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Facile synthesis of nickel hydroxide-graphene nanocomposites for insulin detection with enhanced electro-oxidation properties

机译:用于胰岛素检测的氢氧化镍-石墨烯纳米复合材料的简便合成,具有增强的电氧化性能

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摘要

This study describes a facile and effective one-pot route to synthesize structurally uniform and electrochemically active nickel hydroxide-graphene nanocomposites (Ni(OH)(2)-GN) and investigates the electrocatalytic activity toward the oxidation of insulin. Graphene here was used to tether Ni2+ precursor onto surfaces and eventually grow Ni(OH)(2) nanoparticles to form hybrid materials. The synthetic Ni(OH)(2)-GN nanocomposite has a uniform surface distribution, which was characterized with scanning electron microscopy (SEM). Moreover, the composition of synthetic Ni(OH)(2)-GN nanocomposite was characterized by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR spectra). The Ni(OH)(2)-GN were electrochemically treated in 0.1 M NaOH solution through cyclic voltammograms, and then gradually transited into nickel oxyhydroxide-graphene nanocomposites (NiOOH-GN), which demonstrated high catalytic activity and improved stability to insulin oxidation. The steady-state current response increases linearly with insulin concentration from 800 nM to 6400 nM with a fast response time of less than 2 s and a detection limit of 200 nM. The excellent performance of insulin sensor, including long term stability, can be ascribed to the synergistic effects of the large surface area (resulting in high loading ability), dispersing ability and conductivity of graphene and the large surface-to-volume ratio and electrocatalytic activity of Ni(OH)(2) nanoparticles.
机译:这项研究描述了一种简便有效的一锅法来合成结构均匀且具有电化学活性的氢氧化镍-石墨烯纳米复合材料(Ni(OH)(2)-GN),并研究了其对胰岛素氧化的电催化活性。此处使用石墨烯将Ni2 +前体束缚在表面上,并最终生长Ni(OH)(2)纳米颗粒以形成杂化材料。合成的Ni(OH)(2)-GN纳米复合材料具有均匀的表面分布,这是用扫描电子显微镜(SEM)表征的。此外,合成的Ni(OH)(2)-GN纳米复合材料的组成通过X射线光电子能谱(XPS)和傅立叶变换红外光谱(FT-IR光谱)进行了表征。 Ni(OH)(2)-GN在0.1 M NaOH溶液中通过循环伏安图进行电化学处理,然后逐渐过渡为羟基氧化镍-石墨烯纳米复合材料(NiOOH-GN),具有较高的催化活性和对胰岛素氧化的稳定性。稳态电流响应随胰岛素浓度从800 nM线性增加到6400 nM,响应时间少于2 s,检测极限为200 nM。胰岛素传感器的出色性能(包括长期稳定性)可归因于大表面积(导致高负载能力),石墨烯的分散能力和电导率以及大的表面积体积比和电催化活性的协同效应。 Ni(OH)(2)纳米粒子的数量。

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