Effect of Mechanical Strain on Electric Conductance of Molecular Junctions

被引:10
|
作者
Inatomi, Junichi [1 ]
Fujii, Shintaro [1 ]
Marques-Gonzalez, Santiago [1 ]
Masai, Hiroshi [2 ]
Tsuji, Yasushi [2 ]
Terao, Jun [2 ]
Kiguchi, Manabu [1 ]
机构
[1] Tokyo Inst Technol, Grad Sch Sci & Engn, Dept Chem, Meguro Ku, Tokyo 1528511, Japan
[2] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2015年 / 119卷 / 33期
关键词
SINGLE; ELECTRONICS; TRANSPORT;
D O I
10.1021/acs.jpcc.5b04386
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
Electromechanical properties of single molecular junctions are investigated using scanning tunneling microscopy based break junction method. Two types of molecular junctions consisting of pi-conjugated backbones with and without coordinative bonding (i.e., Co((4-aniline)-terpyridine)(2) complex and oligo(phenylene-ethynylene) derivative) are prepared between two Au electrodes. Electronic transport measurements revealed molecular conductance of ca. 10(-4) G(0) (G(0) = 2e(2)/h) for both of the molecular junctions. Then we assessed the electronic transport properties of the two types of molecular junctions under mechanical strain in their compression-elongation cycle. We found significant asymmetric electromechanical response for all covalent systems of the oligo(phenylene-ethynylene) derivative, while the Co complex with the coordinative bonding exhibits symmetric modulation of the electronic transport property in the compression-elongation cycle of the molecular junctions. The asymmetric and symmetric electromechanical behavior can be, respectively, ascribed to rigid covalent bonding in the pi-conjugated backbone and flexible coordinative bonding at the metal center. This study demonstrates potential tunability of the molecular conductance under mechanical stimulus.
引用
收藏
页码:19452 / 19457
页数:6
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