Unusual self-assembly of chloroaluminium phthalocyanine on graphite

被引:3
|
作者
Ma, Hai-yang [1 ,2 ]
Zhao, Yan-ling [2 ]
Zaw, Myo Win [2 ]
Jia, Jin-Feng [1 ]
Zhang, Rui-qin [2 ]
Van Hove, Michel A. [3 ,4 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Phys & Astron, Key Lab Artificial Struct & Quantum Control, Minist Educ, Shanghai 200240, Peoples R China
[2] City Univ Hong Kong, Dept Phys, Hong Kong, Peoples R China
[3] Hong Kong Baptist Univ, Inst Computat & Theoret Studies, Hong Kong, Peoples R China
[4] Hong Kong Baptist Univ, Dept Phys, Hong Kong, Peoples R China
关键词
Weak interactions; Dispersion forces; 2D self-assembly; MOLECULES; DISPERSION; CHEMISTRY;
D O I
10.1016/j.susc.2018.11.010
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
We report an unusual self-assembled layer structure of chloroaluminium phthalocyanine (ClAlPc) molecules on highly ordered pyrolytic graphite (HOPG), in which a close-packed well-ordered monolayer is separated from the substrate by a relatively disordered buffer layer, as revealed using scanning tunneling microscopy (STM). Our close-packed monolayer has a nearly rectangular lattice, instead of the distinctly different square lattice for the more commonly observed well-ordered bilayer structure. This may be due to the dominance of intermolecular interactions within the monolayer when the influence from the substrate is shielded by the buffer layer. Density Functional Theory (DFT) calculations and Reduced Density Gradient (RDG) analysis indicate that the dominant intermolecular interaction within the unusual layer is likely the London dispersion force.
引用
收藏
页码:104 / 110
页数:7
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