Prospects for Resolving Chemical Structure by Atomic Force Microscopy: A First-Principles Study

被引:21
|
作者
Guo, Chun-Sheng [1 ]
Van Hove, Michel A. [1 ]
Zhang, Rui-Qin [1 ]
Minot, Christian [1 ,2 ]
机构
[1] City Univ Hong Kong, Dept Phys & Mat Sci, Hong Kong, Hong Kong, Peoples R China
[2] Univ Paris 06, CNRS, Chim Theor Lab, UMR7616, F-75252 Paris, France
关键词
LARGE SYSTEMS; PSEUDOPOTENTIALS;
D O I
10.1021/la101317s
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In a recent paper, the chemical structure of a molecule was resolved by means of atomic force microscopy (AFM): using a metal tip terminated in a CO molecule, the authors could image the internal bonding arrangement of a pentacene molecule with remarkable spatial resolution (notably better than with other tip terminations), as verified by their first-principles calculations. Here we further explore with first-principles calculations the mechanisms, applicability, and capabilities of this approach for a wider range of situations, by varying the imaged molecule and the tip beyond the experimental cases. In our simulations, a high atomic resolution is found to be dominated by the electronic structure of the last two atoms on the tip apex which are set perpendicularly to the sample molecule. For example, tips terminated in CH4 or pentacene itself (both having a C-H apex) yield similar images, while tips terminated in O-2 or CO give quite different images. While using a CO-terminated tip successfully resolves the chemical structure of pentacene and of other extended planar networks based on C-6 rings, this tip fails to resolve the structures of benzene (with its single C-6 ring) or nonplanar C-6 networks, such as C-60 or small-diameter carbon nanotubes. Defects (such as N substitution for a C-H group) were also found to significantly influence the image resolution. Our findings indicate that further application of this approach requires, for each sample, careful selection of a suitable "imaging" molecule as tip termination.
引用
收藏
页码:16271 / 16277
页数:7
相关论文
共 50 条
  • [21] Efficient First-Principles Simulation of Noncontact Atomic Force Microscopy for Structural Analysis (vol 102, 176101, 2009)
    Chan, T. -L.
    Wang, C. Z.
    Ho, K. M.
    Chelikowsky, James R.
    PHYSICAL REVIEW LETTERS, 2009, 102 (18)
  • [22] First-principles calculation of atomic force in the LSDA plus U formalism
    Park, Se Young
    Choi, Hyoung Joon
    PHYSICAL REVIEW B, 2009, 80 (15):
  • [23] First principles simulations of nanoindentation and atomic force microscopy on silicon surfaces
    Perez, R
    Payne, MC
    Stich, I
    Terakura, K
    MATERIALS THEORY, SIMULATIONS, AND PARALLEL ALGORITHMS, 1996, 408 : 255 - 260
  • [24] A first-principles study of the diffusion of atomic oxygen in nickel
    Nam, Hyo On
    Hwang, Il Soon
    Lee, Kyu Hwan
    Kim, Ji Hyun
    CORROSION SCIENCE, 2013, 75 : 248 - 255
  • [25] First-principles study of the atomic volume of hydrogen in palladium
    Setayandeh, Samaneh Sadat
    Gould, Tim
    Vaez, Aminollah
    McLennan, Keith
    Armanet, Nicolas
    Gray, Evan
    JOURNAL OF ALLOYS AND COMPOUNDS, 2021, 864
  • [26] First-principles simulations of atomic structure and magnetism in Fe nanoparticles
    Postnikov, AV
    Entel, P
    Soler, JM
    NANOPARTICULATE MATERIALS, 2002, 704 : 225 - 230
  • [27] Noncontact atomic force microscopy imaging of atomic structure and cation defects of the polar MgAl2O4 (100) surface: Experiments and first-principles simulations
    Rasmussen, Morten K.
    Foster, Adam S.
    Canova, Filippo F.
    Hinnemann, Berit
    Helveg, Stig
    Meinander, Kristoffer
    Besenbacher, Flemming
    Lauritsen, Jeppe V.
    PHYSICAL REVIEW B, 2011, 84 (23)
  • [29] Atomic Structure, Electronic and Mechanical Properties of Pyrophyllite under Pressure: A First-Principles Study
    Qin, Xinzhan
    Zhao, Jian
    Wang, Jiamin
    He, Manchao
    MINERALS, 2020, 10 (09) : 1 - 14
  • [30] First-principles Study of the Atomic and Electronic Structure of Amorphous ZnO-SiO2
    Kang, Il-Joon
    Woo, Sun-A
    Park, Chul-Hong
    JOURNAL OF THE KOREAN PHYSICAL SOCIETY, 2011, 58 (03) : 604 - 607