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Improving the voltammetric determination of Hg(II): a comparison between ligand-modified glassy carbon and electrochemically reduced graphene oxide electrodes
Date issued
2020-11
Author(s)
DOI
10.3390/s20236799
Abstract
A new thiosemicarbazone ligand was immobilized through a Cu(I)-catalyzed click reaction
on the surface of glassy carbon (GC) and electrochemically reduced graphene oxide (GC-ERGO)
electrodes grafted with phenylethynyl groups. Using the accumulation at open circuit followed by
anodic stripping voltammetry, the modified electrodes showed a significant selectivity and sensibility
for Hg(II) ions. A detection limit of 7 nM was achieved with the GC modified electrodes. Remarkably,
GC-ERGO modified electrodes showed a significantly improved detection limit (0.8 nM), sensitivity,
and linear range, which we attribute to an increased number of surface binding sites and better
electron transfer properties. Both GC and GC-ERGO modified electrodes proved their applicability
for the analysis of real water samples.
on the surface of glassy carbon (GC) and electrochemically reduced graphene oxide (GC-ERGO)
electrodes grafted with phenylethynyl groups. Using the accumulation at open circuit followed by
anodic stripping voltammetry, the modified electrodes showed a significant selectivity and sensibility
for Hg(II) ions. A detection limit of 7 nM was achieved with the GC modified electrodes. Remarkably,
GC-ERGO modified electrodes showed a significantly improved detection limit (0.8 nM), sensitivity,
and linear range, which we attribute to an increased number of surface binding sites and better
electron transfer properties. Both GC and GC-ERGO modified electrodes proved their applicability
for the analysis of real water samples.
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