arXiv subjects

U. Staub

Publications and source records attributed to U. Staub.

At least 55 records · Page 3Linked to original sources

arXiv2011

Femtosecond dynamics of the collinear-to-spiral antiferromagnetic phase transition in CuO

We report on the ultrafast dynamics of magnetic order in a single crystal of CuO at a temperature of 207 K in response to strong optical excitation using femtosecond resonant x-ray diffraction. In the experiment, a femtosecond laser pulse induces a sudden, nonequilibrium increase in magnetic disorder. After a short delay ranging from 400 fs to 2 ps, we observe changes in the relative intensity of the magnetic ordering diffraction peaks that indicate a shift from a collinear commensurate phase to a spiral incommensurate phase. These results indicate that the ultimate speed for this antiferromagnetic re-orientation transition in CuO is limited by the long-wavelength magnetic excitation connecting the two phases.

cond-mat.str-el↗

arXiv2011

Competing Ferri- and Antiferromagnetic Phases in Geometrically Frustrated LuFe2O4

We present a detailed study of magnetism in LuFe2O4, combining magnetization measurements with neutron and soft x-ray diffraction. The magnetic phase diagram in the vicinity of T_N involves a metamagnetic transition separating an antiferro- and a ferrimagnetic phase. For both phases the spin structure is refined by neutron diffraction. Observed diffuse magnetic scattering far above T_N is explained in terms of near degeneracy of the magnetic phases.

cond-mat.str-el↗

arXiv2011

Origin of the large polarization in multiferroic YMnO$_3$ thin films revealed by soft and hard x-ray diffraction

We investigated the magnetic structure of an orthorhombic YMnO3 thin film by resonant soft x-ray and hard x-ray diffraction. We observed a temperature-dependent incommensurate magnetic reflection below 45 K and a commensurate lattice-distortion reflection below 35 K. These results demonstrate that the ground state is composed of coexisting E-type and cycloidal states. Their different ordering temperatures clarify the origin of the large polarization to be caused by the E-type antiferromagnetic states in the orthorhombic YMnO3 thin film.

cond-mat.str-el↗

arXiv2011

Triakontadipole and high-order dysprosium multipoles in the antiferromagnetic phase of DyB$_2$C$_2$

Resonant soft x-ray Bragg diffraction at the Dy M$_{4,5}$ edges has been used to study Dy multipoles in the combined magnetic and orbitally ordered phase of DyB$_2$C$_2$. The analysis incorporates both the intra-atomic magnetic and quadrupolar interactions between the 3d core and 4f valence shells. Additionally, we introduce to the formalism the interference of magnetic and nonmagnetic oscillators. This allows a determination of the higher order multipole moments of rank 1 (dipole) to 6 (hexacontatetrapole). The strength of the Dy 4f multipole moments have been estimated at being between 7 and 78 % of the quadrupolar moment.

cond-mat.str-el↗

arXiv2010

Doping and temperature dependence of Mn 3d states in A-site ordered manganites

We present a systematic study of the electronic structure in A-site ordered manganites as function of doping and temperature. The energy dependencies observed with soft x-ray resonant diffraction (SXRD) at the Mn L_{2,3} edges are compared with structural investigations using neutron powder diffraction as well as with cluster calculations. The crystal structures obtained with neutron powder diffraction reflect the various orbital and charge ordered phases and show an increase of the Mn-O-Mn bond angle as function of doping and temperature. Cluster calculations show that the observed spectral changes in SXRD as a function of doping are more pronounced than expected from an increase in bandwitdh due to the increase in Mn-O-Mn bond angle, and are best described by holes that are distributed at the neighbouring oxygen ions. These holes are not directly added to the Mn 3d shell, but centered at the Mn site. In contrast, the spectral changes in SXRD as function of temperature are best described by an increase of magnetic correlations. This demonstrates the strong correlations between orbitals and magnetic moments of the 3d states.

cond-mat.str-el↗

arXiv2009

Direct observation of charge order and orbital glass state in multiferroic LuFe2O4

Geometrical frustration of the Fe ions in LuFe2O4 leads to intricate charge and magnetic order and a strong magnetoelectric coupling. Using resonant x-ray diffraction at the Fe K edge, the anomalous scattering factors of both Fe sites are deduced from the (h/3 k/3 l/2) reflections. The chemical shift between the two types of Fe ions equals 4.0(1) eV corresponding to full charge separation into Fe2+ and Fe3+. Polarization and azimuthal angle dependence of the superlattice reflections demonstrates the absence of anisotropic scattering revealing random orientations of the Fe2+ orbitals characteristic of an orbital glass state.

cond-mat.str-el↗

arXiv2008

Magnetic and electronic Co states in layered cobaltate GdBaCo2O5.5-x

We have performed non-resonant x-ray diffraction, resonant soft and hard x-ray magnetic diffraction, soft x-ray absorption and x-ray magnetic circular dichroism measurements to clarify the electronic and magnetic states of the Co3+ ions in GdBaCo2O5.5. Our data are consistent with a 3+ Py Co HS state at the pyramidal sites and a 3+ Oc Co LS state at the octahedral sites. The structural distortion, with a doubling of the a axis (2ap x 2ap x 2ap cell), shows alternating elongations and contractions of the pyramids and indicates that the metal-insulator transition is associated with orbital order in the t2g orbitals of the 3+ Py Co HS state. This distortion corresponds to an alternating ordering of xz and yz orbitals along the a and c axes for the 3+ Py Co . The orbital ordering and pyramidal distortion lead to deformation of the octahedra, but the 3+ Oc Co LS state does not allow an orbital order to occur for the 3+ Oc Co ions. The soft x-ray magnetic diffraction results indicate that the magnetic moments are aligned in the ab plane but are not parallel to the crystallographic a or b axes. The orbital order and the doubling of the magnetic unit cell along the c axis support a non-collinear magnetic structure. The x-ray magnetic circular dichroism data indicate that there is a large orbital magnetic contribution to the total ordered Co moment.

cond-mat.str-el↗

arXiv2008

A Resonant soft x-ray powder diffraction study to determine the orbital ordering in A-site ordered SmBaMn2O6

Soft X-ray resonant powder diffraction has been performed at the Mn L2,3 edges of A-site ordered SmBaMn2O6. The energy and polarization dependence of the (1/2 1/2 0) reflection provide direct evidence for a (x2-z2)/(y2-z2) type orbital ordering in contrast to the single layer manganite. The temperature dependence of the reflection indicates an orbital reorientation transition at 210 K, below which the charge and orbital ordered MnO2 sheets show AAAA type of stacking. The concurring reduction of the ferromagnetic super exchange correlations leads to further charge localization.

cond-mat.str-el↗

arXiv2007

Manipulating the magnetic structure by electric fields in multiferroic ErMn2O5

Based on measurements of soft x-ray magnetic diffraction under in-situ applied electric field, wereport on significantly manipulation and exciting of commensurate magnetic order in multiferroic ErMn2O5. The induced magnetic scattering intensity arises at the commensurate magnetic Bragg position whereas the initial magnetic signal almost persists. We demonstrate the possibility to imprint a magnetic response function in ErMn2O5 by applying electric field.

cond-mat.str-el↗

arXiv2007

Direct observation of oxygen superstructures in manganites

We report the observation of superstructures associated with the oxygen 2p-states in two prototypical manganites using x-ray diffraction at the oxygen K-edge. We determine the nature of the orderings and discuss our picture with respect to novel theoretical models. In the stripe order system Bi0.31 Ca0.69 MnO3, hole-doped O states are found to be orbitally ordered, at the same propagation vector as the Mn orbital ordering, but no evidence is found to support a picture of oxygen charge stripes at this periodicity. In La 7/8 Sr 1/8 MnO3, we observe a 2p charge ordering described by alternating hole-poor and hole-rich MnO planes that is consistent with recent predictions.

cond-mat.str-el↗

arXiv2007

Role of oxygen vacancies in Cr-doped SrTiO3 for resistance-change memory

Transition-metal oxides exhibiting a bistable resistance state are attractive for non-volatile memory applications. The relevance of oxygen vacancies (VO) for the resistance-change memory was investigated with x-ray fluorescence, infrared microscopy, and x-ray absorption spectroscopy using Cr-doped SrTiO3 as example. We propose that the microscopic origin of resistance switching in this class of materials is due to an oxygen-vacancy drift occurring in close proximity to one of the electrodes.

cond-mat.mtrl-sci↗

arXiv2007

Resistive Switching in Cr doped SrTiO3: An X-ray Absorption Spectroscopy study

X-ray absorption spectroscopy was used to study the microscopic origin of conductance and resistive switching in chromium doped strontium titanate (Cr:SrTiO3). Differences in the x-ray absorption near edge spectroscopy (XANES) at the Cr K-edge indicate that the valence of Cr changes from 3+ to 4+ underneath the anode of our sample device after the application of an electric field. Spatially resolved x-ray fluorescence microscopy ($μ$-XRF) maps show that the Cr4+ region retracts from the anode-Cr:SrTiO3 interface after a conducting state has been achieved. This interface region is studied with extended x-ray absorption fine structure (EXAFS) and the results are compared with structural parameters obtained from density functional theory (DFT) calculations. They confirm that oxygen vacancies which are localized at the octahedron with a Cr at its center are introduced at the interface. It is proposed that the switching state is not due to a valence change of chromium but caused by changes of oxygen vacancies at the interface.

cond-mat.mtrl-sci↗

arXiv2006

Manipulating 4f quadrupolar pair interactions in TbB2C2 using a magnetic field

Resonant soft x-ray Bragg diffraction at the Tb M4,5 edges and non resonant Bragg diffraction have been used to investigate orbitals in TbB2C2. The Tb 4f quadrupole moments are ordered in zero field below T_N and show a ferroquadrupolar alignment dictated by the antiferromagnetic order. With increasing applied field along [110] the Tb 4f magnetic dipole moments rotate in a gradual manner toward the field. The quadrupole moment is rigidly coupled to the magnetic moment and follows this field-induced rotation. The quadrupolar pair interaction is found to depend on the specific orientation of the orbitals as predicted theoretically and can be manipulated with an applied magnetic field.

cond-mat.str-el↗

arXiv2006

What drives the charge/orbital ordering in La0.5Sr1.5MnO4: Jahn-Teller distortion versus orbital ordering

Temperature dependences of a magnetic and an orbital Bragg reflection at the Mn L2 and L3 edges of La0.5Sr1.5MnO4 have been collected. The temperature evolution of the orbital reflection depend strongly on the x-ray energy and reflects the different order parameteres for orbitals and Jahn-Teller distortions. The gradual increase of the orbital order parameter indicates that the orbital order and not the Jahn-Teller distortion drives the metal-insulator transition. Correspondingly, the orbital-orbital (super) exchange interaction dominates over the Jahn-Teller strain-field interaction.

cond-mat.str-el↗

arXiv2006

Role of magnetic and orbital ordering at the metal-insulator transition in NdNiO3

Soft x-ray resonant scattering at the Ni L2,3 edges is used to test models of magnetic and orbital-ordering below the metal-insulator transition in NdNiO3. The large branching ratio of the L3 to L2 intensities of the (1/2,0,1/2) reflection and the observed azimuthal angle and polarization dependence originates from a non collinear magnetic structure. The absence of an orbital signal and the non collinear magnetic structure show that the nickelates are materials for which orbital ordering is absent at the metal-insulator transition.

cond-mat.str-el↗

arXiv2006

High-order Dy multipole motifs observed in DyB2C2 with resonant soft x-ray Bragg diffraction

Resonant soft x-ray Bragg diffraction at the Dy M4,5 edges has been exploited to study Dy multipole motifs in DyB2C2. Our results are explained introducing the intra-atomic quadrupolar interaction between the core 3d and valence 4f shell. This allows us to determine for the first time higher order multipole moments of dysprosium $4f$ electrons and to draw their precise charge density. The Dy hexadecapole and hexacontatetrapole moment have been estimated at -20% and +30% of the quadrupolar moment, respectively. No evidence for the lock-in of the orbitals at T_N has been observed, in contrast to earlier suggestions. The multipolar interaction and the structural transition cooperate along c but they compete in the basal plane explaining the canted structure along [110].

cond-mat.str-el↗

arXiv2004

EPR study of some rare-earth ions (Dy3+, Tb3+ and Nd3+) in YBa2Cu3O6 compound

We investigate the low temperature X-band electron paramagnetic resonance (EPR) of YBa2Cu3O6 compounds with x = 6.0 doped with Dy3+, Tb3+, and Nd3+. The EPR spectra of Dy3+ and Tb3+ have been identified. The EPR of Tb3+ is used also to study the effect of suppression of high Tc superconductivity. The EPR of Nd3+ is probably masked by the intense resonance of Cu2+. All experimental EPR results compare well with theoretical estimations.

cond-mat.supr-con↗

arXiv2000

Magnetic Phase Transitions in the double spin-chains compound $\rm LiCu_2O_2$

We report high-resolution x-ray diffraction, muon-spin-rotation spectroscopic and specific heat measurements in the double spin-chains compound $\rm LiCu_2O_2$. The x-ray diffraction results show that the crystal structure of $\rm LiCu_2O_2$ ~is orthorhombic down to T=10K. Anisotropic line-broadening of the diffraction peaks is observed, indicating disorder along the spin chains. Muon spin relaxation and specific heat measurements show that $\rm LiCu_2O_2$ ũndergoes a phase transition to a magnetic ordered state at $\rm T_1\sim24K$. The specific heat data exhibits a second $\rm λ$-like peak at $\rm T_2\sim22.5 K$, which increases with increasing magnetic field similarly way to that found in spin-ladder compounds.

cond-mat.str-el↗