Abstract
Considering the formidable explosive power and human carcinogenicity of nitroaromatic explosives, the implementation of an accurate and sensitive detection technology is imperative for ensuring public safety and monitoring post-blast environmental contamination. In the present work, a versatile and selective electrochemical sensor based on dummy molecularly imprinted poly (3,4-ethylenedioxythiophene)/laser-induced graphene (MIPEDOT/LIG) was successfully developed and the specific detection of multiple nitroaromatic explosives was realized in the single sensor. The accessible and nontoxic trimesic acid (TMA) and superior 3, 4-ethylenedioxythiophene (EDOT) were selected as the dummy-template and the functional monomer, respectively. The interaction between the functional monomer and the template, and the morphology, electrochemical properties and detection performance of the sensor were comprehensively investigated by ultraviolet–visible spectroscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy, cyclic voltammetry, and differential pulse voltammetry. Benefiting from the alliance of TMA and EDOT, the MIPEDOT/LIG sensor manifested outstanding selectivity and sensitivity for 2,4,6-trinitrotolueen (TNT), 2,4,6-trinitrophenol (TNP), 2,4-dinitrotoluene (DNT), 1,3,5-trinitrobenzene (TNB), 2,4-dinitrophenol (DNP), and 1,3-dinitrobenzene (DNB) (representative nitroaromatic explosives) with limits of determination of 1.95 ppb, 3.06 ppb, 2.49 ppb, 1.67 ppb, 1.94 ppb, and 4.56 ppb, respectively. The sensor also exhibited extraordinary reliability and convenience for environmental sample detection. Therefore, a perfect combination of versatility and selectivity in the MIPEDOT/LIG sensor was achieved. The findings of this work provide a new direction for the development of multi-target electrochemical sensors using a versatile dummy template for explosives detection.
Published Version
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