Enhanced Dry Reforming of Methane Catalysis by Ni at Heterointerfaces between Thin MgAlOx and Bulk ZrO2

Author:

Wang Jin1ORCID,Kayode Gbolade O.2,Hirayama Yuki3,Shpasser Dina1,Ogino Isao3,Montemore Matthew M.2ORCID,Gazit Oz M.1ORCID

Affiliation:

1. Department of Chemical Engineering Technion- Israel Institute of Technology Haifa 3200003 Israel

2. Department of Chemical and Biomolecular Engineering Tulane University New Orleans LA 70118 USA

3. Faculty of Engineering Hokkaido University N13 W8, Kita-ku Sapporo Hokkaido 060-8628 Japan

Abstract

AbstractThe catalytic performance of supported metals is greatly influenced by the interaction with the support material. The role of the support becomes even more important when dealing with metal nanoparticles and high reaction temperatures. Herein, we show that interfacial sites between two metal oxides, MgAlOx and ZrO2 can bestow high stability as well as enhanced reactivity to nickel (Ni) nanoparticles. We use the MgAlOx as thin oxides on an underlying bulk ZrO2. We demonstrate the effect of the metal‐support interactions (MSI) in different support locations on the performance in dry reforming of methane (DRM). We find that the rate of DRM catalysis produces a concave‐down trend with respect to Ni loading with a maximum at ~0.8–1.1 % wt Ni. Measuring the Ni2p3/2 binding energy (BE), we find a similar concave‐down trend whereas for the Mg2p BE we find a concave‐up trend with respect to the Ni loading both with the maximum and minimum centered at 0.8–1.1 % wt Ni, respectively. These trends were correlated with the stability of Ni calculated by DFT. Overall, our results suggest that heterointerfacial sites can be used to tailor moderate MSI, which can be used in the design of DRM catalyst with significantly increased activity and high stability.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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