Diffusion versus sticking anisotropy: Anisotropic growth of organic molecular films

被引:20
作者
Berkebile, Stephen
Koller, Georg
Hlawacek, Gregor
Teichert, Christian
Netzer, Falko P.
Ramsey, Michael G.
机构
[1] Karl Franzens Univ Graz, Inst Phys, A-8010 Graz, Austria
[2] Univ Min & Met Leoben, Inst Phys, A-8700 Leoben, Austria
基金
奥地利科学基金会;
关键词
surface diffusion; growth; self-assembly; sticking; near edge extended X-ray absorption tine structure (NEXAFS); molecular beam epitaxy; titanium oxide; aromatics;
D O I
10.1016/j.susc.2006.06.044
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The molecular/crystal orientation and morphology of active molecular structures is a key determinant for the function of nanoscaled organic devices, yet little is known regarding the processes that govern thin film growth. Here, we show that either sticking or diffusion anisotropy can control the growth depending on preparation conditions. This is illustrated by an investigation into the growth of sexiphenyl (6P) on the anisotropic TiO2(110)-(1 x 1) single crystal surface. The great differences in crystallite orientation and morphology observed are explained by the domination of the growth kinetics by either sticking or diffusion anisotropy depending on growth temperature. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:L313 / L317
页数:5
相关论文
共 16 条
[1]   Dipole-assisted self-assembly of light-emitting p-nP needles on mica [J].
Balzer, F ;
Rubahn, HG .
APPLIED PHYSICS LETTERS, 2001, 79 (23) :3860-3862
[2]   Polymer crystallization on pre-patterned substrates [J].
Dorenbos, G ;
Sommer, JU ;
Reiter, G .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (02) :784-791
[3]   Simulations of denuded-zone formation during growth on surfaces with anisotropic diffusion [J].
Ebner, C ;
Park, KB ;
Nielsen, JF ;
Pelz, JP .
PHYSICAL REVIEW B, 2003, 68 (24)
[4]   POLARIZED ELECTROLUMINESCENCE FROM ORIENTED P-SEXIPHENYL VACUUM-DEPOSITED FILM [J].
ERA, M ;
TSUTSUI, T ;
SAITO, S .
APPLIED PHYSICS LETTERS, 1995, 67 (17) :2436-2438
[5]   Single crystalline nature of para-sexiphenyl crystallites grown on KCl(100) [J].
Haber, T ;
Oehzelt, M ;
Resel, R ;
Andreev, A ;
Thierry, A ;
Sitter, H ;
Smilgies, DM ;
Schaffer, B ;
Grogger, W ;
Resel, R .
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2006, 6 (03) :698-703
[6]   Para-sexiphenyl thin films on KCl(100) surfaces: Growth morphologies and their individual epitaxial order [J].
Haber, T ;
Andreev, A ;
Thierry, A ;
Sitter, H ;
Oehzelt, M ;
Resel, R .
JOURNAL OF CRYSTAL GROWTH, 2005, 284 (1-2) :209-220
[7]   The nucleation of pentacene thin films [J].
Heringdorf, FJMZ ;
Reuter, MC ;
Tromp, RM .
APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING, 2004, 78 (06) :787-791
[8]   Highly oriented growth of p-sexiphenyl molecular nanocrystals on rubbed polymethylene surface [J].
Hu, WS ;
Lin, YF ;
Tao, YT ;
Hsu, YJ ;
Wei, DH .
MACROMOLECULES, 2005, 38 (23) :9617-9624
[9]   Substrate-mediated electronic structure and properties of sexiphenyl films [J].
Ivanco, J ;
Winter, B ;
Netzer, TR ;
Ramsey, MG .
ADVANCED MATERIALS, 2003, 15 (21) :1812-1815
[10]   Ultrathin film growth of p-phenylene oligomers on alkali halide substrates [J].
Kintzel, EJ ;
Smilgies, DM ;
Skofronick, JG ;
Safron, SA ;
Van Winkle, DH .
JOURNAL OF CRYSTAL GROWTH, 2006, 289 (01) :345-350