Spectroelectrochemical study of the electrosynthesis of Pt nanoparticles/poly(3,4-(ethylenedioxythiophene) composite

UV-Visible, NIR and Raman spectroelectrochemistry techniques have been used for the in-situ study of Pt nanoparticles (PtNPs) electrosynthesis on an electrochemically generated poly(3,4-ethylenedioxythiophene) film. Two electrochemical steps have been used to obtain in a reproducible way PtNPs with...

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Detalles Bibliográficos
Autores: Fernández Blanco, Ana Cristina, Ibáñez Martínez, David, Colina, Álvaro, Ruiz Fernández, Virginia, Heras, Aránzazu
Tipo de recurso: artículo
Estado:Versión enviada para evaluación y publicación
Fecha de publicación:2014
País:España
Institución:Universidad de Burgos (UBU)
Repositorio:Repositorio Institucional de la Universidad de Burgos (RIUBU)
OAI Identifier:oai:riubu.ubu.es:10259/3854
Acceso en línea:http://hdl.handle.net/10259/3854
Access Level:acceso abierto
Palabra clave:Conducting polymers
PEDOT
Platinum nanoparticles
Electrochemistry
Spectroelectrochemistry
Química analítica
Chemistry, Analytic
Descripción
Sumario:UV-Visible, NIR and Raman spectroelectrochemistry techniques have been used for the in-situ study of Pt nanoparticles (PtNPs) electrosynthesis on an electrochemically generated poly(3,4-ethylenedioxythiophene) film. Two electrochemical steps have been used to obtain in a reproducible way PtNPs with catalytic properties towards methanol oxidation: 1) deposition of Pt nuclei on the polymer modified electrode, 2) growth of these nuclei to form nanoparticles yielding drastic changes in the spectroscopic signal and a significant increase of the amount of Pt. A two steps procedure facilitates an interfacial growth mechanism of the nuclei over a diffusion controlled growth. Evolution of UV-Visible and NIR spectra during these two PtNPs synthesis steps helps to understand and explain the mechanism of generation of these nanoparticles. Besides, Energy Dispersive X-Ray analysis and Scanning Electron Microscopy images registered of the composite after each step of synthesis confirm the conclusions extracted from spectroelectrochemistry data