| Literature DB >> 24719231 |
Ashleigh E Baber1, Xiaofang Yang, Hyun You Kim, Kumudu Mudiyanselage, Markus Soldemo, Jonas Weissenrieder, Sanjaya D Senanayake, Abdullah Al-Mahboob, Jerzy T Sadowski, Jaime Evans, José A Rodriguez, Ping Liu, Friedrich M Hoffmann, Jingguang G Chen, Darío J Stacchiola.
Abstract
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.Entities:
Keywords: CO oxidation; IR spectroscopy; mixed oxides; scanning tunneling microscopy; surface chemistry
Year: 2014 PMID: 24719231 DOI: 10.1002/anie.201402435
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336