Determination of silver ions in distilled water by stripping voltammetry at a Nafion-coated gold electrode in combination with quartz crystal microbalance and electrochemical impedance spectroscopy.

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Talanta Pub Date : 2025-01-01 Epub Date: 2024-10-09 DOI:10.1016/j.talanta.2024.127006
Tingting Han, Sini Chen, Songlin Yang, Tao Song, Xuliang Lin, Qin Yu, Dongxue Han, Johan Bobacka, Li Niu
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引用次数: 0

Abstract

Here, we propose a stripping voltammetric method for Ag+ ion determination in distilled water utilizing screen-printed Au electrodes coated with Nafion (Nafion/Au screen-printed electrodes). The concentration of Ag+ in pure water was determined by linear sweep voltammetry (LSV) after silver deposition on the Nafion/Au electrode. The anodic stripping peak current increased linearly with the concentration of Ag+ ion in the range from 1 ppm to 22 ppm. The LSV oxidative peak current was increased by extending the silver deposition time from 300 s to 500 s. Repetitive LSV measurements revealed satisfactory reproducibility of the Nafion/Au screen-printed electrodes. The detection mechanism was elucidated by recording mass changes of the Nafion/Au electrode with a quartz crystal microbalance (QCM), and by determining changes in the low-frequency capacitance of the Nafion/Au electrode by electrochemical impedance spectroscopy (EIS). The observed changes in mass and capacitance confirmed Ag+ accumulation and release processes at the Nafion/Au electrodes, in good agreement with stripping voltammetry. The combination of stripping voltammetry, QCM and EIS allowed a detailed characterization of the ion transfer, deposition and stripping processes at the Nafion/Au electrodes in presence of Ag+ ions. The Nafion/Au screen-printed electrode enabled voltammetric determination of low Ag+ concentrations in distilled water, without any sample pretreatment nor addition of supporting electrolyte.

结合石英晶体微天平和电化学阻抗光谱法,通过在镀有纳菲昂的金电极上进行剥离伏安法测定蒸馏水中的银离子。
在此,我们提出了一种利用涂有 Nafion 的丝网印刷金电极(Nafion/Au 丝网印刷电极)测定蒸馏水中 Ag+ 离子的剥离伏安法。在 Nafion/Au 电极上沉积银后,采用线性扫描伏安法(LSV)测定纯水中的 Ag+ 浓度。在 1 ppm 至 22 ppm 的范围内,阳极剥离峰电流随 Ag+ 离子浓度的增加而线性增加。通过将银沉积时间从 300 秒延长到 500 秒,LSV 氧化峰电流也随之增加。重复 LSV 测量显示,Nafion/Au 丝网印刷电极的再现性令人满意。通过石英晶体微天平 (QCM) 记录 Nafion/Au 电极的质量变化,以及通过电化学阻抗光谱 (EIS) 确定 Nafion/Au 电极的低频电容变化,阐明了检测机制。观察到的质量和电容变化证实了 Ag+ 在 Nafion/Au 电极上的积累和释放过程,这与剥离伏安法十分吻合。结合剥离伏安法、QCM 和 EIS,可以详细描述 Ag+ 离子存在时 Nafion/Au 电极的离子转移、沉积和剥离过程。Nafion/Au 丝网印刷电极可对蒸馏水中的低浓度 Ag+ 进行伏安测定,无需对样品进行任何预处理,也无需添加支撑电解质。
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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