Interpretation of X-ray Absorption Spectroscopy in the Presence of Surface Hybridization

Abstract

X-ray absorption spectroscopy yields direct access to the electronic and geometric structure of hybrid inorganic-organic interfaces formed upon adsorption of complex molecules at metal surfaces. The unambiguous interpretation of corresponding spectra is challenged by the intrinsic geometric flexibility of the adsorbates and the chemical interactions with the interface. Density-functional theory (DFT) calculations of the extended adsorbate-substrate system are an established tool to guide peak assignment in X-ray photoelectron spectroscopy (XPS) of complex interfaces. We extend this to the simulation and interpretation of X-ray absorption spectroscopy (XAS) data in the context of functional organic molecules on metal surfaces using dispersion-corrected DFT calculations within the transition potential approach. On the example of X-ray absorption signatures for the prototypical case of 2H-porphine adsorbed on Ag(111) and Cu(111) substrates, we follow the two main effects of the molecule/surface interaction on XAS: (1) the substrate-induced chemical shift of the 1s core levels that dominates in physisorbed systems and (2) the hybridization-induced broadening and loss of distinct resonances that dominates in more chemisorbed systems.

arXiv comment13 pages, 4 figures

References in corpus (3)

• Stabilizing a Molecular Switch at Solid Surfaces: A Density-Functional Theory Study of Azobenzene at Cu(111), Ag(111), and Au(111)
• Temperature-dependent templated growth of porphine thin films on the (111) facets of copper and silver
• Interfacial charge rearrangement and intermolecular interactions: Density-functional theory study of free-base porphine adsorbed on Ag(111) and Cu(111)

Cited by in corpus (3)

• Binding and Electronic Level Alignment of $\mathbf{\pi }$-Conjugated Systems on Metals
• Efficient Simulation of Near-Edge X-ray Absorption Fine Structure (NEXAFS) in Density-Functional Theory: Comparison of Core-Level Constraining Approaches
• Characterizing Molecule-Metal Surface Chemistry with Ab-Initio Simulation of X-ray Absorption and Photoemission Spectra