K. Fauth

Lowering of the L10 ordering temperature of FePt nanoparticles by He+ ion irradiation

Arrays of FePt particles (diameter 7nm) with mean interparticle distances of 60nm are prepared by a micellar technique on Si substrates. The phase transition of these magnetic particles towards the chemically ordered L10 phase is tracked for 350kV He+ ion irradiated samples and compared to a nonirradiated reference. Due to the large separation of the magnetically decoupled particles the array can be safely annealed without any agglomeration as usually observed for more densely packed colloidal FePt nanoparticles. The He+ ion exposure yields a significant reduction of the ordering temperature by more than 100K.

A guideline for atomistic design and understanding of ultrahard nanomagnets.

Magnetic nanoparticles are of immense current interest because of their possible use in biomedical and technological applications. Here we demonstrate that the large magnetic anisotropy of FePt nanoparticles can be significantly modified by surface design. We employ X-ray absorption spectroscopy offering an element-specific approach to magnetocrystalline anisotropy and the orbital magnetism. Experimental results on oxide-free FePt nanoparticles embedded in Al are compared with large-scale density functional theory calculations of the geometric- and spin-resolved electronic structure, which only recently have become possible on world-leading supercomputer architectures. The combination of both approaches yields a more detailed understanding that may open new ways for a microscopic design of magnetic nanoparticles and allows us to present three rules to achieve desired magnetic properties. In addition, concrete suggestions of capping materials for FePt nanoparticles are given for tailoring both magnetocrystalline anisotropy and magnetic moments.

How well does total electron yield measure x-ray absorption in nanoparticles?

The possibility to quantitatively analyze total electron yield (TEY) spectra as a measure of the x-ray absorption cross section from supported magnetic nanoparticles is explored by a combination of experiments and Monte Carlo simulations. Unless the particles are very small, it is found that saturation effects are important and can lead to a severe underestimation of the magnetic moments, when the magneto-optical sum rules are straightforwardly applied to experimental data. However, unlike for planar samples the possibility to examine and correct the saturation effects by varying the x-ray angle of incidence is not given, the absorption profiles are largely unaffected in their shape. The Monte Carlo simulations, appropriately conducted for the material under investigation, provide an estimate of the saturation effects occurring in nanoparticle TEY data.

The X-ray microscopy beamline UE46-PGM2 at BESSY

The Max Planck Institute for Metal Physics in Stuttgart and the Helmholtz Center Berlin operate a soft X‐ray microscopy beamline at the storage ring BESSY II. A collimated PGM serves as monochromator for a scanning X‐ray microscope and a full field X‐ray microscope at the helical undulator UE46. The selection between both instruments is accomplished via two switchable focusing mirrors. The scanning microscope (SM) is based on the ALS STXM microscope and fabricated by the ACCEL company. The full field microscope (FFM) is currently in operation at the U41‐SGM beamline and will be relocated to its final location this year.

Vortex dynamics in Permalloy disks with artificial defects: suppression of the gyrotropic mode

The dynamics of magnetic vortices in thin Permalloy disks having artificial defects in the form of small holes at different locations within the disk has been investigated by means of frequency-domain spatially resolved ferromagnetic resonance. It is found that the vortex can be effectively captured by such a defect. Consequently the commonly observed gyrotropic vortex motion in an applied microwave field of 1mT is suppressed. However, if in addition a static magnetic field of at least 4.3mT is applied, the vortex core is nucleated from the artificial defect and a modified gyrotropic motion starts again.

Strong influence of defects on the electronic structure of Pt adatoms and clusters on graphite

Abstract We study the specific impact of defects such as step edges at the graphite surface on the electronic configuration of adsorbed Pt atoms and Pt 8 clusters. Surface diffusion is strongly reduced by depositing Pt and Pt 8 into a thin rare gas layer. In this configuration a very narrow adatom Pt 4f spectrum is found at an exceptionally small binding energy, similar to Pt surfaces. Both, adatom and cluster spectra are strongly shifted towards higher binding energy when allowed to diffuse towards defects like step edges. The strong shifts are indicative of a chemical reaction at the step edges and are conjectured to be part of the particle size dependent binding energy shifts typically observed for transition metal clusters grown on the surface of graphite.

Dual nature of magnetic dopants and competing trends in topological insulators

Topological insulators interacting with magnetic impurities have been reported to host several unconventional effects. These phenomena are described within the framework of gapping Dirac quasiparticles due to broken time-reversal symmetry. However, the overwhelming majority of studies demonstrate the presence of a finite density of states near the Dirac point even once topological insulators become magnetic. Here, we map the response of topological states to magnetic impurities at the atomic scale. We demonstrate that magnetic order and gapless states can coexist. We show how this is the result of the delicate balance between two opposite trends, that is, gap opening and emergence of a Dirac node impurity band, both induced by the magnetic dopants. Our results evidence a more intricate and rich scenario with respect to the once generally assumed, showing how different electronic and magnetic states may be generated and controlled in this fascinating class of materials.

Enhancement of L10 phase formation in FePt nanoparticles by nitrogenization

FePt particles 6 nm in size are produced by argon/nitrogen sputtering and gas-phase condensation. Marked changes in the atomic structure and morphology of the particles occur upon addition of nitrogen to the sputter gas. Electron energy loss spectroscopy and x-ray absorption spectroscopy show that nitrogen is incorporated in the particles in molecular and compound form. In situ sintering of the particles drives out the nitrogen causing enhanced diffusion leading to the preference of the L10 structure over the multiply twinned icosahedral structure, which forms in the absence of nitrogen in the sputter gas.

Magnetic and electronic properties of the interface between half metallic Fe3O4 and semiconducting ZnO

We have investigated the magnetic depth profile of an epitaxial Fe3O4 thin film grown directly on a semiconducting ZnO substrate by soft x-ray resonant magnetic reflectometry (XRMR) and electron energy loss spectroscopy (EELS). Consistent chemical profiles at the interface between ZnO and Fe3O4 are found from both methods. Valence selective EELS and XRMR reveal independently that the first monolayer of Fe at the interface between ZnO and Fe3O4 contains only Fe3+ ions. Besides this narrow 2.5 A interface layer, Fe3O4 shows magnetic bulk properties throughout the whole film making highly efficient spin injection in this system feasible.

X-ray absorption measurements on nanoparticle systems: self-assembled arrays and dispersions

X-ray absorption spectroscopy methods are presented as a useful tool to determine local structure, composition and magnetic moments as well as to estimate the effective anisotropy of substrate supported self-assembled arrays of wet-chemically synthesized FePt nanoparticles. A compositional inhomogeneity within the nanoparticles yields reduced magnetic moments with respect to the corresponding bulk material and may also hinder the formation of the chemically ordered L10 phase in FePt nanoparticles. The latter is indicated by a reduced effective anisotropy, which is one order of magnitude smaller than expected from the known value of the corresponding bulk material.As a new approach, measurements of the x-ray absorption near-edge structure of Fe-oxide nanoparticles in dispersion are presented and ageing effects are discussed on the basis of multiplet calculations.