利用激光划线技术制作的金改性碳电极用于益生菌活性的电化学分析

IF 3.4 Q2 CHEMISTRY, ANALYTICAL
Juliana L. M. Gongoni, George Chumanov, Thiago R. L. C. Paixão, Dr. Carlos D. Garcia
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引用次数: 0

摘要

本文介绍了一种简单、快速(<15 分钟)、分两步对纸板基底进行激光划线的方法,用于制造金属纳米粒子修饰的碳电极。第一个划线步骤是将纸板基底图案化(促进多孔碳电极的形成)。第二步是通过水溶液中阳离子的化学还原过程产生金属纳米粒子。在这些实验中,考虑到铜、银、镍、钴、锌和金对所生产的碳材料的电气性能和成分的影响,对它们的效果进行了评估。这些实验表明,尽管电阻发生了显著变化(普通电极的电阻为 138 ± 7 Ω,金改性电极的电阻仅为 53 ± 3 Ω),但所生产材料的形态或成分仅发生了微不足道的变化(普通纸板的 IG/ID 为 1.2 ± 0.3,钴改性电极的 IG/ID 为 1.8 ± 0.3)。为了证明所提策略的适用性,我们将金改性电极组装成电化学传感器,并将其用于测量各种商业样品中活微生物的代谢活性,只需 100 µL 样品和 10 分钟的培养时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Au-Modified Carbon Electrodes Produced by Laser Scribing for Electrochemical Analysis of Probiotic Activity

Au-Modified Carbon Electrodes Produced by Laser Scribing for Electrochemical Analysis of Probiotic Activity

A simple and fast (<15 min), two-step laser scribing of cardboard substrates is described as a method for fabricating carbon electrodes modified with metallic nanoparticles. The first scribing step patterned a cardboard substrate (promoting the formation of porous carbon electrodes). The second step was included to produce metallic nanoparticles via a chemical reduction process of cations from an aqueous solution. For these experiments, the effects of copper, silver, nickel, cobalt, zinc, and gold were evaluated considering their effect on the electrical properties and the composition of the carbon materials produced. These experiments revealed that, despite significant changes in resistance (from 138±7 Ω for plain electrodes to just 53±3 Ω for Au-modified electrodes), only marginal changes were observed in the morphology or composition of the material produced (IG/ID ranged from 1.2±0.3 for the plain cardboard to 1.8±0.3 for the cobalt-modified electrodes). To demonstrate the applicability of the proposed strategy, Au-modified electrodes were assembled into electrochemical sensors and applied to measure the metabolic activity of live microorganisms in various commercial samples, requiring only 100 μL of sample and 10 min of incubation time.

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CiteScore
2.60
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