Samuel D. Oberdick

Origin of reduced magnetization and domain formation in small magnetite nanoparticles

The structural, chemical, and magnetic properties of magnetite nanoparticles are compared. Aberration corrected scanning transmission electron microscopy reveals the prevalence of antiphase boundaries in nanoparticles that have significantly reduced magnetization, relative to the bulk. Atomistic magnetic modelling of nanoparticles with and without these defects reveals the origin of the reduced moment. Strong antiferromagnetic interactions across antiphase boundaries support multiple magnetic domains even in particles as small as 12–14 nm.

Magnetostatic effects on switching in small magnetic tunnel junctions

Perpendicular CoFeB/MgO/CoFeB magnetic tunnel junctions with diameters under 100 nm are investigated by conductive atomic force microscopy. Minor loops of the tunnel magnetoresistance as a function of applied magnetic field reveal the hysteresis of the soft layer and an offset due to the magnetostatic field of the hard layer. Within the hysteretic region, telegraph noise is observed in the tunnel current. Simulations show that in this range, the net magnetic field in the soft layer is spatially inhomogeneous, and that antiparallel to parallel switching tends to start near the edge, while parallel to antiparallel reversal favors nucleation in the interior of the soft layer. As the diameter of the tunnel junction is decreased, the average magnitude of the magnetostatic field increases, but the spatial inhomogeneity across the soft layer is reduced.

Gravity driven current during the coalescence of two sessile drops

Coalescence of liquid drops is critical in many phenomena such as emulsion stability, inkjet printing, and coating applications. For sessile drops on a solid surface, the coalescence process is more complicated than the coalescence of drops suspended in a fluid medium as a result of the coupling of the contact line motions to the fluid flow. In this paper, we use video microscopy to track the evolution of the interfaces and contact lines as well as the internal fluid motion within a merged sessile droplet. In this study, the fluids in the coalescing drops are miscible and have similar surface tensions and drop volumes but different viscosities and densities. Coalescence occurs in three stages. During the first stage, rapid healing of the bridge between the drops occurs just after they touch. In the second stage, slower rearrangement of the liquids occurs. We show that these intermediate rearrangements are driven by gravity even for density differences of the two fluids as small as 1%. For the systems exam...

Particle moment canting in CoFe 2 O 4 nanoparticles

Polarization-analyzed small-angle neutron scattering methods are used to determine the spin morphology in high crystalline anisotropy, 11 nm diameter CoFe2O4 nanoparticle assemblies with randomly oriented easy axes. In moderate to high magnetic fields, the nanoparticles adopt a uniformly canted structure, rather than forming domains, shells, or other arrangements. The observed canting angles agree quantitatively with those predicted from an energy model dominated by Zeeman and anisotropy competition, with implications for the technological use of such nanoparticles.

Spin canting across core/shell Fe3O4/MnxFe3−xO4 nanoparticles

Magnetic nanoparticles (MNPs) have become increasingly important in biomedical applications like magnetic imaging and hyperthermia based cancer treatment. Understanding their magnetic spin configurations is important for optimizing these applications. The measured magnetization of MNPs can be significantly lower than bulk counterparts, often due to canted spins. This has previously been presumed to be a surface effect, where reduced exchange allows spins closest to the nanoparticle surface to deviate locally from collinear structures. We demonstrate that intraparticle effects can induce spin canting throughout a MNP via the Dzyaloshinskii-Moriya interaction (DMI). We study ~7.4 nm diameter, core/shell Fe3O4/MnxFe3−xO4 MNPs with a 0.5 nm Mn-ferrite shell. Mössbauer spectroscopy, x-ray absorption spectroscopy and x-ray magnetic circular dichroism are used to determine chemical structure of core and shell. Polarized small angle neutron scattering shows parallel and perpendicular magnetic correlations, suggesting multiparticle coherent spin canting in an applied field. Atomistic simulations reveal the underlying mechanism of the observed spin canting. These show that strong DMI can lead to magnetic frustration within the shell and cause canting of the net particle moment. These results illuminate how core/shell nanoparticle systems can be engineered for spin canting across the whole of the particle, rather than solely at the surface.

Formation of FePt nanodots by wetting of nanohole substrates

Large area arrays of FePt nanodots are fabricated on patterned substrates made of SiOx, SiNx and TiNx. The templates have a depth of ∼10 nm and a pitch of ∼20 nm with 18 nm wide holes. FePt is sputtered on the nanohole arrays, then back-etched, leaving a highly ordered array of FePt nanodots behind. To promote phase transformation to the L10 phase, the samples are annealed at temperatures of 550-650° C. During annealing, the FePt strongly dewets SiOx and SiNx substrates, causing sintering and coalescence of the FePt nanodots, but the nanodots remain highly ordered on the TiNx substrate. The nanodot arrays on TiNx are characterized magnetically before and after annealing. The out-of-plane coercivity increases by ∼1 kOe, suggesting partial transformation to the L10 phase. We also show that a capping layer can be sputtered on top of the nanodot arrays prior to annealing to prevent dewetting.

Formation of FePt nanoparticle arrays using nanohole templates

This study investigates the synthesis and characterization of FePt nanodot arrays. The FePt nanometer-scale thin film is deposited on SiOx substrate by RF sputtering and heat treated by rapid thermal annealing at 650°C for 20 min. Scanning electron microscopy, X-ray diffraction, and alternating gradient force microscopy are employed to determine the structural and magnetic hysteresis properties of the nanodots.