Environmental contamination by heavy metals (HMs) remains a critical concern; among them, Pb2+ is distinguished by its toxicity, bioaccumulation, and persistence. Here, we present disposable, noble-metal-free screen-printed carbon electrodes (SPCEs) functionalized with MoS2 nanosheets covalently conjugated to newly synthesized Schiff bases (SB1, SB2) via a monochloroacetic-acid linker, affording a chemically defined MoS2–SB interface for enhanced Pb2+ sensing in water. Using square-wave anodic stripping voltammetry (SWASV) under optimized conditions in PBS (pH 4.0), the MoS2@SB2/SPCE exhibits markedly higher currents than both bare and other modified electrodes. The sensor achieves an area-normalized sensitivity of 220.344 μA μM–1 cm–2, a limit of detection of 0.267 μM, and a primary linear range of 1–5 μM for Pb2+. This covalent interfacial design couples the high surface area and conductivity of MoS2 with SB2 driven chelation, yielding good selectivity, device-to-device reproducibility, and reliable performance in tap water samples. Our results outline a viable path for the low-cost and on-site monitoring of lead ions in complex water matrices.

Enhanced Electrochemical Detection of Lead Ions Using Schiff Base/MoS2 Modified Screen-Printed Electrodes

Iannazzo, Daniela
Primo
;
Celesti, Consuelo
;
Bucolo, Federica
;
Giofre', Salvatore V.;Vasi, Sebastiano;Morganti, Dario;Abid, Khouloud
Penultimo
;
Neri, Giovanni
Ultimo
2025-01-01

Abstract

Environmental contamination by heavy metals (HMs) remains a critical concern; among them, Pb2+ is distinguished by its toxicity, bioaccumulation, and persistence. Here, we present disposable, noble-metal-free screen-printed carbon electrodes (SPCEs) functionalized with MoS2 nanosheets covalently conjugated to newly synthesized Schiff bases (SB1, SB2) via a monochloroacetic-acid linker, affording a chemically defined MoS2–SB interface for enhanced Pb2+ sensing in water. Using square-wave anodic stripping voltammetry (SWASV) under optimized conditions in PBS (pH 4.0), the MoS2@SB2/SPCE exhibits markedly higher currents than both bare and other modified electrodes. The sensor achieves an area-normalized sensitivity of 220.344 μA μM–1 cm–2, a limit of detection of 0.267 μM, and a primary linear range of 1–5 μM for Pb2+. This covalent interfacial design couples the high surface area and conductivity of MoS2 with SB2 driven chelation, yielding good selectivity, device-to-device reproducibility, and reliable performance in tap water samples. Our results outline a viable path for the low-cost and on-site monitoring of lead ions in complex water matrices.
2025
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3343133
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