Self-assembled monolayers of 4-aminothiophenol on copper surfaces studied by grazing-incidence X-ray absorption spectroscopy

Citation
O. Schlieben et J. Hormes, Self-assembled monolayers of 4-aminothiophenol on copper surfaces studied by grazing-incidence X-ray absorption spectroscopy, J SYNCHROTR, 6, 1999, pp. 793-795
Citations number
16
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
JOURNAL OF SYNCHROTRON RADIATION
ISSN journal
09090495 → ACNP
Volume
6
Year of publication
1999
Part
3
Pages
793 - 795
Database
ISI
SICI code
0909-0495(19990501)6:<793:SMO4OC>2.0.ZU;2-G
Abstract
Self-Assembled Monolayers (SAMs) of 4-Aminothiophenol on copper surfaces ha ve been investigated, using Grazing Incidence X-Ray Absorption Spectroscopy (GIXAS). The surface sensitivity of this technique allows us to characteri ze the chemisorption process by XANES and EXAFS measurements in fluorescenc e mode at the sulfur- and copper-g-edge. Our results are consistent with 4- Aminothiophenol (4-ATP) bound to the surface through the sulfur headgroup. From EXAFS analysis two different interatomic distances between sulfur and next neighbour copper atoms d(S-Cu1) 2.26 Angstrom and d(S-Cu2) = 3.1 Angst rom could be determined. Data indicates occupation of deep three-fold hollo w positions of sulfur with significant reconstruction of first layer copper atoms on preferably textured (111)-surfaces. Adsorption of 4-ATP as disulf ide, described in a "sulfur-pairing model", is not supported by absorption data in the XANES region. EXAFS analysis on the other hand gives some evide nce for the presence of a sulfur dimer moiety, with a sulfur-sulfur spacing of d(S-S) = 2.1 Angstrom. Depending on the preparation procedure, oxidatio n of thiol-molecules occurs, leading to a coexistence of sulfate-ions and i ntact 4-ATP on metal surfaces due to partial cleavage of the S-C bond.