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<dc:title>Spectroelectrochemical study of the electrosynthesis of Pt nanoparticles/poly(3,4-(ethylenedioxythiophene) composite</dc:title>
<dc:creator>Fernández Blanco, Ana Cristina</dc:creator>
<dc:creator>Ibáñez Martínez, David</dc:creator>
<dc:creator>Colina, Álvaro</dc:creator>
<dc:creator>Ruiz Fernández, Virginia</dc:creator>
<dc:creator>Heras, Aránzazu</dc:creator>
<dc:subject>Conducting polymers</dc:subject>
<dc:subject>PEDOT</dc:subject>
<dc:subject>Platinum nanoparticles</dc:subject>
<dc:subject>Electrochemistry</dc:subject>
<dc:subject>Spectroelectrochemistry</dc:subject>
<dc:subject>Química analítica</dc:subject>
<dc:subject>Chemistry, Analytic</dc:subject>
<dc:description>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</dc:description>
<dc:description>Ministerio de Ciencia y Tecnologia (CTQ2010-17127, V.R. Programa Ramon y Cajal), Junta de Castilla y Leon (GR71, BU349-U13), and Academy of Finland (V.R., Academy Research Fellow) is gratefully acknowledged. C. F-B. thanks Ministerio de Educacion, Cultura y Deporte for a predoctoral FPU fellowship. D.I. is grateful for his FPI-MICINN agreement of the Ministerio de Economia y Competitividad. ICTS of Complutense University of Madrid (Spain) and PCT-UBU of Burgos University (Spain) are also acknowledged for SEM images and EDX analysis, respectively.</dc:description>
<dc:date>2015-09-29T09:29:32Z</dc:date>
<dc:date>2015-09-29T09:29:32Z</dc:date>
<dc:date>2014-11</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/submittedVersion</dc:type>
<dc:identifier>0013-4686</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/3854</dc:identifier>
<dc:identifier>10.1016/j.electacta.2014.08.004</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Electrochimica Acta. 2014, V. 145, p. 139–147</dc:relation>
<dc:relation>http://dx.doi.org/10.1016/j.electacta.2014.08.004</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/GR71</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/BU349-U13</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINCYT/CTQ2010-17127</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Elsevier</dc:publisher>
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