Structural evolution of trimesic acid (TMA)/Zn2+ ion network on Au(111) to final structure of (10√3 x 10√3)

被引:1
|
作者
Kim, Jandee [1 ,2 ]
Lee, Jaesung [1 ]
Rhee, Choong Kyun [1 ]
机构
[1] Chungnam Natl Univ, Dept Chem, Daejeon 34134, South Korea
[2] Korea Atom Energy Res Inst, Nucl Chem Res Div, Daejeon 34057, South Korea
基金
新加坡国家研究基金会;
关键词
Metal-organic coordination; Network; Trimesic acid; Zn; Au(111); SCANNING-TUNNELING-MICROSCOPY; ORIENTED PYROLYTIC-GRAPHITE; WEAK HYDROGEN-BONDS; COORDINATION CHEMISTRY; SELF-ORGANIZATION; TEREPHTHALIC ACID; CU(100) SURFACE; NANOSTRUCTURES; SUBSTRATE; ARCHITECTURES;
D O I
10.1016/j.susc.2015.10.021
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
Presented is a scanning tunneling microscopy (STM) study of structural evolution of TMA/Zn2+ ion network on Au(111) to the final structure of (10 root 3 x 10 root 3) during solution phase post-modification of pristine trimesic acid (TMA) network of a (5 root 3 x 5 root 3) structure with Zn2+ ions. Coordination of Zn2+ ions into adsorbed TMA molecules transforms crown-like TMA hexamers in pristine TMA network to chevron pairs in TMA/Zn2+ ion network. Two ordered transient structures of TMA/Zn2+ ion network were observed. One is a (5 root 7 x 5 root 7) structure consisting of Zn2+ ion-containing chevron pairs and Zn2+ ion-free TMA dimers. The other is a (5 root 39 x 5 root 21) structure made of chevron pairs and chevron-pair-missing sites. An STM image showing domains of different stages of crystallization of chevron pairs demonstrates that the TMA/Zn2+ network before reaching to the final one is quite dynamic. The observed structural evolution of the TMA/Zn2+ ion network is discussed in terms of modification of configurations of adsorbed TMA as accommodating Zn2+ ions and re-ordering of Zn2+ ion-containing chevron pairs. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 134
页数:6
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