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Molecular Modeling of Defect Structures in Pentacene

Published online by Cambridge University Press:  11 February 2011

Paul K. Miska
Affiliation:
Department of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109–2136, U.S.A. Materials Research Society, 506 Keystone Drive, Warrendale, PA 16066, U.S.A.
Lawrence F. Drummy
Affiliation:
Department of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109–2136, U.S.A. Materials Research Society, 506 Keystone Drive, Warrendale, PA 16066, U.S.A.
David C. Martin
Affiliation:
Department of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109–2136, U.S.A. Materials Research Society, 506 Keystone Drive, Warrendale, PA 16066, U.S.A.
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Abstract

We have studied defect structures in the crystalline organic molecular semiconductor pentacene. Our investigations included the calculation of free surface energies on low index planes. It was found that that the (001) surface had the lowest energy ∼50 mJ/m2, roughly half that of the other low index planes, (100) and (010) ∼120 mJ/m2 and ∼140 mJ/m2 respectively. These calculations were then compared to experimental data from vapor grown crystals using optical microscopy, Scanning Electron Microscopy (SEM) and High Resolution Transmission Electron Microscopy (HRTEM). We also modeled dislocations dipoles of varying Burgers vector and dipole length. It was found that dislocations were accommodated by extensive molecular deformation near the defect core, as well as a well defined stacking fault that occurred down the length of the dipole. Finally, we investigated low angle tilt grain boundaries. It was seen that low angle boundaries relaxed through molecular deformation in the first layer of molecules at the boundary as well as bending of the (001) planes.

Type
Research Article
Copyright
Copyright © Materials Research Society 2003

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References

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