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  • 1990-1994  (2)
  • second harmonic generation  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1983-1988 
    ISSN: 0887-6266
    Keywords: second harmonic generation ; optical anisotropy ; spin-cast polymer film ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The nonlinear susceptibilities (χ(2)33, χ(2)31), and the refractive index anisotropy, of a main chain accordion polymer, BCSC (see the text for the complete chemical formula), have been measured by the techniques of second harmonic generation (SHG) and waveguiding. A large birefringence, which is induced in the BCSC film by the spin-coating process, is almost removed by electric field poling. Our results demonstrate the fundamental difference between the birefringence associated with quadrupolar orientational order and the dipolar order associated with SHG. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2615-2624 
    ISSN: 0887-6266
    Keywords: second harmonic generation ; correlated dipolar orientation ; trapped charges ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Second harmonic generation (SHG) in three corona-poled, pure, bulk polymers is studied as a function of temperature. It is found that this technique readily yields dynamical information that is complementary to that obtained from the technique of dielectric relaxation (DR). The SHG results are compared to those from DR in the same temperature ranges above Tg. It is found that in the temperature ranges examined, the relaxation times obtained from SHG are several orders fo magnitude longer than those measured by dielectric relaxation. This is explained as being due to the strong correlation between oriented dipoles and to trapped charges injected by the poling process. Fitting measured data to the Williams-Landau-Ferry (WLF) equation indicates that more free volume is needed in SHG for dipolar reorientation than is needed in DR. An SHG relaxation elongation phenomenon at constant temperature is found to occur in the pure bulk polymers and is similar to that found in chromophore-doped polymers previously studied. The SHG technique is developed as a new tool to directly study the reorientational dynamics of polar polymer segments. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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