Restructuring of Porphyrin Networks Driven by Self-Assembled Octanoic Acid Monolayer on Au(111)

被引:10
|
作者
Kim, Yongman [1 ,2 ]
Kim, YoungJae [1 ,2 ]
Park, Jeong Young [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
[2] Inst for Basic Sci Korea, Ctr Nanomat & Chem React, Daejeon 34141, South Korea
关键词
LIQUID-SOLID INTERFACE; SCANNING-TUNNELING-MICROSCOPY; MOLECULES; OXIDATION; GRAPHITE; SURFACE; OCTAETHYLPORPHYRIN; ARCHITECTURES; TEMPERATURE; DIRECTION;
D O I
10.1021/acs.langmuir.0c00333
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report time-dependent surface restructuring of bicomponent domain structures of 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphine (H2OEP) and cobalt(II) 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphine (CoOEP) (H-2/Co OEP) driven by self-assembled octanoic acid on the surface of Au(111). Scanning tunneling microscopy (STM) visualized molecular adsorption/desorption and rearrangement of supramolecular architectures in real-time in a solution of octanoic acid. We found that unique domain structures emerged at an initial state guided by adsorbed octanoic acid on the Au surface. Moreover, the desorption of octanoic acid occurred in solution, leading to the surface restructuring of porphyrin molecular networks. This molecular evidence is well- manifested in the time-dependent phase transitions, monitored by in situ STM.
引用
收藏
页码:3792 / 3797
页数:6
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