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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 84 (1998), S. 181-188 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The alignment behavior of nematic liquid crystal (LC) on the surface of four types of polyimide (PI) films, three aromatic PIs and a PI with an alicyclic dianhydride, exposed to linearly polarized light of long wavelength (366 nm) was investigated by polarizing microscopy. It was found that the alignment of the LC was induced by all of the exposed PIs and the alignment direction of the LC was perpendicular to the polarization direction of the linearly polarized light. The degree of uniformity of LC alignment increased with increasing exposure energy incident on PI films. To produce the uniform alignment state, the PI with an alicyclic dianhydride had to be exposed to higher energy than aromatic PIs. Ultraviolet (UV) -visible spectroscopy indicated that the absorbance changes of the aromatic PIs were much smaller than that of the PI with an alicyclic dianhydride when uniform alignment of the LC was caused. Furthermore, both UV-visible and infrared spectroscopy showed the change in the absorbance of the aromatic PI with a diphenyl ether diamine was still very small even though it was exposed to linearly polarized light with a large dose. These results demonstrate that the aromatic PIs are more favorable as a photosensitive alignment layer and the uniform alignment of the LC can be induced without significant destruction of the chemical structure of PI with a diphenyl ether diamine. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 72 (1998), S. 545-547 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Homogeneous alignment of a nematic liquid crystal (LC) was induced by a polyimide (PI) film containing diphenyl ether component exposed to linearly polarized light at 366 nm. Ultraviolet-visible absorption spectra showed that the change in the absorption of the PI was very small after exposure; the preliminary result indicated that the homogeneous alignment of a LC could be induced without significant change in the PI structure. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 84 (1998), S. 4573-4578 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The alignment of a nematic liquid crystal (LC) could be induced by three polyimide (PI) films exposed to linearly polarized ultraviolet (UV) light of long wavelength (366 nm). The alignment could also be modified by changing the direction of polarization of the linearly polarized light (LPL). Infrared (IR) and UV-visible spectroscopy indicated that among the three PI films the PI with a benzophenone moiety and the PI with a diphenyl methane moiety were sensitive to UV radiation and susceptible to remarkable ablation after irradiation with LPL in air. Polarized UV-visible spectroscopy indicated that dichroism of the PI films was caused by LPL and altered by changing the polarization of the LPL. Furthermore, the PI films irradiated under vacuum showed little reduction in intensity of IR bands, which is in sharp contrast to the marked decreases in samples irradiated in atmospheres containing oxygen. This proves that oxygen is necessary to the ablative process of the PI films. Our results indicate that the mechanism of LC alignment on the photosensitive PI films is photoinduced anisotropic oxidative ablation of the PI films. In contrast, the PI film with a diphenyl ether moiety was quite stable under similar irradiation conditions even though the irradiated PI film could also induce alignment of the LC molecules. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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