Structure, surface chemistry and electrochemical de-alloying of bimetallic PtxAg100-x nanoparticles: Quantifying the changes in the surface properties for adsorption and electrocatalytic transformation upon selective Ag removal

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Título: Structure, surface chemistry and electrochemical de-alloying of bimetallic PtxAg100-x nanoparticles: Quantifying the changes in the surface properties for adsorption and electrocatalytic transformation upon selective Ag removal
Autor/es: Weber, Isabella | Solla-Gullón, José | Brimaud, Sylvain | Feliu, Juan M. | Behm, R. Jürgen
Grupo/s de investigación o GITE: Electroquímica de Superficies | Electroquímica Aplicada y Electrocatálisis
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Química Física | Universidad de Alicante. Instituto Universitario de Electroquímica
Palabras clave: Bimetallic nanoparticles | Electrochemical de-alloying | Segregation | In situ spectro-electrochemistry | PtAg | CO electrooxidation
Área/s de conocimiento: Química Física
Fecha de publicación: 15-may-2017
Editor: Elsevier
Cita bibliográfica: Journal of Electroanalytical Chemistry. 2017, 793: 164-173. doi:10.1016/j.jelechem.2016.11.062
Resumen: We investigated the structure and surface chemistry of bimetallic PtAg nanoparticles, which were prepared by a water-in-oil microemulsion synthesis procedure, as well as the changes therein induced by electrochemical (surface) de-alloying, by a combination of electrochemical and in situ FTIR and online differential electrochemical mass spectrometry (DEMS) measurements. Based on transmission electron microscopy the resulting nanoparticles have a narrow size distribution with a mean diameter of around 6 nm, and increasing Ag contents lead to a broadening of the particle size distribution and a loss of the preferential formation of {100} facets observed for Pt nanoparticles. Evaluation of the hydrogen adsorption and CO oxidation characteristics and of the CO adsorption properties (IR) reveals detailed information on the surface composition of the bimetallic nanoparticles before and after electrochemical de-alloying, including also the distribution of Pt and Ag atoms in the surface. Furthermore, relevant information about the modifications in the chemical properties of Pt atoms/sites induced by the presence of Ag is extracted. For the as-prepared nanoparticles we find Ag surface enrichment, while de-alloying results in a core-shell structure with a PtAg core and a Pt shell, whose chemical properties are close to, but not identical, with those of polycrystalline Pt. More general, the study demonstrates that Hupd measurements are not suitable to identify the Pt surface content in such kind of bimetallic nanoparticles.
Patrocinador/es: This work was supported by the Deutsche Forschungsgemeinschaft via the project BE 1201/17-1 and by the Ministerio de Economía y Competitividad (project CTQ2013-44083-P) and Generalitat Valenciana (project PROMETEOII/2014/013).
URI: http://hdl.handle.net/10045/67758
ISSN: 1572-6657 (Print) | 1873-2569 (Online)
DOI: 10.1016/j.jelechem.2016.11.062
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2016 Elsevier B.V.
Revisión científica: si
Versión del editor: http://dx.doi.org/10.1016/j.jelechem.2016.11.062
Aparece en las colecciones:INV - EQSUP - Artículos de Revistas
INV - LEQA - Artículos de Revistas

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