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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 79 (1996), S. 9326-9333 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The in-plane optical loss was correlated with molecular orientation in a unidirectionally stretched poly(ethylene terephthalate-co-isophthalate) copolyester film. X-ray scattering was applied to ascertain the anisotropic and amorphous natures of the stretched film. The film was adhered onto a silicon wafer to fabricate a planar waveguide. Multiple TE and TM propagation modes were obtained on the planar waveguide using a prism coupler at 632.8 nm yielding in-plane refractive indices of 1.6545 and 1.5464, parallel and transverse to the stretch direction, respectively. For each waveguide mode, a propagation streak was generated and registered on photographic film. The in-plane linear attenuation coefficient, α(parallel)≡{ln[I(O)/I(x(parallel))]}/x(parallel), was derived from the propagation streak. The optical path of each mode was determined and used to normalize α(parallel). For the TE modes, α(parallel) increased with the mode number and was highly anisotropic, i.e., α(parallel) (parallel to the stretch direction)≤α(parallel) (transverse to the stretch direction). However, for the TM modes, α(parallel) was found to be a constant smaller than those of the TE modes, and was independent of mode number as well as molecular orientation. The bulk α(parallel) was extrapolated to remove the surface loss contributions for the planar waveguide. Dipole interaction between the stretched copolyester, surface irregularities, and the TE or TM polarization was analyzed to delineate the in-plane optical loss behavior. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 77 (1995), S. 3938-3941 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The electronic properties of the ladder polymer BBL are investigated using steady state and transient photoconductivity techniques. The photocurrent response of the polymer film in the surface cell and sandwich cell configurations are compared along with the absorption spectra and the results correlated with the surface and bulk morphology. The steady state photocurrent shows a nonlinear response with respect to the electric field, and the photocurrent spectral response is accompanied by a significant tailing in the infrared region. The photocurrent is also studied as a function of photon intensity and chopper frequency. A long lived transient photocurrent ((approximately-greater-than)100 ms) is present on exposure to nanosecond laser pulses revealing the presence of deep traps. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 1507-1514 
    ISSN: 0887-6266
    Keywords: poly(p-phenylenebenzobisthiazole) ; Mylar ; polymeric film ; waveguide ; refractive index ; linear attenuation coefficient ; optical anisotropy ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Extruded thin films of a liquid-crystalline charge-conjugated rigid-rod polymer poly(p-phenylenebenzobisthiazole), PBT, and a semicrystalline thermoplastic polyethylene-terephthalate (Mylar) were fabricated and examined for film thickness, refractive index, and linear attenuation coefficient. Optical waveguide modes were successfully induced on the polymeric films using a prism coupler at λ = 633 and 1300 nm. Highly consistent thickness values were obtained for the polymeric films. In addition, the anisotropic nature of the optical properties was determined using TE and TM propagation modes. A refractive index as high as 2.3 was observed on PBT film. The refractive index data suggested that the PBT and Mylar films were optically anisotropic with refractive indices n⊥ (out-of-plane) invariably smaller than n∥ (in-plane). Large anisotropy was also discovered in the linear attenuation coefficient α, with α∥/α⊥ ≈ 50 for the Mylar films. Complementary polarimetric and spectroscopic interference measurements were also applied to investigate the optical anisotropy of the extruded polymeric films. © 1992 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2925-2933 
    ISSN: 0887-6266
    Keywords: ionic conductivity ; DC conductivity ; rigid-rod polymer ; depletion measurement ; X-ray scattering ; anisotropic ; polymer electrolyte ; polyelectrolyte ; conducting polymers ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The conductivity study results of lithium-doped sulfonated PBI, a conjugated rigid rod polymer, poly[(1,7-dihydrobenzo[1,2-d:4,5-d′]dimidazole-2,6-diyl)-2-(2-sulfo)-p-phenylene], derivatized with pendants of propane sulfonate Li+ ionomer are reported. The room-temperature DC four-probe conductivity parallel to the surface of cast films was as large as 8.3 × 10-3 S/cm. Similar measurements with an eight-probe configuration showed no difference between bulk and surface conductivity. The ionic nature of the conductivity was indicated by constant voltage depletion experiments and by secondary ion mass spectroscopy measurements of the residues near the electrodes. The DC two-probe conductivity measured transverse to the sample surface was three to four orders of magnitude smaller than longitudinal conductivity, while the AC two-probe conductivity was even less. Electron microscopy indicated that the films had a layered structure parallel to the surfaces. This structural anisotropy was confirmed by refractive index values obtained from wave-guide experiments and by wide angle X-ray scattering. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2925-2933, 1997
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1941-1950 
    ISSN: 0887-6266
    Keywords: rigid-rod polymer ; cation ; dialysis ; molecular weight ; cast ; aggregated ; isotropic ; anisotropic ; film ; depletion measurement ; ionic conductivity ; x-ray scattering ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly[(1,7-dihydrobenzo[1,2-d:4,5-d′] diimidazole-2,6-diyl)-2-(2-sulfo)-p-phenylene], a conjugated rigid-rod polymer, was derivatized with pendants of propane-sulfonated ionomers. The derivatized rigid-rod polymer was soluble in aprotic solvents as well as in water for isotropic solutions that were processed into isotropic films. Direct-current electrical conductivity σ of the films was measured using the four-probe technique. Room-temperature σ as high as 2.9 × 10-4S/cm was achieved on pristine isotropic films without using dopants. When the rigid-rod polymer concentration exceeded 25 wt %, the isotropic solution could be transformed into a liquid-crystalline solution that allowed deformations to be applied to produce anisotropic films. Significant increase in σ was obtained in a sheared film along both the parallel direction (∥) and the transverse direction (⊥) with a σ∥/σ⊥ = 5. Additionally, enhanced σ was realized in films heat-treated at about 100°C, in the derivatized polymer with higher molecular weight from dialysis, and in substituting the sulfonated ion Na+ by H+ in the pendants of the polymers. Constant-voltage measurements were applied to the polymers to monitor the σ stability for ascertaining the nature of the conductivity. No electronic contribution in σ was detected. Instead, a monotonically decreasing σ was consistently observed indicative of ionic conductivity. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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