Electrochemical detection of nitrite based on glassy carbon electrode modified with gold-polyaniline-graphene nanocomposites
First, polyaniline-graphene oxide (GO-PANI) nanocomposites were prepared by the in situ polymerization of aniline in the presence of graphene oxide (GO). Next, the GO-PANI nanocomposites were reduced to polyaniline-graphene (G-PANI) nanocomposites by a green electrochemical reduction method. Finally...
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Published in | RSC advances Vol. 4; no. 11; pp. 57842 - 57849 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.01.2014
|
Subjects | |
Online Access | Get full text |
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Summary: | First, polyaniline-graphene oxide (GO-PANI) nanocomposites were prepared by the
in situ
polymerization of aniline in the presence of graphene oxide (GO). Next, the GO-PANI nanocomposites were reduced to polyaniline-graphene (G-PANI) nanocomposites by a green electrochemical reduction method. Finally, a thin layer of nearly monodispersed Au nanoparticles with a uniform size (∼12 nm) was coated on the surface of the G-PANI nanocomposites. Moreover, the as-prepared Au-polyaniline-graphene (Au-G-PANI) nanocomposites can be used as a sensing electrode material for the electrochemical detection of nitrite (NO
2
−
). Compared with other common modified electrodes, the Au-G-PANI/GCE shows an obvious oxidation peak of NO
2
−
with a larger peak current, and gives a wider linear range from 0.1 to 200 μmol L
−1
, with a detection limit of 0.01 μmol L
−1
(
S
/
N
= 3). Besides, the oxidation process of NO
2
−
on the Au-G-PANI/GCE is proven to be a surface-controlled process involving the transfer of two electrons. The present study widens the applications of graphene-based nanocomposite materials in the electrochemical detection of environmental pollutants.
This study reports possible interferences for the detection of NO
2
−
on a Au-G-PANI/GCE. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c4ra08543d |