Self-Assembled Structures of Benzoic Acid on Au(111) Surface

被引:9
|
作者
Thu-Hien Vu [1 ,2 ]
Wandlowski, Thomas [2 ]
机构
[1] Hanoi Univ Sci & Technol, Int Training Inst Mat Sci ITIMS, 1 Dai Co Viet, Hanoi, Vietnam
[2] Univ Bern, Dept Chem & Biochem, Freiestr 3, CH-3012 Bern, Switzerland
关键词
Self-assembly; gold single crystals; cyclic voltammetry; EC-STM; benzoic acid; SCANNING-TUNNELING-MICROSCOPY; IN-SITU STM; SUPRAMOLECULAR NETWORKS; INTERFACE STRUCTURE; ISOPHTHALIC ACID; ADSORPTION; DYNAMICS; NANOSTRUCTURES; ELECTRODES; MOLECULES;
D O I
10.1007/s11664-017-5358-3
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Electrochemical scanning tunneling microscopy combined with cyclic voltammetry were employed to explore the self-assembly of benzoic acid (BA) on a Au(111) substrate surface in a 0.1-M HClO4 solution. At the negatively charged surface, BA molecules form two highly ordered physisorbed adlayers with their phenyl rings parallel to the substrate surface. High-resolution scanning tunneling microscopy images reveal the packing arrangement and internal molecular structures. The striped pattern and zigzag structure of the BA adlayers are composed of parallel rows of dimers, in which two BA molecules are bound through a pair of O-H center dot center dot center dot O hydrogen bonds. Increasing the electrode potential further to positive charge densities of Au(111) leads to the desorption of the physisorbed hydrogen-bonded networks and the formation of a chemisorbed adlayer. BA molecules change their orientation from planar to upright fashion, which is accompanied by the deprotonation of the carboxyl group. Furthermore, potential-induced formation and dissolution of BA adlayers were also investigated. Structural transitions between the various types of ordered adlayers occur according to a nucleation and growth mechanism.
引用
收藏
页码:3463 / 3471
页数:9
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