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Formation of Highly Ordered Self-assembled Monolayers by -Conjugated Tolanethioacetates on Au(111)

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dc.contributor.author노재근-
dc.date.accessioned2021-08-03T22:19:33Z-
dc.date.available2021-08-03T22:19:33Z-
dc.date.created2021-06-30-
dc.date.issued2009-03-16-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/62308-
dc.description.abstractSurface structure and adsorption conditions of tolanethioacetate (TTA) self-assembled monolayers (SAMs) on Au(111) in catalytic tetrabutylammonium cyanide (TBACN) solution were examined by scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (XPS). We found that SAM formation by adsorption of TTA molecules on Au(111) strongly depends on experimental conditions for the deprotection of acetyl group. Molecular-scale STM imaging revealed that TTA molecules on Au(111) can form well-ordered SAMs in TBACN catalytic medium compared to in pure solvent. The adsorption of TTA molecules on Au(111) in catalytic TBACN solution at 50 °C for 24 h led to the formation of long-range ordered phase containing rod-like domains, which can be described as a (2 × √7)R62° structure. On the other hand, the adsorption of TTA molecules on Au(111) at room temperature led to the formation of different packing structure, which can be described as a (√3 × √8)R50° structure. In addition, XPS measurements showed a strong S 2p peak at 162 eV for TTA SAMs on Au(111), implying that TTA SAMs were formed via chemical reactions between the sulfur atoms and gold surfaces.-
dc.publisher일본응용물리학회-
dc.titleFormation of Highly Ordered Self-assembled Monolayers by -Conjugated Tolanethioacetates on Au(111)-
dc.typeConference-
dc.contributor.affiliatedAuthor노재근-
dc.identifier.bibliographicCitationFifth International Conference on Molecular Electronics (M&BE5)-
dc.relation.isPartOfFifth International Conference on Molecular Electronics (M&BE5)-
dc.citation.titleFifth International Conference on Molecular Electronics (M&BE5)-
dc.citation.conferencePlace일본 미야자키-
dc.type.rimsCONF-
dc.description.journalClass1-
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