Carmen Munuera

Reversible Resistive Switching and Multilevel Recording in La0.7Sr0.3MnO3 Thin Films for Low Cost Nonvolatile Memories

On the basis of a scanning probe microscopy strategy, we propose a combined methodology capable to program nonvolatile multilevel data and read them out in a noninvasive manner. In the absence of the common two-electrode cell geometry, this nanoscale approach permits, in addition, investigating the relevance of inherent film properties. We demonstrate the feasibility of modifying the local electronic response of La(0.7)Sr(0.3)MnO(3) to obtain nanostructures with switchable resistance embedded in low cost oxide thin films, which constitutes a promising approach for fabricating high density nonvolatile memories.

Grafting of Monocarboxylic Substituted Polychlorotriphenylmethyl Radicals onto a COOH-Functionalized Self-Assembled Monolayer through Copper (II) Metal Ions

A monocarboxylic substituted polychlorotriphenylmethyl radical (PTMCOOH) has been grafted onto a COOH-functionalized SAM (mercaptohexadecanoic acid, MHDA SAM), using copper (II) metal ions as linkers between the carboxyl groups of the SAM and the ligand. The metal-radical adlayer has been characterized thoroughly using different surface analysis techniques, such as contact angle, IRRAS, XPS, SPR, ToF-SIMS, SFM, and NEXAFS. The magnetic character was confirmed by EPR. The density of unoccupied states was investigated using X-ray absorption spectroscopy. A low-energy peak in the NEXAFS spectrum directly revealed the presence of partially occupied electronic levels, thus proving the open-shell character of the grafted ligands. SEM measurements on a laterally patterned sample prepared by muCP of MHDA in a matrix of hexadecane thiolate (a CH 3-terminated SAM) was performed to demonstrate that the metal-assisted anchoring of the open-shell ligand occurs selectively on the COOH terminated SAM. These results represent an easy and new approach to anchor organic radicals on surfaces and constitute a first step toward the growth of magnetic metal-organic radical-based frameworks on solid substrates.

Exploring the Tilt-Angle Dependence of Electron Tunneling across Molecular Junctions of Self-Assembled Alkanethiols

Electronic transport mechanisms in molecular junctions are investigated by a combination of first-principles calculations and current-voltage measurements of several well-characterized structures. We study self-assembled layers of alkanethiols grown on Au(111) and form tunnel junctions by contacting the molecular layers with the tip of a conductive force microscope. Measurements done under low-load conditions permit us to obtain reliable tilt-angle and molecular length dependencies of the low-bias conductance through the alkanethiol layers. The observed dependence on tilt-angle is stronger for the longer molecular chains. Our calculations confirm the observed trends and explain them as a result of two mechanisms, namely, a previously proposed intermolecular tunneling enhancement as well as a hitherto overlooked tilt-dependent molecular gate effect.

Scanning force microscopy three-dimensional modes applied to conductivity measurements through linear-chain organic SAMs

We present here a new approach, based on the use of three-dimensional operation modes of scanning force microscopy. The protocol used reveals the advantages of independent but simultaneous data acquisition to discriminate between different interaction regimes and obtain accurate measurements. The procedure is applied to investigate the conducting characteristics of submonolayer linear-chain organic films for which the bare metallic substrate provides an excellent in situ reference for molecular lattice periodicity, film thickness determination and conductivity measurements.

Nanomechanical properties of surface-modified titanium alloys for biomedical applications

The mechanical properties of the oxide layers developed at elevated temperature on three vanadium-free titanium alloys of interest for biomedical applications were investigated by means of the nanoindentation technique. The as-received alloys (Ti-13Nb-13Zr, Ti-15Zr-4Nb and Ti-7Nb-6Al) and their oxide scales formed by reaction with air at 750 degrees C for several oxidation times were analysed comparatively. In particular, the hardness and the Youngs modulus exhibit larger values for the thermally oxidized alloys than for the untreated specimens. However, the Ti-7Nb-6Al alloy shows a different tendency to that of the TiNbZr alloys, which seems to be related to a different oxide layer growth as a function of the oxidation time.

Contrast inversion in non-contact Dynamic Scanning Force Microscopy: What is high and what is low?

The present work proves that when non-contact Dynamic Scanning Force Microscopy (DSFM) is performed in ambient conditions wrong height measurements of heterogeneous samples can be obtained. In some extreme cases even contrast inversion can be observed. Alkanethiol islands on Au (111) have been used as model system, where contrast inversion is observed with different DSFM modes and various data acquisition parameters. To understand this effect, spectroscopy measurements have been used to show that contrast inversion is really a consequence of the differences in the interaction measured between tip and sample on the bare Au substrate and on the alkanethiol islands. We propose that this interaction is mainly induced by liquid necks forming between tip and sample, which is much stronger on the hydrophilic Au substrate than on the hydrophobic alkanethiol islands.

Quantitative electrostatic force microscopy on heterogeneous nanoscale samples

Locally resolved electrostatic force spectroscopy is combined with Kelvin force microscopy to compare the results obtained using either the force or the frequency as signal source for tip-sample interaction. A two-component locally heterogeneous sample—islands of octadecanethiol molecules self-assembled on Au(111)—is used as a nanometer scale model system. On this kind of sample, electrostatic force spectroscopy as well as Kelvin force microscopy clearly demonstrate that local and quantitative electrostatic force microscopy has to be implemented with the frequency as the signal source.

Phase separation enhanced magneto-electric coupling in La0.7Ca0.3MnO3/BaTiO3 ultra-thin films.

We study the origin of the magnetoelectric coupling in manganite films on ferroelectric substrates. We find large magnetoelectric coupling in La0.7Ca0.3MnO3/BaTiO3 ultra-thin films in experiments based on the converse magnetoelectric effect. The magnetization changes by around 30–40% upon applying electric fields on the order of 1 kV/cm to the BaTiO3 substrate, corresponding to magnetoelectric coupling constants on the order of α = (2–5)·10−7 s/m. Magnetic anisotropy is also affected by the electric field induced strain, resulting in a considerable reduction of coercive fields. We compare the magnetoelectric effect in pre-poled and unpoled BaTiO3 substrates. Polarized neutron reflectometry reveals a two-layer behavior with a depressed magnetic layer of around 30 Å at the interface. Magnetic force microscopy (MFM) shows a granular magnetic structure of the La0.7Ca0.3MnO3. The magnetic granularity of the La0.7Ca0.3MnO3 film and the robust magnetoelastic coupling at the La0.7Ca0.3MnO3/BaTiO3 interface are at the origin of the large magnetoelectric coupling, which is enhanced by phase separation in the manganite.

Low temperature metal free growth of graphene on insulating substrates by plasma assisted chemical vapor deposition

Direct growth of graphene films on dielectric substrates (quartz and silica) is reported, by means of remote electron cyclotron resonance plasma assisted chemical vapor deposition r-(ECR-CVD) at low temperature (650°C). Using a two step deposition process- nucleation and growth- by changing the partial pressure of the gas precursors at constant temperature, mostly monolayer continuous films, with grain sizes up to 500 nm are grown, exhibiting transmittance larger than 92% and sheet resistance as low as 900 Ω·sq-1. The grain size and nucleation density of the resulting graphene sheets can be controlled varying the deposition time and pressure. In additon, first-principles DFT-based calculations have been carried out in order to rationalize the oxygen reduction in the quartz surface experimentally observed. This method is easily scalable and avoids damaging and expensive transfer steps of graphene films, improving compatibility with current fabrication technologies.

Atomically Flat Ultrathin Cobalt Ferrite Islands

A route for fabricating structurally perfect cobalt ferrite magnetic nanostructures is demonstrated. Ultrathin islands of up to 100 μm(2) with atomically flat surfaces and free from antiphase boundaries are developed. The extremely low defect concentration leads to a robust magnetic order, even for thicknesses below 1 nm, and exceptionally large magnetic domains. This approach allows the evaluation of the influence of specific extrinsic effects on domain wall pinning.