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首页> 外文期刊>Electrochimica Acta >Copper Metallization of Gold Nanostructure Activated Polypyrrole by Electroless Deposition
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Copper Metallization of Gold Nanostructure Activated Polypyrrole by Electroless Deposition

机译:无电沉积金纳米结构活化聚吡咯的铜金属化

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We report on the study of novel polymeric electrodes made by the selective, electroless plating, of Copper (Cu) films on gold (Au) nanostructure-modified polypyrrole (Ppy). The main aim of the work is to define the effect of Au nanoparticle seed preparation method on its catalytic properties for Cu electroless deposition. The Au nanostructures were produced by two different techniques, namely, cluster beam deposition from a magnetron sputtering/gas condensation source (with precise size and composition control) and electrochemical deposition. To carry out the research, polypyrrole films were first synthesized by electro-polymerization on Au (200 nm)/SiO2/Si substrates, followed by modification of the polymer surface by either electroplating of Au nanoparticles or Au-923 clusters deposition from a magnetron cluster source. The gold nanoparticle modified electrodes were subjected to copper electroless deposition for different time intervals. The morphology, growth and nucleation kinetics of the resulting copper film were studied by environmental scanning electron microscopy-Energy dispersive X-ray spectroscopy (ESEM-EDS), atomic force microscopy (AFM) and X-ray fluorescence (XRF). Although both nanoparticle type showed similar incubation time, a faster catalytic response, once deposition had been initiated, was observed when the polypyrrole film was modified with Au-923 clusters. The incubation time was independent of cluster size and type. This could be explained by a simple model assuming that the incubation time depends on similar parameters for both nanoparticle types, such as metal-metal (Au-Cu) binding energy, crystallographic misfit (Au-Cu) and lateral growth of the copper film. Further discussion is presented in this paper in attempt to explain the different growth rate of Cu film catalysed by the Au-923 clusters and electroplated Au nanoparticles. (C) 2017 Elsevier Ltd. All rights reserved.
机译:我们报告了通过在金(Au)纳米结构改性聚吡咯(PPY)上的选择性化学电镀,铜(Cu)膜的选择性化学电镀的新型聚合物电极研究。该工作的主要目的是确定Au纳米粒子种子制备方法对铜化学沉积催化性能的影响。 Au纳米结构由两种不同的技术生产,即从磁控溅射/气体缩合源(具有精确尺寸和组合对照)和电化学沉积的簇束沉积。为了进行研究,首先通过在Au(200nm)/ SiO 2 / Si底物上的电聚合来合成聚吡咯膜,然后通过从磁控管簇的α-923沉积的电镀来改变聚合物表面来源。金纳米颗粒改性电极对不同的时间间隔进行铜化学沉积。通过环境扫描电子显微镜 - 能量分散X射线光谱(ESEM-EDS),原子力显微镜(AFM)和X射线荧光(XRF)研究了所得铜膜的形态,生长和成核动力学。虽然纳米粒子型显示出类似的孵育时间,但是一旦引发了更快的催化反应,一旦开始沉积,当用Au-923簇改性聚吡咯膜时,观察到沉积。孵化时间与簇大小和类型无关。这可以通过一种简单的模型来解释,假设孵育时间取决于纳米颗粒类型的类似参数,例如金属 - 金属(Au-Cu)结合能量,结晶错位(Au-Cu)和铜膜的横向生长。本文提出了进一步的讨论,以试图解释Au-923簇和电镀Au纳米粒子催化的Cu膜的不同生长速率。 (c)2017 Elsevier Ltd.保留所有权利。

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