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Epitaxial growth of sexi-thiophene and para-hexaphenyl and its implications for the fabrication of self-assembled lasing nano-fibres

机译:六噻吩和对六苯基的外延生长及其对制备自组装激光纳米纤维的影响

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摘要

Over the last few years, epitaxially grown self-assembled organic nano-structures became of increasing interest due to their high potential for implementation within opto-electronic devices. Exemplarily, the epitaxial growth of the rod-like molecules para-hexaphenyl (p-6P) and α-sexi-thiophene (6T) is discussed within this review. Both molecules tend to crystallize in highly asymmetric elongated entities which are also called nano-fibres. It is demonstrated that the obtained needle orientations and morphologies result from a complex interplay between various parameters e.g. substrate surface symmetry, molecular adsorption, crystal structure and contact plane. The interplay and its implications on the fabrication of self-assembled waveguiding nano-fibres and optical resonator structures are discussed and substantiated by a comparison with the reported literature. In further consequence, it is demonstrated that a precise control on the molecular adsorption geometry and the crystal contact plane represents a fundamental key parameter for the fabrication of self-assembled nano-fibres. As both parameters are basically determined by the chosen molecule-substrate material couple, the possible spectrum of molecular building blocks for the fabrication of waveguiding and lasing nano-structures can be predicted by the discussed growth model. A possible expansion of this common valid concept is presented by the utilization of organic-organic heteroepitaxy. Based on the reported p-6P/6T heterostructures which have been fabricated on various substrate surfaces, it is substantiated that the fabrication of organic-organic interfaces can be effectively used to gain control on the molecular adsorption geometry. As the proposed strategy still lacks a precise control of the obtained crystal contact plane, further strategies are discussed which potentially lead to a controlled fabrication of opto-electronic devices based on self-assembled organic nano-structures.
机译:在过去的几年中,由于外延生长的自组装有机纳米结构在光电器件中的实现潜力很大,因此引起了越来越多的关注。示例性地,在本综述中讨论了棒状分子对六苯基(p-6P)和α-sexi-噻吩(6T)的外延生长。两种分子都倾向于在高度不对称的细长实体(也称为纳米纤维)中结晶。证明了所获得的针的取向和形态是由各种参数(例如,参数)之间复杂的相互作用产生的。基材表面对称性,分子吸附,晶体结构和接触面。通过与已报道的文献进行比较,讨论并证实了相互作用及其对自组装波导纳米纤维和光学谐振器结构制造的影响。进一步的结果表明,对分子吸附几何形状和晶体接触平面的精确控制是制造自组装纳米纤维的基本关键参数。由于两个参数基本上都由所选的分子-基底材料对决定,因此通过讨论的生长模型可以预测用于制造波导和激射纳米结构的分子构件的光谱。通过利用有机-有机异质外延,可以提出这种通用有效概念的可能扩展。基于已报道的在各种基材表面上制备的p-6P / 6T异质结构,证实有机-有机界面的制备可有效地用于控制分子吸附几何形状。由于所提出的策略仍然缺乏对所获得的晶体接触面的精确控制,因此讨论了进一步的策略,这些策略可能导致基于自组装有机纳米结构的光电器件的受控制造。

著录项

  • 来源
    《Semiconductor science and technology》 |2013年第5期|1-31|共31页
  • 作者

    Clemens Simbrunner;

  • 作者单位

    Institute of Semiconductor and Solid State Physics, Johannes Kepler University, Altenbergerstrasse 69, A-4040 Linz, Austria;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 01:30:50

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