National Institute Of Materials Physics - Romania

CdTe nanowires were electrodeposited in ion track membranes with pore diameters in the range 100-2000 nm. Acidic and basic baths were tested for obtaining materials with good stoichiometry. The cyclic voltammograms were compared for the case of deposition on a carbon rotating disc and on the porous membrane substrates, the differences being attributed to the additional resistance induced by the pores. For larger pores a tendency of growing hollow structures was observed.

Our fluorescence study gave information on the presence of chemical defects and irregularities in crystal structure, offering a good tool for quality evaluation of organic crystalline materials. We have analysed the correlation between the bulk or thin film samples' quality determined by experimental parameters (thermal gradient, moving speed of the growth interface, crucible configuration, slow or fast solidification rates) and the fluorescence characteristics for pure meta-dinitrobenzene and meta-dinitrobenzene doped with 8 hydroxyquinoline or 1,3 dihydroxybenzene. The comparative study of the position and shape of the fluorescence emissions for pure and controlled doped materials nave us information on the chemical defects.

Electrochemical polymerization of aniline in an HCl solution on a single-walled carbon nanotubes (SWNTs) film has been studied by Raman and FTIR spectroscopy. It is shown that this method leads to a covalent functionalization of SWNTs with polyaniline (PANI). A careful study in Raman scattering shows that the increase in the intensity of the band at 178cm(-1) associated with radial breathing modes of SWNTs bundles suggests an additional nanotubes roping with PANI as a binding agent. A post chemical treatment with the NH4OH solution of polymer-functionalized SWNTs involves an internal redox reaction between PANI and carbon nanotubes. As a result, the polymer chain undergoes a transition from the semi-oxidized state into a reduced one. (C) 2004 Elsevier Ltd. All rights reserved.

At room temperature, soluted C-60 in pyrrolidine and N-methyl-2-pyrrolidinone associates slowly in stable aggregates. The process originates in the charge transfer from the solvent molecules as electron donors towards fullerene. In the aggregate phase the intermolecular interactions lead to a large reduction in parent I-h C-60 symmetry such that a modified phonon spectrum is observed. Using the surface-enhanced Raman scattering we demonstrate that the Raman range below 800 cm(-1) is most diagnostic for aggregate assignment. In particular, the strong decrease of the radial breathing mode and appearance of new bands at 110 and 93 cm(-1) due to the interball interactions must be noticed.

SERS and FTIR spectra of M and S composites, provided by adding of single-walled carbon nanotubes (SWNTs) to the polyaniline (PANI) solution and chemical polymerization of aniline, respectively are different. The difference originates in the irreversible transformation of SWNTs in the polymerization medium. This explains the similarity of SERS and FTIR spectra of PANI/SWNTs and PANI/C-60 composites, chemically synthesized. For M composites, strong hindrance effects are evidenced by band at 773-755 cm(-1) associated to the vibration of deformation of the benzene and quinoid ring. The charge transfer is illustrated for all compounds by absorption band at 1144 cm(-1).

Photoluminescence (PL) spectra of C-60 solutions in N-methyl-2-pyrrolidinone (NMP) show a drastic increase of the PL intensity if the solutions are stored longer periods of time. Two distinct spectral components, one in the red (1.92-2.00 eV) and another in the green (2.18-2.3 eV) were identified in the whole PL emission. Their weights depend on C-60 concentration and on storage time. The two emissions come from two successive processes running with different kinetics. Charge transfer, leading to (C-60, NMP) loose molecular complexes and a slow aggregation process of these entities seems to originate the red and green emission, respectively. Similar PL properties are found when pyrrolidine (P) is used as solvent.

Lead chalcogenides (PbS, PbSe, PbTe) are narrow band gap semiconductors which have been studied in the field of IR detection and thermoelectric devices. The template method is a general approach for synthesizing nanomaterials within the pores of membranes. The membranes employed contain cylindrical pores with monodisperse diameters, and corresponding cylindrical nanostructures are obtained. The aim of the present study was to prepare PbSe1-xTex nanorod arrays using electrodeposition. The process was investigated by cyclic voltammetry and electrochemical impedance spectroscopy. The resulted PbSe1-xTex nanostructures were characterized using scanning electron microscopy (SEM) as well as energy dispersive X-ray analysis (EDAX).

In this paper, we present Raman studies of different carbon nanotubes systems like single-walled nanotubes (SWNTs), multi-walled nanotubes (MWNTs) or composites prepared with different conjugated or non-conjugated polymers. We have focused our studies on the interactions that can take place in these systems and in general modify the characteristics of individual tubes. By introducing Van der Waals interactions between tubes, we are able to interpret experimental Raman spectra. In the case of SWNTs, we have put in evidence the so-called "bundle'' effect that consists of an upshift of the frequency of the RBM of 10 to 16 cm(-1), depending on the size of the bundles. In MWNTs, one can calculate the low frequency Raman modes observed experimentally. We found that they originate from the radial breathing modes of isolated tubes with an upshift that depends on the number of shells constituting the tube and we were then able to calculate the intensity of such modes. Finally, in polymer/nanotubes composites, we demonstrate that interactions take place between the two constituents in two different cases: PPV/SWNTs and PANI/SWNTs. The role of the method of preparation of composites is particularly put in evidence.

CdxPb1-xS (0 less than or equal to x less than or equal to 1) thin films were prepared on glass substrates using the chemical bath deposition method. The structural, electrical, and photoelectrical properties of the films were investigated, and all were dependent on the x value. For x > 0.5 (high Cd content), the films show a poor crystallinity and weak photoconductivity. For x < 0.5 (high Pb content), the films exhibit a good crystallinity, with an average size of the crystallites of 100 nm, and good photoconductivity. The threshold voltage of photoconductivity is shifted to lower wavelengths with increasing Cd content. The experimental results point toward possible ternary deposition on some composition ranges (near pure PbS or CdS); whereas, for the rest, the deposited film is rather a mixture of phases [not CdxPb1-xS but (CdS)(x)(PbS)(1-x)]. (C) 2004 The Electrochemical Society.

The glassy composition As25Te35Si40 was investigated by differential scanning calorimetry (DSC), X-ray diffraction (XRD), Raman spectroscopy, and infrared absorption (IR) measurements. X-ray diffraction patterns at room temperature and at temperatures around T-g were recorded and the radial distribution functions have been calculated. A continuous random network model for the ideal homogeneous glass structure has been proposed.