| Literature DB >> 21727402 |
Shintaro Fujii1, Masamichi Fujihira.
Abstract
H- and Cl-terminal groups of bicyclo[2.2.2]octane (BCO) derivatives in a mixed self-assembled monolayer (SAM) on Au(111) were imaged using a modified Si tip with a CaF(2) nanocluster to differentiate the two terminals, which have different electronegativities. In order to achieve this we fabricated a new sample holder, on which a CaF(2) single crystal and the mixed SAM on Au(111) could be mounted side by side. We transferred the holder with the two samples into a ultrahigh vacuum (UHV) atomic force microscopy (AFM) chamber. Upon cleaving the CaF(2) single crystal under UHV, a fresh and clean CaF(2)(111) surface parallel with the SAM surface appeared within 2 mm of the separation. The modified Si tip was prepared by repeatedly making contact between a Si tip and the CaF(2)(111) surface. The resulting modified tip could image the atomic periodicity of a Ca(2+) and an F(-) sublattice on the CaF(2)(111) surface depending on the sign of the tip-terminating ion, i.e. an F(-) and a Ca(2+) ion, respectively, as reported previously (Foster et al 2002 Phys. Rev. B 66 235417). Using the modified Si tip with the known tip-terminating ion, we observed the Cl-terminal in the surrounding H-terminals in the mixed SAM by noncontact (NC) AFM. Here, the Cl-terminal is negatively charged due to its electronegativity and thus the BCO moiety with the Cl-terminal is terminated by a C(δ+)-Cl(δ-) permanent dipole, while the H-terminal is almost neutral. The Cl-terminal appeared brighter (more attractive) and darker (more repulsive) than the surrounding H-terminals in NC-AFM images depending on the sign of the tip-terminating ion, i.e. a Ca(2+) and an F(-) on the modified tip, respectively, although the relationship between the image contrast and the sign of the tip-terminating ion was not always perfect because of the instability of the tip-terminating ion on the nanocluster. The present method can be used to distinguish terminal groups with different electronegativities.Entities:
Year: 2006 PMID: 21727402 DOI: 10.1088/0957-4484/17/7/S03
Source DB: PubMed Journal: Nanotechnology ISSN: 0957-4484 Impact factor: 3.874