Publications

Iron and nitrogen doped TiO2 nanoparticles were synthesized and investigated with the aim to obtain photocatalytic systems with enhanced visible light efficiency. In a first step, commercially available Degussa P25 was impregnated with iron (0.3, 0.5, and 1 at. %) and nitrogen under hydrothermal conditions. In the second step, Fe-N doped TiO2 was synthesized by a hydrothermal route starting with TiCl3, FeCl3 center dot 6H(2)O and Urea, at 200 degrees C for 2 h. All samples were post annealed at 400 degrees C for 2h. The X-ray diffraction (XRD) revealed a two phase nanoscaled composition (Anatase and Rutile) of Degussa P25 and a single phase-nanoscaled Anatase content of the hydrothermally synthesized (1at.%) Fe-N doped TiO2 sample. The presence of Fe and nitrogen in samples was confirmed by Mossbauer and X-ray photoelectron spectroscopy measurements (XPS). Transmission electron microscopy (TEM) revealed the structure, particle dimension and morphology. The photocatalytic measurements (based on degradation of Methylene Blue) evidenced the most efficient composition in TiO2 Degussa P25 series as corresponding to 1 at.% Fe, in both UV and visible spectrum. At the same time, the hydrothermal synthesized sample (1at.%) Fe-N doped TiO2 exhibits the best activity in visible spectral region. The nanoscaled systems were synthesized in view of tests on textile materials.

Samples of Ni57-xNdxFe18Ga25 with x=2 and 4 were prepared in ribbon form by rapid quenching via melt spinning route. The samples were analyzed by X-ray diffraction (XRD), magnetic measurements and Mossbauer spectroscopy, both in the as-quenched form and after thermal annealing at 900 degrees C for 2 min and 400 degrees C for 2 hours. For x=2 the Nd atoms are completely dissolved in the Ni-Fe-Ga matrix, while for x=4 the additional occurrence of the secondary 2:17 phase could be resolved. These findings were supported by the analysis of hyperfine magnetic field distributions obtained from the non-linear least-squares fitting of the Mossbauer spectra.

The elastic and structural properties of thermal barrier coatings of Cr2AlC DC sputtered from elemental targets onto Si(100) substrate at 200 degrees C are studied. The material was subsequently submitted to re-crystallization procedure by annealing the film at 650 degrees C and 700 degrees C in high vacuum and in air for 30 min. As-deposited and annealed films are shown to be homogeneous and dense over large areas. The re-crystallization process was monitored using X-ray diffraction and Raman spectroscopy. As-deposited films have an amorphous-like Cr-C-Al solid solution structure and annealed samples crystallize into single-phase hexagonal Cr2AlC. While XRD analysis and Raman spectroscopy of samples annealed in-air show the presence of 5% Cr2O3, the high vacuum samples annealed at 650 degrees C and 700 degrees C are fully crystallized and comprise only single-phase Cr2AlC hexagonal structure. Oxygen presence in the in-air annealed sample is shown to cause an elongation of the hexagonal unit cell along the c axis which coincides with the direction of stacking of Cr6C octahedral building blocks with alternate Al layers. Whereas the average grain size is shown to increase upon annealing, lattice microstrain, calculated using the integral breadth method, is seen to decrease by almost 70% in the annealed films. Raman spectra of as-deposited films show characteristic MAX-phase bands with broad, overlapping peaks in the region of 120-400 cm(-1) but also peaks in the range of 550-900 cm(-1), attributed to other Raman-active modes of the Cr2AlC structure. After annealing, the Raman peaks corresponding to Cr2AlC single-phase are narrower, more intense and better defined than in the as-deposited case. The occurrence of the disorder-induced D carbon band is observed in the Raman spectrum of the as-deposited film while, after high vacuum annealing, a sharp and relatively intense peak attributed to the carbon G band is observed that suggests that there may be carbon nanoclustering in the coatings upon annealing. This observation is consistent with and comes as a confirmation of previously reported ab initio modelling of possible Cr2AlC off-stoichiometric structures.

In the present work we study the optical, struc-tural and morphological properties of CdS-doped glass films, deposited by Pulsed Laser Deposition (PLD) method. The glass target used for ablation was prepared by conventional melt-quenching technique and the semiconductor dopant, CdS powder, was embedded in the borosilicate melt glass host by continuous stirring. In order to improve the properties of the films, the laser wavelength was modified. Photoluminescence emission (PL) of CdSdoped glass films revealed a broad band located in the visible range. The structural analysis was carried out by micro-Raman spectroscopy, pointing out specific vibration modes for Si-O-Si bonds as well as for CdS dopant. The morphology and the chemical characterization of the films were investigated by Scanning Electron Microscopy (SEM), Energy Dispersive X-ray spectroscopy (EDX) and Atomic Force Microscopy (AFM).

NiO/mesoporous SnO2 was deposited by incipient wetness impregnation of the SnO2 powder prepared by hydrothermal synthesis route templated by Brij (R) 35. The sensing properties were acquired and the dependence on the operating temperature of the sensitive material was pointed out. Sensitive selectivity towards H2S detection was highlighted at 350 degrees C.

In this study, one side aligned PANI coated micro-fibers were fabricated in order to develop a novel actuator configuration. Thus, electrospun PMMA fibers were coated only on one side with a thin gold layer guiding in this way the deposition of PANI (only on the side with gold considering an adequate PANI deposition time). Further, the half-metalized fibers were employed as working microelectrodes for electrochemical deposition of PANI. The prepared PANI coated fibers present actuation properties when they are in contact with an electrolyte like 1 M H2SO4. By switching the potential between +1.4 and -0.2 V, the fiber strips move due to the swelling/shrinking and anisotropic deposition of PANI film.

An Ag:HAp (x(Ag) = 0.5) powder was deposited by thermal evaporation technique as coating on a silicon substrate previously covered with a polydimethylsiloxane (PDMS) layer. The Ag: HAp-PDMS layers were characterized by Scanning ElectronMicroscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS), and Fourier Transform Infrared Spectroscopy (FT-IR). By infrared spectroscopy analysis, the phase composition of the Ag: HAp-PDMS layers was investigated. The antimicrobial activity of Ag: HAp-PDMS layers was tested against Escherichia coli, Staphylococcus aureus, and Candida albicans microbial strains. The microbial activity decreases significantly for the surveyed time intervals on Ag: HAp-PDMS layers.

The influence of light illumination on the programming of a capacitor floating gate memory based on Ge nanocrystals in HfO2 was studied. The capacitor was fabricated on a c-Si substrate by magnetron sputtering deposition of a layer sequence of HfO2/Ge-HfO2/HfO2 and post-growth rapid thermal annealing for nanocrystals formation at 600 degrees C. The illumination of the structure was performed through a semi-transparent Au contact (20% transparency). A maximum value of the light- induced change of 90% in C-V curve was obtained for 5 mW/cm(2) illumination during +5 V writing programming. The effect of the light exposure on the relative change of the C-V curve can be increased by reducing the writing time at 1 min.

Wetting properties of wool textiles were studied either for the raw samples or for those functionalized via covering them at low temperature with nanoparticles of titanium dioxide or zinc oxide. Oxygen plasma pretreatment was performed before deposition. Characterization used optical examination, scanning electron microscopy, infrared spectroscopy, thermogravimetry, X-ray diffraction. Wetting properties were tested under static conditions by estimating the water contact angle. The sessile drop method was applied. The deposited matter represents 3 to 8 wt%, covering rather uniformly the fiber surface. Treated samples show mostly lower values of contact angle than the pristine ones. Cassie-Baxter model is discussed in relation to the equilibrium contact angle of the support.

In this paper the holes' mobility for the configuration FTO/TiO2/CH3NH3PbI3/SpiroMeOTAD/Au was measured for the first time by the Photo-CELIV method. The TiO2 dense film was deposited by reactive sputtering at room temperature on FTO glass substrates. High crystalized perovskite films were deposited from solutions in one step by spin coating. Spiro-MeOTAD molecular glass was used as holes transporting layer. The highest holes' mobility from TiO2 thin film through the perovskite and Spiro MeOTAD film to the top gold electrode was of Order 8.5x10(-7) cm(2)/Vs.