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Bioinspired Synthesis of a Soft-Nanofilament-Based Coating Consisting of Polysilsesquioxanes/Polyamine and Its Divergent Surface Control

机译:聚倍半硅氧烷/多胺组成的基于软纳米丝的涂层的生物启发合成及其表面控制

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The synthesis of polysilsesquloxanes coating with controllable one-dimensional nanostructure on substrates remains a major long-term challenge by conventional solution-phase method. The hydrolytic polycondensation of organosilanes in solution normally produces a mixture of incomplete cages, ladderlike, and network structures, resulting in the poor control of the formation of specific nanostructure. This paper describes a simple aqueous process to synthesize nanofilament-based coatings of polysilsesquioxanes possessing various organo-functional groups (for example, thiol, methyl, phenyl, vinyl, and epoxy). We utilized a self-assembled nanostructured polyamine layer as a biomimetically catalytic scaffold/template to direct the formation of one-dimensional nanofilament of polysilsesquioxanes by temporally and spatially controlled hydrolytic polycondensation of organosilane. The surface nanostructure and morphology of polysilsesquioxane coating could be modulated by changing hydrolysis and condensation reaction conditions, and the orientation of nanofilaments of polysilsesquioxanes on substrates could be controlled by simply adjusting the self-assembly conditions of polyamine layer. The nanostructure and polyamine@ polysilsesquioxane hybrid composition of nanofilament-based coatings were examined by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The template role of nanostructured polyamine layer for the formation of polysilsesquioxane nanofilament was confirmed by combining thin film X-ray diffraction (XRD) and XPS measurements. Moreover, these nanotextured coatings with various organo-functional groups could be changed into superhydrophobic surfaces after surface modification with fluorocarbon molecule.
机译:传统溶液相方法在基底上具有可控的一维纳米结构的聚倍半硅氧烷涂层的合成仍然是一个长期的主要挑战。溶液中有机硅烷的水解缩聚通常会产生不完整的笼,梯状和网状结构的混合物,导致对特定纳米结构形成的控制较差。本文介绍了一种简单的水性工艺,用于合成具有各种有机官能团(例如,硫醇,甲基,苯基,乙烯基和环氧基)的聚倍半硅氧烷的纳米丝基涂层。我们利用自组装的纳米结构聚胺层作为仿生催化支架/模板,以通过有机硅烷的时空控制水解缩聚来指导聚倍半硅氧烷的一维纳米丝的形成。通过改变水解和缩合反应条件,可以调节聚倍半硅氧烷涂层的表面纳米结构和形貌,并可以通过简单调节聚胺层的自组装条件来控制聚倍半硅氧烷的纳米丝在基材上的取向。通过扫描电子显微镜(SEM),透射电子显微镜(TEM)和X射线光电子能谱(XPS)检验了纳米丝基涂层的纳米结构和多胺聚倍半硅氧烷杂化组合物。通过结合薄膜X射线衍射(XRD)和XPS测量,证实了纳米结构聚胺层在形成聚倍半硅氧烷纳米丝中的模板作用。而且,这些具有各种有机官能团的纳米纹理涂层在用碳氟化合物分子进行表面改性后可以变成超疏水表面。

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