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Indications of chemical bond contrast in AFM images of a hydrogen-terminated silicon surface

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  • Hatem Labidi

    (University of Alberta
    National Institute for Nanotechnology, National Research Council of Canada)

  • Mohammad Koleini

    (University of Alberta
    National Institute for Nanotechnology, National Research Council of Canada)

  • Taleana Huff

    (University of Alberta)

  • Mark Salomons

    (National Institute for Nanotechnology, National Research Council of Canada)

  • Martin Cloutier

    (National Institute for Nanotechnology, National Research Council of Canada)

  • Jason Pitters

    (National Institute for Nanotechnology, National Research Council of Canada)

  • Robert A. Wolkow

    (University of Alberta
    National Institute for Nanotechnology, National Research Council of Canada)

Abstract

The origin of bond-resolved atomic force microscope images remains controversial. Moreover, most work to date has involved planar, conjugated hydrocarbon molecules on a metal substrate thereby limiting knowledge of the generality of findings made about the imaging mechanism. Here we report the study of a very different sample; a hydrogen-terminated silicon surface. A procedure to obtain a passivated hydrogen-functionalized tip is defined and evolution of atomic force microscopy images at different tip elevations are shown. At relatively large tip-sample distances, the topmost atoms appear as distinct protrusions. However, on decreasing the tip-sample distance, features consistent with the silicon covalent bonds of the surface emerge. Using a density functional tight-binding-based method to simulate atomic force microscopy images, we reproduce the experimental results. The role of the tip flexibility and the nature of bonds and false bond-like features are discussed.

Suggested Citation

  • Hatem Labidi & Mohammad Koleini & Taleana Huff & Mark Salomons & Martin Cloutier & Jason Pitters & Robert A. Wolkow, 2017. "Indications of chemical bond contrast in AFM images of a hydrogen-terminated silicon surface," Nature Communications, Nature, vol. 8(1), pages 1-7, April.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms14222
    DOI: 10.1038/ncomms14222
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