TY - JOUR
T1 - One-pot synthesis of poly(3,4-Ethylenedioxythiophene)-Pt nanoparticle composite and its application to electrochemical H2o2 sensor
AU - Chang, Li Chi
AU - Wu, Huan Nung
AU - Lin, Chia Yu
AU - Lai, Yi Hsuan
AU - Hu, Chih Wei
AU - Ho, Kuo Chuan
N1 - Funding Information:
This work was sponsored by the National Research Council of Taiwan under grant number NSC 99-2221-E-002-183.
PY - 2012
Y1 - 2012
N2 - Poly(3,4-ethylenedioxythiophene)-Pt nanoparticle composite was synthesized in one-pot fashion using a photo-assisted chemical method, and its electrocatalytic properties toward hydrogen peroxide (H2O2) was investigated. Under UV irradiation, the rates of the oxidative polymerization of EDOT monomer along with the reduction of Pt4+ ions were accelerated. In addition, the morphology of PtNPs was also greatly influenced by the UV irradiation; the size of PtNPs was reduced under UV irradiation, which can be attributed to the faster nucleation rate. The immobilized PtNPs showed excellent electrocatalytic activities towards the electroreduction of hydrogen peroxide. The resultant amperometric sensor showed enhanced sensitivity for the detection of H2O2as compared to that without PtNPs, i.e., only with a layer of PEDOT. Amperometric determination of H2O2 at -0.55 V gave a limit of detection of 1.6 μM (S/N = 3) and a sensitivity of 19.29 mA cm-2 M-1 up to 6 μM, with a response time (steady state, t95) of 30 to 40 s. Energy dispersive X-ray analysis, transmission electron microscopic image, cyclic voltammetry (CV), and scanning electron microscopic images were utilized to characterize the modified electrode. Sensing properties of the modified electrode were studied both by CV and amperometric analysis.
AB - Poly(3,4-ethylenedioxythiophene)-Pt nanoparticle composite was synthesized in one-pot fashion using a photo-assisted chemical method, and its electrocatalytic properties toward hydrogen peroxide (H2O2) was investigated. Under UV irradiation, the rates of the oxidative polymerization of EDOT monomer along with the reduction of Pt4+ ions were accelerated. In addition, the morphology of PtNPs was also greatly influenced by the UV irradiation; the size of PtNPs was reduced under UV irradiation, which can be attributed to the faster nucleation rate. The immobilized PtNPs showed excellent electrocatalytic activities towards the electroreduction of hydrogen peroxide. The resultant amperometric sensor showed enhanced sensitivity for the detection of H2O2as compared to that without PtNPs, i.e., only with a layer of PEDOT. Amperometric determination of H2O2 at -0.55 V gave a limit of detection of 1.6 μM (S/N = 3) and a sensitivity of 19.29 mA cm-2 M-1 up to 6 μM, with a response time (steady state, t95) of 30 to 40 s. Energy dispersive X-ray analysis, transmission electron microscopic image, cyclic voltammetry (CV), and scanning electron microscopic images were utilized to characterize the modified electrode. Sensing properties of the modified electrode were studied both by CV and amperometric analysis.
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U2 - 10.1186/1556-276X-7-319
DO - 10.1186/1556-276X-7-319
M3 - Article
C2 - 22716478
AN - SCOPUS:84864011444
SN - 1931-7573
VL - 7
JO - Nanoscale Research Letters
JF - Nanoscale Research Letters
M1 - 319
ER -