Improvement of oxygen reduction activity and stability on a perovskite oxide surface by electrochemical potential

Sanaz Koohfar; Masoud Ghasemi; Tyler Hafen; Georgios Dimitrakopoulos; Dongha Kim; Jenna Pike; Singaravelu Elangovan; Enrique D Gomez; Bilge Yildiz

doi:10.1038/s41467-023-42462-5

Improvement of oxygen reduction activity and stability on a perovskite oxide surface by electrochemical potential

Nat Commun. 2023 Nov 8;14(1):7203. doi: 10.1038/s41467-023-42462-5.

Authors

Sanaz Koohfar^{1

2}, Masoud Ghasemi^{3

4}, Tyler Hafen⁵, Georgios Dimitrakopoulos⁶, Dongha Kim⁶, Jenna Pike⁵, Singaravelu Elangovan⁵, Enrique D Gomez^{3

4}, Bilge Yildiz^{7

8

9}

Affiliations

¹ Laboratory for Electrochemical Interfaces, Massachusetts Institute of Technology, Cambridge, MA, USA.
² Department of Nuclear Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
³ Department of Chemical Engineering, The Pennsylvania State University, University Park, PA, USA.
⁴ Department of Materials Science and Engineering, The Pennsylvania State University, University Park, PA, USA.
⁵ OxEon Energy, LLC, North Salt Lake, UT, USA.
⁶ Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
⁷ Laboratory for Electrochemical Interfaces, Massachusetts Institute of Technology, Cambridge, MA, USA. byildiz@mit.edu.
⁸ Department of Nuclear Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA. byildiz@mit.edu.
⁹ Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA. byildiz@mit.edu.

Abstract

The instability of the surface chemistry in transition metal oxide perovskites is the main factor hindering the long-term durability of oxygen electrodes in solid oxide electrochemical cells. The instability of surface chemistry is mainly due to the segregation of A-site dopants from the lattice to the surface. Here we report that cathodic potential can remarkably improve the stability in oxygen reduction reaction and electrochemical activity, by decomposing the near-surface region of the perovskite phase in a porous electrode made of La_1-xSr_xCo_1-xFe_xO₃ mixed with Sm_0.2Ce_0.8O_1.9. Our approach combines X-ray photoelectron spectroscopy and secondary ion mass spectrometry for surface and sub-surface analysis. Formation of Ruddlesden-Popper phase is accompanied by suppression of the A-site dopant segregation, and exsolution of catalytically active Co particles onto the surface. These findings reveal the chemical and structural elements that maintain an active surface for oxygen reduction, and the cathodic potential is one way to generate these desirable chemistries.