首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >In situ & controlled preparation of platinum nanoparticles dopping into graphene sheets@cerium oxide nanocomposites sensitized screen printed electrode for nonenzymatic electrochemical sensing of hydrogen peroxide
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In situ & controlled preparation of platinum nanoparticles dopping into graphene sheets@cerium oxide nanocomposites sensitized screen printed electrode for nonenzymatic electrochemical sensing of hydrogen peroxide

机译:原位和受控制备掺杂到石墨烯片中的铂纳米粒子@氧化铈纳米复合材料的敏化丝网印刷电极,用于过氧化氢的非酶电化学传感

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摘要

A quick, selective and sensitive electrochemical sensor for nonenzymatic hydrogen peroxide (H2O2) detecting was fabricated. It was based on the in situ & controlled preparation of platinum nanoparticles (Pt) dopping into graphene sheets@cerium oxide (GS@CeO2) nanocomposites sensitized screen printed electrode (SPE). Different sizes of Pt were dopped into GS@CeO2 nanocomposites by using a simple electroless plating method. X-ray powder diffractometer (XRD) combines with Fourier transform infrared spectrum (FTIR) were used to characterize the composition of the hybrid nanomaterials. Electrochemical impedance spectroscopy (EIS) and Scanning electron microscopy (SEM) were employed to study the interfacial properties and morphologies of different electrodes. The electrochemical properties of electrochemical sensor were investigated by cyclic voltammetry (CV) and chronoamperometry (i-t curve) methods. After all experimental parameters were optimized, the GS@CeO2-Pt hybrid nanomaterials modified SPE (SPE I GS@CeO2-Pt) showed a good performance towards the electrocatalytic reduction of H2O2. A wide linear detection range (LDR) extends from 1.0 x 10(-3) mM to 10.0 mM (R = 0.9999) and a low limit of detection (LOD) of 0.43 x 10(-3) mM (S/N = 3) were achieved. The sensor was also simple, stable and reliable. It was applied to the determination of H2O2 in contact lens care solutions with good accuracy and recovery. (C) 2016 Elsevier B.V. All rights reserved.
机译:制作了一种快速,选择性和灵敏的非酶法过氧化氢(H2O2)检测电化学传感器。它基于原位和受控制备的掺杂到石墨烯片@氧化铈(GS @ CeO2)纳米复合材料敏化丝网印刷电极(SPE)中的铂纳米粒子(Pt)。通过使用简单的化学镀方法将不同尺寸的Pt掺入GS @ CeO2纳米复合材料中。 X射线粉末衍射仪(XRD)结合傅立叶变换红外光谱(FTIR)被用来表征杂化纳米材料的组成。电化学阻抗谱(EIS)和扫描电子显微镜(SEM)用于研究不同电极的界面特性和形态。通过循环伏安法(CV)和计时电流法(i-t曲线)研究了电化学传感器的电化学性能。优化所有实验参数后,GS @ CeO2-Pt杂化纳米材料改性的SPE(SPE I GS @ CeO2-Pt)对H2O2的电催化还原表现出良好的性能。宽线性检测范围(LDR)从1.0 x 10(-3)mM扩展到10.0 mM(R = 0.9999),检测下限(LOD)为0.43 x 10(-3)mM(S / N = 3 )达成。该传感器还简单,稳定且可靠。它已以良好的准确度和回收率用于测定隐形眼镜护理液中的H2O2。 (C)2016 Elsevier B.V.保留所有权利。

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