α-Sexithiophene on Cu(1 1 0) and Cu(1 1 0)–(2 × 1)O: An STM and NEXAFS study

Abstract

The adsorption of α-sexithiophene (6T) on Cu(1 1 0), Cu(1 1 0)–(2 × 1)O and the mesoscopically patterned Cu–O striped surface have been studied by STM (scanning tunnelling microscopy), XPS (X-ray photoelectron spectroscopy) and NEXAFS (near edge X-ray absorption fine structure). The molecular resolution of the STM allowed to determine the orientation and local order of the molecules in the submonolayer and monolayer regime. It is shown that the 6T molecules align with their long molecular axis along the densely packed copper rows on Cu(1 1 0) and along the Cu–O rows on the Cu(1 1 0)–(2 × 1)O surface. On the striped phase with alternating copper and Cu–O regions the molecules adsorb first on the Cu regions and after complete filling of these regions, on the Cu–O. The orientation is the same on both areas as on the respective pristine surfaces with the only exception that the molecules reorient by 90° if the width of the copper regions is smaller than the molecular length. The NEXAFS measurements allowed for a determination of the adsorption geometry of the molecules: while 6T lies flat on the surface on clean copper, the molecular planes are inclined with an angle as high as 39° with respect to the substrate on (2 × 1)O. For the latter, this inclination angle is 4° higher than in the bulk crystal structure of 6T observed for thicker films to release stress and allow commensurability with the substrate lattice, while for the former it is a result of the aromatic system bonding to the Cu(1 1 0) surface, as confirmed by XPS.