National Institute Of Materials Physics - Romania

Hybrid ferromagnetic/piezoelectric core-shell nanoparticles and ceramics have potential for a wide range of applications due to their tunability, electronic and magnetic properties. In this study, we designed a core-shell-type nanostructure of composition CoFe2O4/BNT-BT0.08, where BNT-BT0.08 is the abbreviation of bismuth, sodium titanate (Bi0.5Na0.5TiO3, BNT) doped with 8 mol% barium titanate (BaTiO3, BT). This multiferroic composite was prepared by covering CoFe2O4 nanoparticles with a shell of BNT-BT0.08 using the sol-gel technique. Scanning and transmission electron microscopy confirmed formation of a core-shell structure. The results of microstructure, dielectric, piezoelectric and magnetic investigations demonstrated that this heterostructure shows simultaneously electrical and magnetic behavior, at room temperature. XRD pattern of core-shell composite CoFe2O4/BNT-BT0.08 powder reveals only cubic CoFe2O4 and rhombohedral Bi0.5Na0.5TiO3 phases. CoFe2O4/BNT-BT0.08 core-shell nanostructure sample shows high values of permittivity (epsilon >= 600) together with high dielectric losses (tan delta >= 1) in the low-frequency range (nu <= 10(4) Hz). PFM and polarization hysteresis indicated a ferroelectric domains structure and remnant polarization of similar to 2.6 A mu C/cm(2) for the ceramics pellets samples of CoFe2O4/BNT-BT0.08. The present study reveals the possibility of coating nanoparticles onto nanometer-sized core particles, using controlled sol-gel process, in order to prepare multifunctional core-shell composites for piezoelectric and magnetoelectronic sensors.

Herein, the spectral and transport properties in the finite phosphorene lattice are investigated using the tight-binding model in the presence of Anderson disorder potential. The focus is on the zig-zag edge states localization, provided by the numerically calculated inverse participation number. At low disorder, the zig-zag states undergo a localization process, keeping their 1D character, while further increasing the disorder leads to delocalization due to hybridization with the extended 2D states. The disorder-induced changes in the electronic conductance, from one zig-zag edge to the other, are also discussed.

The demand of calcium phosphate bioceramics for biomedical applications is constantly increasing. Efficient and cost-effective production can be achieved using naturally derived materials. In this work, calcium phosphate powders, obtained from dolomitic marble and Mytilus galloprovincialis seashells by a previously reported and improved Rathje method were used to fabricate microporous pellets through cold isostatic pressing followed by sintering at 1200 degrees C. The interaction of the developed materials with MC3T3-E1 pre-osteoblasts was explored in terms of cell adhesion, morphology, viability, proliferation, and differentiation to evaluate their potential for bone regeneration. Results showed appropriate cell adhesion and high viability without distinguishable differences in the morphological features. Likewise, the pre-osteoblast proliferation overtime on both naturally derived calcium phosphate materials showed a statistically significant increase comparable to that of commercial hydroxyapatite, used as reference material. Furthermore, evaluation of the intracellular alkaline phosphatase activity and collagen synthesis and deposition, used as markers of the osteogenic ability of these bioceramics, revealed that all samples promoted pre-osteoblast differentiation. However, a seashell-derived ceramic demonstrated a higher efficacy in inducing cell differentiation, almost equivalent to that of the commercial hydroxyapatite. Therefore, data obtained demonstrate that this naturally sourced calcium-phosphate material holds promise for applications in bone tissue regeneration.

We investigated the magnetic and thermodynamic properties of rolled tantalum in superconducting state. The magnetization shows a crossover from type I to type II superconductivity as the magnetic field increases beyond the thermodynamic critical field. In both regimes, the sample shows a substantial irreversibility of the magnetization which we attribute to the pinning of the entities that characterize the intermediate and mixed states. Magnetic relaxation data taken in the intermediate state shows an important contribution of the quantum tunnelling below 3.7 K.

The recent advances in genetic engineering demand the development of conceptually new methods to prepare and identify efficient vectors for the intracellular delivery of different nucleotide payloads ranging from short single-stranded oligonucleotides to larger plasmid double-stranded circular DNAs. Although many challenges still have to be overcome, polymers hold great potential for intracellular nucleotide delivery and gene therapy. We here develop and apply the postpolymerization modification of polyhydrazide scaffolds, with different degree of polymerization, for the preparation of amphiphilic polymeric vehicles for the intracellular delivery of a circular plasmid DNA. The hydrazone formation reactions with a mixture of cationic and hydrophobic aldehydes proceed in physiologically compatible aqueous conditions, and the resulting amphiphilic polyhydrazones are directly combined with the biological cargo without any purification step. This methodology allowed the preparation of stable polyplexes with a suitable size and zeta potential to achieve an efficient encapsulation and intracellular delivery of the DNA cargo. Simple formulations that performed with efficiencies and cell viabilities comparable to the current gold standard were identified. Furthermore, the internalization mechanism was studied via internalization experiments in the presence of endocytic inhibitors and fluorescence microscopy. The results reported here confirmed that the polyhydrazone functionalization is a suitable strategy for the screening and identification of customized polymeric vehicles for the delivery of different nucleotide cargos.

Highly defected SiO2 nanotubes (SiO2-NT) were obtained by a simple sol-gel procedure followed by calcination. Boron-doped diamond (BDD) polycrystalline films coated with SiO2-NT were used as working electrodes and, unexpectedly, cyclic voltammetric experiments have shown that the concentration of both positive and negative defects at the surface is high enough to enable redox processes involving positively charged Ru(bpy)(3)(2+/3+) to occur. Conversely, no electrochemical activity was put into evidence for Fe (CN)(6)(3/4) species, most likely as a result of the strong electrostatic repulsion exerted by the negatively charged SiO2 surface. The concentration of surface defects was further increased by a subsequent thermal treatment in a hydrogen atmosphere which, as EIS measurements have shown, significantly promotes Ru (bpy)(3)(2+) anodic oxidation. Digital simulation of the voltammetric responses demonstrated that this treatment does not lead to a similar increase of the number of electron-donor sites. It was also found that methanol anodic oxidation at hydrogenated SiO2-NT-supported platinum results in Tafel slopes of 116-220 mV decade(-1), comparable to those reported for both conventional PtRu and Pt-oxide catalysts. (C) 2018 Elsevier B.V. All rights reserved.

The influence of single-walled carbon nanotubes enriched in semiconductor (S-SWNTs) and metallic (M-SWNTs) tubes on the photoluminescence (PL) of polyaniline (PANI), electrosynthesized in the presence of the H2SO4 and HCl solutions, is reported. The emission bands peaked at 407-418 and 440-520 nm indicate that the electropolymerization of aniline (ANI) leads to the formation of short and longer macromolecular chains (MCs), respectively. We demonstrate that the reaction product consists of ANI tetramers (TT) and trimers (TR) as well as PANI-salt. Using Raman scattering and IR absorption spectroscopy, a covalent functionalization of SWNTs with shorter and longer MCs of PANI-salt is demonstrated. The presence of S-SWNTs and M-SWNTs induces a decrease in ANI TT weight in the reaction product mass consisting in S-SWNTs and M-SWNTs covalently functionalized with PANI-emeraldine salt (ES) and PANI-leucoemeraldine salt (LS), respectively. A PANI PL quenching is reported to be induced of the S-SWNTs and M-SWNTs. A de-excitation mechanism is proposed to explain PANI PL quenching.

In this work we report on a new 1-1 composite coaxial nanostructure containing nanotubes of CoFe2O4 and BET-BT0.08 prepared by a template-based fabrication technique using the sol-gel chemistry. In this regard, CoFe2O4/BNT-BT0.08 core-shell nanotubes were prepared using a polycarbonate membrane template and sols precursors of CoFe2O4 and BNT-BT0.08. The deposition of nanotubes was performed by pore wetting of the porous membranes via capillary action and subsequent pyrolysis. The studies with scanning electron microscopy and transmission electron microscopy (TEM) revealed that the composite material is characterized by the 1-D tubular structure. Analysis by X-ray diffraction, high-resolution TEM imaging and selected-area electron diffraction pattern demonstrated that the synthetic composite nanotube CoFe2O4/BNT-BT0.08 has crystalline structure with cubic CoFe2O4 and rhombohedral BNT-BT0.08 phases. CoFe2O4/BNT-BT0.08 coaxial nanotubes show dielectric properties, piezoelectric and ferromagnetic behavior.

This paper presents a comparative study between the properties of the heterostructures realized with single/multi layer organic (zinc phthalocyanine or/and fullerene) prepared on Si substrate between flat or patterned aluminum (Al) layer metallic electrode and multi layer ZnO/Au/ZnO transparent conductor electrode (TCE). The UV-Nanoimprint Lithography was used for the realization of a 2D array of nanostructures (holes/pillars) characterized by a periodicity of 1.1 mu m and cylindrical shape: diameter = 400 nm and depth/height = 300 nm. The effect of the electrode patterning on the properties of the organic heterostructures was analyzed. For the samples with patterned Al electrode was remarked a slight red shift of the peaks in the reflection spectra determined by an increased interaction between the organic molecules in the delimited region of the patterned holes. The shape of the emission spectra at excitation with UV light showed a narrow intense peak around 500 nm associated with the intense resonance phenomena between the energy of the incident light and the surface plasmons in the patterned Al layer. The TCE followed the morphology of the organic film on which it was deposited. The significant differences between the morphology of the top layer in the heterostructures realized on flat and patterned Al are correlated with the total thickness of the successively deposited layers and with the particularities of the molecular arrangement, leading to the preservation or deleting of patterning. An injection contact behavior was evidence for most heterostructures built on flat and patterned Al. The slight increase in current at an applied bias <1 V in the heterostructure Si/Al/ZnPc/TCE is attributed to the larger interfacial area between the patterned Al electrode and ZnPc layer compared to the interface area between flat Al and ZnPc. A buffer layer of 1,4,5,8-naphthalen-tetracarboxylic dianhydride (NTCDA), sandwiched between the flat metallic electrode and organic film in the heterostructure Si/Al/C60/ZnPc/TCE has determined an increase in the current at low applied voltages. (C) 2018 Elsevier B.V. All rights reserved.

Pristine and (SiC + Te)-added MgB2 powders, green and spark plasma sintered (SPS) compacts were investigated from the viewpoint of quasi-static and dynamic (Split-Hopkinson Pressure Bar, SHPB) compressive mechanical properties The amount of the additive (SiC + Te) was selected to be the optimum one for maximization of the superconducting functional parameters. Pristine and added MgB2 show very similar compressive parameters (tan delta, fracture strength, Vickers hardness, others) and fragment size in the SHPB test. However, for the bulk SPSed samples the ratio of intergranular to transgranular fracturing changes, the first one being stronger in the added sample. This is reflected in the quasi-static K-IC that is higher for the added sample. Despite this result, sintered samples are brittle and have roughly similar fragmentation behavior as for brittle engineering ceramics. In the fragmentation process, the composite nature of our samples should be considered with a special focus on MgB2 blocks (colonies) that show the major contribution to fracturing. The Glenn-Chudnovsky model of fracturing under dynamic load provides the closest values to our experimental fragment size data.