期刊
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY
卷 253, 期 -, 页码 -出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ecoenv.2023.114694
关键词
Electrochemical sensing; Transition metal carbides; Electrocatalyst; Nanosensor; Real samples
In this study, a simple synthesis method was designed to prepare an electrochemical sensor based on sulfur-doped graphitic carbon nitride supported transition metal carbide interface. The synthesized Mo2C/SCN nanocatalyst was characterized using X-ray diffraction and scanning electron microscopy, showing its suitability for nano-molar electrochemical sensor applications. The modified glassy carbon electrode with Mo2C/SCN exhibited simultaneous and interference-free detection of uric acid and folic acid with good detection limits.
Till to date, the application of sulfur-doped graphitic carbon nitride supported transition metal carbide interface for electrochemical sensor fabrication was less explored. In this work, we designed a simple synthesis of mo-lybdenum carbide sphere embedded sulfur doped graphitic carbon nitride (Mo2C/SCN) catalyst for the nano -molar electrochemical sensor application. The synthesized Mo2C/SCN nanocatalyst was systematically characterized using X-ray diffraction (XRD) and scanning electron microscopy (SEM) with elemental mapping. The SEM images show that the porous SCN network adhered uniformly on Mo2C, causing a loss of crystallinity in the diffractogram. The corresponding elemental mapping of Mo2C/SCN shows distinct peaks for carbon (41.47%), nitrogen (32.54%), sulfur (1.37%), and molybdenum (24.62%) with no additional impurity peaks, reflecting the successful synthesis. Later, the glassy carbon electrode (GCE) was modified by Mo2C/SCN nano -catalyst for simultaneous sensing of uric acid (UA) and folic acid (FA). The fabricated Mo2C/SCN/GCE is capable of simultaneous and interference free electrochemical detection of UA and FA in a binary mixture. The limit of detection (LOD) calculated at Mo2C/SCN/GCE for UA and FA was 21.5 nM (0.09 - 47.0 mu M) and 14.7 nM (0.09 - 167.25 mu M) respectively by differential pulse voltammetric (DPV) technique. The presence of interferons has no significant effect on the sensor's performance, making it suitable for real sample analysis. The present method can be extended to fabricate an electrochemical sensor for various molecules.
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