Silver residues as a possible key to a remarkable oxidative catalytic activity of nanoporous gold

被引:112
作者
Moskaleva, Lyudmila V. [1 ]
Roehe, Sarah [1 ]
Wittstock, Arne [1 ]
Zielasek, Volkmar [1 ]
Kluener, Thorsten [2 ]
Neyman, Konstantin M. [3 ,4 ,5 ]
Baeumer, Marcus [1 ]
机构
[1] Univ Bremen, Inst Angew & Phys Chem, D-28334 Bremen, Germany
[2] Carl von Ossietzky Univ Oldenburg, Inst Reine & Angew Chem, D-26111 Oldenburg, Germany
[3] ICREA, Barcelona 08010, Spain
[4] Univ Barcelona, IQTCUB, E-08028 Barcelona, Spain
[5] Univ Barcelona, Dept Quim Fis, E-08028 Barcelona, Spain
关键词
MOLECULAR-OXYGEN ADSORPTION; DENSITY-FUNCTIONAL THEORY; CO OXIDATION; AU(321) SURFACE; CARBON-MONOXIDE; AU; AU(111); NANOPARTICLES; O-2; DFT;
D O I
10.1039/c0cp02372h
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
Recently, several forms of unsupported gold were shown to display a remarkable activity to catalyze oxidation reactions. Experimental evidence points to the crucial role of residual silver present in very small concentrations in these novel catalysts. We focus on the catalytic properties of nanoporous gold (np-Au) foams probed via CO and oxygen adsorption/co-adsorption. Experimental results are analyzed using theoretical models represented by the flat Au(111) and the kinked Au(321) slabs with Ag impurities. We show that Ag atoms incorporated into gold surfaces can facilitate the adsorption and dissociation of molecular oxygen on them. CO adsorbed on top of 6-fold coordinated Au atoms can in turn be stabilized by co-adsorbed atomic oxygen by up to 0.2 eV with respect to the clean unsubstituted gold surface. Our experiments suggest a linking of that most strongly bound CO adsorption state to the catalytic activity of np-Au. Thus, our results shed light on the role of silver admixtures in the striking catalytic activity of unsupported gold nanostructures.
引用
收藏
页码:4529 / 4539
页数:11
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