Monolayers of MoS${}_2$ on Ag(111) as decoupling layers for organic molecules: resolution of electronic and vibronic states of TCNQ

Abstract

The electronic structure of molecules on metal surfaces is largely determined by hybridization and screening by the substrate electrons. As a result, the energy levels are significantly broadened and molecular properties, such as vibrations are hidden within the spectral lineshapes. Insertion of thin decoupling layers reduces the linewidths and may give access to the resolution of electronic and vibronic states of an almost isolated molecule. Here, we use scanning tunneling microscopy and spectroscopy to show that a single layer of MoS${}_2$ on Ag(111) provides a semiconducting band gap that may prevent molecular states from strong interactions with the metal substrate. We show that the lowest unoccupied molecular orbital (LUMO) of tetra-cyano-quino-dimethane (TCNQ) molecules is significantly narrower than on the bare substrate and that it is accompanied by a characteristic satellite structure. Employing simple calculations within the Franck-Condon model, we reveal their vibronic origin and identify the modes with strong electron-phonon coupling.

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• Electronic Structure of Epitaxial Single-Layer MoS${}_2$
• Dynamic Jahn-Teller effect in electron transport through single C60 molecules
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Cited by in corpus (3)

• Surface Sensitive Raman Response of Metal-Supported Monolayer MoS${}_2$
• Variations of vibronic states in densely-packed structures of molecules with intramolecular dipoles
• Electronic Properties of Tetraazaperopyrene Derivatives on Au(111): Energy Level Alignment and Interfacial Band Formation