Dynamic multinuclear sites formed by mobilized copper ions in NO x selective catalytic reduction

Author:

Paolucci Christopher1ORCID,Khurana Ishant2ORCID,Parekh Atish A.2ORCID,Li Sichi1ORCID,Shih Arthur J.2ORCID,Li Hui1ORCID,Di Iorio John R.2ORCID,Albarracin-Caballero Jonatan D.2ORCID,Yezerets Aleksey3ORCID,Miller Jeffrey T.2ORCID,Delgass W. Nicholas2ORCID,Ribeiro Fabio H.2ORCID,Schneider William F.1ORCID,Gounder Rajamani2ORCID

Affiliation:

1. Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, IN 46556, USA.

2. Charles D. Davidson School of Chemical Engineering, Purdue University, 480 Stadium Mall Drive, West Lafayette, IN 47907, USA.

3. Cummins Inc., 1900 McKinley Avenue, MC 50183, Columbus, IN 47201, USA.

Abstract

X-ray vision spies copper on the move Copper ions in zeolites help remove noxious nitrogen oxides from diesel exhaust by catalyzing their reaction with ammonia and oxygen. Paolucci et al. found that these copper ions may move about during the reaction (see the Perspective by Janssens and Vennestrom). Zeolite catalysts generally fix metals in place while the reacting partners flow in and out of their cagelike structures. In this case, though, x-ray absorption spectroscopy suggested that the ammonia was mobilizing the copper ions to pair up as they activated oxygen during the catalytic cycle. Science , this issue p. 898 ; see also p. 866

Funder

National Science Foundation

U.S. Department of Energy

Cummins, Inc.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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