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Chemically enhancing block copolymers for block-selective synthesis of self-assembled metal oxide nanostructures

机译:化学增强嵌段共聚物,用于嵌段选择性合成自组装金属氧化物纳米结构

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摘要

We report chemical modification of self-assembled block copolymer thin films by ultraviolet light that enhances the block-selective affinity of organometallic precursors otherwise lacking preference for either copolymer block. Sequential precursor loading and reaction facilitate formation of zinc oxide, titanium dioxide, and aluminum oxide nanostructures within the polystyrene domains of both lamellar- and cylindrical-phase modified polystyrene-block-poly(methyl methacrylate) thin film templates. Near-edge X-ray absorption fine structure measurements and Fourier transform infrared spectroscopy show that photo-oxidation by ultraviolet light creates Lewis basic groups within polystyrene, resulting in an increased Lewis base-acid interaction with the organometallic precursors. The approach provides a method for generating both aluminum oxide patterns and their corresponding inverses using the same block copolymer template.
机译:我们报道了通过紫外光对自组装嵌段共聚物薄膜的化学修饰,该薄膜增强了有机金属前体的嵌段选择性亲和力,否则对任一共聚物嵌段都缺乏偏好。顺序的前体负载和反应有助于在层状和圆柱相改性的聚苯乙烯嵌段聚(甲基丙烯酸甲酯)薄膜模板的聚苯乙烯域内形成氧化锌,二氧化钛和氧化铝纳米结构。近边缘X射线吸收精细结构测量和傅立叶变换红外光谱表明,紫外线的光氧化作用会在聚苯乙烯内产生Lewis碱性基团,从而导致Lewis酸与有机金属前体的相互作用增加。该方法提供了使用相同的嵌段共聚物模板来生成氧化铝图案和它们的对应逆的方法。

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