National Institute Of Materials Physics - Romania

In this paper, the interaction of poly(vinylidene fluoride) (PVDF) with single-walled carbon nanotubes (SWNTs) highly separated in metallic (M) and semiconducting (S) tubes is studied by resonant Raman scattering and FTIR spectroscopy. In this order, the PVDF/SWNTs membranes were prepared by the evaporation of dimethylformamide (DMF) from PVDF solutions containing i) the as-prepared SWNTs samples, i.e., as mixtures of metallic (33%) and semiconducting (66%) tubes (M + S-SWNTs), ii) SWNTs highly separated in metallic tubes (98%, M-SWNTs), and iii) SWNTs highly separated in semiconducting tubes (99%, S-SWNTs). An increase in the PVDF beta phase weight, highlighted by the increase in the absorbance of IR band at 843 cm(-1), is reported to take place in the presence of M + S-SWNTs and S-SWNTs. An increase of the PVDF gamma crystalline phase weight is reported for the PVDF/M + S-SWNTs, PVDF/M-SWNTs and PVDF/S-SWNTs membranes. Using Raman scattering, a donor-acceptor interaction is invoked to take place at the interface PVDF/M + S-SWNTs and PVDF/S-SWNTs. In the case of the membranes based on PVDF and M-SWNTs, the changes reported in Raman spectra of the two constituents are explained on the base induction-interaction forces between the permanent dipole of PVDF and induced dipole of M-SWNTs. (C) 2016 Elsevier B.V. All rights reserved.

Raman enhancement in a layered structure of Bib was studied under optical excitation near the edge of the fundamental absorption band. This phenomenon simultaneously appears at a low temperature with the generation of the excitonic photoluminescence (PL) band, unequally across the Raman spectrum, i.e. in the Stokes and anti-Stokes Raman branches, being dependent on the superposition of the excitation laser line to the excitonic emission band. Performed with the use of different resonant laser light excitations, this effect is regarded as a signature of the exciton-phonon interaction, which is interpreted in terms of a stimulated Raman scattering process (SRS), resulting from the mixing inside of the sample to two optical fields, the pump laser light and the excitonic PL light. (C) 2016 Elsevier B.V. All rights reserved.

Un-doped and Tb3+-doped calcium and strontium aluminates (CaAl2O4, CaAl2O4:Tb3+, SrAl2O4, SrAl2O4: Tb3+) were synthesized by a new soft chemical method the precursor route via the thermal decomposition of tartarate compounds. The complex precursors have been characterized by elemental chemical analysis, infrared spectroScopy (IR), luminescence spectroscopy and thermal analysis. X-ray diffraction (XRD), scanning electron microscopy (SEM), IR and Raman spectroscopy (RS) were used for the structural and morphological characterization of un-doped and doped alkaline-earth aluminate powders. Photoluminescence (PL) and Thermoluminescence (TL) properties of the aluminates were also investigated. The XRD patterns confirmed the formation of low-temperature structures: hexagonal structure for CaAl2O4 and monoclinic structure for SrAl2O4, with average crystallite size of 64 nm and 46 nm for CaAl2O4 and SrAl2O4, respectively. Microstructural analysis by SEM showed the homogeneous microstructure and fine particle size of the powder obtained by precursor method. (C) 2016 Elsevier Ltd. All rights reserved.

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.

The hematite films were prepared via anodic electrodeposition on FTO and FTO/mesoporous TiO2 substrates. The hematite photoanodes were characterized by X-ray diffraction and scanning electron microscopy. The performance of the prepared hematite photoanodes was assessed based on photocurrent-voltage curves and electrochemical impedance spectra. The modification of the hematite surface with nickel oxide nanoparticles improved the performance of the hematite photoanode while phosphorous doped hematite photoanode shows poor photoactivity. The onset of water oxidation photocurrent was cathodically shifted for hematite photoanodes prepared on FTO/TiO2 substrate.

The aim of our study was to synthesize and evaluate the physicochemical and biological properties of composite films based on poly(lactic-co-glycolic acid) copolymer and quercetin (PLGA/Q) microspheres. During our experiments, we firstly synthesized the PLGA/Q microspheres by using an oil-in-water emulsion-diffusion-evaporation method. Subsequently, the as-prepared composite material was subjected to the matrix assisted pulsed laser evaporation (MAPLE) technique, in order to obtain the PLGA/Q coatings. Relevant compositional and microstructural features of the synthesized samples were obtained by means of Fourier transform infrared spectroscopy (FTIR) and AFM (atomic force microscopy). The long-term biocompatibility of the synthesized films was in vitro evaluated by cellular viability and immunofluorescence assays.

The "avalanche" up-conversion properties of the glass-ceramics containing (Ho3+, Yb3+)doped LiYF4 nanocrystals have been studied by comparison to the corresponding nanocrystals and polycrystalline powder samples. Under 810 nm laser light pumping, all the samples showed "green" ((H-2(11/2), 4S(3/2)) -> I-4(15/2)) up-conversion luminescence. The pump power threshold for the avalanche mechanism is about 75mW for the nanocrystalline or polycrystalline powder samples indicating a weak influence of the nanosize related effects is but smaller of about 43mW for the nano-glass ceramic due to the high "local" Yb3+ concentrations.

Two methods were used for the synthesis of composites based on reduced graphene oxide (RGO) and poly(para-phenylene vinylene) (PPV) in un-doped and doped state, respectively, i.e. the annealing conversion (AC) of the PPV precursor solution (PS) at 300 degrees C and the electropolymerization (E) of alpha, alpha, alpha', alpha'-tetrabromo-p-xylene. In the case of the E method, a decrease in the distyrylbenzene (DSB) weight onto the RGO sheet surface in favor of PPV in doped state is demonstrated by the s and p polarized IR spectroscopy. The change of the orientation angle of the transition dipole moment vector for the IR bands at 835 and 964 cm(-1), in the case of the AC of the PPV PS, is a result of the p-p* interactions between the phenyl groups of PPV and the RGO sheets. The photoluminescence (PL) bands at 2.42 and 2.26 eV indicate the formation of PPV macromolecular chains (MCs) with lengths of 5 and 710 repeating units (RUs), respectively. The anisotropic PL studies performed on the composites RGO/PPV in un-doped and doped state, respectively, highlight an increase of the wrapping angle of RGO sheets with PPV MCs with lengths of 5 RUs, when graphene concentration increases.

Thin films of carbon were synthesized by ns pulsed laser deposition in vacuum on silicon substrates, starting from graphite targets. Further on, the films were irradiated with a picosecond laser source emitting in visible at 532 nm. After tuning of laser parameters, we obtained a film surface covered by laser induced periodical surface structures (LIPSS). They were investigated by optical, scanning electron and atomic force microscopy. It was observed that changing the irradiation angle influences the LIPSS covered area. At high magnification it was revealed that the LIPSS pattern was quite complex, being composed of other small LIPSS islands, interconnected by bridges of nanoparticles. Raman spectra for the non-irradiated carbon films were typical for a-C type of diamond-like carbon, while the LIPSS spectra were characteristic to nano-graphite. The pristine carbon film was hydrophilic, while the LIPSS covered film surface was hydrophobic. (C) 2016 Elsevier B.V. All rights reserved.