National Institute Of Materials Physics - Romania

Spectral emission of a Xenon discharge in the presence of NaCl powder is strongly modified and dominated by the XeCl excimer band at 308 nm. Materials introduced in gas electrical discharges interact with the reactive species produced in the plasma: electrons, ions and metastable atoms. In this paper, the influence of ions and metastable atoms of a capacitive RF Xenon discharge plasma (20W, 30MHz) 5 Torr on the structure of a NaCl powder introduced in the discharge has been investigated.

Iron local environment was investigated by EXAFS in Fe- and (Fe, Eu)-doped TiO(2) photocatalysts, prepared by hydrothermal and high-energy ball milling (HEBM) routes. In the case of the hydrothermal samples, the substitution of Ti(4+) by Fe(3+) ions was evidenced. For the samples prepared by HEBM, the iron environment corresponds to mixed metallic and oxidized (FeO, alpha-Fe(2)O(3)) configurations, without a clear evidence of iron incorporation into the TiO(2) lattice. This could be related to the catalyst contamination by iron microparticles detached from the balls during milling process.

Thin films of phosphate glasses were prepared by pulsed laser deposition in oxygen atmosphere on ITO-coated glass and silicon substrates respectively, using a Nd:YAG laser (266 nm). The targets were Li(2)O-Al(2)O(3)-P(2)O(5) bulk glasses doped with Pr and Nd. Infrared transmission-, energy dispersive X-ray- and X-ray photoemission spectroscopy investigations carried out on targets as well as on the deposited films proved a satisfactory compositions transfer on both substrates. Scanning electron microscopy and atomic force microscopy show continuous films with glassy spheres. Processes where substrates were positioned perpendicularly to targets produced discontinuous drops free films.

Fe(III)-doped TiO2 aerogels are prepared by acid catalyzed sol-gel method followed by supercritical drying, and then heat treatment. Raman spectra together with X-ray diffraction (XRD) and selected area electron diffraction (SAED) patterns of the iron-doped TiO2 aerogel samples revealed the existence of both anatase and brookite crystalline phases. It was found that the brookite phase formation is favored by the increase of the iron content in the dried samples. XRD measurements show that the lattice constant c of anatase phase decreases with the dopant addition, while the value of a remains essentially unchanged. The microstructure of the investigated samples is relatively compact with small mesopores as revealed from transmission electron microscopy (TEM). The most enhanced photocatalytic activity was exhibited by the TiO2 aerogel sample with 1.8 at.% Fe(III) whose apparent rate constant of the salicylic acid photodegradation was found to be of almost six times higher than that of Degussa P25.

Fabrication of Au-Ti Schottky structure on GaAs semi-insulating wafer was related to an ultra-high vacuum deposition condition and low vacuum annealing in low vacuum and temperature range T=320-360 degrees C. There are presented representative I-V characteristics in dark and in different light (power levels). The spectral response has a maximum in Delta lambda = (850-950) nm corresponding to a band-to-band transition. The complex dependence of optical generated non-equilibrium carriers is related to the equivalent state density at the conduction band edge (in T(3/2) factor) and in exponential distribution factor exp (-(E-F)/kT).

ZnO:Co thin Films are prepared by electrochemical deposition at different overpotentials and investigated by scanning electron microscopy, X-ray photoelectron spectroscopy and Kerr magnetometry (MOKE). Increse of structural disorder and crystallite re-orientation are observed for cobalt doped samples (especially for those obtained at - 750 and at - 800 mV overpotentials). MOKE magnetometry revealed room temperature ferromagnetic behaviour only for ZnO:Co deposited at - 850 mV. These are the samples with the less cobalt content and lowest structural perturbation of the ZnO matrix by cobalt.

We report the formation of stable C-70 aggregate forms in o-dichlorobenzene/N-methyl-2-pyrrolidinone (DCB/NMP) and o-dichlorobenzene/acetonitrile (DCB/ACN) mixtures and their characterization by UV-VIS absorption spectroscopy and photoluminescence. As NMP acts on C-70 both as a solvent and reactant due to the unpaired electrons of the amidic nitrogen atom, molecular complexes (C-70/NMP) that aggregate slowly are formed by the binding of the NMP molecule to the fullerene cage. This interaction is seen in the UV-VIS absorption spectra of C-70 in DCB/NMP solvent mixtures by a gradual modification of the absorption spectra when increasing the NMP concentration. On the other hand, DCB and ACN combined form it typical solvent/non-solvent mixture favoring an intense aggregation of fullerenes. This yields to the C-70 clusters formations, having different size, similar to a precipitation process. Their characteristic is an abrupt variation in the absorbance appearing when the ACN is used in a greater extent. This different behavior of C-70 aggregation in DCB/NMP and DCB/ACN mixtures is also seen in their luminescence spectra recorded at different excitation wavelengths. While the PL spectra of C-70 solvated in DCB/NMP solution keeps almost the same modified shape irrespective the NMP concentration, the luminescence spectra Of C-70 in DCB/ACN mixture partially regains the powder C-70 PL signature as the ACN concentration is increased.

Hybrid material based on PbI2 intercalated with 2,2'-bypiridine (BIPY) was investigated by correlated studies of photoluminescence. infrared absorption and Raman spectroscopy. The PbI2(BIPY) intercalated compound has been synthesized by the chemical reaction of K1 and Pb(NO3)(2) in aqueous BIPY solution The optical studies reveal different properties for the hybrid material in comparison with those of pure PbI2 and BIPY. In the photoluminescence spectrum of the intercalated compound. recorded at liquid nitrogen temperature a new intense hand emission with maximum at 2 07 eV is observed. The excitation spectrum reveals it broad hand featured by several maxima at 2.77, 3.34 and 3 70 eV. New absorption bands at about 1589, 1489, 1435, 1312, 1009 cm(-1) are observed in the IR spectrum of PbI2(BIPY). The Raman spectrum of intercalated compound discloses new lines at 67, 83, 127 cm(-1) and the shift of two Raman lines from 994 cm(-1) to 1010 cm(-1) and from 1045 cm(-1) to 1060 cm(-1). A charge transfer process, leading to the formation of lead-BIPY coordination complexes. is considered its responsible for the strong host-guest interaction revealed by almost all experimental data

Functionalization of PbI2 with polyaniline-emeraldine base (PANI-EB) or polyaniline-emeraldine salt (PANI-ES) is demonstrated by Raman spectroscopy. Two functionalization methods were used: electrochemical polymerization of aniline onto the PbI2 modified Pt electrode and the mechanico-chemical reaction between PANI and PbI2. The functionalization induces changes in the Raman spectrum of PbI2 that consist in the appearance of new Raman lines with the peaks at 80, 144 and 170 cm(-1) The first line is the signature of the "stacking faults" that disrupt the stacking sequence of layers I-Pb-I atomic layers along the c crystalline axis by the intercalation of polymer molecules The bands at 144 and 170 cm(-1) are attributed to a vibrational mode associated to the Pb-NHR"(2) (R" = C6H4) bond.

TiO2:Fe thin films prepared by pulsed laser deposition exhibit in some case light dependent saturation magnetization, as determined from Kerr magnetometry measurements performed in dark or by illuminating the sample. This phenomenon is Studied in correlation with local atomic Structure investigated by extended X-ray absorption fine structure, composition and chemical state analyzed by X-ray photoelectron spectroscopy and by Xray absorption near-edge structure. It is found that light-controllable magnetism is a property of a mixture of Fe and oxidized Fe clusters embedded in the anatase TiO2 matrix.