Abstract
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 molybdenum carbide sphere embedded sulfur doped graphitic carbon nitride (Mo2C/SCN) catalyst for the nanomolar 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 nanocatalyst 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 μM) and 14.7 nM (0.09 – 167.25 μM) 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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•Electrochemical sensing interface based on sulfur-doped graphitic carbon nitride supported transition metal carbide.•Structural and morphological studies showed effective synthesis.•Simultaneous sensing and nanomolar detection of uric acid (UA) and folic acid (FA).•Limit of detection of 21.5 nM and 14.7 nM for UA and FA respectively by differential pulse voltammetric method.•Real time application to measure UA and FA in real samples of fruits and vegetables.