Publications

Styrene, methyl methacrylate and glycidyl methacrylate vinyl monomers were grafted onto chitosan by surfactant-free emulsion copolymerization using potassium persulfate as initiator. The grafted compounds were characterized by X-ray diffraction, FTIR spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM) and zeta potential measurements. X-ray diffraction showed changes in the crystallinity pattern of chitosan after the copolymerization reaction. Evidence of grafting was confirmed by FTIR spectroscopy. From zeta potential measurements it is found that the surfaces of graft copolymers latex particles have positive charges resulting from the cationic chitosan molecules. The morphology evaluated by SEM, TEM and AFM proves that in the absence of chitosan, latexes of vinyl homopolymers contain quasi-monodispersed spheres with average diameter of about 400 nm or 250 nm while the graft copolymers latexes are formed by clustered irregular beads with average diameter around 100 nm.

Persistent, oscillatory charge and spin currents are shown to be driven by a two-component terahertz laser pulse in a one-dimensional mesoscopic ring with Rashba and Dresselhaus spin-orbit interactions (SOI) linear in the electron momentum. The characteristic interference effects result from the opposite precession directions imposed on the electron spin by the two SOI couplings. The time dependence of the currents is obtained by solving numerically the equation of motion for the density operator, which is later employed in calculating statistical averages of quantum operators on few electron eigenstates. The parameterization of the problem is done in terms of the SOI coupling constants and of the phase difference between the two laser components. Our results indicate that the amplitude of the oscillations is controlled by the relative strength of the two SOI's, while their frequency is determined by the difference between the excitation energies of the electron states. Furthermore, the oscillations of the spin current acquire a beating pattern of higher frequency that we associate with the nutation of the electron spin between the quantization axes of the two SOI couplings. This phenomenon disappears at equal SOI strengths, whereby the opposite precessions occur with the same probability. (c) 2012 Elsevier B.V. All rights reserved.

Amorphous titania thin films with increasing Fe content have been prepared by RF magnetron sputtering. X-ray absorption spectroscopy revealed modifications of both local structures/environment of the Ti and Fe atoms, with formation of phases containing amorphous material and a magnetite-like phase. The temperature dependence of the electrical conductivity of the films was investigated for temperatures higher than half of the Debye temperature (T > 391 K). It was found that the electrical conductivity in the amorphous Fe/TiO2 films obeys the Meyer-Neldel rule. The origin of this behavior is explained on the basis of the multiphonon-assisted hopping model.

We investigate the role of chromium and phosphorous oxides on the growth and magnetic properties of crystallized Fe-containing borosilicate glasses as well as their evolution under different thermal processing. The glasses have the ratio between SiO2 and Fe2O3 in the range 1.49 to 2.68 and Al2O3/MgO as intermediate/modifier oxides. X-ray diffraction and Mossbauer spectroscopy data revealed the presence of magnetite as the major crystalline phase in all as-prepared samples but additional amounts of hematite and of Fe-rich paramagnetic phases are also visible in some samples. The magnetic response is correlated with the disorder observed in the different sites (tetrahedral and octahedral) of the magnetite.

Standard zero-field cooling (zfc) magnetization relaxation measurements over a large temperature T interval were performed for YB2Cu3O7 films with BaZrO3 nanorods parallel to the c axis having the matching field B-Phi similar to 2.3 T. A rich non-monotonous T dependence of the normalized magnetization relaxation rate S at low external magnetic fields H (oriented along the nanorods) was observed. For H = 2 kOe, for example, S(T) clearly exhibits two maxima, located around T = 30 K and T = 62 K, as well as a pronounced S(T) deep at T similar to 77 K. It is shown that the first S(T) maximum may have an extrinsic origin, related to the occurrence of thermo-magnetic instabilities in the low-T domain, the second one is due to a crossover between the non-glassy vortex creep regime involving double vortex kink formation and variable range vortex hopping, whereas the S(T) deep at high T is generated by the accommodation of nearly isolated vortices to the nanorods in the presence of the T dependent macroscopic current induced in the specimen. (C) 2012 Elsevier B.V. All rights reserved.

A current of electrons traversing a landscape of localized spins possessing non-coplanar magnetic order gains a geometrical (Berry) phase, which can lead to a Hall voltage independent of the spin-orbit coupling within the material-a geometrical Hall effect. Here we show that the highly correlated metal UCu5 possesses an unusually large controllable geometrical Hall effect at T < 1.2 K due to its frustration-induced magnetic order. The magnitude of the Hall response exceeds 20% of the nu = 1 quantum Hall effect per atomic layer, which translates into an effective magnetic field of several hundred Tesla acting on the electrons. The existence of such a large geometric Hall response in UCu5 opens a new field of enquiry into the importance of the role of frustration in highly correlated electron materials.

Given the evolution of imaging techniques in the biomedical field is becoming more necessary to develop sensitive markers, less toxic and not least more economical. Upconverting luminescent nanocrystals doped with rare earth ions, excited in infrared and emitting in visible, are considered real concurrent to classical fluorescent markers, featuring a number of advantages in rapport with them. The aim of this study is to prepare NaYF4 nanoparticles doped with erbium and ytterbium for biological applications in bioimaging techniques. After synthesis, upconverting nano particles were coated with SiO2 for surface sealing and passivation. The nano particles were characterized by X-ray diffraction, luminescence spectroscopy, electronic microscopy and dynamic light scattering. The interaction of the nanoparticles with mimicking cell membrane models was studied. NaYF4 nanoparticles showed a good size distribution and good emission efficiency. The uncoated nanoparticles increase the fluidity of the lipid monolayer, while the effect of the silica coated nanoparticles is substantially reduced.