Structures of a film of the long-chain n-alkane n-C44H90 on a Cu (100) surface

被引:27
作者
Hosoi, Y [1 ]
Sakurai, Y
Yamamoto, M
Ishii, H
Ouchi, Y
Seki, K
机构
[1] Nagoya Univ, Grad Sch Sci, Dept Chem, Chikusa Ku, Nagoya, Aichi 4648602, Japan
[2] Showa Univ, Coll Arts & Sci, Dept Chem, Shinagawa Ku, Tokyo 1428555, Japan
[3] Nagoya Univ, Res Ctr Mat Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
关键词
low energy electron diffraction (LEED); infrared absorption spectroscopy; epitaxy; growth; copper; alkanes; low index; single crystal surfaces;
D O I
10.1016/S0039-6028(02)01855-1
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
Structures of a film of a long-chain n-alkane, tetratetracontane (n-C44H90; TTC) on a Cu(100) single-crystal surface were investigated by a combination of infrared reflection absorption spectroscopy (IRRAS) and low energy electron diffraction (LEED). Vacuum vapor deposition was used to prepare epitaxially grown films. Measurements of the stepwise increase in film thickness revealed the structural changes in TTC film during film growth. IRRAS investigations revealed that three phases appear during film growth, as previously observed for TTC deposited on Au(111) and Ag(111) surfaces. In the first layer, which consists of TTC molecules directly adsorbed on a Cu(100) surface, the molecules assume a flat-on structure with the carbon skeleton plane of TTC parallel to the surface (flat-on phase). The next layer consists of slightly disordered molecules including a gauche conformation (gauche phase). Finally, a film with molecular packing close to that in the crystalline state is formed with further deposition (quasi-crystalline phase). LEED investigations indicated that (1) the first layer forms a regular unit cell with a lamellar structure, (2) the molecular arrangement shows a transition upon the completion of the first layer, which can be ascribed to subdivision of the lamella into antiphase domains, and (3) the surfaces of the gauche and quasi-crystalline phases do not have two dimensional order. Since the molecule itself has a one-dimensional periodic structure, it is necessary to consider both the intramolecular and intermolecular periodicity for detailed analysis by LEED. Simulation of the LEED pattern by a kinematic theory indicated that the intramolecular rather than the intermolecular periodicity dominates the LEED pattern. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:157 / 174
页数:18
相关论文
共 59 条
[41]   SCANNING TUNNELING MICROSCOPY IMAGING OF ALKANE BILAYERS ADSORBED ON GRAPHITE - MECHANISM OF CONTRAST [J].
THIBAUDAU, F ;
WATEL, G ;
COUSTY, J .
SURFACE SCIENCE, 1993, 281 (1-2) :L303-L307
[42]  
Ulman A., 1991, INTRO ULTRATHIN ORGA
[43]   Surface "architecture" with large organic molecules: interface order and epitaxy [J].
Umbach, E ;
Glockler, K ;
Sokolowski, M .
SURFACE SCIENCE, 1998, 402 (1-3) :20-31
[44]   Formation of two-dimensional crystals of alkanes on the Au(111) surface in neat liquid [J].
Uosaki, K ;
Yamada, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (16) :4090-4091
[45]   High-resolution imaging of n-alkane crystals by atomic force microscopy [J].
Valdre, G ;
Allessandrini, A ;
Muscatello, U ;
Valdre, U .
PHILOSOPHICAL MAGAZINE LETTERS, 1998, 78 (03) :255-261
[46]  
Van Hove M.A., 1986, Low Energy Electron Diffraction: Experiment, Theory, and Surface Structure Determination
[47]   SCANNING-TUNNELING-MICROSCOPY STUDIES OF SOLVENT EFFECTS ON THE ADSORPTION AND MOBILITY OF TRIACONTANE TRIACONTANOL MOLECULES ADSORBED ON GRAPHITE [J].
VENKATARAMAN, B ;
BREEN, JJ ;
FLYNN, GW .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (17) :6608-6619
[48]   DIRECT OBSERVATION OF LONG-CHAIN ALKANE BILAYER FILMS ON GRAPHITE BY SCANNING TUNNELING MICROSCOPY [J].
WATEL, G ;
THIBAUDAU, F ;
COUSTY, J .
SURFACE SCIENCE, 1993, 281 (1-2) :L297-L302
[49]  
Weiss K, 1999, J MOL STRUC-THEOCHEM, V458, P143, DOI 10.1016/S0166-1280(98)00357-1
[50]   Energetics and kinetics of the physisorption of hydrocarbons on Au(111) [J].
Wetterer, SM ;
Lavrich, DJ ;
Cummings, T ;
Bernasek, SL ;
Scoles, G .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (46) :9266-9275