Tunable Two-Dimensional Binary Molecular Networks

被引:76
作者
Huang, Yu Li [1 ]
Chen, Wei [1 ,2 ]
Li, Hui [1 ]
Ma, Jing [3 ]
Pflaum, Jens [4 ]
Wee, Andrew Thye Shen [1 ]
机构
[1] Natl Univ Singapore, Dept Phys, Singapore 117542, Singapore
[2] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[3] Nanjing Univ, Key Lab Mesoscop Chem MOE, Nanjing 210093, Peoples R China
[4] Univ Wurzburg, Bavarian Ctr Appl Energy Res, Inst Expt Phys 6, D-97047 Wurzburg, Germany
基金
中国国家自然科学基金;
关键词
binary networks; hydrogen bonding; scanning tunneling microscopy; self-assembly; SCANNING-TUNNELING-MICROSCOPY; HONEYCOMB NETWORKS; SELF-ORGANIZATION; POROUS NETWORK; CYANURIC ACID; THIN-FILMS; SURFACE; PHTHALOCYANINE; PORPHYRIN; MELAMINE;
D O I
10.1002/smll.200901291
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel approach to constructing tunable and robust 2D binary molecular nanostructures on an inert graphite surface is presented. The guest molecules are embedded into a host molecular matrix and constrained via the formation of multiple intermolecular hydrogen bonds. By varying the binary molecular ratio and the molecular geometry, various molecular arrays with tunable intermolecular distances are fabricated. The results suggest a promising route for the fabrication of ordered and stable molecular nanostructure arrays for molecular sensors, molecular spintronic devices, and molecular p-n nanojunctions.
引用
收藏
页码:70 / 75
页数:6
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