CO chemisorption on the surfaces of the golden cages

被引:31
|
作者
Huang, Wei [3 ,4 ]
Bulusu, Satya [1 ,2 ]
Pal, Rhitankar [1 ,2 ]
Zeng, Xiao Cheng [1 ,2 ]
Wang, Lai-Sheng [5 ]
机构
[1] Univ Nebraska, Dept Chem, Lincoln, NE 68588 USA
[2] Univ Nebraska, Ctr Mat & Nanosci, Lincoln, NE 68588 USA
[3] Washington State Univ, Dept Phys, Richland, WA 99354 USA
[4] Pacific NW Natl Lab, Chem & Mat Sci Div, Richland, WA 99352 USA
[5] Brown Univ, Dept Chem, Providence, RI 02912 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2009年 / 131卷 / 23期
基金
美国国家科学基金会;
关键词
adsorption; carbon compounds; chemisorption; gold; metal clusters; photoelectron spectra; solid-state phase transformations; spin-orbit interactions; surface chemistry; CARBON-MONOXIDE ADSORPTION; CLUSTER ANIONS; AU CLUSTERS; PHOTOELECTRON-SPECTROSCOPY; VIBRATIONAL SPECTROSCOPY; SATURATED ADSORPTION; MOLECULAR-OXYGEN; OXIDATION; SIZE; O-2;
D O I
10.1063/1.3273326
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 a joint experimental and theoretical study of CO chemisorption on the golden cages. We find that the Au-17- cage is highly robust and retains its cage structure in Au-17(CO)(-). On the other hand, the Au-16- cage is transformed to a structure similar to Au-17- upon the adsorption of CO. Au-18- is known to consist of two nearly degenerate structures, i.e., a cage and a pyramidal isomer, which coexist in the cluster beam. However, upon CO chemisorption only the cage isomer is observed while the pyramidal isomer no longer exists due to its less favorable interaction with CO, compared to the cage isomer. We find that inclusion of the spin-orbit effects is critical in yielding simulated spectra in quantitative agreement with the experimental data and providing unequivocal structural information and molecular insights into the chemical interactions between CO and the golden cages.
引用
收藏
页数:6
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