Bromide Adsorption on Pt(111) over a Wide Range of pH: Cyclic Voltammetry and CO Displacement Experiments
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http://hdl.handle.net/10045/79218
Títol: | Bromide Adsorption on Pt(111) over a Wide Range of pH: Cyclic Voltammetry and CO Displacement Experiments |
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Autors: | Mello, Gisele A.B. | Briega-Martos, Valentín | Climent, Victor | Feliu, Juan M. |
Grups d'investigació o GITE: | Electroquímica de Superficies |
Centre, Departament o Servei: | Universidad de Alicante. Departamento de Química Física | Universidad de Alicante. Instituto Universitario de Electroquímica |
Paraules clau: | Bromide adsorption | Pt(111) | pH | Cyclic voltammetry | CO displacement |
Àrees de coneixement: | Química Física |
Data de publicació: | 23-de juliol-2018 |
Editor: | American Chemical Society |
Citació bibliogràfica: | The Journal of Physical Chemistry C. 2018, 122(32): 18562-18569. doi:10.1021/acs.jpcc.8b05685 |
Resum: | Bromide adsorption on Pt(111) is investigated by means of cyclic voltammetry and CO displacement experiments at different pH values. In acidic pH, bromide adsorption is strongly overlapped with hydrogen desorption process. However, as the pH increases, hydrogen adsorption process displaces toward negative potentials while bromide adsorption remains nearly in the same potential region. In consequence, both processes decouple at higher pH values. The structural transition from Pt(111)-(1×1) to Pt(111)(3×3)-4Br is pH independent, in the SHE scale, and not observed for pH > 9.1. Values of pztc are extracted from the combination of voltammetric and CO displaced charges. An alternative approach to obtain charge curves is based on the coincidence of the curves at the structural transition characteristic of the bromide adlayer completion. Pztc values obtained from different approaches with and without bromide are compared, and their dependence on pH discussed. A thermodynamic analysis is carried out to obtain hydrogen Gibbs excess and charge number from the Esin Markov analysis. |
Patrocinadors: | This work has been financially supported by the MCINN-FEDER (Spain) through Project CTQ2016-76221-P. V.B.-M. thankfully acknowledges to MINECO the award of a predoctoral grant (BES-2014-068176, Project CTQ2013-44803-P). G.A.B.M. expresses thanks for the postdoctorate fellowship from CNPq (Grant No. PDE 233268/2014-6). |
URI: | http://hdl.handle.net/10045/79218 |
ISSN: | 1932-7447 (Print) | 1932-7455 (Online) |
DOI: | 10.1021/acs.jpcc.8b05685 |
Idioma: | eng |
Tipus: | info:eu-repo/semantics/article |
Drets: | © 2018 American Chemical Society |
Revisió científica: | si |
Versió de l'editor: | https://doi.org/10.1021/acs.jpcc.8b05685 |
Apareix a la col·lecció: | INV - EQSUP - Artículos de Revistas |
Arxius per aquest ítem:
Arxiu | Descripció | Tamany | Format | |
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2018_Mello_etal_JPhysChemC_final.pdf | Versión final (acceso restringido) | 2,07 MB | Adobe PDF | Obrir Sol·licitar una còpia |
2018_Mello_etal_JPhysChemC_accepted.pdf | Accepted Manuscript (acceso abierto) | 853,75 kB | Adobe PDF | Obrir Vista prèvia |
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