Rubrene (CH) was adsorbed with submonolayer coverage on Pt(111), Au(111), and graphene-covered Pt(111). Adsorption phases and vibronic properties of CH consistently reflect the progressive reduction of the molecule-substrate hybridization. Separate CH clusters are observed on Pt(111) as well as broad molecular resonances. On Au(111) and graphene-covered Pt(111) compact molecular islands with similar unit cells of the superstructure characterize the adsorption phase. The highest occupied molecular orbital of CH on Au(111) exhibits weak vibronic progression while unoccupied molecular resonances appear with a broad line shape. In contrast, vibronic subbands are present for both frontier orbitals of CH on graphene. They are due to different molecular vibrational quanta with distinct Huang-Rhys factors.
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http://dx.doi.org/10.3762/bjnano.11.100 | DOI Listing |
Front Chem
July 2023
Institute of Chemical Sciences and Engineering (ISIC), École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Recent state-to-state experiments of methane scattering from Ni(111) and graphene-covered Ni(111) combined with quantum mechanical simulations suggest an intriguing correlation between the surface-induced vibrational energy redistribution (SIVR) during the molecule/surface scattering event and the catalytic activity for methane dissociation of the target surface (Werdecker, Phys. Rev. Res.
View Article and Find Full Text PDFBeilstein J Nanotechnol
August 2020
Institut für Physik, Technische Universität Ilmenau, D-98693 Ilmenau, Germany.
Rubrene (CH) was adsorbed with submonolayer coverage on Pt(111), Au(111), and graphene-covered Pt(111). Adsorption phases and vibronic properties of CH consistently reflect the progressive reduction of the molecule-substrate hybridization. Separate CH clusters are observed on Pt(111) as well as broad molecular resonances.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!