Arantxa Fraile Rodríguez

Resistance switching at the nanometre scale in amorphous carbon

The electrical transport and resistance switching mechanism in amorphous carbon (a-C) is investigated at the nanoscale. The electrical conduction in a-C thin films is shown to be captured well by a Poole–Frenkel transport model that involves nonisolated traps. Moreover, at high electric fields a field-induced threshold switching phenomenon is observed. The following resistance change is attributed to Joule heating and subsequent localized thermal annealing. We demonstrate that the mechanism is mostly due to clustering of the existing sp2 sites within the sp3 matrix. The electrical conduction behaviour, field-induced switching and Joule-heating-induced rearrangement of atomic order resulting in a resistance change are all reminiscent of conventional phase-change memory materials. This suggests the potential of a-C as a similar nonvolatile memory candidate material.

Combined temperature-programmed reaction and in situ x-ray scattering studies of size-selected silver clusters under realistic reaction conditions in the epoxidation of propene

The catalytic activity and dynamical shape changes in size-selected nanoclusters at work are studied under realistic reaction conditions by using a combination of simultaneous temperature-programmed reaction with in situ grazing-incidence small angle x-ray scattering. This approach allows drawing a direct correlation between nanocatalyst size, composition, shape, and its function under realistic reaction conditions for the first time. The approach is illustrated in a chemical industry highly relevant selective partial oxidation of propene on a monodisperse silver nanocatalyst. The shape of the catalyst undergoes rapid change already at room temperature upon the exposure to the reactants, followed by a complex evolution of shape with increasing temperature. Acrolein formation is observed around 50 degrees C while the formation of the propylene oxide exhibits a sharp onset at 80 degrees C and is leveling off at 150 degrees C. At lower temperatures acrolein is produced preferentially to propylene oxide; at temperatures above 100 degrees C propylene oxide is favored.

Artificial kagome spin ice: dimensional reduction, avalanche control and emergent magnetic monopoles

Artificial spin-ice systems consisting of nanolithographic arrays of isolated nanomagnets are model systems for the study of frustration-induced phenomena. We have recently demonstrated that monopoles and Dirac strings can be directly observed via synchrotron-based photoemission electron microscopy, where the magnetic state of individual nanoislands can be imaged in real space. These experimental results of Dirac string formation are in excellent agreement with Monte Carlo simulations of the hysteresis of an array of dipoles situated on a kagome lattice with randomized switching fields. This formation of one-dimensional avalanches in a two-dimensional system is in sharp contrast to disordered thin films, where avalanches associated with magnetization reversal are two-dimensional. The self-organized restriction of avalanches to one dimension provides an example of dimensional reduction due to frustration. We give simple explanations for the origin of this dimensional reduction and discuss the disorder dependence of these avalanches. We conclude with the explicit demonstration of how these avalanches can be controlled via locally modified anisotropies. Such a controlled start and stop of avalanches will have potential applications in data storage and information processing.

Direct observation of transverse and vortex metastable magnetic domains in cylindrical nanowires

The study has been performed under the framework of the Projects No. MAT2013-48054-C2-1-R, MAT2016-76824-C3-1-R, MAT-2015-68772-P, MAT2015-64110-C2-2-P supported by the MINECO from Spain and DURSI 2014SGR220 supported by the Catalan Government. J.A.F.-R. acknowledges financial support from MINECO and the ESF through the “Ayudas para contratos predoctorales para la formacion de doctores 2014.”

Magnetization Ratchet in Cylindrical Nanowires

The unidirectional motion of information carriers such as domain walls in magnetic nanostrips is a key feature for many future spintronic applications based on shift registers. This magnetic ratchet effect has so far been achieved in a limited number of complex nanomagnetic structures, for example, by lithographically engineered pinning sites. Here we report on a simple remagnetization ratchet originated in the asymmetric potential from the designed increasing lengths of magnetostatically coupled ferromagnetic segments in FeCo/Cu cylindrical nanowires. The magnetization reversal in neighboring segments propagates sequentially in steps starting from the shorter segments, irrespective of the applied field direction. This natural and efficient ratchet offers alternatives for the design of three-dimensional advanced storage and logic devices.

Direct observation of enhanced magnetism in individual size- and shape-selected 3d transition metal nanoparticles

Magnetic nanoparticles are critical building blocks for future technologies ranging from nanomedicine to spintronics. Many related applications require nanoparticles with tailored magnetic properties. However, despite significant efforts undertaken towards this goal, a broad and poorly understood dispersion of magnetic properties is reported, even within monodisperse samples of the canonical ferromagnetic 3d transition metals. We address this issue by investigating the magnetism of a large number of size-and shape-selected, individual nanoparticles of Fe, Co, and Ni using a unique set of complementary characterization techniques. At room temperature, only superparamagnetic behavior is observed in our experiments for all Ni nanoparticles within the investigated sizes, which range from 8 to 20 nm. However, Fe and Co nanoparticles can exist in two distinct magnetic states at any size in this range: (i) a superparamagnetic state, as expected from the bulk and surface anisotropies known for the respective materials and as observed for Ni, and (ii) a state with unexpected stable magnetization at room temperature. This striking state is assigned to significant modifications of the magnetic properties arising from metastable lattice defects in the core of the nanoparticles, as concluded by calculations and atomic structural characterization. Also related with the structural defects, we find that the magnetic state of Fe and Co nanoparticles can be tuned by thermal treatment enabling one to tailor their magnetic properties for applications. This paper demonstrates the importance of complementary single particle investigations for a better understanding of nanoparticle magnetism and for full exploration of their potential for applications.

Geometric frustration in a hexagonal lattice of plasmonic nanoelements

We introduce the concept of geometric frustration in plasmonic arrays of nanoelements. In particular, we present the case of a hexagonal lattice of Au nanoasterisks arranged so that the gaps between neighboring elements are small and lead to a strong near-field dipolar coupling. Besides, far-field interactions yield higher-order collective modes around the visible region that follow the translational symmetry of the lattice. However, dipolar excitations of the gaps in the hexagonal array are geometrically frustrated for interactions beyond nearest neighbors, yielding the destabilization of the low energy modes in the near infrared. This in turn results in a slow dynamics of the optical response and a complex interplay between localized and collective modes, a behavior that shares features with geometrically frustrated magnetic systems.

Data-mining and informatics approaches for environmental contaminants

New and emerging environmental contaminants are chemicals that have not been previously detected or …

Influence of nanostructural features on the properties of magnetic nanoparticles

Magnetic nanostructures may exhibit novel magnetic phenomena that do not occur in the corresponding …