J. Camarero

Molecular vs. inorganic spintronics: the role of molecular materials and single molecules

Molecular spintronics is a new and emerging sub-area of spintronics that can benefit from the achievements obtained in molecular electronics and molecular magnetism. The two major trends of this area are the design of molecular analogs of the inorganic spintronic structures, and the evolution towards single-molecule spintronics. The former trend opens the possibility to design cheaper spintronic devices compatible with plastic technology, while the second takes advantage of the possibility to tailor molecules with control down to the single spin. In this highlight these two trends will be compared with the state-of-the-art achieved in the conventional inorganic spintronic systems.

Time-resolved magnetic domain imaging by x-ray photoemission electron microscopy

X-ray photoemission electron microscopy (X–PEEM) is a powerful imaging technique that can be used to perform element selective magnetic domain imaging on heterogeneous samples with different magnetic layers, like spin valves and tunnel junctions. We have performed nanosecond time-resolved X–PEEM measurements, on the permalloy layer of a Ni80Fe20 (5 nm)/Cu (10 nm)/Co (5 nm) trilayer deposited on Si(111). We used the pump-probe mode, synchronizing a magnetic pulse from a microcoil with the x-ray photon bunches delivered by the BESSY synchrotron in single bunch mode. Images could be acquired during and after the 20 ns long and 80 Oe high field pulses. The nucleation and subsequent growth of reversed domains in the permalloy could be observed, demonstrating the feasibility of element selective and time-resolved domain imaging using X–PEEM.

Highly asymmetric magnetic behavior in exchange biased systems induced by noncollinear field cooling

A detailed study of the angular dependence of the magnetization reversal in polycrystalline ferromagnetic (FM)/antiferromagnetic Co/IrMn bilayers with noncollinear FM and unidirectional anisotropies shows a peculiar asymmetric magnetic behavior. The anisotropy configuration is set via a field cooling (FC) procedure with the magnetic field misaligned with respect to the easy magnetization direction of the FM layer. Different magnetization reversal modes are observed for either positive or negative angles with respect to the FC direction. The angular dependence of both coercivity and exchange bias also clearly displays the broken symmetry of the induced noncollinearity. Our findings are reproduced with a modified Stoner–Wohlfarth model including the induced anisotropy configuration. Our results highlight the importance of the relative angle between anisotropies in exchange bias systems, opening a new path for the tailoring of their magnetic properties.

Influence of surfactants on atomic diffusion

Abstract We have used Monte Carlo simulations with realistic interatomic potentials, combined with experimental results obtained by He diffraction (thermal energy atom scattering) and STM to investigate the effect of a surfactant agent such as Pb on the mechanisms of atomic diffusion involved in epitaxial metal growth. We find that the main role of the surfactant is to hinder fast diffusion by hopping over the surface, which is the dominant mechanism on a compact face such as Cu(111), and to promote exchange. As a side effect, this facilitates interlayer diffusion and hence layer-by-layer growth, because islands are smaller and have rougher borders; adatoms reaching an edge have more opportunities to cross them by exchange with a step atom.

Thickness-dependent coercivity of ultrathin Co films grown on Cu(111)

By using the magneto-optic Kerr effect (MOKE) we have investigated the coercivity of ultrathin epitaxial Co films grown by molecular beam epitaxy with the aid of Pb as the surfactant on Cu(111). We find two different regimes: below ~6 ML (ML≡monolayer), the coercive field Hc increases continuously, whereas for thicker layers it falls at a rate that is inversely proportional to the film thickness. While this latter behaviour is typical for bulk systems, we show that the initial one is an effect of reduced dimensionality, reflecting the variation of the Curie temperature of the magnetic films in the same thickness range. This phenomenon could have important implications for atomic-scale engineering of magnetic materials.

Tailoring magnetic anisotropy in epitaxial half metallic La0.7Sr0.3MnO3 thin films

We present a detailed study on the magnetic properties, including anisotropy, reversal fields, and magnetization reversal processes, of well characterized half-metallic epitaxial La0.7Sr0.3MnO3 (LSMO) thin films grown onto SrTiO3 (STO) substrates with three different surface orientations, i.e., (001), (110), and (11−8). The latter shows step edges oriented parallel to the [110] (in-plane) crystallographic direction. Room temperature high resolution vectorial Kerr magnetometry measurements have been performed at different applied magnetic field directions in the whole angular range. In general, the magnetic properties of the LSMO films can be interpreted with just the uniaxial term, with the anisotropy axis given by the film morphology, whereas the strength of this anisotropy depends on both structure and film thickness. In particular, LSMO films grown on nominally flat (110)-oriented STO substrates presents a well defined uniaxial anisotropy originated from the existence of elongated in-plane [001]-orient...

Dynamics of Magnetic Domain Wall Motion after Nucleation: Dependence on the Wall Energy

The dynamics of magnetic domain wall motion in the FeNi layer of a FeNi/Al2O3/Co trilayer has been investigated by a combination of x-ray magnetic circular dichroism, photoelectron emission microscopy, and a stroboscopic pump-probe technique. The nucleation of domains and subsequent expansion by domain wall motion in the FeNi layer during nanosecond-long magnetic field pulses was observed in the viscous regime up to the Walker limit field. We attribute an observed delay of domain expansion to the influence of the domain wall energy that acts against the domain expansion and that plays an important role when domains are small.

Magnetic relaxation of exchange biased Pt/Co multilayers studied by time-resolved Kerr microscopy

Magnetization relaxation of exchange biased (Pt/Co)5/Pt/IrMn multilayers with perpendicular anisotropy was investigated by time-resolved Kerr microscopy. Magnetization reversal occurs by nucleation and domain wall propagation for both descending and ascending applied fields, but a much larger nucleation density is observed for the descending branch, where the field is applied antiparallel to the exchange bias field direction. These results can be explained by taking into account the presence of local inhomogeneities of the exchange bias field.

Room temperature in-plane ⟨100⟩ magnetic easy axis for Fe3O4/SrTiO3(001):Nb grown by infrared pulsed laser deposition

We examine the magnetic easy-axis directions of stoichiometric magnetite films grown on SrTiO{sub 3}:Nb by infrared pulsed-laser deposition. Spin-polarized low-energy electron microscopy reveals that the individual magnetic domains are magnetized along the in-plane 〈100〉 film directions. Magneto-optical Kerr effect measurements show that the maxima of the remanence and coercivity are also along in-plane 〈100〉 film directions. This easy-axis orientation differs from bulk magnetite and films prepared by other techniques, establishing that the magnetic anisotropy can be tuned by film growth.We examine the magnetic easy-axis directions of stoichiometric magnetite films grown on SrTiO3:Nb by infrared pulsed-laser deposition. Spin-polarized low-energy electron microscopy reveals that the individual magnetic domains are magnetized along the in-plane film directions. Magneto-optical Kerr effect measurements show that the maxima of the remanence and coercivity are also along in-plane film directions. This easy-axis orientation differs from bulk magnetite and films prepared by other techniques, establishing that the magnetic anisotropy can be tuned by film growth.

Influence of domain wall interactions on nanosecond switching in magnetic tunnel junctions

We have obtained microscopic evidence of the influence of domain wall stray fields on the nanosecond magnetization switching in magnetic trilayer systems. The nucleation barrier initiating the magnetic switching of the soft magnetic