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Atomic scale modification of metal surfaces to impact the surface-catalyzed growth of polymethylene films.

机译:金属表面的原子尺度改性,以影响聚亚甲基薄膜的表面催化生长。

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This dissertation focuses on the preparation of highly insulating ultrathin films of polymethylene [-(CH2)n-; PM] onto metal surfaces. The work develops a new surface-catalyzed method to grow linear PM films directly from a gold surface modified at the atomic level by the underpotential deposition (upd) of a highly ordered metal (sub)monolayer. Modification of the gold surface with upd provides a convenient strategy for tailoring the catalytic properties of the metal surface and therefore, altering the kinetics of polymer film growth and the properties of the surface-catalyzed PM films. For example, the upd of copper enhances the polymer growth over that on an unmodified gold surface while the effect of silver depends greatly on the upd coverage with >0.9 of a silver monolayer completely preventing PM growth.; This work develops a new strategy to pattern metal surfaces with highly insulating, chemically inert polymer films by exploiting the selectivity of upd metals toward the polymer growth. We have demonstrated the ability to direct the growth of PM into well-defined patterns at the micron-scale by first patterning upd layers on the gold surface through a process that involves microcontact printing.; Kinetics studies of PM formation on Cu(upd)/Au show an exponential growth trend for the polymer chains at short times and a linear growth trend at long times, suggesting two types of propagating chains, those that terminate and those that are living or resistant to termination. A possible mechanism in which copper adatoms catalyze living PM growth has been proposed. This “living” character enables an unprecedented control over film thickness and uniformity. Micron-thick PM films formed through this living mechanism provide excellent barrier protection toward the underlying metal substrate as measured by electrochemical impedance spectroscopy (EIS).; The final part of this work explores the use of sequential upd to design a new type of bimetallic catalytic surface. Through the sequential upd of copper and silver, we can produce metal surfaces with well-controlled surface compositions of both catalytically active and inactive metals that enable a fine tuning of the thickness and properties of PM films.
机译:本论文着重于制备高绝缘性的聚亚甲基[-(CH 2 n -]超薄膜。 PM]粘贴到金属表面上。这项工作开发了一种新的表面催化方法,可以通过高度有序的金属(亚)单分子层的欠电势沉积(upd)直接从原子级修饰的金表面直接生长线性PM膜。用upd修饰金表面可为调整金属表面的催化性能提供便利的策略,从而改变聚合物膜生长的动力学和表面催化的PM膜的性能。例如,与未改性的金表面上的铜相比,铜的增加促进了聚合物的生长,而银的作用在很大程度上取决于大于0.9的银单层的覆盖率,从而完全阻止了PM的生长。这项工作开发了一种新的策略,通过利用向上金属对聚合物生长的选择性,在具有高度绝缘性,化学惰性的聚合物薄膜的金属表面上形成图案。我们已经证明了通过在涉及微接触印刷的过程中首先在金表面上构图上覆层的图案,可以将PM的生长引导成微米级的清晰图案。在Cu(upd)/ Au上形成PM的动力学研究表明,聚合物链在短时间内呈指数增长趋势,在长时间上呈线性增长趋势,这表明有两种传播链,即终止的链和活动的或抗性的链。终止。已经提出了铜原子催化活性PM生长的可能机理。这种“活着”的特性可以前所未有地控制薄膜的厚度和均匀性。通过这种活性机理形成的微米级厚的PM膜可通过电化学阻抗谱(EIS)对下层金属基材提供出色的阻隔保护。这项工作的最后一部分探讨了使用顺序更新设计新型双金属催化表面的方法。通过依次增加铜和银,我们可以生产出金属表面,其催化活性和惰性金属的表面组成均得到良好控制,从而可以微调PM膜的厚度和性能。

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