期刊
IEEE SENSORS JOURNAL
卷 22, 期 15, 页码 14952-14958出版社
IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/JSEN.2022.3184509
关键词
Tungsten diselenide; carbon black; sensor; dopamine; ascorbic acid; uric acid
资金
- Scientific and Technology Research Council of Turkey (TUBITAK)
In this study, a nanocomposite of two-dimensional WSe2 nanosheets with carbon black was prepared and used for electrode modification for the simultaneous electrochemical detection of AA, DA, and UA. The modified electrode exhibited enhanced electrocatalytic properties, wide linear ranges, and low detection limits for the target analytes. Additionally, it demonstrated high reproducibility and stability.
The developmentof sensitive and selective electrodes for electrochemical detection of ascorbic acid (AA), dopamine (DA) and uric acid (UA) is essential for early diagnosis and effective treatment. In this work, a nanocomposite of two-dimensional WSe2 nanosheets with carbon black (WSe2@C) was prepared by facile hydrothermal method and used to modify a glassy carbon electrode (GCE) to fabricate an electrochemical sensing platform for simultaneous determination of AA, DA and UA. The as- prepared nanocomposite was characterized in terms of structural and morphological analyses through X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The electrochemical and electrocatalytic behaviors of the modified electrode (GCE-WSe2@C) were investigated using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques. The sensing performance of GCE-WSe2@Celectrodewas tested againstAA, DAandUA, resulting in enhanced electrocatalytic properties compared to GCE-WSe2 and GCE-C electrodes. The GCE-WSe2@C electrode displayed wide linear ranges of 8.0 - 2456 mu M for AA, 1.0 - 49.0 & 72.8 - 381.4 mu M for DA and 1.0 - 24.8 & 36.9 - 185.2 mu M for UA with low detection limits of 3.2, 0.18 and 0.42 mu M, respectively. In addition, the developed electrode demonstrated high reproducibility and stability for electrochemical detection of AA, DA and UA.
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