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首页> 外文期刊>Applied Surface Science >Chemical identification with non-contact atomic force microscopy of xenon atoms adsorbed on graphene on Pt(111) surfaces
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Chemical identification with non-contact atomic force microscopy of xenon atoms adsorbed on graphene on Pt(111) surfaces

机译:用氙原子的非接触原子力显微镜吸附在Pt(111)表面上的石墨烯上的非接触原子力显微镜

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Functionalization of atomic force microscopy (AFM) tips has been revealed as a powerful tool to achieve an enhanced resolution allowing to resolve intramolecular features. Such functionalization can be performed by placing different species at the apex, as Xe adatoms. Functionalized tips could be useful to investigate molecules adsorbed on graphene (Gr) surfaces, where the molecule-graphene interaction is expected to be low. In particular, the Gr/Pt(111) interface has been shown to present a low molecule-substrate interaction that keeps the properties of the adsorbed molecule close to the free-molecule state. In this work, we have investigated the adsorption of Xe on graphene on Pt(111) surfaces, a necessary previous step to the in-situ functionalization of tips with Xe on these surfaces. For this purpose, we have employed a home-made cantilever-based non-contact atomic force microscope (ncAFM) operated under ultrahigh vacuum conditions at 5 K. Our results show the growth of well-ordered Xe islands in the submonolayer regime. Then, we show that force spectroscopy can be used to distinguish these islands from the bare graphene areas without the need of atomic resolution. Finally, the extraction of single Xe adatoms from the surface and the corresponding tip functionalization have been explored.
机译:原子力显微镜(AFM)提示的官能化已被揭示为实现增强的分辨率允许解决分子内特征的强大工具。通过将不同的物种放置在顶点,如XE Adatoms,可以通过将这种官能化进行。官能化尖端可用于研究吸附在石墨烯(GR)表面上的分子,其中分子 - 石墨烯相互作用预期低。特别地,已经显示GR / Pt(111)界面呈现低分子底物相互作用,其使吸附分子的性质保持接近自由分子状态。在这项工作中,我们研究了在Pt(111)表面上的石墨烯上的吸附,这是对这些表面上的XE原位函数化的必要前一步。为此目的,我们采用了在5 k的超高真空条件下运行的自制悬臂的非接触原子力显微镜(NCAFM)。我们的结果显示了亚诺伊洛氏植物制度中有序XE岛的增长。然后,我们表明力光谱可用于将这些岛屿与裸石墨烯区域区分开而不需要原子分辨率。最后,已经探讨了从表面和相应的尖端功能化的单XE吸附物的提取。

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