Observation of direct vibrational excitation in gas-surface collisions of CO with Au(111): a new model system for surface dynamics

被引:23
|
作者
Schaefer, Tim [1 ,2 ]
Bartels, Nils [1 ,2 ]
Golibrzuch, Kai [1 ,2 ]
Bartels, Christof [1 ,2 ]
Koeckert, Hansjochen [1 ,2 ]
Auerbach, Daniel J. [1 ,2 ,3 ]
Kitsopoulos, Theofanis N. [1 ,2 ,4 ,5 ]
Wodtke, Alec M. [1 ,2 ,3 ]
机构
[1] Univ Gottingen, Inst Phys Chem, Gottingen, Germany
[2] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
[3] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[4] Univ Crete, Dept Chem, Iraklion, Greece
[5] IESL FORTH, Iraklion, Greece
关键词
BORN-OPPENHEIMER APPROXIMATION; TO-STATE SCATTERING; ENERGY-TRANSFER; DISSOCIATIVE ADSORPTION; CHEMICAL-DYNAMICS; METAL-SURFACES; ASSOCIATIVE DESORPTION; TRANSLATIONAL ENERGY; MOLECULES; GOLD;
D O I
10.1039/c2cp43351f
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
We report vibrational excitation of CO from its ground (v = 0) to first excited (v = 1) vibrational state in collision with Au(111) at an incidence energy of translation of E-I = 0.45 eV. Unlike past work, we can exclude an excitation mechanism involving temporary adsorption on the surface followed by thermalization and desorption. The angular distributions of the scattered CO molecules are narrow, consistent with direct scattering occurring on a sub-ps time scale. The absolute excitation probabilities are about 3% of those expected from thermal accommodation. The surface temperature dependence of excitation, which was measured between 373 and 973 K, is Arrhenius-like with an activation energy equal to the energy required for vibrational excitation. Our measurements are consistent with a vibrational excitation mechanism involving coupling of thermally excited electron-hole pairs of the solid to CO vibration.
引用
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页码:1863 / 1867
页数:5
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