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Atomic-scale surface science phenomena studied by scanning tunneling microscopy

机译:通过扫描隧道显微镜研究的原子尺度表面科学现象

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摘要

Following the development of the scanning tunneling microscope (STM), the technique has become a very powerful and important tool for the field of surface science, since it provides direct real-space imaging of single atoms, molecules and adsorbate structures on surfaces. From a fundamental perspective, the STM has changed many basic conceptions about surfaces, and paved the way for a markedly better understanding of atomic-scale phenomena on surfaces, in particular in elucidating the importance of local bonding geometries, defects and resolving non-periodic structures and complex co-existing phases. The so-called "surface science approach", where a complex system is reduced to its basic components and studied under well-controlled conditions, has been used successfully in combination with STM to study various fundamental phenomena relevant to the properties of surfaces in technological applications such as heterogeneous catalysis, tribology, sensors or medical implants. In this tribute edition to Gerhard Ertl, we highlight a few examples from the STM group at the University of Aarhus, where STM studies have revealed the unique role of surface defects for the stability and dispersion of Au nanoclusters on TiO_2, the nature of the catalytically active edge sites on MoS_2 nanoclusters and the catalytic properties of Au/Ni or Ag/Ni surfaces. Finally, we briefly review how reaction between complex organic molecules can be used to device new methods for self-organisation of molecular surface structures joined by comparatively strong covalent bonds.
机译:随着扫描隧道显微镜(STM)的发展,该技术已成为表面科学领域非常强大且重要的工具,因为它可以对表面上的单个原子,分子和吸附结构进行直接的真实空间成像。从根本上讲,STM改变了许多有关表面的基本概念,并为更好地了解表面上的原子尺度现象铺平了道路,尤其是在阐明局部键合几何形状,缺陷和解决非周期性结构的重要性方面和复杂的共存阶段。所谓的“表面科学方法”是将复杂系统简化为基本组成部分并在良好控制的条件下进行研究的方法,已成功地与STM结合使用,以研究与技术应用中的表面特性相关的各种基本现象例如多相催化,摩擦学,传感器或医疗植入物。在此致Gerhard Ertl的致敬版本中,我们重点介绍了奥尔胡斯大学STM组的一些示例,其中STM研究揭示了表面缺陷对于TiO_2上Au纳米团簇的稳定性和分散性的独特作用,即催化性质MoS_2纳米簇上的活性边缘位点和Au / Ni或Ag / Ni表面的催化性能。最后,我们简要回顾了复杂的有机分子之间的反应如何可用于装备通过相对强的共价键连接的分子表面结构自组织的新方法。

著录项

  • 来源
    《Surface Science》 |2009年第12期|1315-1327|共13页
  • 作者单位

    Interdisciplinary Nanoscience Center (iNANO), Department of Physics and Astronomy, Aarhus University, Ny Munkegade Building 520, DK 8000 Aarhus C, Denmark;

    Interdisciplinary Nanoscience Center (iNANO), Department of Physics and Astronomy, Aarhus University, Ny Munkegade Building 520, DK 8000 Aarhus C, Denmark;

    Interdisciplinary Nanoscience Center (iNANO), Department of Physics and Astronomy, Aarhus University, Ny Munkegade Building 520, DK 8000 Aarhus C, Denmark;

    Interdisciplinary Nanoscience Center (iNANO), Department of Physics and Astronomy, Aarhus University, Ny Munkegade Building 520, DK 8000 Aarhus C, Denmark;

    Interdisciplinary Nanoscience Center (iNANO), Department of Physics and Astronomy, Aarhus University, Ny Munkegade Building 520, DK 8000 Aarhus C, Denmark;

    Interdisciplinary Nanoscience Center (iNANO), Department of Physics and Astronomy, Aarhus University, Ny Munkegade Building 520, DK 8000 Aarhus C, Denmark;

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  • 正文语种 eng
  • 中图分类
  • 关键词

    scanning tunneling microscopy; catalysis; au nanoclusters; hydrotreating; MoS_2 nanoclusters; steam reforming; self-assembly;

    机译:扫描隧道显微镜催化;金纳米簇;加氢处理MoS_2纳米团簇;蒸汽重整;自组装;

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