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Raman Investigation (raman + investigation)
Selected AbstractsAn ab initio, Infrared, and Raman Investigation of Phosphate Ion Hydration.CHEMINFORM, Issue 1 2004Cory C. Pye No abstract is available for this article. [source] Raman spectroscopy of Bi-Te thin filmsJOURNAL OF RAMAN SPECTROSCOPY, Issue 2 2008V. Russo Abstract The deposition of micro- and nanocrystalline bismuth telluride thin films with tailored structure and composition is of interest in view of improving the well-known material thermoelectric properties. Only a few works exist that discuss Raman scattering of Bi2Te3 crystals and films, while a Raman characterization of other phases, i.e. other lesser known compounds of the Bi-Te system, such as tsumoite (BiTe) and pilsenite (Bi4Te3), is still completely lacking. We here present a Raman investigation of Bi-Te polycrystalline thin films with controlled structure (stoichiometry and growth orientation), morphology and phase composition, produced by nanosecond pulsed laser deposition. Interpretation of Raman spectra from Bi-Te films was supported by scanning electron microscopy, energy dispersive spectroscopy (EDS) and X-Ray diffraction measurements, together with the predictions of the group theory. In this way, the first Raman characterization of Bi-rich phases (namely BiTe and Bi4Te3) has been obtained. For Bi-Te compositions characterized by a high Bi or Te content, Raman spectra reveal that segregation of elemental Bi or Te occurs. Copyright © 2008 John Wiley & Sons, Ltd. [source] Raman spectroscopy and molecular simulation investigations of adsorption on the surface of single-walled carbon nanotubes and nanospheresJOURNAL OF RAMAN SPECTROSCOPY, Issue 6 2007Maher S. Amer Abstract Raman spectroscopy has, for long, been utilized to investigate material systems on the micro and mesoscales. Recently, the technique has proven its ability in exploring systems on the nanoscale. In this paper, we review our recent work on the Raman investigation of molecular adsorption from liquid mixtures on surfaces of single-walled carbon nanotubes and fullerene nanospheres, emphasizing the following major research findings: the development of a Raman-based technique capable of sensing local chemical interactions on the surface of carbon nanotubes and spheres; the molecular simulation results supporting the Raman investigation; the possibility of creating mesostructures based upon mixtures of carbon nanotubes and nanospheres that are crucial for selective adsorption. The current findings represent a major new thrust for the development of new nanostructured materials with superior adsorption capabilities and unique applications. Copyright © 2007 John Wiley & Sons, Ltd. [source] In situ micro Raman investigation of electrochemically formed halide and pseudohalide films on mercury electrodes,JOURNAL OF RAMAN SPECTROSCOPY, Issue 3 2002Alexandre G. Brolo Oxidation of pure mercury electrodes was followed by in situ surface-unenhanced Raman spectroscopy. A special spectroelectrochemical cell allowed the observation of spectral features of the oxidation products using a Raman microprobe. The electrochemical behaviour of mercury in basic solution, halide (F,, Cl,, Br, and I,) and pseudohalide (SCN,) media was investigated. Insoluble films were formed during the anodic processes in all these systems. The identities of the electrochemically generated films were clearly determined from the Raman spectra. The main product of the electrochemical oxidation of mercury in basic solutions was solid HgO. The anodic behaviour of mercury in the presence of halide yielded insoluble Hg2X2 compounds (where X is the halide). The time dependence of the Raman signals indicated a diffusion-controlled growth of the halide films. The oxidation of mercury in SCN, solutions also produced a solid precipitate [Hg2(SCN)2]. Raman bands due to soluble mercury(II) thiocyanate complexes [Hg(SCN)x2,x], present in the electrochemical diffusion layer, were also observed. Copyright © 2002 John Wiley & Sons, Ltd. [source] H2O2 -mediated oxidation of tetrahydrobiopterin: Fourier transform Raman investigations provide mechanistic implications for the enzymatic utilization and recycling of this essential cofactorJOURNAL OF RAMAN SPECTROSCOPY, Issue 8 2002Jeremy Moore The oxidation of (6R)- L - erythro -5,6,7,8-tetrahydrobiopterin (6BH4) by H2O2 was examined by Fourier transform Raman spectroscopy. Initial investigations indicated that oxidation proceeds by incorporation of the H2O2 into the 6BH4 molecule without the formation of any additional water. In addition, the pyrimidine ring is affected with the shift of the double bond from the N1,C2 to the C2,N3 position. Such rearrangements of this double bond are observed after the production of either a carbinolamine or quinonoid species. Using deuterium exchange experiments, it was possible to substantiate that the oxidation of 6BH4 initially proceeds by the formation of a 4a-OH-carbinolamine intermediate prior to its spontaneous dehydration yielding the quinonoid dihydro species (qBH2). Furthermore, the hydrogen on the hydroxyl group of the carbinolamine interacts with the oxygen of the carbonyl group at the C4 position of the pyrimidine ring. It is proposed that this interaction facilitates the dehydration of the carbinolamine, thus explaining its instability. Furthermore, a mechanism for the dehydration reaction is suggested, wherein the 4a-hydroxyl group forms an H-bond to the carbonyl group, thus making the oxygen of the hydroxyl group more susceptible to attack by the proton at position N5 of the pyrazine ring, resulting in qBH2 production concomitant with the loss of a water molecule. Upon increasing the concentration of H2O2 the qBH2 converts to 7,8-BH2, which is further oxidized to L -biopterin. Taken together, our results do not support an earlier proposed mechanism implicating a hydroperoxide intermediate in this oxidation reaction. Copyright © 2002 John Wiley & Sons, Ltd. [source] | ||||||||||