Chemisorption and dissociation of single oxygen molecules on Ag(110)

被引:0
|
作者
Hahn, JR
Ho, W
机构
[1] Univ Calif Irvine, Dept Phys & Astron, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2005年 / 123卷 / 21期
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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
The chemisorption of single oxygen molecules on Ag(110) and the dissociation of the adsorbed molecules induced by tunneling electrons were studied at 13 K using a variable-low-temperature scanning tunneling microscope. Two predominant types of chemisorbed O-2 molecules were identified, one with the O-2 molecular axis aligned along the [001] direction of the substrate [O-2(001)], and the other with the molecular axis aligned along the [1 (1) over bar0] direction [O-2(1 (1) over bar0)]. Tunneling of electrons between the scanning tunneling microscope tip and O-2(001) caused the molecule either to rotate or dissociate, depending on the direction of electron tunneling. In contrast, electron tunneling caused O-2(1 (1) over bar0) to dissociate regardless of tunneling direction. In addition to O-2(001) and O-2(1 (1) over bar0), several other oxygen species and their dynamical behaviors were observed. (c) 2005 American Institute of Physics.
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页数:6
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