4.6 Article

Green reduction and uniform assembly of silver nanoparticles on polydopamine functionalized sulfur-doped graphitic carbon nitride nanosheets for highly sensitive H2O2 detection via nonenzymatic approach

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DOI: 10.1016/j.colsurfa.2023.132383

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Pyrolysis; Polydopamine; Nanocomposite; Electrochemical sensors; Hydrogen peroxide

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In this study, a novel enzyme-free hydrogen peroxide sensor electrode based on silver nanoparticles decorated polydopamine/sulfur-doped graphitic carbon nano-composite was developed. The sensor exhibited outstanding sensing ability with rapid response, high sensitivity, wide detection range, and low limit of detection. The practicality of the sensor was confirmed through testing commercial milk and mouthwash samples.
In this study, we demonstrate a new strategy to fabricate an enzyme-free hydrogen peroxide (H2O2) sensor electrode based on silver nanoparticles (AgNPs) decorated polydopamine/sulfur-doped graphitic carbon nano-composite (denoted as AgNPs@PDA/S-g-C3N4). The S-g-C3N4 nanosheets are derived from the pyrolysis of tri-thiocyanouric acid, followed by thermal exfoliation. A mussel-inspired PDA nanolayer enhances the solubility and high dispersion of S-g-C3N4 nanosheets and AgNPs in aqueous phase synthesis. The amine and catecholic functional groups of PDA are the major nucleation sites for Ag+ ions adsorption and ascorbic acid was further used as a green reducing agent for the growth of AgNPs. PDA adhesion layer can effectively connect the AgNPs and S-g-C3N4 nanosheets via electrostatic interaction to increase the stability and biocompatibility of the ternary composite structure. Various spectroscopy and microscopy techniques confirmed the formation of AgNPs@PDA/ S-g-C3N4 nanocomposite. Our AgNPs@PDA/S-g-C3N4 nanocomposite fabricated disposable sensor exhibited outstanding sensing ability to H2O2 reduction at-0.65 V (vs. Ag/AgCl), which is confirmed through an amperometric detection method. The sensor exhibits rapid response (2 s) to H2O2 sensing with high sensitivity (1020 mu A mM-1 cm-2), wide detection range (0.002-23 mM) and low limit of detection of 0.086 mu M. The practicality of the H2O2 sensor was evaluated with commercial milk and mouthwash samples, which retained satisfactory recoveries. Thus, our results indicate that the PDA functionalization not only enhances the S-g-C3N4 solubility but also increases the interfacial charge transport in AgNPs@PDA/S-g-C3N4 nanocomposite material which develops a potential sensing method for nonenzymatic H2O2 sensor. Due to the effective surface modification strategies, such as PDA nanocoating and AgNPs deposition, the exfoliated S-g-C3N4 nanosheets gained excellent electrochemical properties, facilitating potential candidates in electrochemical applications.

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