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A model electrode of well-defined geometry prepared by direct laser-induced decoration of nanoporous templates with Au-Ag@C nanoparticles

机译:用Au-Ag @ C纳米粒子直接激光诱导的纳米多孔模板装饰制备明确的几何体的模型电极

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摘要

We present an original type of model electrode system consisting of bimetallic Au-Ag nanoparticles embedded in an amorphous carbon matrix with an extremely well-defined geometry of parallel, straight, cylindrical macropores. The samples are prepared in one step by direct laser deposition of the metal/carbon composite onto the inner walls of a porous 'anodic' alumina matrix serving as a template. The coating is homogeneous from top to bottom of the pores, and the amount of material deposited can be tuned by the duration of the deposition procedure. As a test system, we demonstrate that a bimetallic Ag-Au@C system is catalytically active for the electrochemical oxidation of glucose in alkaline solution, the anodic reaction of a direct glucose fuel cell. Furthermore, the electrocatalytic current density increases with the amount of Ag-Au@C NPs deposited, up to a point at which the pores are clogged with it. This type of model system allows for the systematic study of geometric effects in fuel cell electrodes. It can be generalized to a number of different nanoparticle compositions, and thereby, to various electrocatalytic reactions.
机译:我们提出了一种原始类型的模型电极系统,由嵌入无定形碳基质中的双金属Au-Ag纳米粒子组成,具有极明确定义的平行,直圆柱宏级的几何形状。通过将金属/碳复合材料的直接激光沉积在多孔'阳极'氧化铝基质的内壁上以一步进行制备,用作模板。涂层从孔的顶部到底部均匀,并且可以通过沉积过程的持续时间来调节沉积的材料的量。作为测试系统,我们证明了一种双金属Ag-Au @ C系统对于碱性溶液中葡萄糖的电化学氧化,直接葡萄糖燃料电池的阳极反应是催化活性的。此外,电催化电流密度随着沉积的Ag-Au @ C nps的量而增加,直到孔隙堵塞的点。这种类型的模型系统允许系统研究燃料电池电极中的几何效应。它可以推广到许多不同的纳米颗粒组合物,从而推广到各种电催化反应。

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