抗坏血酸
电化学
催化作用
化学
基质(水族馆)
选择性
密度泛函理论
贵金属
限制
无机化学
电极
物理化学
计算化学
食品科学
工程类
机械工程
生物化学
海洋学
地质学
作者
Fuguo Ge,Yujian Sun,Kai Wang,Guijun Ma,Fengxia Li,Qiang Bai,Yun Liu,Ning Sui
标识
DOI:10.1016/j.microc.2024.110745
摘要
The low activity of nanozymes poses a significant scientific challenge, limiting their application. Developing noble metal-based nanozymes with high activity is considered as an effective strategy to address this issue. In this study, core–shell Au@PdNi was synthesized by co-precipitating Pd2+ and Ni2+ on Au cores. The oxidase (OXD)-like property of Au@PdNi was thoroughly investigated, revealing a specific activity reaching 194.2 U mg−1. The high OXD-like activity was attributed to several factors elucidated through experimental analysis and Density Functional Theory (DFT) calculations. Firstly, the core–shell structure of Au@PdNi provides a substantial surface area for catalytic reactions. Secondly, the presence of nickel enhances the current density of the material, augmenting its catalytic activity. Lastly, the electronic interplay between the Au core and the PdNi shell layer improves the binding and reaction kinetics with the target substrate. The Au@PdNi nanozyme demonstrated remarkable performances in colorimetric and electrochemical detection of ascorbic acid (AA), exhibiting high sensitivity and selectivity. Moreover, a portable electrochemical sensor was fabricated for the determination of AA in spiked fruit samples, demonstrating satisfactory recovery rates in real sample analysis.
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