Electrocatalytic Oxidative Coupling of Methane on NiFe Exsolved Perovskite Anode: Effect of Water

Author:

Kim Jaesung1,Ferree Matthew1,Gunduz Seval1,Millet Jean‐Marc M.2,Aouine Mimoun2,Co Anne C.3,Ozkan Umit S.1ORCID

Affiliation:

1. William G. Lowrie Department of Chemical and Biomolecular Engineering The Ohio State University 151 W. Woodruff Ave. Columbus OH 43210 USA

2. Institut de Recherche sur la Catalyse et l'Environnement de Lyon UMR 5256 Université Claude-Bernard Lyon 1 69626 Villeurbanne Cedex France

3. Department of Chemistry and Biochemistry The Ohio State University 100 W. 18th Ave. Columbus OH 43210 USA

Abstract

AbstractOxidative coupling of methane (OCM) can be performed electrocatalytically by utilizing solid oxide cells, which provide a readily controlled oxygen supply through dense electrolytes. La0.7Sr0.2Ni0.2Fe0.8O3 (LSNF) perovskite is an effective anode for OCM. Its surface characteristics and electrocatalytic activity can be improved by reduction and the resultant exsolution of bimetallic NiFe nanoparticles from its bulk. X‐ray diffraction (XRD) and environmental transmission electron microscopy proved that the evolution of hetero‐phases under reducing environment resulted in bimetallic NiFe nanoparticles being formed on the surface. A 36 % improvement in C2+ hydrocarbon production rate was achieved due to the reduction of LSNF with the exsolved NiFe nanoparticles. Co‐feeding of H2O enhanced selective conversion of CH4 resulting in the production rate of C2+ hydrocarbons being increased by 56 %. Analysis of impedance spectra and in‐situ DRIFTS under a CH4+H2O atmosphere provided an understanding for the enhancement on the electrocatalytic OCM.

Funder

Basic Energy Sciences

National Science Foundation

Publisher

Wiley

Subject

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

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