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

## TL;DR

This paper extends density-functional theory simulations to interpret X-ray absorption spectra of organic molecules on metal surfaces, accounting for surface hybridization effects to improve spectral analysis.

## Contribution

It introduces a method combining dispersion-corrected DFT with the transition potential approach for XAS interpretation of hybrid interfaces.

## Key findings

- Surface-induced chemical shifts in XAS are dominant in physisorbed systems.
- Hybridization causes broadening and loss of spectral resonances in chemisorbed systems.
- The approach aids in distinguishing between physisorption and chemisorption in XAS data.

## 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.