HOPG表面Pd-Co双金属配合物纳米结构的形成:XPS和AFM研究

Lisandra Arroyo-Ramírez, R. Montano-Serrano, R. Raptis, C. Cabrera
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引用次数: 11

摘要

为制备低温燃料电池氧还原催化剂,以双金属化合物[Et3NH]2[CoPd2(𝜇-4-I-3,5-Me2pz)4Cl4](CoPd2)为分子前驱体,开发了一种新的单源合成Pd-Co纳米颗粒的方法,在高有序热解石墨(HOPG)表面获得分散催化剂。利用x射线光电子能谱(XPS)和原子力显微镜(AFM)技术表征了纳米结构的形成,并确定了HOPG上配合物的组成和形态。高分辨率XPS分析(HR-XPS)结果显示了前驱体的原子成分对应的结合能。当前驱体溶液放置在HOPG表面时,双金属配合物呈现管状结构,并且HOPG表面似乎为纳米结构的自组织提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nanostructural Formation of Pd-Co Bimetallic Complex on HOPG Surfaces: XPS and AFM Studies
A new single source approach was developed to synthesize Pd-Co nanoparticles using a bimetallic compound, [Et3NH]2[CoPd2(𝜇-4-I-3,5-Me2pz)4Cl4](CoPd2), as a molecular precursor to obtain dispersed catalyst on highly ordered pyrolytic graphite (HOPG) surface, in view of preparing oxygen reduction catalysts for low temperature fuel cells. X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) techniques were employed to characterize the nanostructure formations and to determine the composition and morphology of the complex on the HOPG. Results of high resolution XPS analysis (HR-XPS) revealed the binding energies corresponding to the atomic constituents of the precursor. When the precursor solution was placed on the surface of the HOPG, the bimetallic complex assumes a tubular structure and it appears that the surface of the HOPG offers a ground for the self-organization of nanostructural formations.
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