2006
DOI: 10.1016/j.susc.2006.07.039
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The interplay between molecular orientation, film morphology and luminescence properties of tetracene thin films on epitaxial AlOx/Ni3Al(111)

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Cited by 12 publications
(25 citation statements)
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“…Since COMs like Tc have highly anisotropic electronic and chemical structures, their orientation at the interface is of particular importance to achieve an interface morphology that favors efficient IET. As an example, the IET-competing luminescence of Tc on an ultrathin alumina AlO x layer on Ni 3 Al­(111) is completely quenched if the molecules are planar or are at least only moderately inclined with respect to the surface, while the luminescence persists for larger Tc inclinations. This behavior is attributed to the fact that a smaller Tc inclination gives rise to an increased overlap of π orbitals (located above and below the planar Tc core) and the wave function tails of the metal states facilitating, thus, an efficient IET from Tc to the substrate.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Since COMs like Tc have highly anisotropic electronic and chemical structures, their orientation at the interface is of particular importance to achieve an interface morphology that favors efficient IET. As an example, the IET-competing luminescence of Tc on an ultrathin alumina AlO x layer on Ni 3 Al­(111) is completely quenched if the molecules are planar or are at least only moderately inclined with respect to the surface, while the luminescence persists for larger Tc inclinations. This behavior is attributed to the fact that a smaller Tc inclination gives rise to an increased overlap of π orbitals (located above and below the planar Tc core) and the wave function tails of the metal states facilitating, thus, an efficient IET from Tc to the substrate.…”
Section: Introductionmentioning
confidence: 99%
“…Tc structure formation has been widely studied on several different weakly interacting surfaces, including H–Si, ,, Si oxide, ,, AlO x /Ni 3 Al­(111), polystyrene, parylene C, poly­(methyl methacrylate), hexamethyl­disilazane, Mylar, evaporated carbon, and highly oriented pyrolytic graphite . Thanks to the weak coupling to the substrates, the results are largely transferable.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5][6][7][8] It is a comparatively neglected member of the acene family compared to its neighbors anthracene and pentacene, but it is gaining wider attention and light-emitting field-effect transistors have also been recently realized. [1][2][3][4][5][6][7][8] It is a comparatively neglected member of the acene family compared to its neighbors anthracene and pentacene, but it is gaining wider attention and light-emitting field-effect transistors have also been recently realized.…”
Section: Introductionmentioning
confidence: 99%
“…C1s spectra showed strong extra peaks at 283.1 eV and 285~286 eV in addition to the peak 284.3 eV belonging to tetracene 12 . O1s signal intensity was comparable to C1s.…”
Section: (D)mentioning
confidence: 98%