Topological massive Dirac edge modes and long-range superconducting Hamiltonians

We discover novel topological effects in the one-dimensional Kitaev chain modified by long-range Hamiltonian deformations in the hopping and pairing terms. This class of models display symmetry-protected topological order measured by the Berry/Zak phase of the lower-band eigenvector and the winding number of the Hamiltonians. For exponentially decaying hopping amplitudes, the topological sector can be significantly augmented as the penetration length increases, something experimentally achievable. For power-law decaying superconducting pairings, the massless Majorana modes at the edges get paired together into a massive nonlocal Dirac fermion localized at both edges of the chain: a new topological quasiparticle that we call topological massive Dirac fermion. This topological phase has fractional topological numbers as a consequence of the long-range couplings. Possible applications to current experimental setups and topological quantum computation are also discussed

AC Electrokinetics of Salt-Free Multilayered Polymer-Grafted Particles

Interest in the electrical properties of the interface between soft (or polymer-grafted) nanoparticles and solutions is considerable. Of particular significance is the case of polyelectrolyte-coated particles, mainly taking into account that the layer-by-layer procedure allows the control of the thickness and permeability of the layer, and the overall charge of the coated particle. Like in simpler systems, electrokinetic determinations in AC fields (including dielectric dispersion in the 1 kHz–1 MHz frequency range and dynamic electrophoresis by electroacoustic methods in the 1–18 MHz range) provide a large amount of information about the physics of the interface. Different models have dealt with the electrokinetics of particles coated by a single polymer layer, but studies regarding multi-layered particles are far scarcer. This is even more significant in the case of so-called salt-free systems; ideally, the only charges existing in this case consist of the charge in the layer(s) and the core particle itself, and their corresponding countercharges, with no other ions added. The aims of this paper are as follows: (i) the elaboration of a model for the evaluation of the electrokinetics of multi-grafted polymer particles in the presence of alternating electric fields, in dispersion media where no salts are added; (ii) to carry out an experimental evaluation of the frequency dependence of the dynamic (or AC) electrophoretic mobility and the dielectric permittivity of suspensions of polystyrene latex spherical particles coated with successive layers of cationic, anionic, and neutral polymers; and (iii) finally, to perform a comparison between predictions and experimental results, so that it can be demonstrated that the electrokinetic analysis is a useful tool for the in situ characterization of multilayered particles.Spanish Institution, Ministerio de Ciencia, Innovacion y Universidades GC2018-098770-B-I00Junta de Andalucia BF-FQM-141-UGR1

Polylectrolyte- versus membrane-coated electrodes for energy production by Capmix salinity exchange methods

La versión final publicada se puede encontrar en: Journal of Power Sources, 302(20): 387-393 (2016). http://dx.doi.org/10.1016/j.jpowsour.2015.10.076In this paper we analyze the energy and power achievable by means of a re- cently proposed salinity gradient technique for energy production. The method, denominated soft electrode or SE, is based on the potential di erence that can be generated between two porous electrodes coated with cationic and anionic polyelectrolytes. It is related to the Capacitive Donnan Potential (CDP) tech- nique, where the electrical potential variations are mostly related to the Donnan potential, of ion-selective membranes in the case of CDP, and of the polyelec- trolyte coating in SE. It is found that although SE is comparable to CDP in terms of energy production, it presents slower rates of voltage change, and lower achieved power. The separate analysis of the response of positively and neg- atively coated electrodes shows that the latter produces most of the voltage rise and also of the response delay. These results, together with electrokinetic techniques, give an idea on how the two types of polyelectrolytes adsorb on the carbon surface and a ect di erently the di usion layer. It is possible to suggest that the SE technique is a promising one, and it may overcome the drawbacks associated to the use of membranes in CDP.MINECO FIS2013-47666-C3-1-RJunta de Andalucía, PE2012-FQM0694European Union 7th Framework Programme (FP7/2007–2013) under agreement No. 25686

Denaturing for nanoarchitectonics: local and periodic UV-laser photodeactivation of protein biolayers to create functional patterns for biosensing

The nanostructuration of biolayers has become a paradigm for exploiting nanoscopic light-matter phenomena for biosensing, among other biomedical purposes. In this work, we present a photopatterning method to create periodic structures of biomacromolecules based on a local and periodic mild denaturation of protein biolayers mediated by UV-laser irradiation. These nanostructures are constituted by a periodic modulation of the protein activity, so they are free of topographic and compositional changes along the pattern. Herein, we introduce the approach, explore the patterning parameters, characterize the resulting structures, and assess their overall homogeneity. This UV-based patterning principle has proven to be an easy, cost-effective, and fast way to fabricate large areas of homogeneous one-dimensional protein patterns (2 min, 15 × 1.2 mm, relative standard deviation ≃ 16%). This work also investigates the implementation of these protein patterns as transducers for diffractive biosensing. Using a model immunoassay, these patterns have demonstrated negligible signal contributions from non-specific bindings and comparable experimental limits of detection in buffer media and in human serum (53 and 36 ng·mL−1 of unlabeled IgG, respectively)

First steps in the formulation of praziquantel nanosuspensions for pharmaceutical applications

Praziquantel (PZQ), a broad spectrum anthelmintic drug, cannot be found in acceptable dosage forms for elderly patients, paediatric patients, and for veterinary use. In fact, very little has been done up to now in the formulation of liquid dosage forms, being they always formulated for parenteral administration. To beat this important challenge, it was accomplished a comprehensive analysis of the influence of two elementary physicochemical aspects, i.e. surface thermodynamic and electrokinetic properties, on the colloidal stability of PZQ nanosuspensions. The hydrophobic character of the drug, intensely determining the flocculation curves, was confirmed by the thermodynamic characterization. The electrophoretic characterization, in combination with the sedimentation and relative absorbance versus time curves, highlighted that the electrical double layer thickness and the surface charge can play an essential role in the stability of the pharmaceutical colloid. Finally, it was demonstrated that controlling the pH values and the incorporation of electrolytes can help in formulating PZQ aqueous nanosuspensions with appropriate stability and redispersibility behaviours for pharmaceutical use.Fil: Martinez, Noelia Anabel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Fernández Álvarez, Fátima. Universidad de Granada; EspañaFil: Delgado, Ángel V.. Universidad de Granada; EspañaFil: Badillo García, María Luisa. Universidad de Granada; EspañaFil: Raba, Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Cerutti, Estela Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Arias, José L.. Universidad de Granada; Españ

Electroacoustic Characterization of Bidisperse Suspensions

Electroacoustic techniques are promising tools for the size determination and electrokinetic characterization of concentrated colloidal suspensions. When particles are not homogeneous in size and/or density, the dynamic mobility obtained is a kind of average of the mobilities of every particle. In this paper, we try to discern which averaging procedure provides a better description of the dynamic mobility of bidisperse suspensions consisting of a mixture of two very different types of particles. The results show that the amplitude of the sound wave induced by an applied ac field (electrokinetic sonic amplitude) is not just the sum of the amplitudes of the waves generated by every particle but has a larger contribution from the larger particles, although the small size entities considerably influence the behaviour of the latter because of their interference in the fluxes of the fluid and ions around them

Electric Birefringence Spectroscopy of Montmorillonite Particles

Full version available at http://pubs.rsc.org/en/Content/ArticleLanding/2016/SM/C6SM00512H#!divAbstractElectric birefringence (EB) of suspensions of anisotropic particles can be considered an electrokinetic phenomenon in a wide sense, as both liquid motions and polarization of the electrical double layer (EDL) of the particles participate in the process of particle orientation under the applied field. The EB spectrum can be exploited for obtaining information on the dimensions, average value and anisotropy of the surface conductivity of the particles, and concentration and Maxwell-Wagner polarization of the EDLs. It is thus a highly informative technique, applicable to non-spherical particles. In this paper, we investigate the birefringent response of plate-like montmorillonite particles as a function of the frequency and amplitude of the applied AC electric field, for different compositions (pH, ionic strength, particle concentration) of the suspensions. The transient electric birefringence (i.e., the decay of the refractive index anisotropy with time when the field is switched off) is used for estimating the average dimensions of the particle axes, by modeling it as an oblate spheroid. The obtained values are very similar to those deduced from electron microscopy determinations. The frequency spectra show a very distinct behaviour at low (on the order of a few Hz) and high (up to several MHz) frequencies: the $\alpha$ and Maxwell-Wagner-O'Konski relaxations, characteristic of EDLs, are detected at frequencies above 10 kHz, and they can be well explained using electrokinetic models for the polarization of EDLs. At low frequencies, in contrast, the birefringence changes to negative, an anomalous response meaning that the particles tend to orient with their symmetry axis parallel to the field. This anomaly is weaker at basic pHs, high ionic strengths and low concentrations. The results can be explained by considering the polydispersity of real samples: the fastest particles redistribute around the slowest ones, inducing a hydrodynamic torque opposite to that of the field, in close similarity with results previously described for mixtures of anisometric particles with small amounts of spherical nanoparticles.Junta de Andalucía, Spain (PE2012-FQM0694)MINECO, Spain (project No. FIS2013-47666-C3-1-R)Ramón y Cajal Programme (RYC-2014-16901)[EMBARGADO hasta mayo 2017

Chemical, thermal and viscous characterization of high-oleic sunflower and olive pomace acid oils and derived estolides

This work deals with the chemical, thermal and viscous characterization of a variety of estolides, prepared from higholeic sunflower and olive pomace acid oils, using different acid-catalyzed synthesis protocols and reaction times. Estolides with weight-average molecular weights between 1.7 and 3.4 times higher than the original acid oils were obtained. The molecular weight of the estolides was higher when using the sulphuric acid-catalyzed method and a reaction time of 3-6 h. Estolides presented higher freezing temperatures than acid oils. In general, viscosity values are related to estolide molecular weight. Significant increments in viscosities were found in comparison with acid oils. Maximum viscosity values were obtained for estolides prepared using the sulphuric acidcatalyzed method. The largest viscosity increments in olive pomace acid oil-derived estolides were observed during the first 6 hours of reaction, due to an increase in the molecular weight; longer reaction times yielded adverse results. The temperature dependence of viscosity for all estolides studied is significantly larger than for the original acid oils.Este trabajo presenta la caracterización química, térmica y viscosa de estólidos preparados a partir de oleínas ácidas de girasol alto-oleico y de orujo de oliva, utilizando diferentes métodos catalizados por ácidos y diferentes tiempos de reacción. Se obtuvieron estólidos con pesos moleculares promedios en peso entre 1,7 y 3,4 veces más altos que las oleínas de origen. El peso molecular de los estólidos aumenta cuando se utiliza el método catalizado por ácido sulfúrico y un tiempo de reacción de 3-6 h. Los estólidos obtenidos presentan temperaturas de congelación más altas que las oleínas. En general, los valores de viscosidad están relacionados con el peso molecular del estólido. Se encontraron incrementos significativos de viscosidad en comparación con las oleínas. Los valores máximos de viscosidad se obtuvieron para los estólidos preparados con el método catalizado por ácido sulfúrico. En los estólidos derivados de oleína de orujo de oliva se observaron los mayores incrementos de viscosidad durante las 6 primeras horas de reacción, debido al mayor aumento en el peso molecular. Tiempos más largos de reacción dan lugar a resultados desfavorables. La dependencia de la viscosidad con la temperatura de todos los estólidos es más importante que en las oleínas de partida.This work is part of a research project (CTQ2010-15338) sponsored by a MINECO-FEDER programme (70% European cofunding rate). The authors gratefully acknowledge its financial support

Materials selection for optimum energy production by double layer expansion methods

NOTICE: this is the author’s version of a work that was accepted for publication in Journal of Power Sources. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Journal of Power Sources (2014) DOI:http://dx.doi.org/10.1016/j.jpowsour.2013.12.125The capacitive mixing procedure for energy extraction based on Double Layer Expansion (CDLE) belongs to the group of so-called CAPMIX techniques, which aim at obtaining energy from the salinity difference between fresh and sea waters. Specifically, the CDLE technique takes advantage of the voltage rise that occurs when sea water is exchanged for river water in a pair of porous electrodes which jointly behave as an electrical double layer supercapacitor. In this article, we deal with some experimental aspects that are key for optimizing the extracted energy, and have not been analyzed yet with sufficient detail. This investigation will help in evaluating those parameters which we need to be fixed in a future CDLE device. These include the charging potential, the durations of the different cycle steps, the load resistance used, and the porosity and hydrophilicity of the carbon.Departamento de Física Aplicada, Universidad de GranadaThe research leading to these results received funding from the European Union 7th Framework Programme (FP7/2007-2013) under agreement No. 256868. Further financial support from Junta de Andalucía (Spain), project PE-2008-FQM3993 is also gratefully acknowledged