Novel electrochemical sensing platform based on molybdenum disulfide nanosheets-polyaniline composites and Au nanoparticles

被引:114
作者
Huang, Ke-Jing [1 ]
Zhang, Ji-Zong [1 ]
Liu, Yu-Jie [1 ]
Wang, Ling-Ling [1 ]
机构
[1] Xinyang Normal Univ, Coll Chem & Chem Engn, Xinyang 464000, Peoples R China
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2014年 / 194卷
基金
中国国家自然科学基金;
关键词
Graphene-like molybdenum disulfide-polyaniline composites; Au nanoparticles; Electrochemical sensor; Dopamine; GOLD NANOPARTICLES; ELECTRODE MATERIAL; GRAPHENE ANALOG; ASCORBIC-ACID; DOPAMINE; MOS2; SEROTONIN; SENSOR; NANOCOMPOSITE; GENE;
D O I
10.1016/j.snb.2013.12.106
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Two-dimensional (2D) transition metal dichalcogenide nanosheets offer unique electronic properties and attract increasing attention in electrochemical sensing. In this paper, graphene-like MoS2-polyaniline (PANI) composites were synthesized by a facile hydrothermal method and a simple in situ polymerization procedure. MoS2 served as a 2D conductive skeleton that supported a highly electrolytic accessible surface area of redox-active PANI and provided a direct path for electrons. A novel electrochemical sensor was subsequently developed for the determination of dopamine based on MoS2-PANI composites and gold nanoparticles (AuNPs) modified glassy carbon electrode (AuNPs/MoS2-PANI/GCE). The AuNPs/MoS2-PANI/GCE showed an enhanced electrocatalytic activity toward the oxidation of dopamine when compared with bare electrode and other modified electrode. It exhibited a good electrocatalytic oxidation toward dopamine in the linear response range from 1 to 500 mu M with the detection limit of 0.1 mu M (S/N = 3). The developed electrochemical sensor was successfully applied to the dopamine detection in human urine sample, which proved that it was a versatile sensing tool for the detection of DA in real samples. This work indicated that MoS2-PANI composites were promising in electrochemical sensing and catalytic applications. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:303 / 310
页数:8
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