arXiv subjects

G. Kaindl

Publications and source records attributed to G. Kaindl.

At least 19 recordsLinked to original sources

arXiv2008

Temperature-induced reversal of magnetic interlayer exchange coupling

For epitaxial trilayers of the magnetic rare-earth metals Gd and Tb, exchange coupled through a non-magnetic Y spacer layer, element-specific hysteresis loops were recorded by the x-ray magneto-optical Kerr effect at the rare-earth $M_5$ thresholds. This allowed us to quantitatively determine the strength of interlayer exchange coupling (IEC). In addition to the expected oscillatory behavior as a function of spacer-layer thickness $d_Y$, a temperature-induced sign reversal of IEC was observed for constant $d_Y$, arising from magnetization-dependent electron reflectivities at the magnetic interfaces.

cond-mat.mtrl-sci↗

arXiv2008

Resonant soft x-ray scattering from stepped surfaces of SrTiO3

We studied the resonant diffraction signal from stepped surfaces of SrTiO3 at the Ti 2p -> 3d (L2,3) resonance in comparison with x-ray absorption (XAS) and specular reflectivity data. The steps on the surface form an artificial superstructure suited as a model system for resonant soft x-ray diffraction. A small step density on the surface is sufficient to produce a well defined diffraction peak, showing the high sensitivity of the method. At larger incidence angles, the resonant diffraction spectrum from the steps on the surface resembles the spectrum for specular reflectivity. Both deviate from the XAS data in the relative peak intensities and positions of the peak maxima. We determined the optical parameters of the sample across the resonance and found that the differences between the XAS and scattering spectra reflect the different quantities probed in the different signals. When recorded at low incidence or detection angles, XAS and specular reflectivity spectra are distorted by the changes of the angle of total reflection with energy. Also the step peak spectra, though less affected, show an energy shift of the peak maxima in grazing incidence geometry.

cond-mat.str-el↗

arXiv2007

Direct observation of t2g orbital ordering in magnetite

Using soft-x-ray diffraction at the site-specific resonances in the Fe L23 edge, we find clear evidence for orbital and charge ordering in magnetite below the Verwey transition. The spectra show directly that the (001/2) diffraction peak (in cubic notation) is caused by t2g orbital ordering at octahedral Fe2+ sites and the (001) by a spatial modulation of the t2g occupation.

cond-mat.str-el↗

arXiv2007

Effects of impurities on Tamm-like lanthanide-metal surface states

The effects of isolated residual-gas adsorbates on the local electronic structure of the Dy(0001) surface were spatially mapped by scanning tunneling microscopy and spectroscopy at 12 K. Less than 15 A away from an adsorbate, a strong reduction of the intensity and a significant increase of the width of the majority component of the surface state due to impurity scattering were observed, with essentially no change of the minority component; this reflects a high lateral localization of the Tamm-like surface state. Furthermore, an adsorbate-induced state was found that behaves metastable.

cond-mat.mtrl-sci↗

arXiv2005

Surface-electronic structure of La(0001) and Lu(0001)

Most spectroscopic methods for studying the electronic structure of metal surfaces have the disadvantage that either only occupied or only unoccupied states can be probed, and the signal is cut at the Fermi edge. This leads to significant uncertainties, when states are very close to the Fermi level. By performing low-temperature scanning tunneling spectroscopy and ab initio calculations, we study the surface-electronic structure of La(0001) and Lu(0001), and demonstrate that in this way detailed information on the surface-electronic structure very close to the Fermi energy can be derived with high accuracy.

cond-mat.mtrl-sci↗

arXiv2005

Magnetism of ordered Sm/Co(0001) surface structures

The epitaxial system Sm/Co(0001) was studied for Sm coverages up to 1 monolayer (ML) on top of ultrathin Co/W(110) epitaxial films. Two ordered phases were found for 1/3 and 1 ML Sm, respectively. The valence state of Sm was determined by means of photoemission and magnetic properties were measured by magneto-optical Kerr effect. We find that 1 ML Sm causes a strong increase of the coercivity with respect to that of the underlying 10 ML Co film. Element-specific hysteresis loops, measured by using resonant soft x-ray reflectivity, show the same magnetic behaviour for the two elements.

cond-mat.mtrl-sci↗

arXiv2005

X-Ray Scattering at Lanthanide M5 Resonances: Application to Magnetic Depth Profiling

Quantitative analyses of x-ray scattering from thin films of Ho and Dy metal at the M_5 resonances result in values of the optical constants and the magnetic scattering lengths f_m, with f_m as large as 200 r_0. The observation of first- and second-order magnetic satellites allows to separate f_m into circular and linear dichroic contributions. This high magnetic sensitivity, in conjunction with the tunable x-ray probing depth across the resonance can be applied to monitor depth profiles of complex magnetic structures, as e.g. of helical antiferromagnetic domains in a Dy metal film.

cond-mat.other↗

arXiv2005

X-ray magneto-optics of lanthanide materials: principles and applications

Lanthanide metals are a particular class of magnetic materials in which the magnetic moments are carried mainly by the localized electrons of the 4f shell. They are frequently found in technically relevant systems, to achieve, e.g., high magnetic anisotropy. Magneto-optical methods in the x-ray range are well suited to study complex magnetic materials in an element-specific way. In this work, we report on recent progress on the quantitative determination of magneto-optical constants of several lanthanides in the soft x-ray region and we show some examples of applications of magneto-optics to hard-magnetic interfaces and exchange-coupled layered structures containing lanthanide elements.

cond-mat.mtrl-sci↗

arXiv2005

Lifetime Widths of Surface States on Magnetic Lanthanide Metals

Low-temperature scanning tunneling spectroscopy is used to study electronic structure and dynamics of d-like surface states of trivalent lanthanide metals from La to Lu. The magnetic exchange splitting of these states is found to scale with the 4f spin multiplied by an effective exchange-coupling constant that increases with 4f occupancy in an approximately linear way. The dynamics of the surfaces states, as revealed by the lifetime width, is dominated by electron-phonon scattering in the occupied region and by electron-magnon scattering in the unoccupied region, respectively.

cond-mat.other↗

arXiv2005

Electronic Structure and Dynamics of Quantum-Well States in thin Yb-Metal Films

Quantum-well states above the Fermi energy in thin Yb(111)-metal films deposited on a W(110) single crystal were studied by low-temperature scanning tunneling spectroscopy. These states are laterally highly localized and give rise to sharp peaks in the tunneling spectra. A quantitative analysis of the spectra yields the bulk-band dispersion in Gamma - L direction as well as quasi-particle lifetimes. The quadratic energy dependence of the lifetimes is in quantitative agreement with Fermi-liquid theory.

cond-mat.other↗

arXiv2005

Spectroscopy of stripe order in La1.8Sr0.2NiO4 using resonant soft x-ray diffraction

Strong resonant enhancements of the charge-order and spin-order superstructure-diffraction intensities in La1.8Sr0.2NiO4 are observed when x-ray energies in the vicinity of the Ni L2,3 absorption edges are used. The pronounced photon-energy and polarization dependences of these diffraction intensities allow for a critical determination of the local symmetry of the ordered spin and charge carriers. We found that not only the antiferromagnetic order but also the charge-order superstructure resides within the NiO2 layers; the holes are mainly located on in-plane oxygens surrounding a Ni2+ site with the spins coupled antiparallel in close analogy to Zhang-Rice singlets in the cuprates.

cond-mat.str-el↗

arXiv2004

Rashba Effect at Magnetic Metal Surfaces

We give experimental and theoretical evidence of the Rashba effect at the magnetic rare-earth metal surface Gd(0001). The Rashba effect is substantially enhanced and the Rashba parameter changes its sign when a metal-oxide surface layer is formed. The experimental observations are quantitatively described by ab initio calculations that give a detailed account of the near-surface charge density gradients causing the Rashba effect. Since the sign of the Rashba splitting depends on the magnetization direction, the findings open up new opportunities for the study of surface and interface magnetism.

cond-mat.mtrl-sci↗

arXiv2003

Magneto-optics of Gd and Tb in the soft x-ray resonance regions

We present x-ray absorption spectra around the 3d-4f and 4d-4f excitation thresholds of in-plane magnetized Gd and Tb films measured by total electron yield using circularly polarized synchrotron radiation. By matching the experimental spectra to tabulated absorption data far below and above the thresholds, the imaginary parts of the complex refractive index are determined quantitatively. The associated real parts for circularly polarized light propagating nearly parallel or antiparallel to the magnetization direction are obtained through the Kramers-Kronig relations. The derived magnetooptical parameters are used to calculate soft x-ray reflectivity spectra of a magnetized Gd film at the 3d-4f threshold, which are found to compare well with our experimental spectra.

cond-mat.mtrl-sci↗

arXiv2003

Metal-insulator Crossover Behavior at the Surface of NiS_2

We have performed a detailed high-resolution electron spectroscopic investigation of NiS$_2$ and related Se-substituted compounds NiS$_{2-x}$Se$_x$, which are known to be gapped insulators in the bulk at all temperatures. A large spectral weight at the Fermi energy of the room temperature spectrum, in conjunction with the extreme surface sensitivity of the experimental probe, however, suggests that the surface layer is metallic at 300 K. Interestingly, the evolution of the spectral function with decreasing temperature is characterized by a continuous depletion of the single-particle spectral weight at the Fermi energy and the development of a gap-like structure below a characteristic temperature, providing evidence for a metal-insulator crossover behavior at the surfaces of NiS$_2$ and of related compounds. These results provide a consistent description of the unusual transport properties observed in these systems.

cond-mat.str-el↗

arXiv2002

Prediction of huge X-ray Faraday rotation at the Gd N_4,5 threshold

X-ray absorption spectra in a wide energy range around the 4d-4f excitation threshold of Gd were recorded by total electron yield from in-plane magnetized Gd metal films. Matching the experimental spectra to tabulated absorption data reveals unprecedented short light absorption lengths down to 3 nm. The associated real parts of the refractive index for circularly polarized light propagating parallel or antiparallel to the Gd magnetization, determined through the Kramers-Kronig transformation, correspond to a magneto-optical Faraday rotation of 0.7 degrees per atomic layer. This finding shall allow the study of magnetic structure and magnetization dynamics of lanthanide elements in nanosize systems and dilute alloys.

cond-mat.mtrl-sci↗

arXiv2001

The distribution of the doped holes in La2-xSrxCu1-yRuyO4-(delta)

We present a systematic study of the perovskite-related system La2-xSrxCu1-yRuyO4 using Cu-L2,3, Ru-L2,3, and O-K x-ray absorption spectroscopy (XAS). This system can be regarded as a solid solution of the two superconductors La2-xSrxCuO4 and Sr2RuO4, and thus the question as to the destination of the holes induced by Sr doping is central to our understanding of these novel systems. The comparison of the experimental data with state-of-the-art crystal-field-multiplet calculations shows clearly that the charge balance for x/2y >1 is predominantly achieved by an increase of the Ru valence from Ru(IV) to Ru(V), while Cu remains in the Cu(II) oxidation state.

cond-mat.str-el↗

arXiv2001

Localisation of doped holes in edge-shared CuO_2 chain cuprates: consequences for dynamic spectral weight transfer

We present a joint experimental and theoretical study of the electronic structure of the cuprate chain systems A_(1-x)CuO_2 (A=Ca,Sr,Ba), as measured using O-K and Cu-L_3 x-ray absorption spectroscopy. The doping-dependent behaviour in these systems is radically different to that in conventional 2D cuprate networks formed from corner sharing CuO_4 plaquettes, and follows from the strongly suppressed inter-plaquette hybridisation resulting from the 90 degree Cu-O-Cu interaction pathway in the chain systems. Spectroscopically, this results in (a) a classical mixed-valent scenario whereby the different final states in the Cu-L_3 spectra can be used directly to 'read-off' the Cu valency and (b) a drastic reduction in the dynamic spectral weight transfer from the upper Hubbard band to the low energy scale in the O-K spectra. The final picture emerges of localisation of the doped holes, with the chain then comprised of a mixture of pure Cu(II)O_4 and Cu(III)O_4 plaquettes.

cond-mat.str-el↗

arXiv2001

The electronic structure of the doped one-dimensional transition metal oxide Y1-xCaxBaNiO5 studied using x-ray absorption

A strong anisotropic distribution of the holes in Ni 3d and O 2p orbitals is observed in the polarization dependent O1s and Ni2p3/2 x-ray absorption spectroscopy of the linear-chain nickelate Y1-xCaxBaNiO5 (x = 0, 0.05, 0.1, 0.2), which demonstrates the one-dimensional nature of the electronic state in these compounds. Furthermore, the additional holes introduced by Ca-doping occupy both O 2p and Ni 3d orbitals along the NiO5 chains. By comparing the experimental Ni 2p3/2 absorption spectra of Y1-xCaxBaNiO5 to those from charge transfer multiplet calculations we can derive the orbital character of the additional holes to be of ca. 60% O2p and ca. 40% Ni 3d.

cond-mat.str-el↗