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Deposition of cationic polymer micelles on planar and patterned silicon dioxide surfaces.

机译:在平面和有图案的二氧化硅表面上沉积阳离子聚合物胶束。

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摘要

The deposition of PS-PVPH+ polymer micelles from a pH 1 aqueous solution onto Si wafers has been studied using a simple dip-coating technique. It has been found that the rate of evaporation of the solvent and the rate of withdrawal have a considerable influence on the density and ordering of the adsorbed micelles. The highest density and degree of ordering (as judged by the 2D pair correlation function) is achieved when solvent evaporation dominates the deposition process, but a fairly homogeneous distribution of polymer micelles can be achieved over a distance of at least 3–4 mm by controlling the solvent evaporation rate and the rate of substrate withdrawal. We did not observe any significant effect of added KCl (up to 0.1 M) during the deposition process or soaking in 1 M KCl after deposition. The attachment of these micelles is quite robust as they cannot be washed off in pH 1 water (with or without KCl) without significant mechanical assistance. However we did find that the micelles are rather easily caused to dewet and partially aggregate under the influence of 65°C water vapor.; The concept of graphoepitaxy is applied to the deposition of cationic polymer micelles from the solution phase onto a Si/SiO2 surface with 100 nm deep ion-etched trenches of variable widths. It has been found that the micelle density is substantially higher and the ordering of the micelles is improved for micelles that adsorb in the 100 nm depressions in the width range of ca. 500 to 5000 nm. We ascribe these effects to capillary forces that pull the aqueous solution into the canyons where the micelles can be trapped. While the ordering of the micelles can be substantial, they do not form a perfect hexagonal crystal. If the surface is chemically modified by a Au coating or a layer of sodium poly(styrene sulfonate)) the micelle surface-interaction is strengthened and the degree of ordering is diminished. These results demonstrate that a combination of graphoepitaxy and processing conditions (speed of substrate withdrawal, pH, evaporation of solvent) can be used to make fairly ordered polymer micelle arrays over a space of (at least) several mm.
机译:采用简单的浸涂技术研究了pH 1水溶液中PS-PVPH + 聚合物胶束的沉积。已经发现,溶剂的蒸发速率和排出速率对吸附的胶束的密度和有序性具有相当大的影响。当溶剂蒸发在沉积过程中占主导地位时,可以获得最高的密度和有序度(由2D对关联函数判断),但是通过控制至少在3-4 mm的距离上可以实现相当均匀的聚合物胶束分布溶剂蒸发速率和底物排出速率。我们没有观察到在沉积过程中添加KCl(高达0.1 M)或在沉积后浸泡在1 M KCl中没有任何显着影响。这些胶束的附着力非常强健,因为如果没有明显的机械辅助,它们就无法在pH 1的水中(有或没有KCl的情况下)洗掉。但是,我们确实发现,在65°C水蒸气的作用下,胶束很容易引起润湿和部分聚集。石墨外延的概念适用于阳离子聚合物胶束从溶液相到具有100nm深离子刻蚀宽度可变的沟槽的Si / SiO 2 表面的沉积。已经发现,对于在 ca 的宽度范围内吸附在100nm凹陷中的胶束,胶束的密度显着更高并且胶束的有序性得到了改善。 500至5000 nm。我们将这些影响归因于毛细作用力,毛细作用力将水溶液拉入可以捕获胶束的峡谷中。尽管胶束的排列顺序可能很大,但它们无法形成理想的六边形晶体。如果通过Au涂层或聚苯乙烯磺酸钠层对表面进行化学修饰,则胶束表面相互作用会增强,有序度会降低。这些结果表明,石墨外延和加工条件(底物撤出速度,pH,溶剂蒸发)的组合可用于在(至少)几毫米的空间上制造相当有序的聚合物胶束阵列。

著录项

  • 作者

    Hahn, Jungseok.;

  • 作者单位

    The University of Texas at Austin.;

  • 授予单位 The University of Texas at Austin.;
  • 学科 Chemistry Polymer.; Chemistry Physical.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 p.241
  • 总页数 208
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物);
  • 关键词

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