Influence of intramolecular polar bonds on interface energetics in perfluoro-pentacene on Ag(111)

Physical Review B - Condensed Matter and Materials Physics

Volumn 81, Issue 4, 2010, Pages

  Duhm, Steffen ^a   Hosoumi, Shunsuke ^a   Salzmann, Ingo ^b   Gerlach, Alexander ^c   Oehzelt, Martin ^d   Wedl, Bernhard ^b,e   Lee, Tien Lin ^f,g   Schreiber, Frank ^c   Koch, Norbert ^b   Ueno, Nobuo ^a   Kera, Satoshi ^a  

^a CHIBA UNIVERSITY   (Japan)

^b HUMBOLDT UNIVERSITY   (Germany)

^c UNIVERSITY OF TÜBINGEN   (Germany)

^d JOHANNES KEPLER UNIVERSITY LINZ   (Austria)

^e GRAZ UNIVERSITY OF TECHNOLOGY   (Austria)

^f EUROPEAN SYNCHROTRON RADIATION FACILITY   (France)

^g DIAMOND LIGHT SOURCE LTD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 77954820240     PISSN: 10980121     EISSN: 1550235X     Source Type: Journal    
DOI: 10.1103/PhysRevB.81.045418     Document Type: Article

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58. Note that the (002)-interlayer distance of graphite (d = 3.56 Å) (Ref.), which can be denoted as the prototypical stacked organic molecular crystal, is even slightly larger than the sum of the van der Waals radii.
59. Note that in complex structures (here: island growth plus orientational transition) the exact correlation of the SECO position to a certain organic layer may be difficult (Ref.) since in the valence electron region the UPS spectra are a superposition of emission from sample patches with different spectral feature BEs, whereas the vacuum-level position is an area averaged arithmetic mean of sample patches with different vacuum levels (Refs.). Thus the ionization energy values in Fig. should be dealt with carefully.