Enhanced Electrochemical Detection of Lead Ions Using Schiff Base/MoS <sub>2</sub> Modified Screen-Printed Electrodes

Environmental contamination by heavy metals (HMs) remains a critical concern; among them, Pb<sup>2+</sup> is distinguished by its toxicity, bioaccumulation, and persistence. Here, we present disposable, noble-metal-free screen-printed carbon electrodes (SPCEs) functionalized with MoS<sub>2</sub> nanosheets covalently conjugated to newly synthesized Schiff bases (SB1, SB2) via a monochloroacetic-acid linker, affording a chemically defined MoS<sub>2</sub>-SB interface for enhanced Pb<sup>2+</sup> sensing in water. Using square-wave anodic stripping voltammetry (SWASV) under optimized conditions in PBS (pH 4.0), the MoS<sub>2</sub>@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<sup>-1</sup> cm<sup>-2</sup>, a limit of detection of 0.267 μM, and a primary linear range of 1-5 μM for Pb<sup>2+</sup>. This covalent interfacial design couples the high surface area and conductivity of MoS<sub>2</sub> 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.

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Publication Details

Journal
ACS Omega
Published
2025-11-11
DOI
https://doi.org/10.1021/acsomega.5c07147
Primary Topic
Electrochemical Analysis and Applications
Type
article
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article

Enhanced Electrochemical Detection of Lead Ions Using Schiff Base/MoS 2 Modified Screen-Printed Electrodes

Dario Morganti, Consuelo Celesti, Daniela Iannazzo, Khouloud Abid et al.
ACS Omega
Electrochemical Analysis and Applications
article

Enhanced Electrochemical Detection of Lead Ions Using Schiff Base/MoS 2 Modified Screen-Printed Electrodes

Dario Morganti, Consuelo Celesti, Daniela Iannazzo, Khouloud Abid, G. Neri, Sebastiano Vasi, Zahra Akbari, Federica Bucolo, Salvatore V. Giofrè
article en

Abstract

Environmental contamination by heavy metals (HMs) remains a critical concern; among them, Pb<sup>2+</sup> is distinguished by its toxicity, bioaccumulation, and persistence. Here, we present disposable, noble-metal-free screen-printed carbon electrodes (SPCEs) functionalized with MoS<sub>2</sub> nanosheets covalently conjugated to newly synthesized Schiff bases (SB1, SB2) via a monochloroacetic-acid linker, affording a chemically defined MoS<sub>2</sub>-SB interface for enhanced Pb<sup>2+</sup> sensing in water. Using square-wave anodic stripping voltammetry (SWASV) under optimized conditions in PBS (pH 4.0), the MoS<sub>2</sub>@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<sup>-1</sup> cm<sup>-2</sup>, a limit of detection of 0.267 μM, and a primary linear range of 1-5 μM for Pb<sup>2+</sup>. This covalent interfacial design couples the high surface area and conductivity of MoS<sub>2</sub> 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.

ACS OmegaVol. 10(48)
University of Messina (IT), Ospedale Santa Chiara (IT), Magneto-Inertial Fusion Technologies (United States) (US), Institute for Advanced Energy Technologies (IT), Institute for Chemical and Physical Processes (IT), Institute for Microelectronics and Microsystems (IT)
Openalex Percentile: Top 63%
Electrochemical Analysis and Applications
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