A bromine-catalysis-synthesized poly(3,4-ethylenedioxythiophene)/graphitic carbon nitride electrochemical sensor for
Wei Wu1,2, Ahmat Ali1,2, Ruxangul Jamal1,2
1Key Laboratory of Oil and Gas Fine Chemicals, Ministry of Education, Xinjiang Uygur Autonomous Region, Xinjiang University Urumqi 830046 P. R. China tursunabdir@sina.com.cn jruxangul@sina.com.
Abstract:
In this paper, poly(3,4-ethylenedioxythiophene)/graphitic carbon nitride (PEDOT/g-C3N4) composites were prepared by the bromine catalysed polymerization (BCP) method with varying weight ratios of monomer to g-C3N4. For comparison, solid-state polymerization (SSP) and metal oxidative polymerization (MOP) methods were also used for the synthesis of PEDOT/g-C3N4 composites. Electrochemical determination of heavy metal ions (Cd2+ and Pb2+) was carried out by differential pulse voltammetry (DPV) on composite-modified glass carbon electrodes (GCEs), which were prepared by different methods. The obtained composites were analysed by Fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible absorption spectroscopy (UV-vis), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The results showed that the bromine catalysed polymerization (BCP) method is an effective way to prepare the PEDOT/g-C3N4 composite, and the combination of PEDOT with g-C3N4 can improve the electrochemical activity of electrode materials. And, the composite from the BCP method modified electrode (PEDOT/10 wt% g-C3N4/GCE) exhibited the widest linear responses for Cd2+ and Pb2+, ranging from 0.06-12 μM and 0.04-11.6 μM with detection limits (S/N = 3) of 0.0014 μM and 0.00421 μM, respectively.
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