MoS2 embedded triangular silver nanosheets modified MOF-808 as electrochemical sensing platform for highly sensitive simultaneous detection of ACOP and 4-AP

X射线光电子能谱 检出限 微分脉冲伏安法 循环伏安法 电化学气体传感器 材料科学 电化学 分析化学(期刊) 核化学 扫描电子显微镜 介电谱 选择性 电极 化学工程 化学 色谱法 复合材料 有机化学 催化作用 物理化学 工程类
作者
Xiaoqin Wei,Hao Guo,Mingyue Wang,Zongyan Lu,Zeyun Yang,Lei Sun,Zhiguo Yu,Yinsheng Liu,Wu Yang
出处
期刊:Colloids and Surfaces A: Physicochemical and Engineering Aspects [Elsevier BV]
卷期号:676: 132264-132264 被引量:6
标识
DOI:10.1016/j.colsurfa.2023.132264
摘要

The detection of acetaminophen (ACOP) and its toxic hydrolyzed product p-aminophenol (4-AP) is very significant for clinical diagnosis and quality control of drug formulation. In this study, a novel electrochemical sensor based on MoS2 embedding triangular Ag nanoplates (Tri-AgNPs) coated MOF-808 was developed for simultaneous and sensitive detection of ACOP and 4-AP. The morphology and structure MOF-808@MoS2/Tri-AgNPs nanocomposite were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS) and so on. The electrochemical and electrocatalytic properties of the composite electrode were evaluated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The experimental results demonstrated that the constructed sensor had excellent electrochemical performance for ACOP and 4-AP detection due to the synergistic interaction among MOF-808, MoS2 and Tri-AgNPs. The proposed sensor exhibited a wide linear range (1–450 μM) and low limits of detection for detection of ACOP (0.054 μM) and 4-AP (0.046 μM). At the same time, the sensor also showed outstanding repeatability, reproducibility, stability and selectivity. In addition, MOF-808@MoS2/Tri-AgNPs/GCE was also employed to determine ACOP and 4-AP in acetaminophen tablets and Yellow River water samples with satisfactory recovery rates, which indicated the feasibility of the developed electrochemical sensor in the actual sample analysis.
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