过氧化氢
催化作用
检出限
材料科学
兴奋剂
基质(水族馆)
循环伏安法
电化学
电极
纳米技术
无机化学
分析化学(期刊)
化学
化学工程
光电子学
色谱法
物理化学
有机化学
工程类
地质学
海洋学
生物化学
作者
Beibei Zhu,Dong An,Zhaoshun Bi,Wen Liu,Wei Shan,Yonghai Li,Guohui Nie,Ni Xie,Omar A. Al‐Hartomy,Ahmed A. Al‐Ghamdi,S. Wageh,Wen Chen,Xichang Bao,Xiang Gao,Han Zhang,Meng Qiu
标识
DOI:10.1002/celc.202200050
摘要
Abstract Silver nanoparticles (AgNPs)‐based nanozyme sensors are gaining attention for rapid on‐site H 2 O 2 detection, which is beneficial to disease diagnosis and environmental monitoring. However, the severe agglomeration of AgNPs on the electrodes significantly reduced electrochemical catalytic activity. In this work, we fabricated N‐doped Ti 3 C 2 MXene (named Ag/N−Ti 3 C 2 ) deposited with three‐dimensional flower‐like AgNPs to achieve ultrasensitive H 2 O 2 detection. N doping strategy is employed to improve the conductivity of MXene, and the corresponding catalytic activity of Ag/N−Ti 3 C 2 is enhanced by optimizing the growth process and morphology. The Ag/N−Ti 3 C 2 /glassy carbon electrode (Ag/N‐Ti 3 C 2 /GCE) sensor exhibited a wide H 2 O 2 detection range (0.05–35 mM), a low limit detection (1.53 μM), and 3.1 % relative standard deviation in 50 repeated cyclic voltammetry measurements. The results above indicate that catalytic activity of metal nanozymes could be influenced by the substrate and both materials jointly determine the sensor's performance. As a result, N‐doped MXene is an attractive candidate for biological sensing and other electrocatalytic applications.
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