MoN Nanorod/Sulfur-Doped Graphitic Carbon Nitride for Electrochemical Determination of Chloramphenicol

被引:86
作者
Jaysiva, Ganesamurthi [1 ]
Manavalan, Shaktivel [1 ]
Chen, Shen-Ming [1 ]
Veerakumar, Pitchaimani [2 ,3 ]
Keerthi, Murugan [1 ]
Tu, Huang-Shen [1 ]
机构
[1] Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei 10608, Taiwan
[2] Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan
[3] Acad Sinica, Inst Atom & Mol Sci, Taipei 10617, Taiwan
关键词
molybdenum nitride; graphitic carbon nitride; chloramphenicol; glassy carbon electrode; cyclic voltammetry; TRANSITION-METAL NITRIDES; HYDROGEN EVOLUTION; LIQUID-CHROMATOGRAPHY; SILVER NANOPARTICLES; ELECTRODE MATERIALS; ASSISTED SYNTHESIS; SENSOR; GRAPHENE; NANOSHEETS; EFFICIENT;
D O I
10.1021/acssuschemeng.0c00502
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the present work, we report a one-step pyrolysis synthesis of molybdenum nitride nanorods (MoN NRs) using ammonium heptamolybdate tetrahydrate as a precursor. Properties of MoN NRs have been improved by the sulfur-doped graphitic carbon nitride (MoN(@-GCN) nanocomposite, which has been used to modify the glassy carbon electrode (GCE) for the electrochemical determination of chloramphenicol (CAP). The large surface area of S-GCN-anchored MoN NRs in the nanocomposite demonstrates a synergistic effect of the transport of a kinetic barrier electron and a well-defined redox cycle within the ferricyanide system. In the electrochemical determination of CAP over MoN@S-GCN/GCE, cyclic voltammetry (CV) showed a superior electrochemical response to the CAP concentration, while bare GCE and other modified GCEs showed an inferior electrochemical response. In addition, different concentrations, scanning rates, and pH electrolyte tests have been performed for MoNgS-GCN/GCE, which verified that it is an appropriate candidate for electrochemical detection of CAP. Differential pulse voltammetry (DPV) in the electrochemical determination of CAP exhibits a low detection limit of 6.9 nM and a sensitivity of 1.0557 mu M mu A(-1) cm(-2) for the current response, yielding a linear increase with increasing concentration of CAP from 0.5 to 2450 mu M. Moreover, the proposed sensor shows appreciable selectivity and satisfactory recovery for real samples of milk and eye drop solutions.
引用
收藏
页码:11088 / 11098
页数:11
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