催化作用
Atom(片上系统)
电化学
纳米材料基催化剂
材料科学
纳米颗粒
选择性
金属
检出限
纳米技术
氧化物
光化学
化学
电极
物理化学
嵌入式系统
冶金
生物化学
色谱法
计算机科学
作者
Jiening Wu,Yalin Wu,Liping Lü,Dongtang Zhang,Xiayan Wang
出处
期刊:Talanta open
[Elsevier BV]
日期:2021-11-20
卷期号:4: 100075-100075
被引量:28
标识
DOI:10.1016/j.talo.2021.100075
摘要
Owing to the maximum utilization efficiency of the metal atoms, single-atom catalysts (SACs), which have higher catalytic activity and selectivity than traditional nanocatalysts, have been used as sensing materials for signal amplification and sensitive detection of biomolecules. Recently, single-atom Au catalysts have attracted attention. Au nanoparticles have high catalytic activity, and the loading efficiency on the support can be further increased by downsizing Au nanoparticles to single atoms. Compared with other oxide supports, the higher density of vacancies on the CeO 2 surface can accommodate more Au atoms, and thereby CeO 2 can stabilize more metal atoms. In this paper, we describe an electrochemical sensor based on Au–CeO 2 nanocomposites for ultrasensitive and highly selective detection of H 2 O 2 released from A549 cells by immobilizing single-atom Au on specific facets of CeO 2 . Due to the abundant oxygen vacancies on the surface and the strong interactive effect between Ce ions and Au atoms, this sensor displayed excellent electrochemical performance, with a detection limit of 1.4 nM. The synergistic effect of CeO 2 and Au atoms also resulted in high catalytic activity and stability. This study shows that the single-atom nanozyme sensing strategy can be applied to the sensitive detection of reactive oxygen species. Thus, single-atom sensors have broad application prospects in clinical analysis and physiology.
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