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  Metal-organic interface functionalization via acceptor end groups: PTCDI on coinage metals

Franco-Cañellas, A., Wang, Q., Broch, K., Duncan, D. A., Kumar Thakur, P., Liu, L., et al. (2017). Metal-organic interface functionalization via acceptor end groups: PTCDI on coinage metals. Physical Review Materials, 1(1): 013001. doi:10.1103/PhysRevMaterials.1.013001.

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PhysRevMaterials.1.013001-1.pdf (Verlagsversion), 740KB
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PhysRevMaterials.1.013001-1.pdf
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2017
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APS
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 Urheber:
Franco-Cañellas, Antoni1, Autor
Wang, Qi2, Autor
Broch, Katharina3, Autor           
Duncan, David A.4, Autor
Kumar Thakur, Pardeep4, Autor
Liu, Lijia2, Autor
Kera, Satoshi5, Autor
Gerlach, Alexander1, Autor
Duhm, Steffen2, Autor
Schreiber, Frank1, Autor
Affiliations:
1Institut für Angewandte Physik, Universität Tübingen, Auf der Morgenstelle 10, 72076 Tübingen, Germany, ou_persistent22              
2Institute of Functional Nano & Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University , Suzhou 215123, People’s Republic of China, ou_persistent22              
3Physical Chemistry, Fritz Haber Institute, Max Planck Society, ou_634546              
4Diamond Light Source, Harwell Science and Innovation Campus, Oxfordshire OX11 0DE, United Kingdom, ou_persistent22              
5Department of Photo-Molecular Science, Institute for Molecular Science, Okazaki 444-8585, Japan, ou_persistent22              

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 Zusammenfassung: We present a comprehensive study of the complex interface between perylene-3,4,9,10-tetracarboxylic diimide (PTCDI) and the (111) surfaces of the three coinage metals. The specific structural, electronic, and chemical properties of the interface rendered by the different substrate reactivities are monitored with low-energy electron diffraction (LEED), x-ray standing waves (XSW), and ultraviolet and x-ray photelectron spectroscopy (UPS and XPS). In particular, the balance between molecule-substrate and molecule-molecule interactions is considered when interpreting the core-level spectra of the different interfaces. By presenting additional adsorption distances of the unsubstituted perylene, we showthat the molecular functionalization via end groups with acceptor character facilitates the charge transfer from the substrate but it is not directly responsible for the associated short adsorption distances, demonstrating that this frequently assumed correlation is not necessarily correct.

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Sprache(n): eng - English
 Datum: 2017-03-022017-06-27
 Publikationsstatus: Online veröffentlicht
 Seiten: 6
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1103/PhysRevMaterials.1.013001
 Art des Abschluß: -

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Titel: Physical Review Materials
  Kurztitel : Phys. Rev. Mat.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: College Park, MD : American Physical Society
Seiten: 6 Band / Heft: 1 (1) Artikelnummer: 013001 Start- / Endseite: - Identifikator: ISSN: 2475-9953
CoNE: https://pure.mpg.de/cone/journals/resource/2475-9953