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Spectroscopic Srudies of Model Organic Photovoltaic and Organic Light Emitting Diode Organic-Organic' and Metal-Organic Heterojunctions

机译:模型有机光伏和有机发光二极管“有机-有机”和金属-有机异质结的光谱研究

摘要

The purpose of this Dissertation was to present fundamental approaches to expand the general knowledge of the chemistry that occurs at both the organic-organic' (O-O') and the metal-organic (M-O) interfaces in organic optoelectronic devices. In order to simplify the interactions in the initial studies presented herein, simple model molecules that represent the larger, highly conjugated molecules used in device construction were considered.UPS, reductive-desorption electrochemistry, and Raman surface spectroscopy were used to determine monolayer characteristics of thiophenol and pentafluorothiophenol on Ag. Proposed interfacial orientations and molecular spacing of the TP and F5TP were proposed. Benzene and hexafluorobenzene (F6-benzene) were then condensed and forcibly dewet onto the monolayers in an effort to understand the solid-liquid interfacial interactions. Benzene films on alkanethiol (UDT) and perfluorinated thiophenol (F5TP) were prone to rupturing, and spectroscopically appeared to be liquid-like in character, while molecular spacing of TP and adsorbed benzene on unmodified Ag template ordered benzene films. Polycrystalline films of F6-benzene forms at the interfaces of TP and unmodified substrates. F6-benzene induces a reorientation of F5TP molecules, but is subsequently unable to induce long range order. F6-benzene on UDT appears liquid-like. These studies show that fixed molecules can stimulate order or disorder at a molecular heterojunction, which may have profound effects in device efficiency.In an effort to begin to understand the complicated reaction chemistry that occurs at the organic-metal interfaces in optoelectronic devices, thin benzene films were reacted with typical device cathode metals, Ag, Mg, Al, and Ca, and studied using Raman vibrational spectroscopy. Ag and Mg form metal clusters and some adduct formation. Al undergoes an insertion reaction, forming a substituted benzene ring. Ca reacts with benzene to form a phenyl radical, which then decomposes the film into regions of ordered graphitic carbon. The results of these studies are attributed to atomic properties of the metal atoms.
机译:本文的目的是提出基本方法,以扩展在有机光电器件中有机-有机(O-O')和金属-有机(M-O)界面处发生的化学反应的常识。为了简化此处介绍的初步研究中的相互作用,考虑了代表较大的高度共轭分子的简单模型分子,这些分子用于设备构造中.UPS,还原-解吸电化学和拉曼表面光谱法用于确定苯酚的单层特征和在银上的五氟硫酚。提出了TP和F5TP的界面取向和分子间距。然后将苯和六氟苯(F6-苯)冷凝并强行润湿到单层上,以了解固液界面相互作用。链烷硫醇(UDT)和全氟化硫酚(F5TP)上的苯膜易于破裂,并且在光谱上看起来呈液体状,而未经修饰的Ag模板有序苯膜上TP和吸附的苯的分子间距。 F6-苯的多晶膜在TP和未修饰的底物的界面处形成。 F6-苯诱导F5TP分子重新定向,但随后不能诱导长程有序。 UDT上的F6-苯呈液体状。这些研究表明,固定分子可以刺激分子异质结处的有序或无序,这可能会对器件效率产生深远影响。为了开始理解光电子器件中有机金属界面处发生的复杂反应化学,稀苯薄膜与典型的器件阴极金属Ag,Mg,Al和Ca反应,并使用拉曼振动光谱进行研究。银和镁形成金属团簇并形成一些加合物。 Al进行插入反应,形成取代的苯环。 Ca与苯反应形成苯基,然后将膜分解成有序石墨碳区域。这些研究的结果归因于金属原子的原子特性。

著录项

  • 作者

    Schalnat Matthew Craig;

  • 作者单位
  • 年度 2009
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类
  • 入库时间 2022-08-20 20:35:21

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