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One-pot synthesis of poly (3,4-ethylenedioxythiophene)-Pt nanoparticle composite and its application to electrochemical H(2)O(2) sensor

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 (H(2)O(2)) was investigated. Under UV irradiation, the rates of the oxidative polymerization of EDOT mono...

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Detalles Bibliográficos
Autores principales: Chang, Li-Chi, Wu, Huan-Nung, Lin, Chia-Yu, Lai, Yi-Hsuan, Hu, Chih-Wei, Ho, Kuo-Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475046/
https://www.ncbi.nlm.nih.gov/pubmed/22716478
http://dx.doi.org/10.1186/1556-276X-7-319
Descripción
Sumario: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 (H(2)O(2)) was investigated. Under UV irradiation, the rates of the oxidative polymerization of EDOT monomer along with the reduction of Pt(4+) 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 H(2)O(2) as compared to that without PtNPs, i.e., only with a layer of PEDOT. Amperometric determination of H(2)O(2) 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 mM, with a response time (steady state, t(95)) 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.