National Institute Of Materials Physics - Romania

A series of PtCeTi-SBA-15 catalysts, with different concentrations of Pt (0.25 %, 0.5 %, 1.0 %), were synthesized. New Ti-SBA-15 material was obtained by direct synthesis and used as support in successive immobilization of Pt and Ce precursors, changing their order of addition. The characterization of the catalysts has been achieved taking an ensemble of techniques which showed preservation of the support porous structure, high dispersion of the amorphous metal oxides and Pt?, the formation of metal crystals for samples with 1wt% Pt and variation of Pt? content on surface in condition of ceria addition. The best conversion (100 %) was obtained in oxidation of hydrocarbons (CH4, C3H8 and C6H14) for the samples with 1% Pt and a significant diminish of activity was obtained for catalyst in which Ce was added on PtTi-SBA-15 sample. Differently of these, CO oxidation was totally irrespective of the catalyst composition.

We observe a strong thermally controlled magnon-mediated interlayer coupling of two ferromagnetic layers via an antiferromagnetic spacer in spin-valve type trilayers. The effect manifests itself as a coherent switching as well as collective resonant precession of the two ferromagnets, which can be controlled by varying temperature and the spacer thickness. We explain the observed behavior as due to a strong hybridization of the ferro- and antiferromagnetic magnon modes in the trilayer at temperatures just below the Neel temperature of the antiferromagnetic spacer.

The lack of order in amorphous chalcogenides offers them novel properties but also adds increased challenges in the discovery and design of advanced functional materials. The amorphous compositions in the Si-Ge-Te system are of interest for many applications such as optical data storage, optical sensors and Ovonic threshold switches. But an extended exploration of this system is still missing. In this study, magnetron co-sputtering is used for the combinatorial synthesis of thin film libraries, outside the glass formation domain. Compositional, structural and optical properties are investigated and discussed in the framework of topological constraint theory. The materials in the library are classified as stressed-rigid amorphous networks. The bandgap is heavily influenced by the Te content while the near-IR refractive index dependence on Ge concentration shows a minimum, which could be exploited in applications. A transition from a disordered to a more ordered amorphous network at 60 at% Te, is observed. The thermal stability study shows that the formed crystalline phases are dictated by the concentration of Ge and Te. New amorphous compositions in the Si-Ge-Te system were found and their properties explored, thus enabling an informed and rapid material selection and design for applications.

The magnetic properties of thin-film multilayers [Fe/Py]/FeMn/Py are investigated as a function of temperature and thickness of the antiferromagnetic FeMn spacer using SQUID magnetometry. The observed behavior differs substantially for the structures with 6 nm and 15 nm FeMn spacers. While the 15 nm FeMn structure exhibits exchange pinning of both ferromagnetic layers in the entire measurement temperature interval from 5 to 300 K, the 6 nm FeMn structure becomes exchange de-pinned in the vicinity of room temperature. The depinned state is characterized by a single hysteresis loop centered at zero field and having enhanced magnetic coercivity. The observed properties are explained in terms of finite-size effects and possible ferromagnetic interlayer coupling through the thin antiferromagnetic spacer.

The structural role of V in 28Li(2)O-72SiO(2) (in mol%) lithium silicate glass doped with 0.5 mol% V2O5 was assessed using Si-29 and V-51 Nuclear Magnetic Resonance (NMR), Fourier-transform infrared (FTIR), and X-ray photoelectron (XPS) spectroscopy techniques. Despite the low amount of V2O5 used, the structural information obtained or deduced from the statistical analysis of the NMR data could explain the evolution of glass properties after V2O5 addition. The XPS results indicated that all vanadium exists in 5+ oxidation state. Both the Si-29 NMR and FTIR data point toward an increase in the polymerization of the silicate network, caused by the V2O5 acting as network former, capable to form various QVn tetrahedral units (for n = 0, 1, and 2) in the glasses. These QVn units, which are similar to phosphate units, scavenge the Li+ ions and cause the silicate network to polymerize. However, in an overall balance, the entire glass network is depolymerized due to the additional nonbridging oxygens contributed by the vanadium polyhedra. The addition of vanadium causes the network to expand and increases the ionic conductivity.

NiO-loaded SnO2 powders were prepared involving two chemical procedures. The mesoporous SnO2 support was synthesized by a hydrothermal route using Brij 35 non-ionic surfactant as a template. The nickel loadings of 1 and 10 wt.%. NiO were deposited by the wet impregnation method. The H2S sensing properties of xNiO-(1-x)SnO2 (x = 0, 1, 10%) thick layers deposited onto commercial substrates have been investigated with respect to different potential interfering gases (NO2, CO, CO2, CH4, NH3 and SO2) over a wide range of operating temperatures and relative humidity specific for in-field conditions. Following the correlation of the sensing results with the morphological ones, 1wt.% NiO/SnO2 was selected for simultaneous electrical resistance and work function investigations. The purpose was to depict the sensing mechanism by splitting between specific changes over the electron affinity induced by the surface coverage with hydroxyl dipoles and over the band bending induced by the variable surface charge under H2S exposure. Thus, it was found that different gas-interaction partners are dependent upon the amount of H2S, mirrored through the threshold value of 5 ppm H2S, which from an applicative point of view, represents the lower limit of health effects, an eight-hour TWA.

Gold nanoparticles (similar to 10 nm) were deposited on titanium dioxide nanoparticles (similar to 21 nm) and the material obtained was characterized using IR, UV-Vis, N-2 adsorption-desorption isotherm, DLS, EDS (EDX), TEM, XPS, and XRD techniques. It was found that the methylene blue dye is degraded in the presence of this material when using hydrogen peroxide as the oxidant. Tests were performed at 2, 4, 6, and 24 h, with hydrogen peroxide contents varying from 1 to 5 mg/mL. Longer exposure time and a higher content of oxidant led to the degradation of methylene blue dye at up to 90%. The material can be reused several times with no loss of activity.

The effect of temperature on the features of the crystal and magnetic structures, as well as the magnetic properties of the solid solution of SrFe10.8In1.2O19 hexaferrite was investigated. The appearance of ferroelectric properties was detected at room temperature, which contradicts the generally accepted opinion on the description of the crystal structure of hexaferrites within the framework of the centrosymmetric P6(3)/mmc (No. 194) space group. The reasons of spontaneous polarization in solid solutions of hexaferrites remain controversial. No deviation from the collinear magnetic structure was found in the investigated temperature range from 1.5 to 350 K, while the thermal expansion of the unit cell was practically absent in the range from 1.5 to 50 K. The crystal structure of hexaferrites was considered in the framework of both centrosymmetric P6(3)/mmc and non-centrosymmetric P6(3)mc space groups, which allowed us to associate the emerging spontaneous polarization with unequal distortions of neighboring oxygen polyhedra.

Fibres of poly(methyl methacrylate) were obtained by electrospinning, subjected to coating with a gold layer and then attached on a thin polyethylene terephthalate substrate in order to obtain flexible electrodes for biosensing applications. The morphology of these electrodes, investigated by scanning electron microscopy showed multilayers of random oriented fibres of approx. 400 nm diameter. The electrochemical characterization of these flexible electrodes was performed by cyclic voltammetry and electrochemical impedance spectroscopy in acid and neutral media, in the absence and in the presence of redox probes, proving their superior performance (e.g. 5fold current density value) when compared to planar gold electrodes obtained on silicon wafers. The electrodes obtained from conductive electrospun polymeric fibres nets were tested by cyclic voltammetry and amperometry for the detection of hydrogen peroxide with a sensitivity of 0.84 mA cm-2 mM-1 and a detection limit of 20.40 ?M. The immobilization of the model enzyme glucose oxidase at the surface of the gold-coated electrospun polymeric fibres electrode was investigated and the obtained biosensor was applied for glucose determination in aqueous solutions by fixed potential amperometry with a sensitivity of 3.10 ?A cm-2 mM-1, a detection limit of 0.33 mM, and reduced interferences. Also, the practical applicability of the biosensor was tested for the detection of glucose in artificial sweat and serum samples.

Ferromagnetism in 3d metals is re-examined in a simple band model. It is shown that the molecular field model cannot account for the low values of coercive field in ferromagnetic pure metals, and that the standard Stoner theory of band ferromagnetism incorrectly evaluates the total electronic energy and cannot predict reasonable Curie temperatures. A simple band model for magnetism is formulated, yielding a criterion for ferromagnetism even in absence of a Hubbard term, involving only the density of states (DOS) at the Fermi level, its derivative and the filling of the 3d band. By introducing a double-peaked DOS, one may explain the occurrence of ferromagnetism in bcc Fe, hcp-fcc Co and fcc Ni, the stabilization of fcc-hcp or bcc structures across all 3d elements, the occurrence of antiferromagnetism in chromium, and derive reasonable Curie temperatures. 'Re-entrant' ferromagnetism is predicted at ultrahigh temperatures, suggesting an alternate origin for the geomagnetic field.