First-Principles Analysis of Chirality-Induced Spin Selectivity at Molecule-Metal Interfaces in Photoemission.

Abstract

Spin-resolved photoelectron spectroscopy (PES) probes chirality-induced spin selectivity, yet it remains unclear whether the measured spin polarization reflects molecular chirality itself or the broader electronic structure of the hybrid interface. We present a first-principles analysis of PES spin polarization at chiral molecule-metal interfaces, treating the interface holistically rather than as a metal substrate plus a separate molecular spin filter/polarizer. Using density functional theory within a three-step photoemission framework, we compute the spin polarization generated in the optical-excitation step for (<i>M</i>)- and (<i>P</i>)-heptahelicene adsorbed on Au(111) and Cu(111) and for coronene/Au(111) as a nonchiral control. We find that adsorption strongly reshapes the PES spin polarization relative to the clean metal surface, but opposite enantiomers yield symmetry-related responses. These results indicate that changes in the PES spin polarization are more naturally attributed to the electronic structure of the hybrid interface than to molecular chirality alone.