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  • Articles  (31)
  • Articles: DFG German National Licenses  (31)
  • XPS  (31)
  • Wiley-Blackwell  (31)
  • 1995-1999  (31)
  • 1985-1989
  • 1997  (31)
  • Physics  (31)
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  • Articles  (31)
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  • Articles: DFG German National Licenses  (31)
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  • 1995-1999  (31)
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1993-2001 
    ISSN: 0887-6266
    Keywords: polyaniline ; conducting polymer ; iodine doping ; XPS ; FTIR ; TGA ; WAXD ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyaniline, synthesized by using potassium dichromate as the oxidant, was doped with iodine in order to increase its electrical conductivity. The iodine-doped polyanilines attained a conductivity of 1.83 × 10-3 S/cm, which was about eight orders of magnitude greater than that of intrinsic polyaniline. The iodine-doped polyanilines did not absorb moisture readily when compared to the protonic-acid-doped polyanilines. Fourier transform infrared (FTIR) and x-ray photoelectron spectroscopy (XPS) results indicated that iodine-doping reactions occurred at the N-atoms in the quinoid structural units of the polyaniline molecular chains and consequently formed the charge transfer complexes. The iodine in the iodine-doped polyanilines existed mainly in the forms of I-3 and I-5 anions. As the doping level increased, the relative content of I-5 anions increased. Thermogravimetric analysis (TGA) results showed that there was about 6 wt % of iodine strongly bonded to the polyanilines since they would not evolve even at the structural decomposition temperatures of the polymer backbones. Wide-angle x-ray diffraction spectroscopy (WAXD) results revealed that the intrinsic polyaniline was an amorphous polymer but the regularity of polyaniline chains increased after iodine-doping. The iodine-doped polyanilines also showed a decrease in thermal stability. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1993-2001, 1997
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 629-642 
    ISSN: 0142-2421
    Keywords: XPS ; FTIR ; carbon nitride ; thin film ; simulation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The chemical bonding and microstructure of dual ion beam-deposited CNx films with nitrogen contents in the range 20-33 at.% have been examined by Fourier transform infrared spectroscopy (FTIR) and x-ray photoelectron spectroscopy (XPS). The FTIR spectra together with other published data have been used to construct a model microstructure of the CNx films. The XPS N 1s peak is composed of two components corresponding to N-sp2 C and N-sp3 C bonds. Using the quantified N 1s data and making certain assumptions, the model microstructure has been used as the basis of a C 1s peak simulation in which nine C components have been combined. At an N content of 20 at.% the simulation agrees well with the experimentally recorded XPS C 1s peak. The FTIR spectra, XPS N 1s peak shape and C 1s peak simulations support a microstructure of N substitution into an amorphous sp2/sp3 hybridized carbon structure. Above an N content of ∽20%, a new (nitrile-like) chemical form also emerges in the material, its abundance increasing with N content. It is proposed that this new structure occurs due to the presence, in the surface region of the condensing film, of C≡N dimers, which are formed when a C atom is surrounded by many N atoms. This molecule becomes trapped in the material and bonds to atoms at neighbouring sites. © 1997 by John Wiley & Sons, Ltd.
    Additional Material: 12 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 301-314 
    ISSN: 0142-2421
    Keywords: XPS ; FTIR ; carbon nitride ; thin film ; simulation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The chemical composition and microstructure of dual ion beam-deposited CNx films with nitrogen contents in the range 20-33 at.% have been examined by Fourier transform infrared spectroscopy (FTIR) and x-ray photoelectron spectroscopy (XPS). The FTIR spectra together with other published data have been used to construct a model microstructure of the CNx films. The XPS N 1s peak is composed of two components corresponding to N-sp2 C and N-sp3 C bonds. Using the quantified N 1s data and making certain assumptions, the model microstructure has been used as the basis of a C 1s peak simulation in which nine C components have been combined. At an N content of 20 at.% the simulation agrees well with the experimentally recorded XPS C 1s peak. The FTIR spectra, XPS N 1s peak shape and C 1s peak simulations support a chemical structure of N substitution in an amorphous sp2/sp3 hybridized carbon structure. Above an N content of ∽20%, a new (nitrile-like) chemical form also emerges in the material, its abundance increasing with N content. It is proposed that this new structure occurs due to the presence, in the surface region of the condensing film, of C—N dimers, which are formed when a C atom is surrounded by many N atoms. This molecule becomes trapped in the material and bonds to atoms at neighbouring sites. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 12 Ill.
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  • 4
    ISSN: 0142-2421
    Keywords: carbon nitride ; PVD ; hybridization ; AES ; XPS ; XANES ; ToF-SIMS ; magnetron-sputtered film ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The existence of β-C3N4 with hardness characteristics similar or better than diamond was predicted in 1990 by Liu and Cohen. Many studies have since been devoted to the synthesis of this compound. In the present work, carbon nitride films were deposited by various reactive magnetron sputtering processes of graphite targets in pure nitrogen and characterized by AES, XPS, x-ray adsorption near-edge structure (XANES) and static time-of-flight SIMS (ToF-SIMS). Various bonding states (single and double bond) are observed between carbon and nitrogen atoms and between carbon atoms but there is no evidence in the XANES results for either the presence of carbon-nitrogen triple bonds or a pyridine-like ring structure. Surface N/C ratios were estimated to be close to 0.3. Carbon K-edge XANES lineshapes, the C 1s plasmon-loss structure and the calculated density (2.2 g cm-3) indicate that the films are similar to diamond-like carbon without long-range ordering. The presence of CxNy fragments with 1≤y〈4 and the low abundance of CHx and CHxNy fragments in ToF-SIMS spectra further confirm that the carbon atoms do not adopt a graphite or pyridine-like cyclic two-dimensional structure and that the films are not significantly hydrogenated. A three-phase solid solution model is proposed for the composition of the films: a ‘free’ carbon phase, an sp3 - carbon-nitrided phase and an sp2 - carbon-nitrided phase. The relative proportion of these phases is influenced by the deposition conditions. Enhanced plasma ionization reactive magnetron sputtering leads to higher density and to a higher fraction of the sp3 carbon phase. © 1997 John Wiley & Sons, Ltd.
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  • 5
    ISSN: 0142-2421
    Keywords: XPS ; coating thickness ; global analysis ; multilayers ; curvature ; roughness ; atomic force microscopy ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Approaches are described for the analysis of XPS signals from samples comprising thin conformal coatings on substrates with non-ideal surface topography. In particular, attention is focused on arbitrarily shaped rough or curved substrates. Relations are derived for the relative x-ray photoelectron intensities emitted from various elements in such non-ideal samples. The surface topography of arbitrarily rough samples is analysed by atomic force microscopy to provide a frequency histogram of the local slopes, which is incorporated into a global, multi-element analysis method for interpretation of the observed XPS elemental intensities. An analogous approach is used for the analysis of curved samples. Our algorithms also enable simultaneous analysis of successively coated multilayer structures. When the elemental composition of the individual layers is known, the fit procedure enables determination of the thickness values of single-layer and multilayer coatings. The range of validity of the theory is discussed. © 1997 by John Wiley & Sons, Ltd.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 809-816 
    ISSN: 0142-2421
    Keywords: XPS ; Al-Si alloy ; segregation ; oxide growth ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The oxidation of three aluminium-silicon alloys has been studied as a function of temperature. At temperatures below 473 K a thin passivating oxide film is formed. At higher temperatures the segregation of the trace element magnesium to the surface is observed where it dominates the subsequent oxidation behaviour. In the absence of oxygen, magnesium segregation does not occur. From these results it is concluded that at temperatures in excess of 473 K magnesium segregation controls oxide growth and also that the degree of segregation is temperature dependent. Segregation effects are also observed for sodium, which appears to be concentration limited, and silicon, which is confined to the alumina-rich regions close to the metal surface where the silicon is also oxidized. © 1997 by John Wiley & Sons, Ltd.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 292-294 
    ISSN: 0142-2421
    Keywords: XPS ; Auger parameter ; TiO2 ; catalyst ; chemical state plot ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The analysis by XPS of TiO2 deposited on different substrates (SiO2, MgO, Ag, SnO) shows the existence of shifts in the Ti 2p binding energy and Auger parameter values. The magnitude of these shifts is a function of the support and of the coverage. A systematic representation of these shifts is possible with a chemical state plot. The implications of the existence of such shifts for the characterization of catalysts are discussed. © 1997 by John Wiley & Sons, Ltd.
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  • 8
    ISSN: 0142-2421
    Keywords: XPS ; carbon fiber ; achromatic ; monochromatic ; oxidize ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Amoco M40 PAN-based carbon fibers were electrochemically oxidized in a pilot plant system. The changes in the surface of the fibers were monitored using monochromatic x-ray photoelectron spectroscopy (XPS). A parallel experiment using achromatic x-radiation was conducted for comparison. Other graphitic materials were also studied. Decomposition of the fiber due to x-ray exposure could be effectively eliminated by using the monochromator. The use of monochromatic x-radiation produced considerable narrowing in the linewidth of the graphitic peak. This allowed the curve fitting of the component peaks to be performed with significantly greater confidence. © 1997 John Wiley & Sons, Ltd.
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  • 9
    ISSN: 0142-2421
    Keywords: XPS ; AES ; attenuation length ; IMFP ; elastic scattering ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: We examine substrate/overlayer experiments and the equations commonly used to quantify overlayer thicknesses. Comparisons with accurate Monte-Carlo simulations show that using attenuation lengths (rather than inelastic mean free paths) eliminates most of the error due to elastic scattering without increasing the complexity of the quantification.We give attenutation lengths for 27 elements, calculated by the criterion that systematic errors in such quantifications should be minimized. These are therefore the best attenuation length values to use in layerwise quantification. We show that, provided these attenuation length values are used, the error in estimation of the thickness of an overlayer due to elastic scattering can be limited to ±(5%+1 Å) for an emission angle ≤58° from the surface normal, and ±(10%+1 Å) for an emission angle ≤63° from the surface normal. This accuracy is acceptable for most analytical work. Other methods (such as analytical transport theory) are much more complicated, and achieve a high precision that is often unnecessary in view of other uncertainties typically present in these experiments (such as errors due to surface morphology and diffraction effects). The results presented here, using the full theory, show that the analyst's simple straight-line approximation is in fact of adequate accuracy, provided that the correct values of attenuation length are used.Simple semi-empirical equations are presented, which allow the analyst to estimate the attenuation length for electrons of kinetic energy between 50 and 2000 eV, to a standard uncertainty of 6%. © 1997 John Wiley & Sons, Ltd.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 643-649 
    ISSN: 0142-2421
    Keywords: thermoplastic olefin (TPO) ; valence band ; XPS ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: In this study we evaluate the utility of using x-ray-excited valence band measurements for the determination of the surface composition of simple model thermoplastic olefin systems composed of binary blends of semicrystalline polypropylene (PP) and an amorphous ethylene-propylene copolymer (E-co-P). Blend compositions included combinations of high- and low-molecular-weight (MW) PP and E-co-P composed of 60 wt.% PP/40 wt.% E-co-P and 80 wt.% PP/20 wt.% E-co-P blends. Results demonstrate that experimental valence band spectra for the polyolefin blends can be approximated by a linear combination of the pure-component valence band spectra. Bulk compositions determined from spectra recorded from cryomicrotomed cross-sections were found to be consistent with the bulk component wt.%. The surface compositions of the binary blends were all found to be enriched in PP. Measurements taken from the 60/40 wt.% blends were 10-20% higher in PP concentration than the bulk compositions, and were found to vary depending on the MW combination of the components. No MW dependence was observed for the 80/20 wt.% blends, apparently due to a near saturation of the surface with PP. The development of methods for assessing the surface composition of these types of materials may prove useful in monitoring changes in composition with material formulation and process conditions. Information of this nature could be helpful in permitting an evaluation of potential influences of composition on adhesion. © 1997 by John Wiley & Sons, Ltd
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