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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 786-798 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: In this article we report the characteristics of the new High Energy Spherical Grating Monochromator beam line on the SRS. The instrument, which has no entrance slit, was designed to provide high photon flux with small spot size, in the energy range covering the 1s binding energies of carbon, nitrogen, oxygen, and fluorine. Radiation from a bending magnet is horizontally focused onto the exit slit by a long, Pt-coated meridian cylinder (R=299 m, 2 mrad horiz. aperture, 2° glancing angle). The light is vertically diffracted and focused by one of three interchangeable spherical gratings (1050, 1500, and 1800 lines mm−1) operating in negative order. Finally, the light is refocused by an ellipsoidal mirror. The photon flux, determined with copper and carbon photocathodes, is presented for the three gratings. Useful flux is obtained in the range 250–1200 eV, with intensity maxima for each grating at 600, 700, and 800 eV of 11, 9, and 5×1010 photons s−1 per 100-mA stored beam into a band pass of 0.05%. The influence of contaminants which are present on the optical elements is discussed, together with details of beam line operating conditions which minimize the build up of such contaminants. Photoabsorption and photoemission measurements indicate a high (up to 30%) second order and some third order light content. Resolution determinations obtained from photoabsorption measurements are presented. Although features as narrow as 250 meV have been resolved, the resolving power of the instrument is found to depend strongly on stored beam current. We suggest this may be due to electron beam (i.e., source) blow-up. We critically discuss the suitability of the new facility for surface EXAFS of low Z adsorbates, in particular above the carbon, nitrogen, and oxygen 1s edges, using examples from recent studies which have been undertaken on the beamline.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 2202-2212 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An adsorption calorimeter for studies on well-defined single crystal surfaces under ultrahigh vacuum conditions is now available, based on supersonic molecular beam dosing onto ultrathin metal single crystals. Here we discuss the relationship between the calorimetric heat of adsorption as measured in this system and the related parameters: the differential heat of adsorption, the isosteric heat, and the Arrhenius desorption energy. Coverage-dependent calorimetric heats of adsorption and sticking probabilities for CO on Ni{111}, {110}, and {100} are presented, and comparisons made with literature values for isosteric heats and Arrhenius desorption energies. At intermediate coverages some significant discrepancies occur which are attributed to a temperature-dependent adlayer structure. By combining sticking probability with heat measurements at high coverage, at 300 K, where significant desorption occurs, the desorption preexponential has been accurately determined; differential entropies of adsorption are also obtained. Differences in initial heats of adsorption and in the coverage dependencies for the three crystal planes are discussed, particularly in relation to surface stoichiometry, and to CO–CO interactions.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 2782-2789 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High-resolution spectra have been obtained for the predissociative N–H stretching overtone levels 5ν1 (15 120 cm−1) and 6ν1 (17 670 cm−1) of HN3, cooled in a free-jet expansion. The spectral bandwidth (Doppler limited at 0.007 cm−1 full width at half-maximum (FWHM) is sufficiently narrow to reveal the homogeneous linewidths of individual rovibrational transitions in the 6ν1 band, for which we previously measured the dissociation lifetime in time-domain experiments. Two distinct manifestations of vibrational coupling characterize the spectra: (a) anharmonic mixing of the N–H stretch with other vibrational motions to give a complex spectrum of vibrational eigenstates and (b) homogeneous widths of the resultant states determined by the dissociation lifetime. The results are discussed with reference to previous studies of overtone spectroscopy and intramolecular mixing. Time-domain measurements of dissociation rates are reported for four vibrational levels with zero-order labels 5ν1 +νx. Over the range 15 100 cm−1–17 700 cm−1, the dissociation rate increases monotonically with vibrational energy, with no apparent "mode-specific'' variations. This is interpreted in terms of the highly mixed character of any particular vibrational eigenstate that is excited.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 8789-8797 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: CO adsorption on Ni{110} and on hydrogen precovered Ni{110} surfaces at 180 K has been studied by FT-RAIRS. On a clean Ni{110} surface CO adsorbs at on-top sites upto a coverage of 0.7 ML. At higher coverages the on-top CO band at 2060 cm−1 decreases in intensity with a concomitant increase in a band at 1960 cm−1 which shifts up in frequency. The (2×1)p2mg structure at 1.0 ML CO coverage shows a single band at 1998 cm−1 attributed to CO tilted at bridged sites. FT-RAIRS of CO adsorption on H precovered Ni{110} surfaces shows complex CO site switching within different CO and H coverage regimes. A model is presented involving compression of H into islands of high coverage and both mixed H and CO and unmixed CO islands are formed. CO adsorbs in the unmixed CO islands the same as that on clean Ni{110}. Within the mixed H/CO islands the first layer nickel atoms reconstruct and a new hydrogen desorption state is observed. The CO site switching observed by FT-RAIRS within the various H and CO coverage regimes is discussed in terms of a dominant indirect interaction.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 98 (1993), S. 10106-10106 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 62 (1991), S. 2177-2185 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: The design of an ultrahigh vacuum microcalorimeter enabling calorimetric heats of adsorption to be obtained on single crystal surfaces as a detailed function of coverage is discussed. The system comprises a pulsed supersonic molecular beam source, an ultrathin metal single crystal, and remote infrared temperature sensing. Sticking probabilities and coverages are determined pulsewise by the King and Wells method, and heat capacity calibrations are conducted in situ by laser beam pulsing. Results for CO and O2 on Ni{110} demonstrate excellent sensitivity to adsorption of ∼10−13 moles of gas (∼0.01 monolayer). The heat capacity of the calorimeter is 4.2 μJ K−1.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical & engineering data 19 (1974), S. 320-323 
    ISSN: 1520-5134
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 96 (1974), S. 3328-3330 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 7379-7380 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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