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Synthesis of nickel oxides nanoparticles on glassy carbon as an electron transfer facilitator for horseradish peroxidase: Direct electron transfer and H_2O_2 determination

机译:玻碳上的氧化镍纳米粒子作为辣根过氧化物酶的电子转移促进剂的合成:直接电子转移和H_2O_2的测定

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摘要

In this study, horseradish peroxidaseickel oxides nanoparticles/glassy carbon (HRP/NiO NPs/GC) electrode was prepared by first applying nickel oxides nanoparticles on glassy carbon surface and then horseradish peroxidase immobilized on the NiO NPs. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) have been used as a diagnostic tools to identify the synthesized NiO NPs. Immobilized HRP showed an electrochemical redox behavior pertained to HRP(Fe(III)-Fe(II)) by direct electron transfer between protein and nanoparticles with a formal potential (E~0) of - 55.5 mV (vs. Ag/AgCl and 141.5 mV vs. NHE) in 50 mM phosphate buffer solution (PBS). The anodic charge transfer coefficient (α) and heterogeneous electron transfer rate constant (k_s) were 0.42 and 0.75 s~(-1), respectively. Biocatalytic activity of HRP/NiO NPs/GC electrode for reduction of hydrogen peroxide and application to hydrogen peroxide determination was exemplified.
机译:在这项研究中,辣根过氧化物酶/氧化镍纳米粒子/玻璃碳(HRP / NiO NPs / GC)电极的制备方法是先将氧化镍纳米粒子涂在玻璃碳表面,然后将辣根过氧化物酶固定在NiO NPs上。扫描电子显微镜(SEM)和原子力显微镜(AFM)已被用作诊断工具,以识别合成的NiO NP。固定化的HRP通过蛋白质与具有55.5 mV的形式势(E〜0)(相对于Ag / AgCl和141.5的形式电位)的纳米粒子之间的直接电子转移显示了与HRP(Fe(III)-Fe(II))有关的电化学氧化还原行为50 mM磷酸盐缓冲溶液(PBS)中的mV对NHE)。阳极电荷转移系数(α)和异质电子转移速率常数(k_s)分别为0.42和0.75 s〜(-1)。举例说明了HRP / NiO NPs / GC电极对过氧化氢还原的生物催化活性及其在过氧化氢测定中的应用。

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