Specific surface reactions for identification of platinum surface domains Surface characterization and electrocatalytic tests

The electrochemical properties of bismuth and germanium irreversibly adsorbed on platinum electrodes have been used to screen the surface domains of polycrystalline electrodes. As revealed by the use of stepped surfaces, bismuth adsorbed on (1 1 1) terrace sites shows a redox peak at 0.63 V, whose c...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Electrochimica acta 2005-08, Vol.50 (21), p.4308-4317
Hauptverfasser: RODRIGUEZ, P, HERRERO, E, SOLLA-GULLON, J, VIDAL-IGLESIAS, F. J, ALDAZ, A, FELIU, J. M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The electrochemical properties of bismuth and germanium irreversibly adsorbed on platinum electrodes have been used to screen the surface domains of polycrystalline electrodes. As revealed by the use of stepped surfaces, bismuth adsorbed on (1 1 1) terrace sites shows a redox peak at 0.63 V, whose charge is proportional to the number of (1 1 1) terrace sites, without any interference from bismuth adsorbed on any other site. For the characterization of (1 0 0) terrace sites, adsorption of germanium can be used, since the adatoms adsorbed on the (1 0 0) terrace sites show a redox peak at 0.55 V. Although no other peak is found in this potential region for the germanium adsorbed on other sites, other contributions may give rise to an increase in the current in this region. After the appropriate corrections, the charge for bismuth and germanium redox process in the selected region is proportional to the number of terrace sites with (1 1 1) and (1 00) symmetry, respectively. These relationships can be used to characterize the bidimensional domains of any platinum electrode. Four different platinum nanoparticle electrodes were characterized and the results were used to understand their behaviour towards ammonia oxidation.
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2005.02.087