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    题名: 3-Mercapto-1-propanesulfonic acid and Bis(3-sulfopropyl) Disulfide Adsorbed on Au(111): In Situ Scanning Tunneling Microscopy and Electrochemical Studies
    作者: Jian,ZY;Chang,TY;Yang,YC;Dow,WP;Yau,SL;Lee,YL
    贡献者: 中央大學
    关键词: SELF-ASSEMBLED MONOLAYERS;COPPER ELECTRODEPOSITION;GOLD SURFACES;ADSORPTION;SPECTROSCOPY;CHLORIDE;FILMS;AU;ALKANETHIOLS;DECANETHIOL
    日期: 2009
    上传时间: 2010-06-29 19:44:40 (UTC+8)
    出版者: 化學研究所
    摘要: 3-Mereapto-1-propanesulfonic acid (MPS) and bis(3-sulfopropyl)disulfide (SPS) adsorbed on a Au(111) electrode were studied by using in situ scanning tunneling microscopy (STM). Although the adsorptions of MPS and SPS arc known to be oxidative and reductive, respectively, on an Au(111) electrode, these two admolecules behave similarly in terms of phase evolution, surface coverage, potential for stripping, and characteristics of cyclic voltammetry. However, different adsorption mechanisms of these molecules result in different structures. Raising electrode potential causes more MPS and SPS molecules to adsorb, yielding ordered adlattices between 0.67 and 0.8 V (vs reversible hydrogen electrode). The ordered adlattices of MPS and SPS appear as striped and netlike structures with molecules adsorbed parallel to the Au(111) surface. Switching potential to 0.9 V or more positive still does not result in upright molecular orientation, possibly inhibited by electrostatic interaction between the end group Of -SO3- and the Au(111) electrode. Lowering the potential to 0.4 V disrupted the ordered adlayer. Stripping voltammetric experiments show that MPS and SPS admolecules are desorbed from Au(111) at the same potential, suggesting that these molecules are both adsorbed via their sulfur headgroups. The S-S bond in SPS is likely broken upon its adsorption on Au(111).
    關聯: LANGMUIR
    显示于类别:[化學研究所] 期刊論文

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