Nature of Oxidation of the Au(111) Surface: Experimental and Theoretical Investigation

被引:45
作者
Baker, Thomas A. [1 ]
Xu, Bingjun [1 ]
Liu, Xiaoying [1 ]
Kaxiras, Efthimios [1 ,2 ,3 ]
Friend, Cynthia A. [1 ,2 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[3] Harvard Univ, Dept Phys, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
CO OXIDATION; LOW-TEMPERATURE; CATALYTIC-ACTIVITY; AU/TIO2; CATALYSTS; OXYGEN-ADSORPTION; GOLD CATALYSTS; ATOMIC OXYGEN; PSEUDOPOTENTIALS; CHEMISORPTION; NANOPARTICLES;
D O I
10.1021/jp9052192
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 Au(111) surface is the prototypical inert metal substrate, whose interaction with oxygen remains a controversial issue. Here, we study the effect of dosing temperature and coverage on the absorption of atomic oxygen on this surface, using ab initio molecular dynamics and high-resolution electron energy loss spectroscopy. Two vibrational peaks are observed experimentally at 380 and 580 cm(-1). The lower frequency peak is predominant at low oxygen coverages, while the higher frequency peak grows more pronounced with increasing oxygen coverage. Our simulations reproduce these results and show that oxygen chemisorbed on the surface is the primary species at low coverages or low surface temperatures. An oxide-like species, both on the surface and under the top layer of gold, becomes dominant at higher coverages or temperatures. These results elucidate the nature of oxidation of the Au(111) Surface.
引用
收藏
页码:16561 / 16564
页数:4
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