Ångstromスケール先端強化ラマンイメージングによって明らかになった吸着駆動単分子対称性低下

The vibrational landscape of adsorbed molecules is central to understanding surface interactions at the atomic scale, influencing phenomena from catalysis to molecular electronics. Recent advances in atomic-scale tip-enhanced Raman spectroscopy (TERS) have enabled vibrational mapping of single molecules with subnanometer spatial resolution, providing unprecedented insights into molecule-surface interactions by confining light in plasmonic picocavities. Here, we exploit TERS in a cryogenic scanning tunneling microscope junction to perform Raman hyperspectral mapping of single iron phthalocyanine (FePc) molecules in three nonequivalent adsorption configurations on Ag surfaces. We explore the changes in the vibrational modes of FePc molecules adsorbed on two distinct silver crystal terminations with differing symmetry, Ag(111) and Ag(110), revealing how subtle variations in the adsorption geometry due to substrate anisotropy can strongly influence molecular vibrations, lifting the degeneracy of individual normal modes. Our findings not only demonstrate the first use of subnanometer TERS mapping across different symmetry configurations but also provide a deeper understanding of how site-specific vibrational properties are intimately linked to local atomic environments. This capability paves the way for precisely tailoring surface interactions and controlling chemical reactions on the atomic scale.