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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 3723-3733 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dynamics of supercooled salol (phenyl salicylate) was measured in the time domain using optical Kerr effect techniques. By combining several experimental setups, data spanning more than six decades in amplitude and time (∼100 fs to ∼1 μs) were observed. The data have a complex shape, ranging from high-frequency intramolecular oscillations at short times, to nearly exponential relaxation at long times. As predicted by mode-coupling theory (MCT), the data for some ranges of time appear as power laws. The slowest power law, the von Schweidler power law, has an almost constant exponent of ∼0.59 over the entire temperature range studied (247–340 K). Above the MCT Tc (T〉∼1.17 Tg, where Tg is the laboratory glass transition temperature) for t〉∼1 ps, the decays are shown to be in excellent agreement with the master curve predicted by ideal MCT when higher order terms are included. However, the data do not display the plateau predicted by ideal MCT. To discuss the data at all temperatures, the intermediate time scale portion of the data, 2〈t〈10 to 500 ps (depending on the temperature), is modeled as a power law that falls between the critical decay and the von Schweidler power law. This intermediate power law shows significant temperature dependence with an exponent that decreases to a value of ∼−1 below Tc. Calculations using extended MCT, for a full range of hopping times, demonstrate that the temperature dependence of the intermediate time scale data near and below Tc cannot be explained by extended MCT. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 2710-2719 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present a new time domain technique for studying molecular orientational relaxation in viscous liquids. A molecular velocity gradient (acoustic disturbance) associated with a density change induced by weak absorption of a 1.06 μm excitation pulse, causes molecular alignment through translational–rotational coupling. Using an optical heterodyne detection method, molecular orientational relaxation is monitored. An eightfold experimental cycle, analogous to phase cycles in NMR, is used to separate the DIHARD signal (density induced heterodyne amplified rotational dynamics) from optical Kerr effect (OKE) contributions and thermal lensing effects. Calculations combining the Navier–Stokes equation with translational–rotational coupling are presented that describe the nature of the method. The method is analyzed theoretically and demonstrated with experiments on supercooled salol (phenyl salicylate). DIHARD experiments on salol combined with heterodyne detected OKE experiments are used to examine long time scale orientational relaxation over a wide range of times and temperatures. While OKE experiments measure the time derivative of an orientational correlation function, it is shown that DIHARD directly measures the time dependence of an orientational correlation function. The experimental results are compared to those previously reported in the literature, which were obtained with other methods. © 1999 American Institute of Physics.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 241-248 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The method of stimulated echoes was used to investigate the reorientational mechanism in the selectively deuterated glass-former glycerol, C3D5(OH)3 about 15 K above its calorimetric glass temperature. The reorientation process is fully isotropic. This enables an accurate determination of the decay constant, T1Q, of the quadrupolar spin order in the regime of ultraslow motion. The knowledge of this time constant has made it possible to reliably determine the rotational correlation function. The experimentally obtained evolution time-dependent correlation functions are compared with those from a simulation procedure involving a distribution of molecular jump angles. It is found that in glycerol small angles in the 2°–3° range dominate. They are accompanied by a small, but significant, fraction of larger jump angles. © 1998 American Institute of Physics.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 108 (1998), S. 890-899 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Using deuteron NMR techniques two-, effective three-, and various four-time correlation functions were recorded for supercooled ortho-terphenyl at 10–15 K above the calorimetric glass transition in order to characterize the heterogeneous nature of its primary response. The experimental results could successfully be described within various energy landscape models as well as via continuous time random walk simulations. These theoretical considerations provide a suitable basis for a definition of the term dynamic heterogeneity. We discuss the power but also some limitations of the present multidimensional NMR techniques when applied to amorphous materials. © 1998 American Institute of Physics.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 430-433 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The effect of spin diffusion on the decay of longitudinal magnetization in deuterated glassy systems is investigated. The decay of longitudinal magnetization was measured for different dilutions of amorphous deuterated toluene in protonated toluene. For increasing dilution the magnetization was found to decay more slowly, indicating the importance of spin diffusion also in deuteron spin systems. A strong correlation between the apparent width of the distribution of spin lattice relaxation times and the absolute value of the average spin lattice relaxation time was found. This correlation can be explained in terms of spin diffusion. A simple model is able to reproduce the main features of the observed phenomena. The initial decay rates are shown to be independent of spin diffusion. Conclusions concerning the frequency dependencies of observed average spin lattice relaxation times and width parameters are drawn. © 1995 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 314-319 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: 2H-NMR spin-lattice relaxation times T1 of phenyl ring deuterated toluene have been measured as a function of temperature (75–290 K) at Larmor frequencies between 13.8 and 55.8 MHz. The results are interpreted by assuming a Cole–Davidson rotational correlation time distribution for the α process dominating T1 at temperatures down to about 20 K above the glass transition (Tg=117 K) and one further process at lower temperatures. The latter is analyzed below Tg using a model with temperature dependent librational angles ΔΦ〈13° and mean correlation times τ(approximately-greater-than)10−9 s. Self-diffusion coefficients are determined at temperatures down to 136 K (D=1.5×10−14 m2 s−1) using a static field gradient 1H-NMR method. The product of D and the mean rotational correlation time shows a tendency to increase at the lowest temperatures. © 1996 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Solid State Communications 86 (1993), S. 183-186 
    ISSN: 0038-1098
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics Letters 216 (1993), S. 51-55 
    ISSN: 0009-2614
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 1 (1998), S. 169-172 
    ISSN: 1434-6036
    Keywords: PACS. 61.25.EmMolecular liquids - 61.12.-qNeutron diffraction and scattering - 78.35.+cBrillouin and Rayleigh scattering; other light scattering
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract: The dynamics of supercooled toluene, studied in a GHz-THz range by incoherent neutron and depolarized light scattering, is found to be in full accord with mode coupling predictions. Around the susceptibility minimum, neutron spectra are wavenumber independent and proportional to light scattering data; the fast -relaxation scaling law applies; amplitude and frequency diverge with power laws that extrapolate towards a crossover temperature K.
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 1977-03-01
    Print ISSN: 0011-183X
    Electronic ISSN: 1435-0653
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Published by Wiley
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