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Novel perovskite structured Nd0.5Ba0.5Co1/3Ni1/3Mn1/3O3−δ as highly efficient catalyst for oxygen electrode in solid oxide electrochemical cells

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posted on 2024-01-03, 11:18 authored by Shuang Zhao, Liwen Huang, Min Huang, Wen-Feng LinWen-Feng Lin, Yan Wu

Developing catalytic materials with highly efficient oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is essential for lower-temperature solid oxide fuel cell (SOFC) and electrolysis cell (SOEC) technologies. In this work, a novel triple perovskite material, Nd0.5Ba0.5Co1/3Ni1/3Mn1/3O3−δ, has been developed and employed as a catalyst for both ORR and OER in SOFC and SOEC operations at relatively lower temperatures, showing a low polarization resistance of 0.327 Ω cm2, high-power output of SOFC up to 773 mW cm–2 at 650 °C, and a high current density of 1.57 A cm–2 from SOEC operation at 1.5 V at 600 °C. The relaxation time distribution reveals that Nd0.5Ba0.5Co1/3Ni1/3Mn1/3O3−δ could maintain a slow polarization process at the relatively low operating temperature, offering a significant antipolarization advantage over other perovskite electrode materials. The Nd0.5Ba0.5Co1/3Ni1/3Mn1/3O3−δ electrode provides a low energy barrier of about 0.36 eV in oxygen ion mobility, which is beneficent for oxygen reduction/evolution reaction processes.

Funding

National Natural Science Foundation of China (NSFC, grant no. 22378372)

Sustainable Hydrogen Production from Seawater Electrolysis

Engineering and Physical Sciences Research Council

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History

School

  • Aeronautical, Automotive, Chemical and Materials Engineering

Department

  • Chemical Engineering

Published in

ACS Applied Materials & Interfaces

Volume

15

Issue

51

Pages

59512 - 59523

Publisher

American Chemical Society

Version

  • AM (Accepted Manuscript)

Rights holder

© American Chemical Society

Publisher statement

This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Materials & Interfaces, copyright © 2023 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsami.3c14336

Acceptance date

2023-11-30

Publication date

2023-12-15

Copyright date

2023

ISSN

1944-8244

eISSN

1944-8252

Language

  • en

Depositor

Prof Wen Feng Lin. Deposit date: 19 December 2023

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