Tuning the reactivity of oxide surfaces by charge-accepting adsorbates

被引:52
|
作者
Wang, Yuemin
Xia, Xinyu
Urban, Alexander
Qiu, Hengshan
Strunk, Jennifer
Meyer, Bernd
Muhler, Martin [1 ]
Woell, Christof
机构
[1] Ruhr Univ Bochum, Lehrstuhl Tech Chem, D-44780 Bochum, Germany
[2] Ruhr Univ Bochum, Lehrstuhl Physkal Chem 1, D-44780 Bochum, Germany
[3] Ruhr Univ Bochum, Lehrstuhl Tech Chem, D-44780 Bochum, Germany
[4] Ruhr Univ Bochum, Lehrstuhl Theoret Chem, D-44780 Bochum, Germany
关键词
ab initio calculations; heterogeneous catalysis; microcalorimetry; vibrational spectroscopy; zinc oxide;
D O I
10.1002/anie.200702815
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bridging the materials and pressure gaps : The adsorption of CO on ZnO surfaces becomes much stronger in the presence of preadsorbed CO2 (see picture; O red, Zn gray, C green). The increased strength of the interaction between CO and polycrystalline ZnO powder originates from the formation of tridentate carbonate species on the mixed-terminated (1010) surfaces, which increase the Lewis acidity of neighboring Zn2+ cations. (Figure Presented). © 2007 Wiley-VCH Verlag GmbH &. Co. KGaA.
引用
收藏
页码:7315 / 7318
页数:4
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