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  • 标题:Fabrication of 2D-MoSe 2 incorporated NiO Nanorods modified electrode for selective detection of glucose in serum samples
  • 本地全文:下载
  • 作者:Gayathri Jeevanandham ; Kumaran Vediappan ; Zeid A. ALOthman
  • 期刊名称:Scientific Reports
  • 电子版ISSN:2045-2322
  • 出版年度:2021
  • 卷号:11
  • DOI:10.1038/s41598-021-92620-2
  • 语种:English
  • 出版社:Springer Nature
  • 摘要:Layered molybdenum diselenide (MoSe 2) nanosheets were formed by the weak Van der Waals forces of attraction between Se and Mo atoms. MoSe 2 has a larger space between the adjacent layers and smaller band gaps in the range of 0.85 to ~ 1.6 eV. In this study, MoSe 2 nanosheets decorated nickel oxide (NiO) nanorods have been synthesized by hydrothermal method using sodium molybdate and selenium metal powder. NiO/MoSe 2 composite formation was confirmed by powder X-ray diffraction analysis. In addition, the presence of MoSe 2 nanosheets on NiO nanorods were confirmed by field emission scanning electron microscopy, high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy. The Nyquist plots of NiO/MoSe 2 coated glassy carbon electrode (GCE) was indicated that it had lower charge transfer resistance compared to NiO/GCE and MoSe 2/GCE. Furthermore, as-prepared NiO/MoSe 2/GCE was used to detect glucose in alkaline solution by cyclic voltammetry and amperometry techniques. The NiO/MoSe 2/GCE was exhibited a linear response for the oxidation of glucose from 50 µM to 15.5 mM (R 2  = 0.9842) at 0.5 V by amperometry. The sensor response time and the limit of detection were found to be 2 s and 0.6 µM for glucose. Moreover, selectivity of the NiO/MoSe 2 sensor was tested in the presence of common interferent molecules such as hydrogen peroxide, fructose, lactose, ascorbic acid, uric acid, and dopamine. It was found that NiO/MoSe 2/GCE did not respond to these interfering biomolecules. In addition, NiO/MoSe 2/GCE had shown high stability, reproducibility and repeatability. Finally, the practical application of the sensor was demonstrated by detecting glucose in human blood serum with the acceptable recovery.
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