Water-promoted interfacial pathways in methane oxidation to methanol on a CeO 2 -Cu 2 O catalyst

Author:

Liu Zongyuan1ORCID,Huang Erwei2ORCID,Orozco Ivan2ORCID,Liao Wenjie2ORCID,Palomino Robert M.1ORCID,Rui Ning1ORCID,Duchoň Thomas3ORCID,Nemšák Slavomir4ORCID,Grinter David C.5ORCID,Mahapatra Mausumi1ORCID,Liu Ping12ORCID,Rodriguez José A.12ORCID,Senanayake Sanjaya D.1

Affiliation:

1. Chemistry Division, Brookhaven National Laboratory, Upton, NY 11973, USA.

2. Chemistry Department, Stony Brook University, Stony Brook, NY 11794, USA.

3. Peter-Grünberg-Institut 6, Forschungszentrum Jülich, 52425 Jülich, Germany.

4. Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

5. Diamond Light Source Limited, Diamond House, Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0DE, UK.

Abstract

A water boost for methanol synthesis Model catalysts based on metals and metal oxides can dissociate methane (CH 4 ) at room temperature, converting it directly to methanol (CH 3 OH). Liu et al. show that for one of these catalysts, an “inverted” CeO x -Cu 2 O oxide on Cu(111), water tunes the selectivity from forming CO and CO 2 to forming surface CH 3 O groups, as revealed by ambient-pressure x-ray photoelectron spectroscopy. Theoretical modeling showed that adsorbed water blocks O 2 dissociation and O 2 instead oxidizes the reduced catalyst. Hydroxyl groups from water generate the CH 3 O species from dissociated CH 4 , and water then goes on to form and displace CH 3 OH to the gas phase. Science , this issue p. 513

Funder

U.S. Department of Energy

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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