TY - JOUR
T1 - Prospects for resolving chemical structure by atomic force microscopy
T2 - A first-principles study
AU - Guo, Chun-Sheng
AU - Van Hove, Michel A.
AU - Zhang, Rui-Qin
AU - Minot, Christian
PY - 2010/11/2
Y1 - 2010/11/2
N2 - 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 CH 4 or pentacene itself (both having a C-H apex) yield similar images, while tips terminated in O2 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 C6 rings, this tip fails to resolve the structures of benzene (with its single C 6 ring) or nonplanar C6 networks, such as C60 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. © 2010 American Chemical Society.
AB - 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 CH 4 or pentacene itself (both having a C-H apex) yield similar images, while tips terminated in O2 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 C6 rings, this tip fails to resolve the structures of benzene (with its single C 6 ring) or nonplanar C6 networks, such as C60 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. © 2010 American Chemical Society.
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U2 - 10.1021/la101317s
DO - 10.1021/la101317s
M3 - RGC 21 - Publication in refereed journal
SN - 0743-7463
VL - 26
SP - 16271
EP - 16277
JO - Langmuir
JF - Langmuir
IS - 21
ER -