Current-Driven Magnetic Excitations in Permalloy-Based Multilayer Nanopillars

We study current-driven magnetization switching in nanofabricated Ni84Fe16/Cu/Ni84Fe16 trilayers at 295 K and 4.2 K. The shape of the hysteretic switching diagram at low magnetic field changes from 295 K to 4.2 K. The reversible behavior at higher field involves two phenomena, a threshold current for magnetic excitations closely correlated with the switching current, and a peak in differential resistance characterized by telegraph noise, with average period that decreases exponentially with current and shifts with temperature. We interpret both static and dynamic results at 295 K and 4.2 K in terms of thermal activation over a potential barrier, with a current dependent effective magnetic temperature.Comment: 4 pages, 4 Figure

Detecting Spin-Polarized Currents in Ballistic Nanostructures

We demonstrate a mesoscopic spin polarizer/analyzer system that allows the spin polarization of current from a quantum point contact in an in-plane magnetic field to be measured. A transverse focusing geometry is used to couple current from an emitter point contact into a collector point contact. At large in-plane fields, with the point contacts biased to transmit only a single spin (g < e^2/h), the voltage across the collector depends on the spin polarization of the current incident on it. Spin polarizations of greater than 80% are found for both emitter and collector at 300mK and 7T in-plane field.Comment: related papers at http://marcuslab.harvard.ed

Fabrication and Characterization of Co1−xFex Alloy Nanowires

Co1−xFex alloy nanowires with 40 nm diam and x=0–1.0 were fabricated by electrodeposition in nanopores of alumina templates. The crystalline structure of the nanowires is concentration dependent and shows a transition from the cobalt hexagonal-closed-packed structure (hcp) to a face-centered-cubic structure (fcc) in the concentration range

Investigation of Magnetic Interactions in Large Arrays of Magnetic Nanowires

The magnetic interactions in large arrays of ordered magnetic nanowires with 12-48 nm diameter and 55-95 nm spacing were investigated using modified Henkel plots. The measurements for nanowire arrays ac demagnetized with the field applied parallel to the nanowire axis (the easy magnetization axis) indicate that the dominant interaction during the switching process is the magnetostatic coupling between the nanowires. Nevertheless, while the strength of the magnetostatic interactions increases with the magnetic moment associated with the nanowires, the increase is not linear with respect to the volume of the nanowires. Moreover, the dependence of the remanence curves on the field history suggests that even for magnetic nanowire systems with high geometric anisotropy, the magnetic pole structure of the nanowires can be complex. This conclusion is also supported by the field dependence of the initial magnetization curves. (c) 2008 American Institute of Physics

Investigation of Magnetic Interactions in Large Arrays of Magnetic Nanowires

The magnetic interactions in large arrays of ordered magnetic nanowires with 12-48 nm diameter and 55-95 nm spacing were investigated using modified Henkel plots. The measurements for nanowire arrays ac demagnetized with the field applied parallel to the nanowire axis (the easy magnetization axis) indicate that the dominant interaction during the switching process is the magnetostatic coupling between the nanowires. Nevertheless, while the strength of the magnetostatic interactions increases with the magnetic moment associated with the nanowires, the increase is not linear with respect to the volume of the nanowires. Moreover, the dependence of the remanence curves on the field history suggests that even for magnetic nanowire systems with high geometric anisotropy, the magnetic pole structure of the nanowires can be complex. This conclusion is also supported by the field dependence of the initial magnetization curves. (c) 2008 American Institute of Physics

Modeling of Hysteresis and Magnetization Curves for Hexagonally Ordered Electrodeposited Nanowires

A computational model has been developed to investigate how the magnetostatic interactions affect the hysteresis and magnetization curves for hexagonal arrays of magnetic nanowires. The magnetization coupling between nanowires arises from the stray fields produced by the other nanowires composing the array such that the field at each nanowire is the sum of the external field and the interaction field with the other nanowires. Using only two adjustable parameters: the interaction between nearest neighbors and the width of the Gaussian distribution in switching fields centered around the measuredcoercivity, simulations are compared with the experimentally measuredhysteresis and magnetization curves for electrodepositedCo0.45 Fe0.55 alloy nanowires with diameters from 12 to 48 nm. Excellent agreement is found for all nanowire systems except for the largest diameter arrays where deviations from the Gaussian distribution of switching fields need to be considered

Zero Magnetization States in Electrodeposited Co0.45Fe0.55 Nanowire Arrays

Co0.45Fe0.55 alloy nanowires with 12 to 35 nm diameter and 12 μm length were fabricated by electrodeposition in porous anodic alumina templates. The initial magnetization curves reveal that the zero magnetization state is not unique and is determined by the field history (acdemagnetization process) leading to the zero average moment state. For acdemagnetization processes with the field applied parallel to the nanowire axis, the subsequent magnetization curves suggest that an individual nanowire behaves as a single domain with neighboring nanowires being antiparallel to each other in the zero magnetization state. However, for a demagnetization process with the field applied perpendicular to the nanowires, a different zero magnetization state is created in which the individual nanowires consist of multidomains having opposite axial orientations. These results are consistent with the asymmetric (symmetric) behavior found in the minor hysteresis loops measured after perpendicular (parallel) acdemagnetization on these nanowire arrays

Fabrication and Characterization of Co1−xFex Alloy Nanowires

Co1−xFex alloy nanowires with 40 nm diam and x=0–1.0 were fabricated by electrodeposition in nanopores of alumina templates. The crystalline structure of the nanowires is concentration dependent and shows a transition from the cobalt hexagonal-closed-packed structure (hcp) to a face-centered-cubic structure (fcc) in the concentration range