Artículo
Adsorption of phenylphosphonic acid on rutile TiO2(110)
Köbl, Julia; Wechsler, Daniel; Kataev, Elmar; Williams, Federico José
; Tsud, Nataliya; Franchi, Stefano; Steinruck, Hans Peter; Lytken, Ole
Fecha de publicación:
08/2020
Editorial:
Elsevier Science
Revista:
Surface Science
ISSN:
0039-6028
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
Binding of functionalized organic molecules to oxide surfaces is an important step in the rational design of molecular devices. In the present investigation, we used synchrotron radiation photoelectron spectroscopy and near-edge X-ray absorption fine structure spectroscopy to determine the binding mode, electronic structure and adsorption geometry of phenylphosphonic acid (PPA) on TiO2(110)–(1 × 1). We found that PPA multilayers desorb below 380 K leaving a compact PPA monolayer adsorbed on the surface, which remains stable up to 780 K. In the 380–520 K temperature range, molecules are anchored to the surface via a single P–O–Ti covalent bond (monodentate configuration). Furthermore, the phenyl ring is tilted ~45° with respect to the surface plane and it either forms 45° or is randomly oriented with respect to [001] crystallographic direction. Raising the temperature above 520 K partially transforms the monodentate configuration to a mixed oneand twofold deprotonated bidentate binding mode, presumably after surface hydroxyl groups leave the surface as water molecules. This change in molecular binding does not alter the molecular electronic structure nor the adsorption geometry, which remain essentially unchanged.
Palabras clave:
porfirinas
,
superficies
,
fotoemisión
,
NEXAFS
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Articulos(INQUIMAE)
Articulos de INST.D/QUIM FIS D/L MATERIALES MEDIOAMB Y ENERGIA
Articulos de INST.D/QUIM FIS D/L MATERIALES MEDIOAMB Y ENERGIA
Citación
Köbl, Julia; Wechsler, Daniel; Kataev, Elmar; Williams, Federico José; Tsud, Nataliya; et al.; Adsorption of phenylphosphonic acid on rutile TiO2(110); Elsevier Science; Surface Science; 698; 121612; 8-2020; 121612-121617
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