Substrate-mediated electron tunneling through molecule-electrode interfaces

被引:2
|
作者
Sun, Jia-Tao [1 ]
Chen, Lan [2 ]
Feng, Yuan Ping [3 ]
Wee, Andrew Thye Shen [3 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
[3] Natl Univ Singapore, Dept Phys, Singapore 117542, Singapore
基金
新加坡国家研究基金会;
关键词
ab initio calculations; adsorbed layers; density functional theory; electrodes; electronic density of states; graphite; organic compounds; silver; tunnelling; TRANSPORT; FILM;
D O I
10.1063/1.3650248
中图分类号
O59 [应用物理学];
学科分类号
摘要
Electron tunneling properties at the molecule-electrode interfaces formed by coronene molecules adsorbed on Ag(111) and highly oriented pyrolytic graphite surfaces are investigated by scanning tunneling microscopy and first-principles calculations. Experimentally, the coronene molecules display significant variation in the electronic density of states at the molecular centers on different substrates. An analysis of the electronic structures for both systems by first-principles calculations based on density functional theory reveals that substrate dependent molecular image contrast is ascribed to the resonant tunneling process mediated by geometrically different substrates. Possible consequences for electron transport are briefly discussed. (C) 2011 American Institute of Physics. [doi:10.1063/1.3650248]
引用
收藏
页数:3
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