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A functional graphene oxide-ionic liquid composites-gold nanoparticle sensing platform for ultrasensitive electrochemical detection of Hg2+

机译:用于超灵敏电化学检测Hg2 +的功能性氧化石墨烯-离子液体复合物-金纳米颗粒传感平台

摘要

A simple and sensitive electrochemical assay strategy of stripping voltammetry for mercury ions (Hg2+) detection is described based on the synergistic effect between ionic liquid functionalized graphene oxide (GO-IL) and gold nanoparticles (AuNPs). The AuNPs-GO-IL modified onto glassy carbon electrode (GCE) resulted in highly enhanced electron conductive nanostructured membrane and large electroactive surface area, which was excellently examined by scanning electron microscopy and cyclic voltammetry. After accumulating Hg2+, anodic stripping voltammetry (ASV) was performed, and differential pulse voltammetry (DPV) was employed for signal recording of Hg2+. Several main experimental parameters were optimized, i.e., deposition potential and time of AuNPs were -0.2 V and 180 s, respectively, and accumulation potential and time of Hg2+ were -0.3 V and 660 s, respectively. Under the optimal conditions, this AuNPs-GO-IL-GCE sensor attained a good linearity in a wide range of 0.1-100 nM (R = 0.9808) between the concentration of the Hg2+ standard and peak current. The limit of detection was estimated to be 0.03 nM at a signal-to-noise ratio of 3 sigma. A variety of common coexistent ions in water samples were investigated, showing no obvious interferences on the Hg2+ detection. The practical application of the proposed sensor has been carried out and demonstrated as feasible for determination of trace levels of Hg2+ in drinking and environmental water samples.
机译:基于离子液体功能化氧化石墨烯(GO-IL)和金纳米粒子(AuNPs)的协同效应,描述了一种用于汞离子(Hg2 +)检测的溶出伏安法的简单而灵敏的电化学测定策略。修饰到玻碳电极(GCE)上的AuNPs-GO-IL导致高度增强的电子导电纳米结构膜和大的电活性表面积,这通过扫描电子显微镜和循环伏安法进行了出色的检查。积累Hg2 +后,进行阳极溶出伏安法(ASV),采用差分脉冲伏安法(DPV)记录Hg2 +信号。优化了几个主要的实验参数,即AuNPs的沉积电势和时间分别为-0.2 V和180 s,Hg2 +的累积电势和时间分别为-0.3 V和660 s。在最佳条件下,此AuNPs-GO-IL-GCE传感器在Hg2 +标准溶液的浓度和峰值电流之间的0.1-100 nM(R = 0.9808)的宽范围内均具有良好的线性。在3 sigma的信噪比下,检测极限估计为0.03 nM。对水样中各种常见的共存离子进行了研究,结果表明对Hg2 +的检测无明显干扰。所提出的传感器的实际应用已经进行,并被证明可用于测定饮用水和环境水样品中痕量的Hg2 +。

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