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Electrochemical Behavior of Ferrocenylthiol / Alkanethiol Binary SAM in Ionic Liquids

机译:二茂铁硫醇/烷硫醇二元SAM在离子液体中的电化学行为

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摘要

The redox behavior of the binary self-assembled monolayers (SAMs) of 11-ferrocenyl-1-undecanethiol and 1-undecanthiol on gold substrate was investigated in an ionic liquid (IL), trimethyl-n--hexylammonium bis[(trifluoromethyl)sulfonyl]amide (TMHA-Tf_zN) and HClO_4 aqueous solution. It was found that the total amount of charge for the redox of ferrocenyl groups in the ionic liquid is about 70% of that in the HClO_4 solution, indicating that less number of ferrocenyl groups are involved in the redox in the ionic liquid. A set of impedance measurements indicated that the electron transfer rate between the SAMs and the substrate is lower in the ionic liquid than that in aqueous solution, suggesting a slow and incomplete reconstruction of TMHA-Tf_2N ions at the SAMs/ionic liquid surface.
机译:在离子液体(IL),三甲基-正己基铵双[((三氟甲基))磺酰基中研究了11-二茂铁基-1-十一碳硫醇和1-十一碳硫醇的二元自组装单分子膜(SAMs)在金基底上的氧化还原行为。酰胺(TMHA-Tf_zN)和HClO_4水溶液。发现离子液体中二茂铁基团的氧化还原的电荷总量约为HClO_4溶液中二茂铁基团的氧化还原电荷的总量,表明离子液体中的氧化还原所涉及的二茂铁基团的数目较少。一组阻抗测量结果表明,离子液体中SAM与底物之间的电子转移速率低于水溶液中的电子转移速率,这表明TMHA-Tf_2N离子在SAM /离子液体表面的重建缓慢而不完全。

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  • 来源
    《Molten salts and ionic liquids 16》|2008年|575-581|共7页
  • 会议地点 Honolulu HI(US);Honolulu HI(US)
  • 作者单位

    Department of Materials Science and Engineering, Kyoto University, Yoshida-hommachi, Sakyo-ku, Kyoto 606-8501, Japan;

    Department of Materials Science and Engineering, Kyoto University, Yoshida-hommachi, Sakyo-ku, Kyoto 606-8501, Japan;

    Department of Materials Science and Engineering, Kyoto University, Yoshida-hommachi, Sakyo-ku, Kyoto 606-8501, Japan;

    Department of Materials Science and Engineering, Kyoto University, Yoshida-hommachi, Sakyo-ku, Kyoto 606-8501, Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 熔盐;
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