No Arabic abstract
Magnetometry and neutron scattering have been used to study the magnetic properties of pressure graded Co/Pd multilayers. The grading of the multilayer structure was done by varying the deposition pressure during sputtering of the samples. Magnetic depth profiling by polarized neutron reflectometry directly shows that for pressure-graded samples, the magnetization changes significantly from one pressure region to the next, while control samples sputtered at uniform pressure exhibit essentially uniform magnetic depth profiles. Complementary magnetometry results suggest that the observed graded magnetic profiles are due in part to a decrease in saturation magnetization for regions deposited at progressively higher pressure. Increased deposition pressure is shown to increase coercivity, and for graded samples, the absence of discrete steps in the hysteresis loops implies exchange coupling among regions deposited at different pressures.
Magnetization reversal mechanisms and depth-dependent magnetic profile have been investigated in Co/Pd thin films magnetron-sputtered under continuously varying pressure with opposite deposition orders. For samples grown under increasing pressure, magnetization reversal is dominated by domain nucleation, propagation and annihilation; an anisotropy gradient is effectively established, along with a pronounced depth-dependent magnetization profile. However, in films grown under decreasing pressure, disorders propagate vertically from the bottom high-pressure region into the top low-pressure region, impeding domain wall motion and forcing magnetization reversal via rotation; depth-dependent magnetization varies in an inverted order, but the spread is much suppressed.
Depth-grading of magnetic anisotropy in perpendicular magnetic media has been predicted to reduce the field required to write data without sacrificing thermal stability. To study this prediction, we have produced Co/Pd multilayers with depth-dependent Co layer thickness. Polarized neutron reflectometry shows that the thickness grading results in a corresponding magnetic anisotropy gradient. Magnetometry reveals that the anisotropy gradient promotes domain nucleation upon magnetization reversal - a clear experimental demonstration of the effectiveness of graded anisotropy for reducing write-field.
Ever since its discovery in 1996, ultrafast demagnetization has ignited immense research interest due to its scientific rigor and technological potential. A flurry of recent theoretical and experimental investigations has proposed direct and indirect excitation processes in separate systems. However, it still lacks a unified mechanism and remains highly debatable. Here, for the first time, we demonstrate that instead of either direct or indirect interaction, simultaneous and controlled excitation of both direct and indirect mechanisms of demagnetization are possible in a multilayers composed of repeated Co/Pd bi-layers. Moreover, we were able to modulate demagnetization time (from ~350 fs to ~750 fs) by fluence and thickness dependent indirect excitation due to heat current flowing vertically downward from top layers, which is combined with an altogether different scenario of direct irradiation. Finally, by regulating the pump wavelength we could effectively control the contribution of indirect process, which gives a confirmation to our understanding of the ultrafast demagnetization process.
The formation mechanisms of evaporated Pd islands on the reconstructed Au(111) $22 /times /sqrt{3}$ herringbone surface have been here studied by Scanning Tunneling Microscopy (STM) at room temperature. Atomically resolved STM images at the very early stages of growth provide a direct observation of the mechanisms involved in preferential Pd islands nucleation at the elbows of the herringbone structure. At low Pd coverage the Au(111) herringbone structure remains substantially unperturbed and isolated Pd atoms settled in hollow sites between Au atoms are found nearby the elbows and the distortions of the reconstructed surface. In the same regions, at extremely low coverage (0.003 ML), substituted Pd atoms in lattice sites of the Au(111) surface are also observed, revealing the occurrence of a place exchange mechanism. Substitution seems to play a fundamental role in the nucleation process, forming aggregation centers for incoming atoms and thus leading to the ordered growth of Pd islands on Au(111). Atomically resolved STM images of Pd islands reveal a close-packed arrangement with lattice parameter close to the interatomic distance between gold atoms in the fcc regions of the Au(111) surface. Distortion of the herringbone structure for Pd coverages higher than 0.25 ML indicates strong interaction between the growing islands and the topmost Au(111) layer.
The magnetic properties of (111)-oriented Rh/Co/Pt and Pd/Co/Pt multilayers are investigated by first-principles calculations. We focus on the interlayer exchange coupling, and identify thicknesses and composition where a typical ferromagnet or a synthetic antiferromagnet across the spacer layer is formed. All systems under investigation show a collinear magnetic intralayer order, but the Dzyaloshinskii-Moriya interaction (DMI) is rather strong for Pd-based systems, so that single magnetic skyrmions can be expected. In general, we find a strong sensitivity of the magnetic parameters (especially the DMI) in Rh-based systems, but Pd-based multilayers are less sensitive to structural details.