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Fingerprint of fractional charge transfer at metal/organic interface

2015/02/06 by Sabine-A. Savu, Savu, Sabine-A., Giulio Biddau +13
Chemistry · Engineering · Physics and Astronomy · #Electrochemical Analysis and Applications #FOS: Physical sciences #Materials Science (cond-mat.mtrl-sci) #Molecular Junctions and Nanostructures #Soft Condensed Matter (cond-mat.soft) #Spectroscopy and Quantum Chemical Studies

paper · pdf · doi:10.48550/arxiv.1502.01909

openalex publication_date 2015/02/06 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/28

Abstract

Although physisorption is a widely occurring mechanism of bonding at the organic/metal interface, contradictory interpretations of this phenomenon are often reported. Photoemission and X-ray absorption spectroscopy investigations of nanorods of a substituted pentacene, 2,3,9,10-tetrafluoropentacene, deposited on gold single crystals reveal to be fundamental to identify the bonding mechanisms. We find fingerprints of a fractional charge transfer from the clean metal substrate to the physisorbed molecules. This phenomenon is unambiguously recognizable by a non-rigid shift of the core-level main lines while the occupied states at the interface stay mostly unperturbed, and the unoccupied states experience pronounced changes. The experimental results are corroborated by first-principles calculations.

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