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Author Mete, Ersen ♦ Demiroglu, Ilker ♦ Danisman, M. Fatih ♦ Ellialtioglu, Sinasi
Source arXiv.org
Content type Text
File Format PDF
Date of Submission 2009-12-31
Language English
Subject Domain (in DDC) Computer science, information & general works ♦ Natural sciences & mathematics ♦ Physics
Subject Keyword Condensed Matter - Materials Science ♦ physics:cond-mat
Abstract The structural profiles and electronic properties of pentacene (C$_{22}$H$_{14}$) multilayers on Ag(111) surface has been studied within the density functional theory (DFT) framework. We have performed first-principle total energy calculations based on the projector augmented wave (PAW) method to investigate the initial growth patterns of pentacene (Pn) on Ag(111) surface. In its bulk phase, pentacene crystallizes with a triclinic symmetry while a thin film phase having an orthorhombic unit cell is energetically less favorable by 0.12 eV/cell. Pentacene prefers to stay planar on Ag(111) surface and aligns perfectly along silver rows without any molecular deformation at a height of 3.9 {\AA}. At one monolayer (ML) coverage the separation between the molecular layer and the surface plane extends to 4.1 {\AA} due to intermolecular interactions weakening surface--pentacene attraction. While the first ML remains flat, the molecules on a second full pentacene layer deposited on the surface rearrange so that they become skewed with respect to each other. This adsorption mode is energetically more preferable than the one for which the molecules form a flat pentacene layer by an energy difference similar to that obtained for bulk and thin film phases. Moreover, as new layers added, pentacenes assemble to maintain this tilting for 3 and 4 ML similar to its bulk phase while the contact layer always remains planar. Therefore, our calculations indicate bulk-like initial stages for the growth pattern.
Description Reference: J. Phys. Chem. C, 2010, 114 (6), pp 2724-2729
Educational Use Research
Learning Resource Type Article
Page Count 21


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