4.8 Article

Mapping the force field of a hydrogen-bonded assembly

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NATURE COMMUNICATIONS
卷 5, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms4931

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资金

  1. University of Nottingham High Performance Computing Facility
  2. 973 Programme [2011CB933300]
  3. National Natural Science Foundation of China [51071110, 51271134, 40972044, J1210061, 11328403]
  4. China MOE NCET Programme [NCET-07-0640]
  5. MOE Doctoral Fund [20090141110059]
  6. Fundamental Research Funds for the Central Universities
  7. Engineering and Physical Sciences Research Council (EPSRC) [EP/G007837/1, EP/J500483/1]
  8. Leverhulme Trust, [F00/114 BI]
  9. Royal Society Wolfson Merit Award
  10. Curie fellowship - ACRITAS FP7
  11. EPSRC [EP/G007837/1] Funding Source: UKRI
  12. Engineering and Physical Sciences Research Council [EP/G007837/1] Funding Source: researchfish

向作者/读者索取更多资源

Hydrogen bonding underpins the properties of a vast array of systems spanning a wide variety of scientific fields. From the elegance of base pair interactions in DNA to the symmetry of extended supramolecular assemblies, hydrogen bonds play an essential role in directing intermolecular forces. Yet fundamental aspects of the hydrogen bond continue to be vigorously debated. Here we use dynamic force microscopy (DFM) to quantitatively map the tip-sample force field for naphthalene tetracarboxylic diimide molecules hydrogen-bonded in two-dimensional assemblies. A comparison of experimental images and force spectra with their simulated counterparts shows that intermolecular contrast arises from repulsive tip-sample interactions whose interpretation can be aided via an examination of charge density depletion across the molecular system. Interpreting DFM images of hydrogen-bonded systems therefore necessitates detailed consideration of the coupled tip-molecule system: analyses based on intermolecular charge density in the absence of the tip fail to capture the essential physical chemistry underpinning the imaging mechanism.

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