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Investigating the interfacial dynamics of thin films.

机译:研究薄膜的界面动力学。

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This thesis probes the interfacial dynamics and associated phenomena of thin films. Surface specific tools were used to study the self-assembly of alkanethiols, the mono- and bilayer dynamics of SF6, and the surface motion of poly(methyl methacrylate). Non-pertubative helium atom scattering was the principal technique used to investigate these systems. A variety of other complementary tools, including scanning tunneling microscopy, electron diffraction, Auger spectroscopy, atomic force microscopy, and ellipsometry were used in tandem with the neutral atom scattering studies.; Controlling the spontaneous assembly of alkanethiols on Au(111) requires a better fundamental understanding of the adsorbate-adsorbate and substrate-adsorbate interactions. Our characterization focused on two key components, the surface structure and adsorbate vibrations. The study indicates that the Au(111) reconstruction plays a larger role than anticipated in the low-density phase of alkanethiol monolayers. A new structure is proposed for the 1-decanethiol monolayer that impacts the low-energy vibrational mode. Varying the alkane chain lengths imparts insight into the assembly process via characterization of a dispersionless phonon mode.; Studies of SF6 physisorbed on Au(111) bridge surface research on rare gas adsorbates with complicated dynamical organic thin films. Mono- and bilayer coverages of SF6/Au(111) were studied at cryogenic temperatures. Our experiments probed the surface properties of SF6 yielding insights into substrate and coverage effects. The study discovered a dispersionless Einstein oscillation with multiple harmonic overtones. A second layer of SF6 softened the mode, but did not show any indications of bulk or cooperative interactions. The vibrational properties of SF 6 showed both striking similarities and differences when compared with physisorbed rare gases.; Lastly, this thesis will discuss studies of thin film poly(methyl methacrylate) on Si. The non-pertubative and surface specific nature of helium atom scattering allows for a deft study of the relationship between surface motion and the glass transition temperature. An added parameter in this complex organic system is the film thickness. The confinement effects and enhanced surface displacement were examined as a function of the thermal attenuation of both inelastic and elastic helium atom scattering. The Debye-Waller factor for these thin films of PMMA is similar to the low-density alkanethiol self-assembled monolayers discussed earlier.
机译:本文探讨了薄膜的界面动力学及其相关现象。使用特定于表面的工具研究链烷硫醇的自组装,SF6的单层和双层动力学以及聚甲基丙烯酸甲酯的表面运动。非渗透氦原子散射是研究这些系统的主要技术。与中性原子散射研究相结合,使用了多种其他互补工具,包括扫描隧道显微镜,电子衍射,俄歇光谱,原子力显微镜和椭圆偏振法。控制链烷硫醇在Au(111)上的自发组装需要对被吸附物-被吸附物和底物-被吸附物的相互作用有更好的基本了解。我们的表征集中在两个关键部分,即表面结构和吸附物振动。研究表明,Au(111)重建在烷硫醇单层低密度相中的作用比预期的要大。提出了一种1-癸硫醇单层的新结构,该结构会影响低能振动模式。通过改变无分散声子模式的特征,改变烷烃链的长度可以深入了解组装过程。物理吸附在Au(111)桥面上的SF6的研究复杂动态有机薄膜的稀有气体吸附物的研究。在低温下研究了SF6 / Au(111)的单层和双层覆盖率。我们的实验探查了SF6的表面特性,从而深入了解了基材和覆盖效果。研究发现具有多个谐波泛音的无色散爱因斯坦振荡。 SF6的第二层软化了该模式,但未显示出大量或协作相互作用的迹象。与物理吸附的稀有气体相比,SF 6的振动特性既显示出惊人的相似性,也显示出差异。最后,本文将讨论在硅上的薄膜聚甲基丙烯酸甲酯的研究。氦原子散射的非渗透性和表面比性质允许对表面运动与玻璃化转变温度之间的关系进行深入研究。在这种复杂的有机体系中,增加的参数是膜的厚度。作为非弹性和弹性氦原子散射的热衰减的函数,研究了约束效应和增加的表面位移。这些PMMA薄膜的Debye-Waller因子类似于前面讨论的低密度烷硫醇自组装单层。

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