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Raul Arenal

Publications and source records attributed to Raul Arenal.

At least 19 recordsLinked to original sources

Low-Dose 3D Bonding Mapping Through "Soft" Core-Loss EELS Tomography and Unsupervised Deep Learning

Resolving the 3D chemical configuration of beam-sensitive nanomaterials at high spatial resolution remains a persistent frontier in scanning transmission electron microscopy (STEM). The main limitation lies in the trade-off between high electron dose required for analytical signals and the large number of projections needed for tomographic reconstruction. Here, we achieve dose-efficient 3D bonding mapping of FeO/Fe$_3$O$_4$ core-shell nanocubes with high resolution via electron energy loss spectroscopy (EELS). Our approach relies on two developments. First, a standardless "soft" core-loss EELS methodology exploiting Fe-M$_{2,3}$ edges provides ${\sim}50\times$ higher dose efficiency than conventional Fe-L$_{2,3}$ edges, using the latter only as a source of FeO and Fe$_3$O$_4$ standards. Second, we introduce multi-channel deep image prior with total variation regularization (DIPm-TV), an unsupervised method for spectroscopic tomography that jointly reconstructs multiple channels by exploiting spatial correlations under sparse-view and low-dose conditions. Using simulated datasets, high-quality reconstructions are obtained from as few as nine projections over $-70^\circ$ to $+70^\circ$, without HAADF-STEM signal or symmetry constraints. Applied to FeO/Fe$_3$O$_4$ nanocubes, Fe-M$_{2,3}$ EELS maps show improved SNR and spatial resolution, revealing a thin outer FeO shell surrounding the magnetite shell. DIPm-TV yields ${\sim}1$ nm isotropic resolution oxidation-state volumes preserving cubic morphology, recovering the outer FeO shell, and revealing a small internal void, features not accessible with conventional reconstruction methods. This work establishes a pathway for low-dose 2D and 3D analytical mapping of beam-sensitive materials using shallow core-loss edges, enabling orders-of-magnitude dose reduction while maintaining spectral fidelity and reliable 3D information.

eess.IV

Degenerate monolayer Ising superconductors via chiral-achiral molecule intercalation

Engineering unconventional superconductors is a central challenge in condensed matter physics. Molecule-intercalated TaS2 superlattices have recently been reported to host such states, yet their origin remains debated, underscoring the urgent need for controlled, device-integrated studies. Here, we report that nanometer-thick TaS2 and NbSe2 intercalated with chiral and achiral organic cations instead exhibit robust monolayer-like Ising superconductivity, with no evidence of unconventional pairing. Using high-quality superlattices integrated into devices, we disentangle the roles of interlayer coupling and charge transfer in shaping their superconducting behavior. In TaS2, intercalation induces interlayer decoupling regardless of molecular size or symmetry, yielding monolayer-like Ising superconductivity. NbSe2 instead retains quasi-three-dimensional transport, with a gradual Ising enhancement and near-monolayer behavior only at the largest interlayer spacing. Transport remains reciprocal across all superlattices, consistent with preserved inversion symmetry and incompatible with parity-breaking superconductivity and noncentrosymmetric monolayers. We attribute the behavior to electronically detached monolayers with opposite spin-split bands, coupled through thermal and tunneling processes, which overall preserve inversion symmetry. These findings establish molecular intercalation compounds as a robust, device-ready, platform for engineering advanced superconducting superlattices.

cond-mat.supr-con

Mechanical and electrical properties of a nano-gap or how to play the nano-accordion

In-situ transmission electron microscopy (TEM) has become an important technique to study dynamic processes at highest spatial resolution and one branch is the investigation of phenomena related with electrical currents. Here, we present experimental results obtained from a peculiar in-situ TEM device, which was prepared with the aim to analyze the relationship between (thermo)electric properties and specific crystal orientations of a misfit layered compound. The formation of a nano-sized gap at a grain boundary facilitated a precisely controllable mechanical bending of the device by application of differential heating currents. The devices' electrical properties were found to be substantially influenced by the gap, leading to a high intrinsic voltage. This voltage additionally depends on the vacuum environment and on the history of applied heating currents. These findings are largely attributed to the presence of adsorbed molecules within the gap region. The electrical in-situ TEM studies of this work illustrate that interior surfaces can strongly influence electrical properties even under high vacuum conditions.

cond-mat.mes-hall

Direct Visualization of Temperature-Induced Phase Separation of Completely Miscible Au-Pd Alloy by In-Situ TEM

In-situ transmission electron microscopy (TEM) studies reveal key insights into the structural and chemical evolution of nanoparticles (NPs) under external stimuli like heating and biasing, which is critical for evaluating their suitability in chemical reactions and their tendency towards forming novel NP systems. In this study, starting from a core@shell Au nanotriangle (AuNT)@Pd nanostructure, the formation of a phase-separated bi-metallic Au-Pd NP system at high temperature is reported, despite the fact that Au and Pd are miscible in the entire composition and temperature range. In-situ TEM heating of bare AuNT@Pd core@shell structures up to 1000{\deg}C has been performed. Between 400{\deg}C and 800{\deg}C, an initial alloy formation has been observed. It is also noted that higher initial loading of Pd increases the melting temperature of the bi-metallic system. However, the most important observation is the separation of the nanostructure into Au and Pd phases at temperatures higher than 850{\deg} C for high Pd doping. The extent of Pd separation depends on the amount of initial Pd loading. A Janus Au-Pd nanostructure is formed at the end of the thermal treatments at 1000{\deg} C. The phase-separated NP is observed to be highly stable and could be clearly beneficial for various applications, particularly in catalytic processes.

cond-mat.mtrl-sci

Galvanic intercalation of molecular cations into van der Waals materials

The intercalation of molecular species between the layers of van der Waals (vdW) crystals is a powerful approach to combine the remarkable physical properties of vdW materials with the chemical versatility of organic molecules. However, the full transformative potential of molecular intercalation remains underexplored, largely due to the lack of simple, broadly applicable methods that preserve high crystalline quality down to the few-layer limit. Here, we introduce a simple galvanic approach to intercalate different molecules into various vdW materials under ambient conditions, leveraging the low reduction potential of selected metals. We employ our method, which is particularly well-suited for the in-situ intercalation of few-layer-thick crystals, to intercalate nine vdW materials, including magnets and superconductors, with molecules ranging from conventional alkylammonium ions to metallorganic and bio-inspired chiral cations. Notably, intercalation leads to an unprecedented transition from antiferromagnetic to ferrimagnetic ordering in {\alpha}-RuCl3 and to a molecule-dependent enhancement of the superconducting transition in 2H-TaS2. These results establish our approach as a versatile technique for engineering atomically thin quantum materials and heterostructures, unlocking the transformative effects of molecular intercalation.

cond-mat.mtrl-sci

Toward thermoelectric characterization of (nano)materials by in situ transmission electron microscopy

We explore the possibility to perform an in-situ transmission electron microscopy (TEM) thermoelectric characterization of materials. A differential heating element on a custom in-situ TEM microchip allows to generate a temperature gradient across the studied materials, which are simultaneously measured electrically. A thermovoltage was induced in all studied devices, whose sign corresponds to the sign of the Seebeck coefficient of the tested materials. The results indicate that in-situ thermoelectric TEM studies can help to profoundly understand fundamental aspects of thermoelectricity, which is exemplary demonstrated by tracking the thermovoltage during in-situ crystallization of an amorphous Ge thin film. We propose an improved in-situ TEM microchip design, which should facilitate a full quantitative measurement of the induced temperature gradient, the electrical and thermal conductivities, as well as the Seebeck coefficient. The benefit of the in-situ approach is the possibility to directly correlate the thermoelectric properties with the structure and chemical composition of the entire studied device down to the atomic level, including grain boundaries, dopants or crystal defects, and to trace its dynamic evolution upon heating or during the application of electrical currents

cond-mat.mtrl-sci

Stable CoO$_2$ Nanoscrolls With Outstanding Electrical Properties

Layered CoO$_2$ is of great interest for its promising properties but is meta-stable in its bulk form. CoO$_2$ was synthesized by converting the quasi-one-dimensional crystal structure of bulk Ca$_3$Co$_2$O$_6$ via a hydrothermal treatment. The resulting nanostructures were predominantly nanoscrolls with very thin walls, which exhibit long-term stability. A detailed structural investigation reveals that the CoO$_2$ is found to crystallize in monoclinic form, similar to the related CaCoO$_2$-CoO$_2$ misfit structure. Individual nanoscrolls are characterized electrically and show a p-type semiconducting nature with a high current-carrying capacity of 4$\cdot$10$^5$ A cm$^{-2}$ and an extremely high breakdown voltage of up to 270 kV/cm. The results demonstrate the possibility to stabilize meta-stable materials in low-dimensional forms and a promising application of the nanoscrolls as interconnect in high-voltage electronic circuitry.

cond-mat.mtrl-sci

Support-based transfer and contacting of individual nanomaterials for in-situ nanoscale investigations

Although in-situ transmission electron microscopy (TEM) of nanomaterials has been gaining importance in recent years, difficulties in sample preparation have limited the number of studies on electrical properties. Here, a support-based preparation method of individual 1D and 2D materials is presented, which yields a reproducible sample transfer for electrical investigation by in-situ TEM. Using a mechanically rigid support grid allows the reproducible transfer and contacting to in-situ chips by focused ion beam with minimum damage and contamination. The transfer quality is assessed by exemplary studies of different nanomaterials, including a monolayer of WS2. Preliminary results from in-situ test experiments give an overview of possible studies, which concern the interplay between structural properties and electrical characteristics on the individual nanomaterial level as well as failure analysis under electrical current or studies of electromigration, Joule heating and related effects. The TEM measurements can be enriched by additional correlative microscopy techniques, which allow the study with a spatial resolution in the range of a few microns. Although developed for in-situ TEM, the present transfer method is also applicable to transferring nanomaterials to similar chips for performing further studies or even for using them in potential electrical/optoelectronic/sensing devices.

cond-mat.mes-hall

Quasi 1D Nanobelts from the Sustainable Liquid Exfoliation of Terrestrial Minerals for Future Martian based Electronics

The sky is the limit with regards to the societal impact nanomaterials can have on our lives. However, in this study we show that their potential is out of this world. The planet Mars has an abundant source of calcium sulfate minerals and in our work, we show that these deposits can be the basis of transformative nanomaterials to potentially support future space endeavors. Through a scalable eco-friendly liquid processing technique performed on two common terrestrial gypsum, our simple method presented a cost-efficient procedure to yield the commercially valuable intermediate phase of gypsum, known as bassanite. Through the liquid exfoliation of bassanite powders, suspensions of large aspect ratio anhydrite nanobelts with long-term stability were characterized through scanning electron microscopy and Raman spectroscopy. Transmission electron microscopy showed nanobelts to have a mesocrystal structure, with distinct nanoparticle constituents making up the lattice. Unexpectedly, anhydrite nanobelts had remarkable electronic properties, namely a bandgap that was easily tuned between semiconducting (~2.2 eV) and insulating (~4 eV) behaviors through dimensional control measured via atomic force microscopy. To demonstrate the application potential of our nanobelts; optoelectronic, electrochemical and nanocomposite measurements were made. For the hydrogen evolution reaction and mechanical reinforcement, selenite-based anhydrite nanobelts displayed superlative performances.

physics.app-ph

Room-Temperature Anomalous Hall Effect in Graphene in Interfacial Magnetic Proximity with EuO Grown by Topotactic Reduction

We show that thin layers of EuO, a ferromagnetic insulator, can be achieved by topotactic reduction under titanium of a Eu2O3 film deposited on top of a graphene template. The reduction process leads to the formation of a 7-nm thick EuO smooth layer, without noticeable structural changes in the underlying chemical vapor deposited (CVD) graphene. The obtained EuO films exhibit ferromagnetism, with a Curie temperature that decreases with the initially deposited Eu2O3 layer thickness. By adjusting the thickness of the Eu2O3 layer below 7 nm, we promote the formation of EuO at the very graphene interface: the EuO/graphene heterostructure demonstrates the anomalous Hall effect (AHE), which is a fingerprint of proximity-induced spin polarization in graphene. The AHE signal moreover persists above Tc up to 350K due to a robust super-paramagnetic phase in EuO. This original high-temperature magnetic phase is attributed to magnetic polarons in EuO: we propose that the high strain in our EuO films grown on graphene stabilizes the magnetic polarons up to room temperature. This effect is different from the case of bulk EuO in which polarons vanish in the vicinity of the Curie temperature Tc= 69K.

cond-mat.mtrl-sci

Onion-like Fe3O4/MgO/CoFe2O4 magnetic nanoparticles: new ways to control magnetic coupling between soft/hard phases

The control of the magnetization inversion dynamics is one of the main challenges driving the design of new nanostructured magnetic materials for magnetoelectronic applications. Nanoparticles with onion-like architecture offer a unique opportunity to expand the possibilities allowing to combine different phases at the nanoscale and also modulate the coupling between magnetic phases by introducing spacers in the same structure. Here we report the fabrication, by a three-step high temperature decomposition method, of Fe3O4/MgO/CoFe2O4 onio-like nanoparticles and their detailed structural analysis, elemental compositional maps and magnetic response. The core/shell/shell nanoparticles present epitaxial growth and cubic shape with overall size of (29+-6) nm. These nanoparticles are formed by cubic iron oxide core of (22+-4) nm covered by two shells, the inner of magnesium oxide and the outer of cobalt ferrite of ~1 and ~2.5 nm of thickness, respectively. The magnetization measurements show a single reversion magnetization curve and the enhancement of the coercivity field, from HC~608 Oe for the Fe3O4/MgO to HC~5890 Oe to the Fe3O4/MgO/CoFe2O4 nanoparticles at T=5 K, ascribed to the coupling between both ferrimagnetic phases with a coupling constant of =2 erg/cm2. The system also exhibits exchange bias effect, where the exchange bias field increases up to HEB~2850 Oe at 5 K accompanied with the broadening of the magnetization loop of HC~6650 Oe. This exchange bias effect originates from the freezing of the surface spins below the freezing temperature TF=32 K that pinned the magnetic moment of the cobalt ferrite shell.

cond-mat.mes-hall

Molybdenum diselenide-manganese porphyrin bifunctional electrocatalyst for hydrogen evolution reaction and selective hydrogen peroxide production

Electrochemical reactions for hydrogen and hydrogen peroxide production are essential for energy conversion to diminish energy crisis, but still lack efficient electrocatalysts. Development of non\-noble metal bifunctional electrocatalysts for hydrogen evolution and 2e oxygen reduction reaction to ease reaction kinetics is a challenging task. Integration of single components by employing easy strategies provides a key\-step towards the realization of highly active electrocatalysts. In this vein, MoSe2 owns catalytic active sites and high specific surface area but suffers from insufficient conductivity and high catalytic performance that noble\-metals provide. Herein, MoSe2 was used as a platform for the incorporation of manganese metallated porphyrin. The developed hybrid, namely MoSe2\-MnP, by the initial metal\-ligand coordination and the subsequent grafting with MnP was fully characterized and electrochemically assessed. The bifunctional electrocatalyst lowered the overpotential toward hydrogen evolution, improved reaction kinetics and charge transfer processes and was extremely stable after 10000 ongoing cycles. Simultaneously, rotating ring disk electrode analysis showed that oxygen reduction proceeds through the 2e pathway for the selective production of hydrogen peroxide with a high yield of 97 percent. The new facile modification route can be applied in diverse transition metal dichalcogenides and will help the development of new advanced functional materials.

cond-mat.mtrl-sci

Crystalline Phase Effects on the Nonlinear Optical Response of MoS2 and WS2 Nanosheets

In the present work, some MoS2 and WS2 nanosheets were prepared and characterized. Depending on the preparation procedures, trigonal prismatic (2H) or octahedral (1T) coordination of the metal atoms were obtained, exhibiting metallic (1T) or semiconducting (2H) character. Both MoS2 and WS2 nanosheets were found exhibiting large nonlinear optical (NLO) response, strongly dependent on their metallic (1T) or semiconducting (2H) character. So, the semiconducting character 2H-MoS2 and 2H-WS2 exhibit positive nonlinear absorption and strong self-focusing, while their metallic character counterparts exhibit strong negative nonlinear absorption and important self-defocusing. In addition, the semiconducting MoS2 and WS2 were found exhibiting important and very broadband optical limiting action extended from 450 to 1750 nm. So, by selecting the crystalline phase of the nanosheets, i.e., their semiconduction/metallic character, their NLO response can be greatly modulated. The results of the present work demonstrate unambiguously that the control of the crystalline phase of MoS2 and WS2 provides an efficient strategy for 2D nanostructures with custom made NLO properties for specific optoelectronic and photonic applications.

cond-mat.mtrl-sci

Asymmetrical plasmon distribution in hybrid AuAg hollow/solid coded nanotubes

Morphological control at the nanoscale paves the way to fabricate nanostructures with desired plasmonic properties. We report the nanoengineering of plasmon resonances in 1D hollow nanostructures of two different AuAg nanotubes; completely hollow nanotubes and hybrid nanotubes comprising solid Ag and hollow AuAg segments. Spatially resolved plasmon mapping by electron energy loss spectroscopy (EELS) revealed the presence of high order resonator-like modes and localized surface plasmon resonance (LSPR) modes in both nanotubes. Experimental findings are accurately correlated with boundary element method (BEM) simulations, where both experiments and simulations revealed that the plasmon resonances are intensely present inside the nanotubes due to plasmon hybridization. Based on the experimental and simulated results reported, we show that the novel hybrid AuAg nanotubes possess two significant coexisting features: (i) LSPRs have been generated distinctively from the hollow and solid parts of the hybrid AuAg nanotube, which opens the way to control a broad range of plasmon resonances with one single nanostructure and (ii) the periodicity of the high-order modes are disrupted due to the plasmon hybridization by the interaction of solid and hollow parts, resulting in an asymmetrical plasmon distribution in 1D nanostructures. The asymmetry could be modulated/engineered leading to control coded plasmonic nanotubes.

physics.app-ph

Photo-Rechargeable Li Ion Batteries using TiS2 Cathode

Photo-rechargeable (solar) battery can be considered as an energy harvesting cum storage system, where it can charge the conventional metal-ion battery using light instead of electricity, without having other parasitic reactions. Here we demonstrate a two-electrode lithium ion solar battery with multifaceted TiS2-TiO2 hybrid sheets as cathode. Choice of TiS2-TiO2 electrode ensures the formation of a type II semiconductor heterostructure while the lateral heterostructure geometry ensures high mass/charge transfer and light interactions with the electrode. TiS2 has a higher lithium binding energy (1.6 eV) than TiO2 (1.03 eV), ensuring the possibilities of higher amount of Li ion insertion to TiS2 and hence the maximum recovery with the photocharging, as further confirmed by the experiments. Apart from the demonstration of solar solid-state batteries, the charging of lithium ion full cell with light indicates the formation of lithium intercalated graphite compounds, ensuring the charging of the battery without any other parasitic reactions at the electrolyte or electrode-electrolyte interfaces. Possible mechanisms proposed here for the charging and discharging processes of solar batteries, based on our experimental and theoretical results, indicate the potential of such systems in forthcoming era of renewable energies.

physics.app-ph

Catalysts for the hydrogen evolution reaction in alkaline medium: Configuring a cooperative mechanism at the Ag-Ag$_2$S-MoS$_2$ interface

Designing electrocatalysts for HER in alkaline conditions to overcome the sluggish kinetics associated with the additional water dissociation step is a recognized challenge in promoting the hydrogen economy. To this end, delicately tuning the atomic-scale structure and surface composition of nanoparticles is a common strategy and, specifically, making use of hybrid structures, can produce synergistic effects that lead to highly active catalysts. Here, we present a core-shell catalyst of Ag@MoS$_2$ that shows promising results towards the hydrogen evolution reaction (HER) in both 0.5 M H2SO4 and 0.5 M KOH. In this hybrid structure, the MoS$_2$ shell is strained and defective, and charge transfer occurs between the conductive core and the shell, contributing to the electrocatalytic activity. The shelling process results in a large fraction of Ag$_2$S in the cores, and adjusting the relative fractions of Ag, Ag$_2$S, and MoS$_2$ leads to improved catalytic activity and fast charge-transfer kinetics. We suggest that the enhancement of alkaline HER is associated with a cooperative effect of the interfaces, where the Ag(I) sites in Ag$_2$S drive the water dissociation step, and the formed hydrogen subsequently recombines on the defective MoS$_2$ shell. This study demonstrates the benefits of hybrid structures as functional nanomaterials and provides a scheme to activate MoS$_2$ for HER in alkaline conditions.

cond-mat.mtrl-sci

On the Existence of Photoluminescence and Room-Temperature Spin Polarization in Ambipolar V doped MoS$_2$ Monolayers

Opto-spintronics is an emerging field where ultra-thin magnetic-semiconductors having high spin-valley coupling play an important role. Here, we demonstrate substitutional vanadium (V) doping in MoS$_2$ lattice in different extent, leading to the coexistence of photoluminescence (PL), valleypolarization (~32%), and valley splitting (~28 meV shift in PL with helicity $\sigma^+$ and $\sigma^-$ of light excitation). A large V doping causes semiconductor to metal transition in MoS$_2$ but with medium level causing the existence of photoluminescence with high spin polarization. The ambipolar nature of medium level V doped MoS$_2$ is shown here indicating its potential as an opto-electronic material. The presence of V-dopants and their different level of content are proven by both spectroscopic and microscopic methods.A detailed temperature and power dependent photoluminescence studies along with density functional theory-based calculations in support unravels the emergence of the co-existence of spin-valley coupling and photoluminescence. This study shows the potential of doping MoS$_2$ for deriving new materials for next generation room temperature opto-spintronics.

physics.app-ph

Aberration-corrected transmission electron microscopy with Zernike phase plates

We explore the possibility of applying physical phase plates (PPs) in combination with aberration-corrected transmission electron microscopy. Phase-contrast transfer characteristics are calculated and compared for a thin-film based Zernike PP, a hole-free (HF) or Volta PP and an electrostatic Zach PP, considering their phase-shifting properties in combination with partial spatial coherence. The effect of slightly converging illumination conditions, often used in high-resolution applications, on imaging with PPs is discussed. Experiments with an unheated Zernike PP applied to various nanomaterial specimens and a qualitative analysis clearly demonstrates the general compatibility of PPs and aberration-corrected transmission electron microscopy. Calculations and experiments show the benefits of the approach, among which is a strong phase-contrast enhancement of a large range of spatial frequencies. This allows the simultaneous imaging of atomic-resolution structures and morphological features at the nanometer scale, with maximum phase contrast. The calculations can explain why the HFPP damps contrast transfer at higher spatial frequencies.

physics.ins-det