Investigation of electron-induced cross-linking of self-assembled monolayers by scanning tunneling microscopy

被引:4
|
作者
Stohmann, Patrick [1 ]
Koch, Sascha [1 ]
Yang, Yang [1 ,2 ]
Kaiser, Christopher David [1 ]
Ehrens, Julian [3 ]
Schnack, Juergen [3 ]
Biere, Niklas [4 ]
Anselmetti, Dario [4 ]
Goelzhaeuser, Armin [1 ]
Zhang, Xianghui [1 ]
机构
[1] Univ Bielefeld, Phys Supramol Syst & Surfaces, Fac Phys, D-33615 Bielefeld, Germany
[2] Imperial Coll London, Dept Chem Engn, London SW7 2AZ, England
[3] Univ Bielefeld, Condensed Matter Theory Grp, Fac Phys, D-33615 Bielefeld, Germany
[4] Univ Bielefeld, Expt Biophys & Appl Nanosci, Fac Phys, D-33615 Bielefeld, Germany
基金
欧盟地平线“2020”;
关键词
carbon nanomembranes; electron-induced cross-linking; scanning tunneling microscopy; self-assembled monolayers; subnanometerpores; CARBON NANOMEMBRANES; TERPHENYLTHIOL; IRRADIATION; POLYMORPHISM; MOLECULES; MECHANISM; SURFACES; AU(111); METALS;
D O I
10.3762/bjnano.13.39
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ultrathin membranes with subnanometer pores enabling molecular size-selective separation were generated on surfaces via electron-induced cross-linking of self-assembled monolayers (SAMs). The evolution of p-terphenylthiol (TPT) SAMs on Au(111) surfaces into cross-linked monolayers was observed with a scanning tunneling microscope. As the irradiation dose was increased, the cross- linked regions continued to grow and a large number of subnanometer voids appeared. Their equivalent diameter is 0.5 +/- 0.2 nm and the areal density is approximate to 1.7 x 10(17) m(-2). Supported by classical molecular dynamics simulations, we propose that these voids may correspond to free volumes inside a cross-linked monolayer.
引用
收藏
页码:462 / 471
页数:10
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