双金属片
X射线光电子能谱
合金
纳米颗粒
循环伏安法
透射电子显微镜
扫描电子显微镜
银纳米粒子
化学
纳米技术
电化学
材料科学
核化学
化学工程
分析化学(期刊)
电极
金属
有机化学
冶金
复合材料
工程类
物理化学
作者
P. Arul,Sheng‐Tung Huang,Veerappan Mani,Chih‐Hung Huang
标识
DOI:10.1021/acsanm.2c00435
摘要
An efficient and simple way has been described to prepare gold and silver bimetallic alloy nanoparticles (Au-AgNPs) in an organic framework with a metal-free core. The growth of alloy Au-AgNPs was monitored by UV–visible spectroscopy (UV–vis) and confirmed using various spectral, microscopy, and electrochemical techniques. The field-emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) results revealed that the covalent organic framework (COF) had a uniform flake-like morphology, and the alloy-based Au-AgNPs had a flower-like structure. The results of X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) indicated that Au-AgNPs are metallic in nature and highly crystalline. The surface of a glassy carbon electrode (GCE) was then modified with Au-AgNPs-COF, which was subsequently employed for enzyme-free electrochemical reduction of H2O2. The electrocatalytic cyclic voltammetry performance of the different modified electrodes was in the following order: COF (−14.82 μA) < AgNPs-COF (−26.95 μA) < AuNPs-COF (−31.78 μA) < Au-AgNPs-COF (−46.15 μA). The Au-AgNPs-COF/GCE displayed an excellent electrocatalytic activity toward reduction of H2O2, over a dynamic range of 2.0 nM–1.0 mM with a limit of detection (LOD) of 0.44 nM (S/N = 3). Furthermore, the present sensor showed appreciable selectivity, stability, and reproducibility against the reduction of H2O2. Practicality was demonstrated in fetal bovine serum (FBS), cat blood serum (CBS), and living cells (RAW 264.7).
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