Self-assembly of amino acids on the Cu(001) surface

被引:49
作者
Zhao, XY
Wang, H
Zhao, RG
Yang, WS [1 ]
机构
[1] Peking Univ, Mesoscop Phys Lab, Beijing 100871, Peoples R China
[2] Peking Univ, Dept Phys, Beijing 100871, Peoples R China
来源
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS | 2001年 / 16卷 / 1-2期
基金
中国国家自然科学基金;
关键词
amino acids; single crystal metal surfaces; adsorption; organic molecules; hydrogen bonds; step faceting; chirality; scanning tunneling microscopy (STM);
D O I
10.1016/S0928-4931(01)00276-4
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The major results of a series of our recent investigations on the self-assembly of amino acids on the Cu(001) surface are reviewed in the present paper. It has been found that all eight amino acids studied here adsorb on the surface in their anionic forms and that for most of them, three distinctly different phases of the adsorbates may form, that is, the 2D gas, intermediate and solid phases, In the gas phase, the intermolecular interactions are repulsive and the molecules are "standing" on their carboxylate group "feet" and can diffuse frequently on the surface. In the intermediate phase, the intermolecular interactions are also repulsive and the molecules are also "standing" on the surface; however, the molecules align into short rows. In the solid phase, the molecules "lie" down with their main chain and, in some cases, also the side chain attached to the surface, whereas, hydrogen bonds are likely responsible for stabilization of this phase. In addition to the formation of these phases. some amino acid adsorbates may cause magnificent step faceting and bunching or even chiral restructuring of the surface morphology. These results may have applications in nano-scale materials. nano-technology and probably, also in chiral separations or enantioselective heterogeneous catalysis. (C) 2001 Elsevier Science B.V.. All rights reserved.
引用
收藏
页码:41 / 50
页数:10
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