Dynamics of Pyridine Adsorption on Gold(111) Terraces in Acid Solution from in-Situ Scanning Tunneling Microscopy under Potentiostatic Control

The adsorption of pyridine (Py) on Au(111) terraces produced from aqueous 0.1 M HClO<sub>4</sub> + 10-<sup>3</sup> M Py at 298 K was studied in the potential range 0.15 V < E < 0.55 V (vs SHE) by in-situ scanning tunneling microscopy. When E ≥ E<sub>pzc</sub>, the potential of zero charge of the sub...

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Authors: Andreasen, Gustavo; Vela, María Elena; Salvarezza, Roberto Carlos; Arvia, Alejandro Jorge
Format: Article
Status:Published version
Publication date:1997
Country:Argentina
Institution:UNLP
Repository:SEDICI (UNLP)
Language:English
OAI Identifier:oai:sedici.unlp.edu.ar:10915/85927
Online Access:http://sedici.unlp.edu.ar/handle/10915/85927
Access Level:Open access
Keyword:Ciencias Exactas
Química
Piridinas
Oro
scanning tunneling microscopy
potentiostatic
Metales
Electroquímica
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author Andreasen, Gustavo
author2 Vela, María Elena
Salvarezza, Roberto Carlos
Arvia, Alejandro Jorge
author2_role author
author
author
author_browse Andreasen, Gustavo
Arvia, Alejandro Jorge
Salvarezza, Roberto Carlos
Vela, María Elena
author_facet Andreasen, Gustavo
Vela, María Elena
Salvarezza, Roberto Carlos
Arvia, Alejandro Jorge
author_role author
collection SEDICI (UNLP)
description The adsorption of pyridine (Py) on Au(111) terraces produced from aqueous 0.1 M HClO<sub>4</sub> + 10-<sup>3</sup> M Py at 298 K was studied in the potential range 0.15 V < E < 0.55 V (vs SHE) by in-situ scanning tunneling microscopy. When E ≥ E<sub>pzc</sub>, the potential of zero charge of the substrate, both ordered and disordered domains can be observed. Ordered domains correspond to vertically adsorbed Py molecules forming a (4 × 4) hexagonal lattice with the nearest neighbor distance d = 0.38 nm, and corrugation z = 0.04 nm. The ordered adsorbate structure disappears for E < E<sub>pzc</sub>, but it is recovered several minutes after stepping E backward to E > E<sub>pzc</sub>, as expected for a reversible potential-step-induced surface process. The surface concentration of adsorbed Py molecules resulting from the (4 × 4) lattice is close to 1 × 10-<sup>9</sup> mol/cm<sup>2</sup>, a figure exceeding the average integral surface concentration value obtained from electroadsorption measurements. Therefore, disordered domains would be related to a mobile diluted Py adsorbate coexisting with ordered Py adsorbate domains leading to a nonhomogeneous Py adsorbate layer at the positively charged Au(111) terraces.
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oai_identifier_str oai:sedici.unlp.edu.ar:10915/85927
publishDate 1997
publishDateSort 1997
reponame_str SEDICI (UNLP)
spelling Dynamics of Pyridine Adsorption on Gold(111) Terraces in Acid Solution from in-Situ Scanning Tunneling Microscopy under Potentiostatic Control Andreasen, Gustavo Vela, María Elena Salvarezza, Roberto Carlos Arvia, Alejandro Jorge Ciencias Exactas Química Piridinas Oro scanning tunneling microscopy potentiostatic Metales Electroquímica The adsorption of pyridine (Py) on Au(111) terraces produced from aqueous 0.1 M HClO<sub>4</sub> + 10-<sup>3</sup> M Py at 298 K was studied in the potential range 0.15 V < E < 0.55 V (vs SHE) by in-situ scanning tunneling microscopy. When E ≥ E<sub>pzc</sub>, the potential of zero charge of the substrate, both ordered and disordered domains can be observed. Ordered domains correspond to vertically adsorbed Py molecules forming a (4 × 4) hexagonal lattice with the nearest neighbor distance d = 0.38 nm, and corrugation z = 0.04 nm. The ordered adsorbate structure disappears for E < E<sub>pzc</sub>, but it is recovered several minutes after stepping E backward to E > E<sub>pzc</sub>, as expected for a reversible potential-step-induced surface process. The surface concentration of adsorbed Py molecules resulting from the (4 × 4) lattice is close to 1 × 10-<sup>9</sup> mol/cm<sup>2</sup>, a figure exceeding the average integral surface concentration value obtained from electroadsorption measurements. Therefore, disordered domains would be related to a mobile diluted Py adsorbate coexisting with ordered Py adsorbate domains leading to a nonhomogeneous Py adsorbate layer at the positively charged Au(111) terraces. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas Facultad de Ciencias Exactas http://sedici.unlp.edu.ar/handle/10915/85927
spellingShingle Dynamics of Pyridine Adsorption on Gold(111) Terraces in Acid Solution from in-Situ Scanning Tunneling Microscopy under Potentiostatic Control
Andreasen, Gustavo
Ciencias Exactas
Química
Piridinas
Oro
scanning tunneling microscopy
potentiostatic
Metales
Electroquímica
status_str publishedVersion
title Dynamics of Pyridine Adsorption on Gold(111) Terraces in Acid Solution from in-Situ Scanning Tunneling Microscopy under Potentiostatic Control
title_full Dynamics of Pyridine Adsorption on Gold(111) Terraces in Acid Solution from in-Situ Scanning Tunneling Microscopy under Potentiostatic Control
title_fullStr Dynamics of Pyridine Adsorption on Gold(111) Terraces in Acid Solution from in-Situ Scanning Tunneling Microscopy under Potentiostatic Control
title_full_unstemmed Dynamics of Pyridine Adsorption on Gold(111) Terraces in Acid Solution from in-Situ Scanning Tunneling Microscopy under Potentiostatic Control
title_short Dynamics of Pyridine Adsorption on Gold(111) Terraces in Acid Solution from in-Situ Scanning Tunneling Microscopy under Potentiostatic Control
title_sort Dynamics of Pyridine Adsorption on Gold(111) Terraces in Acid Solution from in-Situ Scanning Tunneling Microscopy under Potentiostatic Control
topic Ciencias Exactas
Química
Piridinas
Oro
scanning tunneling microscopy
potentiostatic
Metales
Electroquímica
topic_facet Ciencias Exactas
Química
Piridinas
Oro
scanning tunneling microscopy
potentiostatic
Metales
Electroquímica
url http://sedici.unlp.edu.ar/handle/10915/85927