Abstract:We studied the sublimation of tetracene single crystals under vacuum and 1 atm inert gas to develop the surface cleaning technique for organic semiconductors. It was found that the microscopic sublimation behavior is strongly dependent on the gas pressure.Nanometer-scale roughening is observed after heating in vacuum, while layer-by-layer sublimation was observed under 1 atm Ar gas. Reflection high energy electron diffraction of the topmost surface showed streak patterns, which shows surface contaminants were … Show more
“…While Vollmer et al ascribed the cause of such defects to a cleavage process with adhesive tape, a disordered top surface layer on the tetracene single crystals was suggested by reflection high-energy electron diffraction experiments even without any mechanical cleavage procedure. 156 A probable molecular rearrangement for the top surface layer of the tetracene single crystal was also claimed through precise X-ray diffraction analyses. 157 ARUPS measurements of more surface insensitive conditions, e.g., under excitation by lower energy photons, may be a possible solution for accessing the valence band structures and hole effective mass of the bulk single crystal tetracene, which was successfully demonstrated for pentacene as discussed in the next subsection.…”
Methodologies and experimental achievements for exploration into electronic band structures of organic semiconductor and hybrid perovskite single crystals are reviewed.
“…While Vollmer et al ascribed the cause of such defects to a cleavage process with adhesive tape, a disordered top surface layer on the tetracene single crystals was suggested by reflection high-energy electron diffraction experiments even without any mechanical cleavage procedure. 156 A probable molecular rearrangement for the top surface layer of the tetracene single crystal was also claimed through precise X-ray diffraction analyses. 157 ARUPS measurements of more surface insensitive conditions, e.g., under excitation by lower energy photons, may be a possible solution for accessing the valence band structures and hole effective mass of the bulk single crystal tetracene, which was successfully demonstrated for pentacene as discussed in the next subsection.…”
Methodologies and experimental achievements for exploration into electronic band structures of organic semiconductor and hybrid perovskite single crystals are reviewed.
“…the in-plane mean crystallite size of C 60 grown at 130 K was only about a fifth to that grown at RT), it was drastically improved to reach the in-plane mean crystallite size of up to about 250 nm as the growth temperature was raised to 343 K. It is noteworthy that the crystallite size even shrunk when the growth temperature was above 363 K. This is presumably ascribed to re-sublimation of the substrate rubrene molecules and/or intermixing of rubrene and C 60 . For the case of tetracene, it was reported that surface roughening occurred by mild heating in vacuum [52]. On the other hand, in the previous literature [33], disordered structures are frequently recognized especially at step edges in the AFM images of the C 60 /RubSC formed at high temperatures, suggesting that formation of amorphous intermixture between C 60 and rubrene competed with assembly into the crystalized domains.…”
Uniform and well-defined interfaces are required for clarification of fundamental processes at internal interfaces between donor and acceptor molecules constituting organic optoelectronic devices. In this study, evolution of a well-ordered molecular interface, epitaxially grown C 60 on the single crystal rubrene (C 42 H 28 ) surface, was accurately investigated by grazing incidence x-ray diffraction (GIXD) techniques. Contrasting to the case of C 60 on the single crystal pentacene forming uniquely aligned epitaxial interfaces, coexistence of two inequivalent crystalline domains of C 60 was identified on the single crystal rubrene. Nevertheless, crystallinity of C 60 /rubrene exhibited even more remarkable improvement to extend its in-plane average crystallite size up to 250 nm as the growth temperature was raised. Probable leading factors determining the structures and crystallinity of the well-defined molecular interfaces are discussed based on close comparison of the present results with the C 60 /pentacene interfaces. The techniques presented herein for enhancement of the crystallinity in epitaxial molecular interfaces are potentially applicable to development in the photoelectric power conversion efficiency of organic photovoltaics (OPVs) via improved charge carrier mobility in donor-acceptor interfaces.
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