Stabilization of Catalytically Active Cu plus Surface Sites on TitaniumCopper Mixed-Oxide Films**

被引:56
作者
Baber, Ashleigh E. [1 ]
Yang, Xiaofang [1 ]
Kim, Hyun You [3 ]
Mudiyanselage, Kumudu [1 ]
Soldemo, Markus [2 ]
Weissenrieder, Jonas [2 ]
Senanayake, Sanjaya D. [1 ]
Al-Mahboob, Abdullah [3 ]
Sadowski, Jerzy T. [3 ]
Evans, Jaime [4 ]
Rodriguez, Jose A. [1 ]
Liu, Ping [3 ]
Hoffmann, Friedrich M. [5 ]
Chen, Jingguang G. [1 ,6 ]
Stacchiola, Dario J. [1 ]
机构
[1] BNL, Dept Chem, Upton, NY 11973 USA
[2] KTH Royal Inst Technol, Stockholm, Sweden
[3] BNL, CFN, Upton, NY 11973 USA
[4] Cent Univ Venezuela, Fac Ciencias, Caracas 1020A, Venezuela
[5] BMCC CUNY, Dept Sci, New York, NY 10007 USA
[6] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
基金
瑞典研究理事会;
关键词
CO oxidation; IR spectroscopy; mixed oxides; scanning tunneling microscopy; surface chemistry; TRANSITION-METAL OXIDES; PHOTOELECTRON-SPECTROSCOPY; PHOTOCATALYTIC ACTIVITY; AMBIENT-PRESSURE; CARBON-MONOXIDE; OXIDATION; COPPER; CO; ADSORPTION;
D O I
10.1002/anie.201402435
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The oxidation of CO is the archetypal heterogeneous catalytic reaction and plays a central role in the advancement of fundamental studies, the control of automobile emissions, and industrial oxidation reactions. Copper-based catalysts were the first catalysts that were reported to enable the oxidation of CO at room temperature, but a lack of stability at the elevated reaction temperatures that are used in automobile catalytic converters, in particular the loss of the most reactive Cu+ cations, leads to their deactivation. Using a combined experimental and theoretical approach, it is shown how the incorporation of titanium cations in a Cu2O film leads to the formation of a stable mixed-metal oxide with a Cu+ terminated surface that is highly active for CO oxidation.
引用
收藏
页码:5336 / 5340
页数:5
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