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以乙二胺四乙酸功能化的金半胱胺自组装单分子层作为新型纳米传感器

Functionalization of gold cysteamine self-assembled monolayer with ethylenediaminetetraacetic acid as a novel nanosensor.

作者信息

Shervedani Reza Karimi, Farahbakhsh Anahita, Bagherzadeh Mojtaba

机构信息

Department of Chemistry, University of Isfahan, Isfahan 81746-73441, Islamic Republic of Iran.

出版信息

Anal Chim Acta. 2007 Mar 28;587(2):254-62. doi: 10.1016/j.aca.2007.01.053. Epub 2007 Jan 25.

Abstract

Electrochemical characterization of gold cysteamine self-assembled monolayer, in situ functionalized with ethylenediaminetetraacetic acid (Au-CA-EDTA SAM), is described by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and Osteryoung square wave voltammetry (OSWV). The results obtained by EIS and CV, in the presence of Fe(CN)(6) redox probe, show that EDTA is successfully grafted to the surface of Au-CA electrode. Reproducible and reversible variation of the R(ct) and DeltaEp as a function of solution pH show that Au-CA-EDTA SAM is stable in a wide range of pH and potentials. Accumulation of the Pb(2+) and Cu(2+) ions on the Au-CA-EDTA SAM electrode is investigated using faradaic currents or impedimetric effects measured by OSWV and EIS, respectively. These results reveal the presence of active complexing functional groups of EDTA on the surface, and thus, the formation of Au-CA-EDTA SAM electrode. The new sensor responds to the Pb(2+) and Cu(2+) separately and simultaneously in a wide linear range of concentrations.

摘要

通过循环伏安法(CV)、电化学阻抗谱(EIS)和奥斯特里杨方波伏安法(OSWV)描述了用乙二胺四乙酸原位功能化的金半胱胺自组装单分子层(Au-CA-EDTA SAM)的电化学特性。在Fe(CN)(6)氧化还原探针存在下,通过EIS和CV获得的结果表明,EDTA成功接枝到Au-CA电极表面。R(ct)和ΔEp随溶液pH值的可重现且可逆变化表明,Au-CA-EDTA SAM在很宽的pH值和电位范围内是稳定的。分别使用OSWV和EIS测量的法拉第电流或阻抗效应研究了Pb(2+)和Cu(2+)离子在Au-CA-EDTA SAM电极上的积累。这些结果揭示了表面存在EDTA的活性络合官能团,从而形成了Au-CA-EDTA SAM电极。这种新型传感器在很宽的浓度线性范围内分别和同时对Pb(2+)和Cu(2+)作出响应。

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