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Register a new userStructural and magnetic characterization of self-assembled iron oxide nanoparticle arrays
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We report about a combined structural and magnetometric characterization of self-assembled magnetic nanoparticle arrays. Monodisperse iron oxide nanoparticles with a diameter of 20 nm were synthesized by thermal decomposition. The nanoparticle suspension was spin-coated on Si substrates to achieve self-organized arrays of particles and subsequently annealed at various conditions. The samples were characterized by x-ray diffraction, bright and dark field high resolution transmission electron microscopy (HRTEM). The structural analysis is compared to the magnetic behavior investigated by superconducting interference device (SQUID) magnetometry. We can identify either multi-phase FeO/g-Fe2O3 or multi-phase FeO/Fe3O4 nanoparticles. The FeO/g-Fe2O3 system shows a pronounced exchange bias effect which explains the peculiar magnetization data obtained for this system.
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We report on self-assembled iron oxide nanoparticle films on silicon substrates. In addition to homogeneously assembled layers, we fabricated patterned trenches of 40-1000 nm width using electron beam lithography for the investigation of assisted self-assembly. The nanoparticles with a diameter of 20 nm +/- 7% were synthesized by thermal decomposition of iron oleate complexes in trioctylamine in presence of oleic acid. Samples with different track widths and nanoparticle concentration were characterized by scanning electron microscopy and by superconducting quantum interference device magnetometry.
We report an easy and broadly applicable method for the controlled self-assembly of atomically precise Au32(nBu3P)12Cl8 nanoclusters into micro-crystals. This enables the determination of emergent optoelectronic properties resulting from long-range order in such assemblies. Compared to the same nanoclusters in glassy, polycrystalline ensembles, we find a 100-fold increase in the electric conductivity and charge carrier mobility as well as additional optical transitions. We show that these effects are due to a vanishing energetic disorder and a drastically reduced activation energy to charge transport in the highly ordered assemblies. This first structure-transport correlation on self-assembled superstructures of atomically precise gold nanoclusters paves the way towards functional materials with novel collective optoelectronic properties.
We report the magnetotransport properties of self-assembled Co@CoO nanoparticle arrays at temperatures below 100 K. Resistance shows thermally activated behavior that can be fitted by the general expression of R exp{(T/T0)^v}. Efros-Shklovskii variable range hopping (v=1/2) and simple activation (hard gap, v=1) dominate the high and low temperature region, respectively, with a strongly temperature-dependent transition regime in between. A giant positive magnetoresistance of >1,400% is observed at 10K, which decreases with increasing temperature. The positive MR and most of its features can be explained by the Zeeman splitting of the localized states that suppresses the spin dependent hopping paths in the presence of on-site Coulomb repulsion.
The radiative heat transfer between gold nanoparticle layers is presented using the coupled dipole method. Gold nanoparticles are modelled as effective electric and magnetic dipoles interacting via electromagnetic fluctuations. The effect of higher-order multipoles is implemented in the expression of electric polarizability to calculate the interactions at short distances. Our findings show that the near-field radiation reduces as the radius of the nanoparticles is increased. Also, the magnetic dipole contribution to the heat exchange becomes more important for larger particles. When one layer is displayed in parallel with respect to the other layer, the near-field heat transfer exhibits oscillatory-like features due to the influence of the individual nanostructures. Further details about the effect of the nanoparticles size are also discussed.
Magnetic skyrmions are nontrivial spin textures which resist external perturbations, being promising candidates for the next generation recording devices. Nevertheless, a major challenge in realizing skyrmion-based devices is the stabilization of ordered arrays of these spin textures under ambient conditions and zero applied field. Here, we demonstrate for the first time the formation and stabilization of magnetic skyrmions on arrays of self-assembled hexagonal nanodomes taking advantage of the intrinsic properties of its curved geometry. Magnetic force microscopy images from the arrays of 100 nm nanodomes showed stable skyrmions at zero field that are arranged following the topography of the nanostructure. Micromagnetic simulations are compared to the experiments to determine the correlation of the domain textures with the topography of the samples. We propose a simple method to nucleate and annihilate skyrmions, opening the possibility for ultra-dense data storage based on the high stability and low energy consumption of the skyrmionic textures.
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