are consistent with the idea that suppression of superconductivity by vortices nucleates local patches of stripe order.

cond-mat.supr-con↗

arXiv2001

Orbital Correlations in Doped Manganites

We review our recent x-ray scattering studies of charge and orbital order in doped manganites, with specific emphasis on the role of orbital correlations in Pr_1-xCa_xMnO_3. For x=0.25, we find an orbital structure indistinguishable from the undoped structure with long range orbital order at low temperatures. For dopings 0.3<x<0.5, we find scattering consistent with a charge and orbitally ordered CE-type structure. While in each case the charge order peaks are resolution limited, the orbital order exhibits only short range correlations. We report the doping dependence of the correlation length and discuss the connection between the orbital correlations and the finite magnetic correlation length observed on the Mn^3+ sublattice with neutron scattering techniques. The physical origin of these domains, which appear to be isotropic, remains unclear. We find that weak orbital correlations persist well above the phase transitions, with a correlation length of 1-2 lattice constants at high temperatures. Significantly, we observe similar correlations at high temperatures in La_0.7Ca_0.3MnO_3, which does not have an orbitally ordered ground state, and we conclude that such correlations are robust to variations in the relative strength of the electron-phonon coupling.

cond-mat.str-el↗

arXiv2001

A Resonant X-ray Scattering Study of Octahedral Tilt Ordering in LaMnO$_3$ and Pr$_{1-x}$Ca$_x$MnO$_3$

We report an x-ray scattering study of octahedral tilt ordering in the manganite series Pr$_{1-x}$Ca$_x$MnO$_3$ with x=0.4 and 0.25 and in LaMnO$_3$. The sensitivity to tilt ordering is achieved by tuning the incident x-ray energy to the L$_I$, L$_{II}$ and L$_{III}$ absorption edges of Pr and La, respectively. The resulting energy-dependent profiles are characterized by a dipole-resonant peak and higher energy fine structure. The polarization dependence is predominantly $σ$-to-$π$ and the azimuthal dependence follows a sin-squared behavior. These results are similar to those obtained in recent x-ray scattering studies of orbital ordering carried out in these same materials at the Mn K edge. They lead to a description of the cross-section in terms of Templeton scattering in which the tilt ordering breaks the symmetry at the rare earth site. The most interesting result of the present work is our observation that octahedral tilt ordering persists above the orbital ordering transition temperatures in all three samples. Indeed, we identify separate structural transitions which may be associated with the onset of orbital and tilt ordering, respectively, and characterize the loss of tilt ordering versus temperature in LaMnO$_3$.

cond-mat.str-el↗

arXiv2000

Correlated Polarons in Dissimilar Perovskite Manganites

We report x-ray scattering studies of broad peaks located at a (0.5 0 0)/(0 0.5 0)-type wavevector in the paramagnetic insulating phases of La_{0.7}Ca_{0.3}MnO_{3} and Pr_{0.7}Ca_{0.3}MnO_{3}. We interpret the scattering in terms of correlated polarons and measure isotropic correlation lengths of 1-2 lattice constants in both samples. Based on the wavevector and correlation lengths, the correlated polarons are found to be consistent with CE-type bipolarons. Differences in behavior between the samples arise as they are cooled through their respective transition temperatures and become ferromagnetic metallic (La_{0.7}Ca_{0.3}MnO_{3}) or charge and orbitally ordered insulating (Pr_{0.7}Ca_{0.3}MnO_{3}). Since the primary difference between the two samples is the trivalent cation size, these results illustrate the robust nature of the correlated polarons to variations in the relative strength of the electron-phonon coupling, and the sensitivity of the low-temperature ground state to such variations.

cond-mat.str-el↗

arXiv2000

Spin Dynamics and Orbital State in LaTiO_3

A neutron scattering study of the Mott-Hubbard insulator LaTiO$_{3}$ (T$_{\rm N}=132$ K) reveals a spin wave spectrum that is well described by a nearest-neighbor superexchange constant $J=15.5$ meV and a small Dzyaloshinskii-Moriya interaction ($D=1.1$ meV). The nearly isotropic spin wave spectrum is surprising in view of the absence of a static Jahn-Teller distortion that could quench the orbital angular momentum, and it may indicate strong orbital fluctuations. A resonant x-ray scattering study has uncovered no evidence of orbital order in LaTiO$_{3}$.

cond-mat.str-el↗

arXiv2000

X-ray Anomalous Scattering Study of a Charge-Ordered State in NaV2O5

Charge ordering of V4+ and V5+ in NaV2O5 has been studied by an X-ray diffraction technique using anomalous scattering near a vanadium K-absorption edge to critically enhance a contrast between the two ions. A dramatic energy dependence of the superlattice intensities is observed below Tc=35 K. Consequently, the charge ordering pattern is the zigzag-type ladders with the unit cell 2a*2b*4c, but not the chain-type originally proposed for the spin-Peierls state. Charge disproportionation suggested in our model as the average valence V^{4.5+-delta_c/2} is observed below T_C, showing continuous variation of delta_c as a function of temperature.

cond-mat.str-el↗

arXiv2000

X-ray Resonant Scattering Studies of Orbital and Charge Ordering in Pr$_{1-x}$Ca$_x$MnO$_3$

We present the results of a systematic x-ray scattering study of the charge and orbital ordering in the manganite series Pr$_{1-x}$Ca$_x$MnO$_3$ with $x$=0.25, 0.4 and 0.5. The temperature dependence of the scattering at the charge and orbital wavevectors, and of the lattice constants, was characterized throughout the ordered phase of each sample. It was found that the charge and orbital order wavevectors are commensurate with the lattice, in striking contrast to the results of earlier electron diffraction studies of samples with $x$=0.5. High momentum-transfer resolution studies of the x=0.4 and 0.5 samples further revealed that while long-range charge order is present, long-range orbital order is never established. Above the charge/orbital ordering temperature T$_o$, the charge order fluctuations are more highly correlated than the orbital fluctuations. This suggests that charge order drives orbital order in these samples. In addition, a longitudinal modulation of the lattice with the same periodicity as the charge and orbital ordering was discovered in the x=0.4 and 0.5 samples. For x=0.25, only long-range orbital order was observed with no indication of charge ordering, nor of an additional lattice modulation. We also report the results of a preliminary investigation of the loss of charge and orbital ordering in the x=0.4 sample by application of a magnetic field. Finally, the polarization and azimuthal dependence of the charge and orbital ordering in these compounds is characterized both in the resonant and nonresonant limits, and compared with the predictions of current theories. The results are qualitatively consistent with both cluster and LDA+U calculations of the electronic structure.

cond-mat.str-el↗

arXiv1999

Oxygen Ordering Superstructures and Structural Phase Diagram of YBa_2Cu_3O_{6+x} Studied by Hard X-ray Diffraction

High energy x-ray diffraction is used to investigate the bulk oxygen ordering properties of YBa_2Cu_3O_{6+x}. Superstructures of Cu-O chains aligned along the b axis and ordered with periodicity ma, along the a axis have been observed. For $x < 0.62$ the only observed superstructure is ortho-II with m=2. At room temperature we find ortho-III (m=3) for $0.72\le x\le 0.82$, ortho-V (m=5) in a mixed state with ortho-II at x=0.62, and ortho-VIII (m=8) at x=0.67. Ortho-II is a 3D ordered structural phase, the remaining ones are essentially 2D. None of the superstructures develops long range ordering. Studies of the ortho-II ordering properties in samples prepared with x=0.5 but by different methods show that finite size domains with internal thermodynamic equilibrium are formed. The crystal perfection as well as the thermal annealing history determine the domain size. The temperature dependence of the observed superstructure ordering is investigated explicitly and a structural phase diagram is presented.

cond-mat.supr-con↗

arXiv1999

Interplay between charge, orbital and magnetic order in Pr_{1-x}Ca_xMnO_3

We report resonant x-ray scattering studies of charge and orbital order in Pr_{1-x}Ca_{x}MnO_3 with x=0.4 and 0.5. Below the ordering temperature, T_O=245 K, the charge and orbital order intensities follow the same temperature dependence, including an increase at the antiferromagnetic ordering temperature, T_N. High resolution measurements reveal, however, that long range orbital order is never achieved. Rather, an orbital domain state is formed. Above T_O, the charge order fluctuations are more highly correlated than the orbital fluctuations. Similar phenomenology is observed in a magnetic field. We conclude that the charge order drives the orbital order at the transition.

cond-mat.str-el↗