4.6 Article

Electrochemical stripping analysis from micro-counter electrode

期刊

ELECTROCHIMICA ACTA
卷 393, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2021.139095

关键词

Indirect electrochemical stripping analysis; Counter-electrode electrochemistry; Voltammetry; Amperometry

资金

  1. China Scholarship Council

向作者/读者索取更多资源

This study presents a new approach to electrochemical stripping analysis, where the target analyte is indirectly analyzed based on the signal obtained from the counter electrode, using an ultramicroelectrode to take advantage of the polarization effect. By utilizing this method, the resolution of signals can be improved and background interference can be reduced, offering a new angle of electroanalysis.
Electrochemical stripping analysis (anodic, cathodic, or adsorptive) is usually based on the pre-concentration of a target analyte on the working electrode surface and then measuring its quantity via its direct quantitative electrochemical transformation (with the electrode refreshed afterwards). In this work, we demonstrate a new approach to carry out electrochemical stripping analysis of non-adsorbing species, thus not based on the analyte being directly pre-concentrated on the working electrode (WE), but on the signal obtained indirectly from the counter electrode (CE) where metal ions are reduced and then electrochemically stripped. Different from the CE with large surface area in classical electrochemical measurements, an ultramicroelectrode is chosen here as CE to purposely exploit the polarization effect. The concept is based on oxidizing the analyte on WE in one compartment of the electrochemical cell while reducing Cu2+ on CE from another compartment connected with an ionic bridge or a less common metal bridge. The deposited Cu on CE is then analyzed by stripping in another three-electrode cell, and the charge shows good linear relationship with the concentration of analyte in the former cell. As the stripping current response (peak) is much clearer than the small current variations corresponding to the direct oxidation of the analyte, it improves the resolution of raw signal. Besides, it may also reduce the background signal from blank solution by filtering the non-Faradaic charge. Like in classical electrochemical stripping analysis, one may also prolong the oxidation time in exchange for higher sensitivity of analysis. This work extends the applications of stripping analysis and offers a new angle of electroanalysis by capturing signals from counter electrode. (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