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  • 1
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 108 (1998), S. 3360-3372 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Amorphous poly(propylene oxide), PPO (molecular weights, 425 and ∼106), complexed with NaClO4 salt has ionic conductivities as high as 10−5 S/cm at room temperature. In an attempt to directly study the dynamics of the Na+ ions, (I=3/2) nuclear magnetic resonance (NMR) spin-lattice relaxation times, T1, and spin–spin relaxation times, T2, at a resonance frequency of 77.0 MHz have been measured over the temperature range from 150 to 390 K. A range of salt compositions [(PPO)nNaClO4; n=8–30] have been investigated. In addition, the glass transition temperature for each sample is reported. The recovery of equilibrium magnetization following a π/2 pulse is biexponential as expected for a spin I=3/2 system in the viscous liquid region. Below Tg a better fit to the magnetization recovery curve can be obtained if Kohlrausch–Williams–Watts (KWW) functions are used in place of the exponential functions. At low temperature the molecular motion has slowed to the point where a common spin temperature is not achieved by ionic diffusion. Two T2 values are observed over a limited temperature region near the T1 minimum. In the remaining low temperature region only the T2 associated with the central transition could be determined because the large 23Na quadrupole coupling constant made detection of the satellite transitions impossible. There is no evidence from the NMR relaxation time data for two Na+ populations. The experimental spin-lattice relaxation times can be analyzed to determine the correlation time for the ionic motion as a function of reciprocal temperature. The correlation time data display a distinct change in behavior at Tg which is interpreted as an indication of a crossover between two ionic transport mechanisms. Plots of T1 as a function of Tg/T indicate that dynamics for T〉Tg are largely determined by the flexibility of the polymer host (the α process) whereas a different process dominates for T〉Tg (presumably the β process). A comparison of correlation times derived from NMR relaxation times and ionic conductivities show a marked difference especially in the region of Tg. The conductivity decreases rapidly while the sodium ion motion continues with a correlation time ∼10−6 s through the glass transition. © 1998 American Institute of Physics.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 9047-9055 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 75 (1994), S. 7482-7488 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: Brillouin light scattering (BLS) has been used to study a series of three thin films of poly(styrene) spin coated onto Si(001) wafers. Poly(styrene) molecular weights M¯w of 30 000 and 600 000 were used, and the film thicknesses h were in the range 1730 A(ring)〈h〈3750 A(ring). It was found that the poly(styrene) films have isotropic elastic symmetry and that all of the films can be described by the same set of two independent elastic constants c11=5.7±0.15 GPa and c44=1.39±0.03 GPa. Both c11 and c44 were determined unambiguously using a least-squares-fitting procedure by observation of the longitudinal guided and Rayleigh modes of the poly(styrene) films. Calculations have been performed of the BLS spectra which include both surface ripple and elasto-optic light scattering mechanisms. From comparisons of the relative mode intensities in the measured and calculated BLS spectra, it is found that the values of the elasto-optic coefficients for poly(styrene) are k11=−1.4±0.4 and k12=−1.6±0.4.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 7474-7482 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Protonic conducting polymeric gel synthesis is motivated by its possible application in various electrochemical devices. This study focuses on the molecular motion of deuterons in gels formed with D3PO4 dissolved in propylene carbonate and a polymer matrix obtained using a free radical polymerization of methyl methacrylate with a cross-linking agent triethylene glycol dimethacrylate. Results are reported for samples containing 11, 23, and 45 mass % D3PO4. The measurements of the diffusion coefficients for deuterons and 31P show conclusively that the deuterons diffuse faster than the phosphorus carrying species. Therefore, the ionic conductivity results from a combination of the vehicular and Grotthus-type mechanisms. Species such as D2PO4−, D3PO4, or D4PO4+ are formed and the motion of the ions represents the vehicular mechanism while deuteron hopping from one species to the others constitutes the Grotthus mechanism. The nuclear magnetic resonance (NMR) spectra are consistent with the deuterons residing in a narrow distribution of sites; activation energies are similar for all samples, indicating that the barrier height to motion is independent of the concentration of D3PO4. This information reinforces the picture that the deuterons are always closely associated with PO4 groups. The correlation times determined from the deuteron nuclear relaxation times do not follow the Vogel–Tamman–Fulcher behavior observed in the conductivity measurements. The temperature dependence of the conductivity follows that of the structural relaxation or α process for T〉1.2Tg, while the NMR correlation time is determined by any motion which modulates the electric field gradient at the deuteron site. Both the α and slow β processes influence the NMR correlation times. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 12 (1979), S. 658-661 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 12 (1979), S. 661-662 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 17 (1984), S. 885-888 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 163-167 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 64 (1988), S. 2038-2043 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: Raman spectra of LiClO4 complexed in poly(propylene-glycol) (PPG) have been obtained for concentrations of the monomer to salt ratio (ether oxygen):Li in the range 30:1–5:1. Splitting of the symmetric stretching mode of the ClO4− anion was observed with an intensity profile that varied with salt concentration. This phenomenon indicates a changing environment about the anion. A two-component band analysis leads to the identification of dissociated ions on one hand and solvent-separated ion pairs on the other. The concentration of ion pairs is relatively low compared to that of the dissociated ions, which are predominant for all concentrations. Despite the observed increase in the absolute number of dissociated ions at higher salt concentration, the electrical conductivity is reported to decrease in the same range. This indicates that the number of "free'' charge carriers is of less importance for the conductivity than the mobility, which is damped in this concentration range. Frequency shifts of the disordered longitudinal-acoustic mode and increased hypersonic velocities, measured with Raman and Brillouin scattering techniques, respectively, indicate increased stiffness of the polymer matrix for increasing salt concentration, which probably results in decreased ion mobility.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 68 (1990), S. 5128-5132 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: The empirical response function introduced by Cole and Davidson for the analysis of dielectric relaxation in the frequency domain has been used in an analogous way to reanalyze ionic conductivity relaxation using the electric modulus representation. The fitting of data for ionic relaxation in AgPO3, 0.1AgI-0.9AgPO3, and 0.4Ca(NO3)2-0.6KNO3 originally fit using a Kohlrausch–Williams–Watts response function has been considerably improved.
    Materialart: Digitale Medien
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