An effective postgrowth electrical tuning, via an oxygen releasing method, to enhance the content of non-noble metals in deposits directly written with gas-assisted focused-electron-beam-induced deposition (FEBID) is presented. It represents a novel and reproducible method for improving the electrical transport properties of Co-C deposits. The metal content and electrical properties of Co-C-O nanodeposits obtained by electron-induced dissociation of volatile Co(CO) precursor adsorbate molecules were reproducibly tuned by applying postgrowth annealing processes at 100 °C, 200 °C, and 300 °C under high-vacuum for 10 min. Advanced thin film EDX analysis showed that during the annealing process predominantly oxygen is released from the Co-C-O deposits, yielding an atomic ratio of Co:C:O = 100:16:1 (85:14:1) with respect to the atomic composition of as-written Co:C:O = 100:21:28 (67:14:19). In-depth Raman analysis suggests that the amorphous carbon contained in the as-written deposit turns into graphite nanocrystals with size of about 22.4 nm with annealing temperature. Remarkably, these microstructural changes allow for tuning of the electrical resistivity of the deposits over 3 orders of magnitude from 26 mΩ cm down to 26 μΩ cm, achieving a residual resistivity of ρ/ρ = 0.56, close to the value of 0.53 for pure Co films with similar dimensions, making it especially interesting and advantageous over the numerous works already published for applications such as advanced scanning-probe systems, magnetic memory, storage, and ferroelectric tunnel junction memristors, as the graphitic matrix protects the cobalt from being oxidized under an ambient atmosphere.

First-order reversal curve diagrams have been used to investigate magnetostatic interactions and average coercivity of individual wires in soft ferromagnetic uniform length nanowire arrays. We present a method for identifying these physical parameters on the out-of-plane first-order reversal curve diagrams: the position of the irreversible part on the critical axis is a good approximation to the average value of the nanowire coercivity and the maximum interaction field is equal to the interaction field at saturation. Their dependence upon material (CoFeB and Ni) and nanowire length are presented. The magnetostatic interactions increase linearly with length, in agreement with a model developed previously. The global array coercivity, obtained from magnetization curves, is generally lower than the apparent average coercivity for individual nanowires. This coercivity reduction increases linearly with the magnetostatic interactions. The general shape of the out-of-plane first-order reversal curve diagrams is compared with those obtained from a theoretical moving Preisach model.

This paper describes a solution-phase route to prepare Ag-Fe 3 O 4 colloidal dimer nanoparticles (NPs) with a dumbbell-like shape. Results show enhancement of the magnetic anisotropy and large coercivity that are explained through the nonzero orbital moment, m orb , and the related strong spin-orbit interaction that can be induced by a lattice distortion of the Fe-O bond lengths. In particular, distortions of the octahedral sites in magnetite result in Fe 3d-O 2p mixing and O 2p to Fe 3d charge transfer which, together with crystal field effects, lifts the electronic degeneracy, leading to a nonzero m orb . dc magnetization and ferromagnetic resonance were employed for analyzing the magnetic response of the reference Fe 3 O 4 NPs and Ag-Fe 3 O 4 dimer NPs samples, showing a very good agreement with the structural characterization.

Assembled Fe3O4 nanoparticles on graphene for enhanced electromagnetic wave losses Appl. Phys. Lett. 101, 153108 (2012) Magnetization reversal and magnetoresistance behavior of perpendicularly magnetized [Co/Pd]4/Au/[Co/Pd]2 nanowires J. Appl. Phys. 112, 073902 (2012) Electric-field control of CoFeB/IrMn exchange bias system J. Appl. Phys. 112, 064120 (2012) Critical effect of spin-dependent transport in a tunnel barrier on enhanced Hanle-type signals observed in threeterminal geometryWe report on the structural and magnetic properties of crystalline bi-phase Co nanowires, electrodeposited into the pores of anodized alumina membranes, as a function of their length. Co nanowires present two different coexistent crystalline structures (fcc and hcp) that can be controlled by the time of pulsed electrodeposition. The fcc crystalline phase grows at the early stage and is present at the bottom of all the nanowires, strongly influencing their magnetic behavior. Both structural and magnetic characterizations indicate that the length of the fcc phase is constant at around 260-270 nm. X-ray diffraction measurements revealed a strong preferential orientation (texture) in the (1 0-1 0) direction for the hcp phase, which increases the nanowire length as well as crystalline grain size, degree of orientation, and volume fraction of oriented material. The first-order reversal curve (FORC) method was used to infer both qualitatively and quantitatively the complex magnetization reversal of the nanowires. Under the application of a magnetic field parallel to the wires, the magnetization reversal of each region is clearly distinguishable; the fcc phase creates a high coercive contribution without an interaction field, while the hcp phase presents a smaller coercivity and undergoes a strong antiparallel interaction field from neighboring wires.

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A new approach to the quantitative and physical analysis of first-order reversal curve (FORC) diagrams is presented. Each hysteron in the FORC method represents a magnetic cluster. Starting with a model for a ferromagnetic, isotropic, and monodomain sphere, and adding anisotropy and domain structure, three different types of “basic hysterons” are obtained: vertical reversible and irreversible, and linear. The FORC diagrams of basic hysterons with a mean interaction field were obtained by simulation. From them, the relationships between the characteristics of the hysterons and the FORC distribution function were extracted. Different sets of hysterons can lead to the same FORC distribution function. A positive mean interaction field tends to merge the hysterons on the FORC diagram, while a negative mean interaction field introduces repulsion between them.

The magnetization reversal processes are discussed for exchangecoupled ferromagnetic hard/soft bilayers made from Co 0.66 Cr 0.22 Pt 0.12 (10 and 20 nm)/Ni (from 0 to 40 nm) films with out-of-plane and in-plane magnetic easy axes respectively, based on room temperature hysteresis loops and first-order reversal curve analysis. On increasing the Ni layer thicknesses, the easy axis of the bilayer reorients from out-of-plane to in-plane. An exchange bias effect, 2 consisting of a shift of the in-plane minor hysteresis loops along the field axis, was observed at room temperature after in-plane saturation. This effect was associated with specific ferromagnetic domain configurations experimentally determined by polarized neutron reflectivity. On the other hand, perpendicular exchange bias effect was revealed from the out-of-plane hysteresis loops and it was attributed to residual domains in the magnetically hard layer.

A set of multi-segmented Fe/Cu nanowires were synthesized by a two-step anodization process of aluminum substrates and a pulsed electrodeposition technique using a single bath. While both Fe segment length and diameter were kept constant to (30 ± 7) and (45 ± 5) nm, respectively, Cu length was varied between (15 ± 5) and (120 ± 10) nm. The influence of the non-magnetic layer thickness variation on the nanowire magnetic properties was investigated through first-order reversal curve (FORC) measurements and micromagnetic simulations. Our analysis confirmed that, in the multi-segmented Fe/Cu nanowires with shorter Cu segments, the dipolar coupling between Fe segments controls the nanowire magnetic behavior, and its performance is like that of a homogenous Fe nanowire array of similar dimensions. On the other hand, multi-segmented Fe/Cu nanowires with larger Cu segments act like a collection of non-interacting magnetic entities (along the nanowire axis), and their global behavior is mainly controlled by the neighbor-to-neighbor nanodisc dipolar interactions.