Formation of an organic film on an electrode via a suspension of redox-active droplets in acidic aqueous solution

IF 4.7 3区 工程技术 Q2 ELECTROCHEMISTRY
Katarzyna Dusilo , Aleksandra Siwiec , Marcin Holdynski , Pekka Peljo , Marcin Opallo
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引用次数: 0

Abstract

Previous electrochemical studies of redox emulsions have been mainly performed in the context of electro-organic synthesis. More recently, this research has been oriented towards applications of emulsions in flow batteries. Such biphasic systems seem to provide a suitable environment for reactions at the liquid–liquid interface. Taking an emulsion consisting of microdroplets of decamethylferrocene solution in a hydrophobic ionic liquid/toluene mixture in acidic aqueous solution as an example, we have demonstrated that an electrochemical redox reaction involving the hydrophobic redox probe occurs at the glassy carbon electrode|organic liquid film interface. This reaction is followed by ion exchange between liquid phases. This effect is explained by the instability of the emulsion. A portion of the organic liquid stays on the electrode surface after transfer to a purely aqueous electrolyte and remains electroactive.

Abstract Image

通过在酸性水溶液中悬浮氧化还原活性液滴在电极上形成有机薄膜
以往对氧化还原乳的电化学研究主要是在电有机合成的背景下进行的。最近,这项研究的方向是乳液在液流电池中的应用。这种双相体系似乎为液-液界面的反应提供了合适的环境。以十甲基二茂铁溶液微滴组成的乳液为例,在酸性水溶液中疏水离子液体/甲苯混合物中,我们证明了疏水氧化还原探针在玻碳电极/有机液膜界面上发生电化学氧化还原反应。这个反应之后是液相之间的离子交换。这种效应可以用乳剂的不稳定性来解释。有机液体的一部分在转移到纯水电解质后停留在电极表面并保持电活性。
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来源期刊
Electrochemistry Communications
Electrochemistry Communications 工程技术-电化学
CiteScore
8.50
自引率
3.70%
发文量
160
审稿时长
1.2 months
期刊介绍: Electrochemistry Communications is an open access journal providing fast dissemination of short communications, full communications and mini reviews covering the whole field of electrochemistry which merit urgent publication. Short communications are limited to a maximum of 20,000 characters (including spaces) while full communications and mini reviews are limited to 25,000 characters (including spaces). Supplementary information is permitted for full communications and mini reviews but not for short communications. We aim to be the fastest journal in electrochemistry for these types of papers.
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