journal article·2015-11-01Open access

Identification of an organic semiconductor superlattice structure of pentacene and perfluoro-pentacene through resonant and non-resonant X-ray scattering

S. Kowarik, A. Hinderhofer, C. Wang, C. Weber, A. Gerlach, A. Hexemer, S. R. Leone, F. Schreiber

AIP Advances· Volume 5· Issue 11

Abstract

Highly crystalline and stable molecular superlattices are grown with the smallest possible stacking period using monolayers (MLs) of the organic semiconductors pentacene (PEN) and perfluoro-pentacene (PFP). Superlattice reflections in X-ray reflectivity and their energy dependence in resonant soft X-ray reflectivity measurements show that PFP and PEN MLs indeed alternate even though the coherent ordering is lost after ∼ 4 ML. The observed lattice spacing of 15.9 Å in the superlattice is larger than in pure PEN and PFP films, presumably because of more upright standing molecules and lack of interdigitation between the incommensurate crystalline PEN and PFP layers. The findings are important for the development of novel organic quantum optoelectronic devices.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Molecular Junctions and Nanostructures · Organic Light-Emitting Diodes Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Humboldt-Universität zu Berlin 1 , Institut für Physik, Newtonstr. 15, 12489 Berlin, Germany

Universität Tübingen 2 , Institut für Angewandte Physik, Auf der Morgenstelle 10, 72076 Tübingen, Germany

Advanced Light Source, Lawrence Berkeley National Laboratory 3 , Berkeley, CA 94720, United States

Departments of Chemistry and Physics, University of California 4 , and Lawrence Berkeley National Laboratory, Berkeley, CA 94720, United States

References (31)

Show source-provided references
1. 2010
2. Appl. Phys. Lett. · 2000 · 76 · 385510.1063/1.126800 ↗
3. Appl. Phys. Lett. · 2006 · 8810.1063/1.2206124 ↗
4. Appl. Phys. Lett. · 1990 · 56 · 67410.1063/1.102733 ↗
5. Adv. Mater. · 2014 · 26 · 458210.1002/adma.201400702 ↗
6. Phys. Rev. Lett. · 2006 · 97 · 810.1103/PhysRevLett.97.237401 ↗
7. Chemphyschem · 2012 · 13 · 62810.1002/cphc.201100737 ↗
8. Thin Solid Films · 1994 · 239 · 21410.1016/0040-6090(94)90854-0 ↗
9. J. Appl. Phys. · 1993 · 73 · 282610.1063/1.353059 ↗
10. Appl. Phys. Lett. · 1993 · 62 · 310210.1063/1.109151 ↗
11. Phys. Rev. Lett. · 1993 · 71 · 209810.1103/PhysRevLett.71.2098 ↗
12. Thin Solid Films · 2014 · 554 · 7410.1016/j.tsf.2013.03.082 ↗
13. Appl. Phys. Lett. · 2009 · 95 · 20310610.1063/1.3256194 ↗
14. MRS Bull. · 2010 · 35 · 44910.1557/mrs2010.583 ↗
15. J. Am. Chem. Soc. · 2004 · 126 · 813810.1021/ja0476258 ↗
16. J. Am. Chem. Soc. · 2007 · 129 · 1031610.1021/ja0730516 ↗
17. Adv. Mater. · 2009 · 21 · 229410.1002/adma.200803328 ↗
18. Thin Solid Films · 2007 · 515 · 560610.1016/j.tsf.2006.12.020 ↗
19. Org. Electron. · 2004 · 5 · 25710.1016/j.orgel.2004.05.001 ↗
20. Phys. Status Solidi - Rapid Res. Lett. · 2008 · 2 · 12010.1002/pssr.200802052 ↗
21. Langmuir · 2008 · 24 · 729410.1021/la800606h ↗
22. J. Appl. Phys. · 2013 · 114 · 04351510.1063/1.4816320 ↗
23. J. Chem. Phys. · 2012 · 136 · 110.1063/1.3677839 ↗
24. J. Chem. Phys. · 2011 · 134 · 110.1063/1.3557476 ↗
25. J. Chem. Phys. · 2013 · 13810.1063/1.4795004 ↗
26. J. Mater. Chem. C · 2013 · 1 · 18710.1039/C2TC00001F ↗
27. J. Phys. Condens. Matter · 2008 · 20 · 18400510.1088/0953-8984/20/18/184005 ↗
28. Eur. Phys. J. Spec. Top. · 2009 · 167 · 1110.1140/epjst/e2009-00930-y ↗
29. J. Phys. Chem. C · 2010 · 114 · 2012010.1021/jp107518f ↗
30. Phys. Rev. B · 2011 · 84 · 110.1103/PhysRevB.84.075479 ↗
31. J. Am. Chem. Soc. · 2004 · 126 · 408410.1021/ja049726b ↗