Dynamic interplay between metal nanoparticles and oxide support under redox conditions

Author:

Frey H.12ORCID,Beck A.23ORCID,Huang X.14ORCID,van Bokhoven J. A.23ORCID,Willinger M. G.1ORCID

Affiliation:

1. Scientific Center of Optical and Electron Microscopy (ScopeM), ETH Zürich, 8093 Zürich, Switzerland.

2. Institute for Chemical and Bioengineering, ETH Zürich, 8093 Zürich, Switzerland.

3. Paul Scherrer Institute, 5232 Villigen, Switzerland.

4. College of Chemistry, Fuzhou University, Fuzhou 350116, P. R. China.

Abstract

The dynamic interactions between noble metal particles and reducible metal-oxide supports can depend on redox reactions with ambient gases. Transmission electron microscopy revealed that the strong metal-support interaction (SMSI)–induced encapsulation of platinum particles on titania observed under reducing conditions is lost once the system is exposed to a redox-reactive environment containing oxygen and hydrogen at a total pressure of ~1 bar. Destabilization of the metal–oxide interface and redox-mediated reconstructions of titania lead to particle dynamics and directed particle migration that depend on nanoparticle orientation. A static encapsulated SMSI state was reestablished when switching back to purely oxidizing conditions. This work highlights the difference between reactive and nonreactive states and demonstrates that manifestations of the metal-support interaction strongly depend on the chemical environment.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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