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Ll. Balcells

Publications and source records attributed to Ll. Balcells.

13 recordsLinked to original sources

Extending Field Limits in Nanoscale Magnetic Imaging with Metamaterial-inspired Magnetic Flux Concentrators

Many nanoscale magnetic imaging techniques are constrained by the maximum magnetic field that can be applied during measurements, due to geometrical limitations or interactions with the probe or the detected signal (e.g., electrons). Here, it is demonstrated that sample-integrated metamaterial-inspired magnetic flux concentrators (MFCs) locally amplify magnetic fields, allowing observation of magnetization processes beyond instrumental limits. Micrometer-sized MFCs fabricated directly on the samples are tested in photoemission electron microscopy experiments employing X-ray magnetic circular dichroism as magnetic contrast mechanism. At low applied fields, substantial amplification factors enable observation of magnetization reversal in a chain of magnetite nanoparticles synthesized by magnetotactic bacteria at an applied field of 8 mT, substantially smaller than the 50 mT predicted by simulations in absence of MFCs. At higher fields, the field enhancement extends the accessible field range by a factor of five, enabling for the first time, imaging of the field-dependent magnetic domain structure evolution of an isolated giant magnetofossil. Finally, we show how MFC geometry and material parameters can be tuned to optimize performance considering sample and experimental constraints, providing a tunable and broadly applicable strategy for extending the accessible field range in a wide variety of nanoscale magnetic imaging techniques.

cond-mat.mtrl-sci

Self-assembled line network in BiFeO3 thin films

In this work we report on the controlled fabrication of a self-assembled line network in highly epitaxial BiFeO3 thin films on top of LaAlO3 in the kinetically limited grown region by RF sputtering. As previously shown in the case of manganite thin films, the remarkable degree of ordering is achieved using vicinal substrates with well-defined step-terrace morphology. Nanostructured BiFeO3 thin films show mixed-phase morphology. Besides typical formation following (100) and (010) axes, some mixed phase nanodomains are detected also in-between the regular line network. These particular microstructures open a playground for future applications in multiferroic nanomaterials.

cond-mat.mtrl-sci

Controlling magnetisation's reversal mechanism and hyperthermia efficiency in core/shell magnetic nanoparticles by tuning the interphase coupling

Magnetic particle hyperthermia, in which colloidal nanostructures are exposed to an alternating magnetic field, is a promising approach to cancer therapy. Unfortunately, the clinical efficacy of hyperthermia has not yet been optimized. Consequently, routes to improve magnetic particle hyperthermia such as designing hybrid structures comprised from different phase materials are actively pursued. Here we demonstrate enhanced hyperthermia efficiency in relative large spherical Fe/Fe-oxide core/shell nanoparticles through the manipulation of interactions between the core and shell phases. Experimental results on exemplary samples with diameters in the range 30-80 nm indicated a direct correlation of hysteresis losses to the observed temperature elevation rate with a maximum efficiency of around 0.9 kW/g. The absolute particle size, the core/shell ratio, and the interposition of a thin wüstite interlayer, are shown to have powerful effects on the specific absorption rate. By comparing our measurements to micromagnetic calculations we have unveiled topologically non-trivial magnetisation reversal modes under which interparticle interactions become negligible, aggregates formation is minimized, and the energy that is converted into heat is increased. This information has been overlooked till date and is in stark contrast to the existing knowledge on homogeneous particles.

cond-mat.mtrl-sci

Switching on superferromagnetism

Recent results in electric-field control of magnetism have paved the way for the design of alternative magnetic and spintronic devices with enhanced functionalities and low power consumption. Among the diversity of reported magnetoelectric effects, the possibility of switching on and off long-range ferromagnetic ordering close to room temperature stands out. Its binary character opens up the avenue for its implementation in magnetoelectric data storage devices. Here we show the possibility to locally switch on superferromagnetism in a wedge-shaped polycrystalline Fe thin film deposited on top of a ferroelectric and ferroelastic BaTiO3 substrate. A superparamagnetic to superferromagnetic transition is observed for confined regions for which a voltage applied to the ferroelectric substrate induces a sizable strain. We argue that electric-field-induced changes of magnetic anisotropy lead to an increase of the critical temperature separating the two regimes so that superparamagnetic regions develop collective long-range superferromagnetic behavior.

cond-mat.mtrl-sci

Spin-orbit effects surfacing on manganites

Spin-orbit coupling in magnetic systems lacking inversion symmetry can give rise to non trivial spin textures. Magnetic thin films and heterostructures are potential candidates for the formation of skyrmions and other non-collinear spin configurations as inversion symmetry is inherently lost at their surfaces and interfaces. However, manganites, in spite of their extraordinarily rich magnetic phase diagram, have not yet been considered of interest within this context as their spin-orbit coupling is assumed to be negligible. We demonstrate here, by means of angular dependent X-ray linear dichroism experiments and theoretical calculations, the existence of a noncollinear antiferromagnetic ordering at the surface of ferromagnetic La$_{2/3}$Sr$_{1/3}$MnO$_3$ thin films whose properties can only be explained by an unexpectedly large enhancement of the spin-orbit interaction. Our results reveal that spin-orbit coupling, usually assumed to be very small on manganites, can be significantly enhanced at surfaces and interfaces adding a new twist to the possible magnetic orders that can arise in electronically reconstructed systems.

cond-mat.str-el

Isothermal anisotropic magnetoresistance in antiferromagnetic metallic IrMn

Antiferromagnetic spintronics is an emerging field; antiferromagnets can improve the functionalities of ferromagnets with higher response times, and having the information shielded against external magnetic field. Moreover, a large list of aniferromagnetic semiconductors and metals with Néel temperatures above room temperature exists. In the present manuscript, we persevere in the quest for the limits of how large can anisotropic magnetoresistance be in antiferromagnetic materials with very large spin-orbit coupling. We selected IrMn as a prime example of first-class moment (Mn) and spin-orbit (Ir) combination. Isothermal magnetotransport measurements in an antiferromagnetic-metal(IrMn)/ferromagnetic-insulator thin film bilayer have been performed. The metal/insulator structure with magnetic coupling between both layers allows the measurement of the modulation of the transport properties exclusively in the antiferromagnetic layer. Anisotropic magnetoresistance as large as 0.15 % has been found, which is much larger than that for a bare IrMn layer. Interestingly, it has been observed that anisotropic magnetoresistance is strongly influenced by the field cooling conditions, signaling the dependence of the found response on the formation of domains at the magnetic ordering temperature.

cond-mat.mtrl-sci

Engineering the microstructure and magnetism of La$_2$CoMnO$_6$ thin films by tailoring oxygen stoichiometry

We report on the magnetic and structural properties of ferromagnetic-insulating La$_2$CoMnO$_6$ thin films grown on top of (001) STO substrates by means of RF sputtering technique. Careful structural analysis, by using synchrotron X-ray diffraction, allows identifying two different crystallographic orientations that are closely related to oxygen stoichiometry and to the features (coercive fields and remanence) of the hysteresis loops. Both Curie temperature and magnetic hysteresis turn out to be dependent on the oxygen stoichiometry. In situ annealing conditions allow tailoring the oxygen content of the films, therefore controlling their microstructure and magnetic properties.

cond-mat.mtrl-sci

Intrinsic robust antiferromagnetism at manganite surfaces and interfaces

Ferromagnetic/metallic manganese perovskites, such as La2/3Sr1/3MnO3 (LSMO)are promising materials for the design and implementation of novel spintronic devices working at room temperature. However, their implementation in practical applications has been severely hampered due to the breakdown of their magnetotransport properties at temperatures well below their magnetic transition temperature. This breakdown has been usually associated to surface and interface related problems but its physical origin has not been clearly established yet. In this work we investigate the interface between La2/3Sr1/3MnO3 (LSMO) thin films and different capping layers by means of x-ray linear dichroism and transport measurements. Our data reveal that, irrespective to the capping material, LSMO/capping layer bilayers exhibit an antiferromegnetic/insulating phase at the interface, likely to originate from a preferential occupancy of Mn 3d 3z2-r2 eg orbitals. This phase, which extends ca. 2 unit cells, is also observed in an uncapped LSMO reference sample thus, pointing to an intrinsic interfacial phase separation phenomenon, likely to be promoted by the structural disruption and symmetry breaking at the LSMO free surface/interface. These experimental observations strongly suggest that the structural disruption at the LSMO interfaces play a major role on the observed depressed magnetotransport properties in manganite-based magnetic tunneling junctions and it is at the origin of the so-called dead layer.

cond-mat.mtrl-sci

Mn valence instability in La2/3Ca1/3MnO3 thin films

A Mn valence instability on La2/3Ca1/3MnO3 thin films, grown on LaAlO3 (001)substrates is observed by x-ray absorption spectroscopy at the Mn L-edge and O K-edge. As-grown samples, in situ annealed at 800 C in oxygen, exhibit a Curie temperature well below that of the bulk material. Upon air exposure a reduction of the saturation magnetization, MS, of the films is detected. Simultaneously a Mn2+ spectral signature develops, in addition to the expected Mn3+ and Mn4+ contributions, which increases with time. The similarity of the spectral results obtained by total electron yield and fluorescence yield spectroscopy indicates that the location of the Mn valence anomalies is not confined to a narrow surface region of the film, but can extend throughout the whole thickness of the sample. High temperature annealing at 1000 C in air, immediately after growth, improves the magnetic and transport properties of such films towards the bulk values and the Mn2+ signature in the spectra does not appear. The Mn valence is then stable even to prolonged air exposure. We propose a mechanism for the Mn2+ ions formation and discuss the importance of these observations with respect to previous findings and production of thin films devices.

cond-mat.mtrl-sci

Exchange bias in laterally oxidized Au/Co/Au nanopillars

Au/Co/Au nanopillars fabricated by colloidal lithography of continuous trilayers exhibit and enhanced coercive field and the appearance of an exchange bias field with respect to the continuous layers. This is attributed to the lateral oxidation of the Co interlayer that appears upon disc fabrication. The dependence of the exchange bias field on the Co nanodots size and on the oxidation degree is analyzed and its microscopic origin clarified by means of Monte Carlo simulations based on a model of a cylindrical dot with lateral core/shell structure.

cond-mat.mtrl-sci

Magnetic dead layers in La2/3Ca1/3MnO3 thin films probed by X-ray magnetic circular dichroism in reflection

Surface magnetic properties of perovskite manganites have been a recurrent topic during last years since they play a major role in the implementation of magnetoelectronic devices. Magneto-optical techniques, such as X-ray magnetic circular dichroism, turn out to be a very efficient tool to study surface magnetism due to their sensitivity to magnetic and chemical variations across the sample depth. Nevertheless, the application of the sum rules for the determination of the spin magnetic moment might lead to uncertainties as large as 40% in case of Mn ions. To overcome this problem we present an alternative approach consisting of using X-ray magnetic circular dichroism in reflection geometry. Fit of the data by using a computer code based in a 4X4 matrix formalism leads to realistic results. In particular, we show that surface and interface roughness are of major relevance for a proper description of the experimental data and a correct interpretation of the results. By using such an approach we demonstrate the presence of a narrow surface region with strongly depressed magnetic properties in La2/3Ca1/3MnO3 thin films.

cond-mat.mtrl-sci

Formation of Mn2+ in La2/3Ca1/3MnO3 Thin Films due to Air Exposure

We report on the chemical stability of La2/3Ca1/3MnO3 thin films. X-ray absorption spectroscopy at the Mn L-edge and O K-edge makes evident deviations from the nominally expected (2/3-1/3) Mn3+/Mn4+ ratio after the growth of thin films on LaAlO3 substrates. As-grown thin films, exhibiting Curie temperature, TC, well below that of the LCMO bulk material, develop an unexpected Mn2+ contribution after a few days of air exposure which increases with time. Moreover, a reduction of the saturation magnetization, MS, is also detected. The similarity of the results obtained by electron yield and fluorescence yield demonstrates that the location of the Mn valence anomalies are not confined to a narrow surface region of the film but can extend throughout the film thickness in case of granular films. High temperature annealing not only improves the magnetic and transport properties of such as-grown films but also recovers the expected 2/3-1/3 Mn3+/Mn4+ ratio, which thereafter is stable to air exposure. Similar results on La2/3Ca1/3MnO3 films grown on SrTiO3 and NdGaO3 substrates demonstrate that there is no direct relation between the observed Mn valence instability and the strain state of the films due to their lattice mismatch with the substrate. A mechanism for the formation of Mn2+ ions formation is discussed.

cond-mat.mtrl-sci

Cationic ordering control of magnetization in Sr2FeMoO6 double perovskite

The role of the synthesis conditions on the cationic Fe/Mo ordering in Sr2FeMoO6 double perovskite is addressed. It is shown that this ordering can be controlled and varied systematically. The Fe/Mo ordering has a profound impact on the saturation magnetization of the material. Using the appropriate synthesis protocol a record value of 3.7muB/f.u. has been obtained. Mossbauer analysis reveals the existence of two distinguishable Fe sites in agreement with the P4/mmm symmetry and a charge density at the Fe(m+) ions significantly larger than (+3) suggesting a Fe contribution to the spin-down conduction band. The implications of these findings for the synthesis of Sr2FeMoO6 having optimal magnetoresistance response are discussed.

cond-mat