Orientation of liquid crystal molecules evaporated onto rubbed and photoaligned polymer surfaces
被引:5
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作者:
Shioda, T
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Tokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, JapanTokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, Japan
Shioda, T
[1
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Okada, Y
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机构:Tokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, Japan
Okada, Y
Takanishi, Y
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机构:Tokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, Japan
Takanishi, Y
Ishikawa, K
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机构:Tokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, Japan
Ishikawa, K
Park, B
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机构:Tokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, Japan
Park, B
Takezoe, H
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机构:Tokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, Japan
Takezoe, H
机构:
[1] Tokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, Japan
[2] Kwangwoon Univ, Dept Electrophys, Seoul 139701, South Korea
来源:
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS BRIEF COMMUNICATIONS & REVIEW PAPERS
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2005年
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44卷
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5A期
Second-harmonic generation (SHG) and polarized ultraviolet-visible (UV-VIS) absorption have been used to study the orientational distribution function of 5CB (4'-n-pentyl-4-cyanobiphenyl) liquid crystal (LC) molecules adsorbed on rubbed and photoaligned photoisomerizable polyamic acid layers. The simultaneous analysis of SHG and polarized UV-VIS absorption data using the maximum entropy method shows that the anisotropic distribution of 5CB molecules along the rubbing direction tilts up from the surface plane as the molecular density increases. More interestingly, the anisotropy is relatively low at the first stage of the evaporation and becomes gradually pronounced, indicating an important role played by the long-range intermolecular interaction among LC molecules for LC surface alignment. No orientation formation of non-liquid crystalline 4CB (4'-n-butyl-4-cyanobiphenyl) molecules on the treated surfaces supports this conclusion. It is important to emphasize that a relatively small fraction of molecules contribute to give a polar order, but the rest form dimers even at the early stage of the evaporation. This tendency is particularly marked on the photoaligned surface; no SHG activity arises irrespective of the amount of evaporated molecules.