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Fabrication of two-dimensional chemically reduced graphene oxide nanosheets for the electrochemical determination of epinephrine
被引:0
|作者:
Susan Immanuel
R Sivasubramanian
机构:
[1] PSG College of Technology,Electrochemical Sensors and Energy Materials Laboratory, Department of Chemistry
[2] PSG Institute of Advanced Studies,Nanotech Research Innovation and Incubation Centre (NRIIC)
来源:
Bulletin of Materials Science
|
2020年
/
43卷
关键词:
Graphene;
epinephrine;
electrochemical sensor;
cyclic voltammetry;
differential pulse voltammetry;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
A simple and selective electrochemical sensor for the determination of epinephrine (EP) was developed using chemically reduced graphene oxide nanosheets (CRGO). The CRGO nanosheets were prepared using modified Hummer’s method and the material was characterized using transmission electron microscope (TEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) and UV–visible spectroscopy, respectively. The CRGO modified glassy carbon electrode (GCE) was employed for the electrochemical studies on EP using cyclic voltammetry (CV). The modified electrode showed significant catalytic activity compared to GO/GCE and bare GCE. The electron transfer kinetics revealed a two electron transfer for all the electrodes with CRGO/GCE exhibiting a high heterogeneous rate constant (0.127 s-1)\documentclass[12pt]{minimal}
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\begin{document}$$^{{-1}})$$\end{document}. The detection was carried out using differential pulse voltammetry (DPV) through reduction of epinephrine chrome to leucoepinephrine chrome. The detection through the electrochemical reduction avoids the interference of similar analytes and improves the selectivity of the sensor. The detection limit was found to be 1.6 μ\documentclass[12pt]{minimal}
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\begin{document}$$\upmu $$\end{document}M with two different linear ranges viz. 10–300 and 400–1300 μ\documentclass[12pt]{minimal}
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\begin{document}$$\upmu $$\end{document}M. Further, the electrode was subjected to stability, reproducibility and interference studies. The reliability of the proposed sensor was tested in the presence of biological serum samples.
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