生物分子
二硫化钼
堆积
材料科学
电化学
检出限
催化作用
电化学气体传感器
钼
选择性
纳米技术
电极
化学工程
化学
有机化学
物理化学
色谱法
工程类
冶金
作者
Aili Zhao,Min Cui,Jingui Wang,Shuai Wang,Yanli Zhao
出处
期刊:Small
[Wiley]
日期:2025-07-26
卷期号:: e04866-e04866
标识
DOI:10.1002/smll.202504866
摘要
Electroactive biomolecules, dopamine (DA) and uric acid (UA), as important biomarkers, often coexist in biological matrices. Due to their similar oxidation potentials, designing electrooxidation catalysts to efficiently detect and distinguish them and establishing structure-activity relationships remain a great bottleneck in the field of electrochemical sensing. Herein, an electrochemical sensor is designed by leveraging molybdenum disulfide nanoflowers embedded within 3D nitrogen-doped porous carbon networks (MoS2@N-3DPC) for sensitive detection and discrimination of DA and UA. In constructing a heterogeneous interface between MoS2 nanoflowers and N-3DPC, the incorporation of N-3DPC not only addresses the stacking issue but also markedly enhances the electrical conductivity. Moreover, the synthesis of petal-like MoS2 shortens the electron and ion transfer pathways. The strong interfacial interaction between N-3DPC and MoS2 effectively enhances the electrocatalytic performance of MoS2@N-3DPC, as demonstrated by electrochemical analysis. The sensor demonstrates wide linear detection ranges (from 0.01 to 989.95 µm for DA and from 0.6 to 1063.4 µm for UA), low limits of detection for DA (3.0 nm) and UA (200.0 nm), as well as high selectivity and stability. Furthermore, such a sensor can be applied to the detection of DA and UA in real biological serum samples, with the results highly correlated with the spectrophotometric method.
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