Novel perovskite structured Nd0.5Ba0.5Co1/3Ni1/3Mn1/3O3−δ as highly efficient catalyst for oxygen electrode in solid oxide electrochemical cells
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
Find out more...History
School
- Aeronautical, Automotive, Chemical and Materials Engineering
Department
- Chemical Engineering
Published in
ACS Applied Materials & InterfacesVolume
15Issue
51Pages
59512 - 59523Publisher
American Chemical SocietyVersion
- AM (Accepted Manuscript)
Rights holder
© American Chemical SocietyPublisher 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.3c14336Acceptance date
2023-11-30Publication date
2023-12-15Copyright date
2023ISSN
1944-8244eISSN
1944-8252Publisher version
Language
- en