Rearrangements in an alkylthiolate self-assembled monolayer using electrostatic interactions between nanoscale asperity and organomercaptan molecules

被引:3
|
作者
Paramonov, Pavel B.
Lyuksyutov, Sergei F. [1 ]
Mayevska, Olga V.
Reagan, Michael A.
Umemura, Kazuo
Tobari, Hiroaki
Hara, Masahiko
Vaia, Richard A.
Juhl, Shane
机构
[1] Univ Akron, Dept Phys, Akron, OH 44325 USA
[2] Univ Akron, Dept Chem, Akron, OH 44325 USA
[3] Univ Akron, Dept Polymer Engn, Akron, OH 44325 USA
[4] Musashi Inst Technol, Dept Environm Energy Engn, Tokyo 1588577, Japan
[5] RIKEN, Wako, Saitama 3510198, Japan
[6] USAF, Res Lab, Mat & Mfg Directorate, WPAFB, Wright Patterson AFB, OH 45433 USA
关键词
D O I
10.1021/la0532858
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chemically induced rearrangements of amphifunctional molecules have been demonstrated using strong nonuniform electric fields (10(8)-10(10)V m(-1)) induced in the vicinity of nanoscale asperities. Electrostatic interactions utilizing these rearrangements of alkylthiolates assembled on Au(111) result in the nanopatterning of raised nanostructure (1.5-9 nm high, 15-100 nm wide) arrays on a second time scale by manipulating an atomic force microscope (AFM) tip above the monolayer. It is suspected that, as a result of the oxidative cleavage initiated by a weak bias of the tip, the S end of the alkylthiolate chain carrying a sulfenium cation is attracted to the (lifting) tip, forming bi- and higher-layer structures in the vicinity of the tip apex. Stabilization of the multiple-layered structures is accomplished via mutual attraction and entanglement of hydrocarbon chains. The rearrangements suggest a novel and general approach for nanoscale architecture in self-assembled systems.
引用
收藏
页码:6555 / 6561
页数:7
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