4.6 Article

Charge effects on the behavior of CTAB adsorbed on Au(111) electrodes in aqueous solutions

期刊

ELECTROCHIMICA ACTA
卷 370, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2021.137737

关键词

-

资金

  1. Ministerio de Ciencia e Innovacion [PID2019-105653GB-100]
  2. Generalitat Valenciana [PROMETEO/2020/063]

向作者/读者索取更多资源

The behavior of adsorbed CTAB on Au(111) electrodes was studied using electrochemical and FTIR experiments in different aqueous solutions. The results showed that the adsorbed layer was stable in acidic solutions. Changes in electrode charge led to changes in electrode capacitance, resulting in characteristic peaks.
The behavior of adsorbed CTAB on Au(111) electrodes has been studied using electrochemical and FTIR experiments in different aqueous solutions. The results show that the adsorbed layer is stable in acidic solutions in the whole potential range of study. The observed electrochemical and FTIR behavior is compatible with the formation of a membrane of CTA(+) on the electrode surface with the polar amino groups in contact with the surface. When the electrode charge is negative, the polar groups are attracted to the surface, so that the capacitance of the electrode is smaller than that recorded for the unmodified Au(111) electrode. As the charge becomes positive, the membrane detaches from the surface and water molecules permeate through it, changing the capacitance of the electrode and giving rise to characteristic peaks in the voltammetric profile. At potentials higher than these peaks, the behavior of the electrode is comparable to that observed for the unmodified electrode. The stability of the membrane is facilitated by the incorporation of anions of the supporting electrolyte. Those anions remain on the membrane even when the electrode is transferred to a different solution, as the electrochemical behavior shows. (C) 2021 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据