MOF-Derived Bimetallic CoFe-PBA Composites as Highly Selective and Sensitive Electrochemical Sensors for Hydrogen Peroxide and Nonenzymatic Glucose in Human Serum

普鲁士蓝 材料科学 沸石咪唑盐骨架 咪唑酯 检出限 纳米复合材料 制作 电化学 线性范围 化学工程 双金属片 生物传感器 金属有机骨架 电极 纳米技术 有机化学 金属 冶金 物理化学 病理 化学 医学 工程类 替代医学 吸附 色谱法
作者
Chen Chen,Dengke Xiong,Minli Gu,Chunxiao Lü,Fei‐Yan Yi,Xinghua Ma
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:12 (31): 35365-35374 被引量:124
标识
DOI:10.1021/acsami.0c09689
摘要

The fabrication of two-dimensional (2D) metal–organic frameworks (MOFs) and Prussian blue analogues (PBAs) combines the advantages of 2D materials, MOFs and PBAs, resolving the poor electronic conductivity and slow diffusion of MOF materials for electrochemical applications. In this work, 2D leaflike zeolitic imidazolate frameworks (Co-ZIF and Fe-ZIF) as sacrificial templates are in situ converted into PBAs, realizing the successful fabrication of PBA/ZIF nanocomposites on nickel foam (NF), namely, CoCo-PBA/Co-ZIF/NF, FeFe-PBA/Fe-ZIF/NF, CoFe-PBA/Co-ZIF/NF, and Fe/CoCo-PBA/Co-ZIF/NF. Such fabrication can effectively reduce transfer resistance and greatly enhance electron- and mass-transfer efficiency due to the electrochemically active PBA particles and NF substrate. These fabricated electrodes as multifunctional sensors achieve highly selective and sensitive glucose and H2O2 biosensing with a very wide detective linear range, extremely low limit of detection (LOD), and good stability. Among them, CoFe-PBA/Co-ZIF/NF exhibits the best sensing performance with a very wide linear range from 1.4 μM to 1.5 mM, a high sensitivity of 5270 μA mM–1 cm–2, a low LOD of 0.02 μM (S/N = 3), and remarkable stability and selectivity toward glucose. What is more, it can realize excellent detection of glucose in human serum, demonstrating its practical applications. Furthermore, this material as a multifunctional electrochemical sensor also manifests superior detection performance against hydrogen peroxide with a wide linear range of 0.2–6.0 mM, a high sensitivity of 196 μA mM–1 cm–2, and a low limit of detection of 1.08 nM (S/N = 3). The sensing mechanism for enhanced performance for glucose and H2O2 is discussed and proved by experiments in detail.
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