National Institute Of Materials Physics - Romania

TiSiC-Cr coatings, with Cr and Si as additional elements, were deposited on Si, C 45 and 316 L steel substrates via cathodic arc evaporation. Two series of coatings with thicknesses in the range of 3.6-3.9 mu m were produced, using either CH4 or C2H2 as carbon containing gas. For each series, different coatings were prepared by varying the carbon rich gas flow rate between 90 and 130 sccm, while maintaining constant cathode currents (110 and 100A at TiSi and Cr cathodes, respectively), substrate bias (-200 V) and substrate temperature (similar to 320 degrees C). The coatings were analyzed for their mechanical characteristics (hardness, adhesion) and tribological performance (friction, wear), along with their elemental and phase composition, chemical bonds, crystalline structure and cross-sectional morphology. The coatings were found to be formed with nano-scale composite structures consisting of carbide crystallites (grain size of 3.1-8.2 nm) and amorphous hydrogenated carbon. The experimental results showed significant differences between the two coating series, where the films formed from C2H2 exhibited markedly superior characteristics in terms of microstructure, morphology, hardness, friction behaviour and wear resistance. For the coatings prepared using CH4, the measured values of crystallite size, hardness, friction coefficient and wear rate were in the ranges of 7.2-8.2 nm, 26-30 GPa, 0.3-0.4 and 2.1-4.8 x 10(-6) mm(3) N-1 m(-1), respectively, while for the coatings grown in C2H2, the values of these characteristics were found to be in the ranges of 3.1-3.7 nm, 41-45 GPa, 0.1-0.2 and 1.4-3.0 x 10(-6) mm(3) N-1 m(-1), respectively. Among the investigated coatings, the one produced using C2H2 at the highest flow rate (130 sccm) exhibited the highest hardness (45.1 GPa), the lowest friction coefficient (0.10) and the best wear resistance (wear rate of 1.4 x 10(-6) mm(3) N-1 m(-1)). (C) 2016 Elsevier B.V. All rights reserved.

The present study is focused on the synthesis, characterization and antifungal evaluation of zinc-doped hydroxyapatite (Zn:HAp) coatings. The Zn:HAp coatings were deposited on a pure Si (Zn:HAp_Si) and Ti (Zn:HAp_Ti) substrate by a sol-gel dip coating method using a zinc-doped hydroxyapatite nanogel. The nature of the crystal phase was determined by X-ray diffraction (XRD). The crystalline phase of the prepared Zn:HAp composite was assigned to hexagonal hydroxyapatite in the P6(3/m) space group. The colloidal properties of the resulting Zn:HAp (x(Zn) = 0.1) nanogel were analyzed by Dynamic Light Scattering (DLS) and zeta potential. Scanning Electron Microscopy (SEM) was used to investigate the morphology of the zinc-doped hydroxyapatite (Zn:HAp) nanogel composite and Zn:HAp coatings. The elements Ca, P, O and Zn were found in the Zn:HAp composite. According to the EDX results, the degree of Zn substitution in the structure of Zn:HAp composite was 1.67 wt%. Moreover, the antifungal activity of Zn:HAp_Si and Zn:HAp_Ti against Candida albicans (C. albicans) was evaluated. A decrease in the number of surviving cells was not observed under dark conditions, whereas under daylight and UV light illumination a major decrease in the number of surviving cells was observed.

We report on the enhancement of critical current density (J(c)) and the unusual behaviour of its dependence on field orientation in YBa2Cu3O7-x (YBCO) nanostructured films by a combination of substrate decoration with Ag nano-dots, of the incorporation of BaZrO3 (BZO) nano-particles and nano-rods, and of multilayer architecture (a thin SrTiO3 layer separating two 1.5 mu m-thick YBCO layers). SrTiO3 insulating layers were 15, 30 or 45 nm thick. The highest improvement of J(c) in applied magnetic fields along the c-axis and smaller than 1 T occurs in the bi-layer with 30 nm-thick STO, but the influence of STO thickness is small. Our thick nanostructured films show significant improvement of J(c) in the magnetic field along the ab-plane direction. The presence of BZO nano-rods, ab-plane defects and nano particles of BZO and Y2O3 was observed in transmission electron microscopy (TEM) images of the film. The peculiarities of artificial pinning centres revealed in the TEM images of the nanostructured films are used to explain an unusual split of the peak in the J(c) dependence on the magnetic field along the ab-plane of YBCO. Effective pinning potentials in high magnetic fields have rather high values for such thick films.

The enhancement of the Raman scattering in Cs3Bi2I9 is evaluated by the ratio I-T/I-300K between the relative intensities of the Raman line peaked at 146cm(-1), when the spectra are recorded in the temperature range of 88-300K, as a signature of exciton-phonon interactions. In the resonant and nonresonant conditions, excitation wavelengths 476, 561, and 660nm, respectively, are used in order to overlap with great accuracy the bands disclosed by diffuse reflection, photoconductivity (PC), photoluminescence (PL), and photoluminescence excitation (PLE) spectra. Based on the experimental analyses, the strength of exciton-phonon interaction is dependent on the defects in the crystal and the type-range interaction of the excitations in an independent Bi2I93- cluster. The noticeable PL band, attributed to excitons trapped on different stacking faults, manifests some defects in crystal that diminish the movement of excitons. This effect significantly decreases the overlaps of excitons with the phonons, resulting in a reduced exciton-phonon coupling.

Fe doped ZnO particles of flower-like shape, hexagonal prisms and hybrid structures flower-prisms have been synthesized by hydrothermal technique, and their luminescence and magnetic properties have been investigated as a function of the morphology changes due to iron dopant (0-0.03 at.% Fe3+). The X-ray diffractograms of Zn1-xFexO powders indicated a hexagonal wurtzite polycrystalline structure. SEM images reveal the change of Zn1-xFexO grains shape from flower-like to hexagonal prisms as the Fe concentration (x) increases from 0 to 3 at.% Fe. Undoped ZnO shown weak room temperatures ferromagnetism, with high coercivity (H-c = 107 Oe) and saturation magnetization M-s of 1.5-10(-3) emu/g. ZnO doped with 1 and 3 at.% Fe presented a significant increase of the magnetization in comparison with the undoped ZnO. For ZnO doped with 3 at.% Fe, Ms = 32.5-10(-3) emu/g and M-rem = 0.78-10(-3) emu/g. Compared with other reports on magnetic properties of undoped and Fe doped ZnO, these results indicated higher coercivity and smaller magnetizations. The drop in the intensity of characteristic green-yellow photoluminescence band of ZnO at about 550-600 nm was attributed to the decrease of the number of oxygen vacancies and interstitial oxygen. By increasing the Fe concentration, the electron paramagnetic resonance (EPR) signal of undoped ZnO decreases due to the decrease of defects concentration. (C) 2017 Elsevier Ltd. All rights reserved.

In this paper, we investigate the influence of Cu, Co, and Al substitutions on the transport properties, and in particular, the magnetoresistive effect in Ni-Fe-Ga ferromagnetic shape memory alloys (FSMAs) prepared as ribbons by melt spinning method and subjected to different thermal treatments. X-ray diffraction, differential scanning calorimetry, magnetometry, and magnetoresistive characterizations were performed. In the range of the martensitic transformation (MT), different FSMA compositions show a rich spectrum of different behaviors. For one of the compositions (Ni52Fe20Co2Ga23Al3), the magnetoresistance (MR) showed a local minimum or, on the contrary, a local maxima of reduced amplitude on cooling, in the range of the MT, depending on the performed thermal treatments. In the same composition, by replacing one Al atom with a Co one, no local extremes are seen, the alloy having a concomitant magneto-structural transition. When the magnetic field was varied, the MR showed a nonmonotonic variation in the martensite phase for some compounds, possibly due to the dynamics of the martensite variants realignment. From the studied compositions, the highest MR found on the MT of -9% for 5 T is for Ni50Fe20Ga27Cu3.

A new facile template method for the preparation of Ni, Co doped ZrO2 self-assembled electrocatalysts for oxygen reduction reaction was employed. The effect of the Ni and Co incorporation into ZrO2 lattice on the structural, texturaL surface chemistry and its activity on ORR was emphasized. As X-ray diffraction reveals, the pseudo-cubic lattice of the tetragonal ZrO2 polymorph (t-ZrO2) is stabilized when Ni and Co are co-doping ZrO2. The results indicate that the synergetic effects arisen from the intimate electronic interaction of the mixed oxides present in the lattice of the zirconia phase, i.e. Nil-xCoxO (or NiO and CoO) in NCZ enhance the electrocatalytic activity of the catalyst. (C) 2017 Elsevier B.V. All rights reserved.

We investigated the evolution of the DC magnetic hysteresis curves of Nb0.89Ti0.11 alloys thermo-mechanically processed by intermediate heat treatments at 900 degrees C in vacuum and cold rolling (similar to 50% thickness reduction). Starting with a rectangular piece (similar to 0.4 mm thick) cut from the as-grown alloy, after the first thermo-mechanical treatment, the specimen exhibits over a wide temperature T interval a peak effect not far from the DC irreversibility line. With a supplemental thermo-mechanical treatment, the peak effect disappears and is substituted by a second magnetization peak ( where the characteristic fields are significantly lower) induced by pinning enhancement. The second magnetization peak was clearly seen at high temperatures only, due to the occurrence of thermo-magnetic instabilities in the low-T domain. In both cases, analysis of magnetic relaxation evidences a crossover towards plastic vortex creep accompanying the maximum in the effective critical current density. These results suggest a common nature of the observed effects, related to the disordering of the vortex system induced by pinning.

In this paper the influence of the heat treatment on the structural and optical properties of oxide single layer and multilayer transparent thin film structures of ITO/Au/ITO, AZO/Au/AZO, TiO2/Au/TiO2 and Bi2O3/Au/Bi2O3 type is studied. The single-layer oxides and respective multilayer structures have been deposited on glass substrates by successive DC magnetron sputtering using metallic targets ln:Sn, Zn:Al, Ti and Bi, in reactive (for the oxide films) or inert (for the metallic Au interlayer films) atmosphere. Good quality transparent conducting thin film structures have been obtained, with resistivity similar to 10(-4) Omega cm and transmittance similar to 75%. The wetting surface properties in function of time exposure at UV radiation (254 nm) have been also studied before and after heat treatment performed at 450 degrees C. (C) 2017 Elsevier Ltd. All rights reserved.

The electronic structure of the SiO2/SiC (0001) interface, buried below SiO2 layers with a thickness from 2 to 4 nm, was explored using soft X-ray angle-resolved photoemission spectroscopy with photon energies between 350 and 1000 eV. The measurements have detected the characteristic k-dispersive energy bands of bulk Silicon Carbide (SiC) below the SiO2 layer without any sign of additional dispersive states, up to an estimated instrumental sensitivity of approximate to 5 x 10(9) cm 2 eV. This experimental result supports the physical picture that the large density of interface traps observed in macroscopic measurements results from dangling bonds randomized by the SiO2 rather than from Shockley-Tamm surface derived states extending into the bulk SiC. Published by AIP Publishing.