Issue 15, 2014

A highly-sensitive electrochemical sensor for the simultaneous detection of Cd2+ and Pb2+ using liquid phase-exfoliated graphene

Abstract

It is quite important to develop sensitive and simple analytical methods for the detection of toxic heavy metal ions, such as Cd2+ and Pb2+. Herein, liquid phase-exfoliated graphene nanosheets were easily prepared through a one-step exfoliation of graphite powder in N-methyl-2-pyrrolidone. The obtained graphene suspension was directly used to modify the surface of a glassy carbon electrode (GCE), constructing a novel and highly-sensitive electrochemical sensor for Cd2+ and Pb2+. Compared with an unmodified GCE, and a reduced graphene oxide-modified GCE, the resulting liquid phase-exfoliated graphene-modified GCE significantly increased the response signals towards Cd2+ and Pb2+, showing remarkable signal amplification effects. The use of this defect-abundant, few-layered graphene sample, with small lateral flake sizes, has led to the beneficial responses observed. The influences of the supporting electrolyte, volume of the graphene suspension, deposition potential and accumulation time were examined. As a result, a sensitive, rapid and convenient electrochemical method was developed for the simultaneous detection of Cd2+ and Pb2+. The detection limits were estimated to be 1.08 μg L−1 and 1.82 μg L−1 for Cd2+ and Pb2+. This new sensor was used in water sample analysis, and the results were consistent with the values obtained by inductively coupled plasma-atomic emission spectroscopy.

Graphical abstract: A highly-sensitive electrochemical sensor for the simultaneous detection of Cd2+ and Pb2+ using liquid phase-exfoliated graphene

Article information

Article type
Paper
Submitted
19 Feb 2014
Accepted
25 Apr 2014
First published
28 Apr 2014

Anal. Methods, 2014,6, 5760-5765

Author version available

A highly-sensitive electrochemical sensor for the simultaneous detection of Cd2+ and Pb2+ using liquid phase-exfoliated graphene

G. Liu, J. Chen, X. Hou and W. Huang, Anal. Methods, 2014, 6, 5760 DOI: 10.1039/C4AY00405A

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