Tunghai University Institutional Repository:Item 310901/22759
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 21921/27947 (78%)
造访人次 : 4205821      在线人数 : 385
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://140.128.103.80:8080/handle/310901/22759


    题名: Local photo-assisted poling of azo copolymer films by scanning probe microscopy
    作者: Chien, F.S.-S., Lin, C.Y., Hsu, C.C.
    贡献者: Department of Physics, Tunghai University
    关键词: AFM;Bound charge;Contact Electrification;Copolymer films;Electrical poling;Electrostatic force microscopy;Glass transition temperature;Non-linear optical material;Optical poling;Physical interactions;Polar chromophores;Polar orientation;Tapping modes
    日期: 2008
    上传时间: 2013-05-21T09:16:02Z (UTC)
    摘要: Azo copolymers are nonlinear-optical materials, in which polar orientation can be induced by optical poling or electrical poling. We report a new efficient approach to performing photo-assisted poling (PAP) by atomic force microscopy (AFM) for azo copolymer films containing disperse-red-1 chromophores, and to characterize the polar orientation by electrostatic force microscopy (EFM) at the submicrometre scale. Both PAP and contact electrification effects can be generated by the physical interaction between the probes and the films. We demonstrated that these two effects can be distinguished by the relationship between the signs of the charges (bound charges and transferred charges) and the probe bias. Finally, we achieve local PAP far below the glass transition temperature by AFM operated in the tapping mode, and the response of the polar chromophores to local PAP can be studied by EFM. ? 2008 IOP Publishing Ltd.
    關聯: Journal of Physics D: Applied Physics 41 (23) , art. no. 235502
    显示于类别:[應用物理學系所] 期刊論文

    文件中的档案:

    档案 大小格式浏览次数
    index.html0KbHTML233检视/开启


    在THUIR中所有的数据项都受到原著作权保护.


    本網站之東海大學機構典藏數位內容,無償提供學術研究與公眾教育等公益性使用,惟仍請適度,合理使用本網站之內容,以尊重著作權人之權益。商業上之利用,則請先取得著作權人之授權。

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈