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http://dx.doi.org/10.5012/bkcs.2011.32.8.2623

Phase Transition of Octaneselenolate Self-assembled Monolayers on Au(111) Studied by Scanning Tunneling Microscopy  

Choi, Jung-Seok (Department of Chemistry and Research Institute for Natural Sciences, Hanyang University)
Kang, Hun-Gu (Department of Chemistry and Research Institute for Natural Sciences, Hanyang University)
Ito, Eisuke (Flucto-order Functions Research Team, RIKEN-HYU Collaboration Center, RIKEN)
Hara, Masahiko (Flucto-order Functions Research Team, RIKEN-HYU Collaboration Center, RIKEN)
Noh, Jae-Geun (Department of Chemistry and Research Institute for Natural Sciences, Hanyang University)
Publication Information
Abstract
We investigated the surface structure and wetting behavior of octaneselenolate self-assembled monolayers (SAMs) on Au(111) formed in a 50 ${\mu}M$ ethanol solution according to immersion time, using scanning tunneling microscopy (STM) and an automatic contact angle (CA) goniometer. Closely-packed, well-ordered alkanethiol SAMs would form as the immersion time increased; unexpectedly, however, we observed the structural transition of octaneselenolate SAMs from a molecular row phase with a long-range order to a disordered phase with a high density of vacancy islands (VIs). Molecularly resolved STM imaging revealed that the missing-row ordered phase of the SAMs could be assigned as a $(6{\times}{\surd}3)R30^{\circ}$ superlattice containing three molecules in the rectangular unit cell. In addition, CA measurements showed that the structural order and defect density of VIs are closely related to the wetting behaviors of octaneselenolate SAMs on gold. In this study, we clearly demonstrate that interactions between the headgroups and gold surfaces play an important role in determining the physical properties and surface structure of SAMs.
Keywords
Octaneselnolate; Self-assembled monolayers; Scanning tunneling microscopy; Phase transition; Contact angle;
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