Issue 9, 2025

Effects of Ce co-doping at the A site of Sm0.5−xSr0.5CoOδ for a high-performance air electrode for solid oxide reversible cells

Abstract

Oxide perovskites, such as SrCoO3, are considered to be promising air electrode catalysts for solid oxide cells. SrCoO3 is composed of non-precious elements and possesses catalytic activity for various reactions, including an oxygen reduction and an oxygen evolution reaction. However, the catalytic activity of this material is typically limited at reduced temperatures. In this study, the catalytic activity of SrCoO3 was improved by co-doping of cerium (Ce) and samarium (Sm) at the A site (Sr site) of SrCoO3. Although Ce was considered the B-site dopant in terms of ionic size and coordination number, a small amount of Ce was successfully substituted at the Sr site, simultaneously with Sm. Oxygen reduction and evolution activity were significantly increased by substitution of a small amount of cerium (∼2.5 mol%) at the A-site. At 973 K, the maximum power density generated from the LaGaO3-supported cell with Ce–Sm co-doped SrCoO3 as an air electrode was 0.62 W cm−2 in fuel cell mode, and the current density in steam electrolysis mode at 1.5 V was 0.93 A cm−2. The increased air electrode activity could be assigned to the improvement in the surface active sites and electrical conductivity of SrCoO3 by simultaneous substitution of Ce with Sm at the A site.

Graphical abstract: Effects of Ce co-doping at the A site of Sm0.5−xSr0.5CoO3±δ for a high-performance air electrode for solid oxide reversible cells

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Article information

Article type
Paper
Submitted
18 Nov 2024
Accepted
16 Jan 2025
First published
17 Jan 2025
This article is Open Access
Creative Commons BY license

J. Mater. Chem. A, 2025,13, 6620-6630

Effects of Ce co-doping at the A site of Sm0.5−xSr0.5CoOδ for a high-performance air electrode for solid oxide reversible cells

S. Khan, A. Staykov, J. Matsuda, M. Kluczny, K. Wu, K. Ninomiya, M. Nishibori, J. T. Song, M. Watanabe, M. Inada and T. Ishihara, J. Mater. Chem. A, 2025, 13, 6620 DOI: 10.1039/D4TA08181A

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