氧化镍电镀和电极表面改性用于谷氨酸的电化学检测

IF 4.7 3区 工程技术 Q2 ELECTROCHEMISTRY
Eun Joong Kim , Chung Mu Kang , Ji-Hyung Han
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引用次数: 0

摘要

通过阴极电镀以及随后在碱性水电解质中进行电化学活化,氧化镍(NiOx)的电化学行为和催化特性得到了增强。通过在 NiOx 表面固定 APTES((3-aminopropyl)triethoxysilane),引入胺基团,从而产生正电荷,实现了对 ʟ -谷氨酸的电化学检测。电化学活化的电镀氧化镍和 APTES 改性表面的协同效应有助于对痕量ʟ-谷氨酸进行有效的电化学检测。APTES 活化的 NiOx 电极对谷氨酸的线性检测范围为 0.2 nM 至 2 mM。这一相对较宽的浓度范围有望用于人体生物液体的分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Nickel oxide electroplating and electrode surface modification for electrochemical detection of glutamate

Nickel oxide electroplating and electrode surface modification for electrochemical detection of glutamate

The electrochemical behavior and catalytic properties of nickel oxide (NiOx) are enhanced through cathodic electroplating and subsequent electrochemical activation in an alkaline aqueous electrolyte. The electrochemical detection of ʟ-glutamate becomes feasible by introducing an amine group through immobilizing APTES ((3-aminopropyl)triethoxysilane) on the NiOx surface, resulting in a positive charge. The synergistic effect of electrochemically activated electroplated NiOx and the APTES-modified surface facilitates the effective electrochemical detection of trace ʟ-glutamate. The APTES-activated NiOx electrode exhibits a linear detection range of 0.2 nM to 2 mM for glutamate. This relatively wide concentration range is promising for the analysis of human biological fluids.

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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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