Direct observation of Oersted-field-induced magnetization dynamics in magnetic nanostripes

We have used time-resolved x-ray photoemission electron microscopy to investigate the magnetization dynamics induced by nanosecond current pulses in NiFe/Cu/Co nanostripes. A large tilt of the NiFe magnetization in the direction transverse to the stripe is observed during the pulses. We show that this effect cannot be quantitatively understood from the amplitude of the Oersted field and the shape anisotropy. High frequency oscillations observed at the onset of the pulses are attributed to precessional motion of the NiFe magnetization about the effective field. We discuss the possible origins of the large magnetization tilt and the potential implications of the static and dynamic effects of the Oersted field on current-induced domain wall motion in such stripes.Comment: Published in Phys. Rev. B 83, 020406 (2011) (Rapid Communications

Iron porphyrin molecules on Cu(001): Influence of adlayers and ligands on the magnetic properties

The structural and magnetic properties of Fe octaethylporphyrin (OEP) molecules on Cu(001) have been investigated by means of density functional theory (DFT) methods and X-ray absorption spectroscopy. The molecules have been adsorbed on the bare metal surface and on an oxygen-covered surface, which shows a $\sqrt{2}\times2\sqrt{2}R45^{\circ}$ reconstruction. In order to allow for a direct comparison between magnetic moments obtained from sum-rule analysis and DFT we calculate the dipolar term $7$, which is also important in view of the magnetic anisotropy of the molecule. The measured X-ray magnetic circular dichroism shows a strong dependence on the photon incidence angle, which we could relate to a huge value of $7$, e.g. on Cu(001) $7$ amounts to -2.07\,\mbo{} for normal incidence leading to a reduction of the effective spin moment $m_s + 7$. Calculations have also been performed to study the influence of possible ligands such as Cl and O atoms on the magnetic properties of the molecule and the interaction between molecule and surface, because the experimental spectra display a clear dependence on the ligand, which is used to stabilize the molecule in the gas phase. Both types of ligands weaken the hybridization between surface and porphyrin molecule and change the magnetic spin state of the molecule, but the changes in the X-ray absorption are clearly related to residual Cl ligands.Comment: 17 figures, full articl

High domain wall velocity at zero magnetic field induced by low current densities in spin-valve nanostripes

Current-induced magnetic domain wall motion at zero magnetic field is observed in the permalloy layer of a spin-valve-based nanostripe using photoemission electron microscopy. The domain wall movement is hampered by pinning sites, but in between them high domain wall velocities (exceeding 150 m/s) are obtained for current densities well below 10^{12} \unit{A/m^2}, suggesting that these trilayer systems are promising for applications in domain wall devices in case of well controlled pinning positions. Vertical spin currents in these structures provide a potential explanation for the increase in domain wall velocity at low current densities.Comment: Published version, Applied Physics Express 2, 023003 (2009) http://dx.doi.org/10.1143/APEX.2.02300

Adatoms and clusters of 3d transition metals on graphene: Electronic and magnetic configurations

We investigate the electronic and magnetic properties of single Fe, Co, and Ni atoms and clusters on monolayer graphene (MLG) on SiC(0001) by means of scanning tunneling microscopy (STM), x-ray absorption spectroscopy, x-ray magnetic circular dichroism (XMCD), and ab initio calculations. STM reveals different adsorption sites for Ni and Co adatoms. XMCD proves Fe and Co adatoms to be paramagnetic and to exhibit an out-of-plane easy axis in agreement with theory. In contrast, we experimentally find a nonmagnetic ground state for Ni monomers while an increasing cluster size leads to sizeable magnetic moments. These observations are well reproduced by our calculations and reveal the importance of hybridization effects and intra-atomic charge transfer for the properties of adatoms and clusters on MLG.Comment: 8 pages (supplementary included), 4 figures, (supplementary included

Exploring the limits of soft x-ray magnetic holography: Imaging magnetization reversal of buried interfaces (invited)

The following article appeared in Journal of Applied Physics 109.7 (2011): 07D357 and may be found at http://scitation.aip.org/content/aip/journal/jap/109/7/10.1063/1.3567035Only a very few experimental techniques can address the microscopic magnetization reversal behavior of the different magnetic layers in a multilayered system with element selectivity. We present an element-selective study of ferromagnetic (FM) [Co/Pt]n multilayers with perpendicular anisotropy exchange-coupled to antiferromagnetic (AFM) FeMn and IrMn films performed with a new experimental set-up developed for both soft x-ray spectroscopy and holography imaging purposes. The spectroscopy analysis allows the quantification of the unpinned (pinned) uncompensated AFM moments, providing direct evidence of its parallel (antiparallel) alignment with respect to the FM moments. The holography experiments give a direct view of both FM and uncompensated AFM magnetic structures, showing that they replicate to each other during magnetization reversal. Remarkably, we show magnetic images for effective thicknesses as small as one monolayer. Our results provide new microscopic insights into the exchange coupling phenomena and explore the sensitivity limits of these techniques. Future trends are also discussed.We acknowledge technical support by the ESRF staff R. Barrett, R. Homs-Regojo, T. Trenit, and G. Retout. A. B. acknowledges support through a Ramo´n y Cajal contract from the Spanish MICINN. This work was supported in part by the Spanish MICINN through Projects CSD2007-00010, and MAT2010-21822 and by Comunidad de Madrid through Project S2009/MAT-1726.Comunidad de Madrid. S2009/MAT-1726/NANOBIOMAGNE

Investigation of magnetic droplet solitons using x-ray holography with extended references

A dissipative magnetic soliton, or magnetic droplet, is a structure that has been predicted to exist within a thin magnetic layer when non-linearity is balanced by dispersion, and a driving force counteracts the inherent damping of the spin precession. Such a soliton can be formed beneath a nano-contact (NC) that delivers a large spin-polarized current density into a magnetic layer with perpendicular magnetic anisotropy. Although the existence of droplets has been confirmed from electrical measurements and by micromagnetic simulations, only a few attempts have been made to directly observe the magnetic landscape that sustains these structures, and then only for a restricted set of experimental parameter values. In this work we use and x-ray holography technique HERALDO, to image the magnetic structure of the [Co/Ni]x4 multilayer within a NC orthogonal pseudo spin-valve, for different range of magnetic fields and injected electric currents. The magnetic configuration imaged at −33 mA and 0.3 T for devices with 90 nm NC diameter reveals a structure that is within the range of current where the droplet soliton exist based on our electrical measurements and have it is consistent with the expected size of the droplet (∼100 nm diameter) and its spatial position within the sample. We also report the magnetisation configurations observed at lower DC currents in the presence of fields (0–50 mT), where it is expected to observe regimes of the unstable droplet formation

Emmet Tieg and Elsie Tieg Interview, September 9, 1997

Emmet Tieg and Elsie Tieg recall how they came to be working their home ranch near the Lewis and Clark National Forest, grazing on Forest Service land with a permit, care and use of the trails on that land, and logging. They describe encounters with hobos, fighting fires, sparse wildlife in the Crazy Mountains, and sheepherding in central Montana.https://scholarworks.umt.edu/lewisandclarknationalforest/1002/thumbnail.jp