Abstract

Heteroatom doped mesoporous carbon materials are promising catalysts for the electrochemical sensing application. Herein, we report highly efficient dual heteroatom-doped hexagonal mesoporous carbon (MC) derived from Santa Barbara Amorphous-15 (SBA-15) hard template for the detection of phenolic isomers. The synthesis involves dopamine hydrochloride (DA)/thiophene complex, which helps to attain perfectly retained N and S dual doped mesoporous carbon (NS-MC) framework. NS-MC exhibits higher surface area (951 m2 g−1) as well as higher pore volume (0.12 cm3 g−1) with huge graphitic, pyridinic and thiophenic defective sites which facilitates the well-resolved simultaneous electrochemical detection of phenolic isomers hydroquinone (HQ) and catechol (CC). Our results demonstrate that as-synthesized NS-MC material had a LOD of 0.63 μM and 0.29 μM for HQ and CC, respectively. From the calibration curve, sensitivities of proposed sensor were found to be 9.44, 2.71 μA μM−1 cm−2 and 20.80, 10.02 μA μM−1 cm−2 for HQ and CC, respectively with good linear ranges of 10–45 μM and 45–115 μM for HQ; 2–16 μM and 16–40 μM for CC. The NS-MC modified electrode exhibited good selectivity over various possible interferences. The present investigation reveals that the proposed NS-MC material is a promising metal-free catalyst which boosted to electrochemically detect both HQ and CC, present in the municipal tap as well as natural river stream water samples.

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