Restructuring of titanium oxide overlayers over nickel nanoparticles during catalysis

Author:

Monai Matteo1ORCID,Jenkinson Kellie2,Melcherts Angela E. M.1ORCID,Louwen Jaap N.1ORCID,Irmak Ece A.2ORCID,Van Aert Sandra2ORCID,Altantzis Thomas3ORCID,Vogt Charlotte1ORCID,van der Stam Ward1ORCID,Duchoň Tomáš4ORCID,Šmíd Břetislav5ORCID,Groeneveld Esther6,Berben Peter6,Bals Sara2ORCID,Weckhuysen Bert M.1ORCID

Affiliation:

1. Inorganic Chemistry and Catalysis Group, Institute for Sustainable and Circular Chemistry and Debye Institute for Nanomaterials Science, Utrecht University, 3584 CG Utrecht, Netherlands.

2. EMAT and NANOlab Center of Excellence, University of Antwerp, 2020 Antwerp, Belgium.

3. ELCAT, University of Antwerp, 2610 Wilrijk, Belgium.

4. Peter-Grünberg-Institut 6, Forschungszentrum Jülich GmbH, 52425 Jülich, Germany.

5. Department of Surface and Plasma Science, Faculty of Mathematics and Physics, Charles University, 180 00 Prague, Czech Republic.

6. BASF Nederland B.V., 3454 PK De Meern, Netherlands.

Abstract

Reducible supports can affect the performance of metal catalysts by the formation of suboxide overlayers upon reduction, a process referred to as the strong metal–support interaction (SMSI). A combination of operando electron microscopy and vibrational spectroscopy revealed that thin TiO x overlayers formed on nickel/titanium dioxide catalysts during 400°C reduction were completely removed under carbon dioxide hydrogenation conditions. Conversely, after 600°C reduction, exposure to carbon dioxide hydrogenation reaction conditions led to only partial reexposure of nickel, forming interfacial sites in contact with TiO x and favoring carbon–carbon coupling by providing a carbon species reservoir. Our findings challenge the conventional understanding of SMSIs and call for more-detailed operando investigations of nanocatalysts at the single-particle level to revisit static models of structure-activity relationships.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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