TY - JOUR
T1 - 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
AU - Khan, Sovann
AU - Staykov, Aleksandar
AU - Matsuda, Junko
AU - Kluczny, Maksymilian
AU - Wu, Kuan Ting
AU - Ninomiya, Kakeru
AU - Nishibori, Maiko
AU - Song, Jun Tae
AU - Watanabe, Motonori
AU - Inada, Miki
AU - Ishihara, Tatsumi
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025/1/17
Y1 - 2025/1/17
N2 - 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.
AB - 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.
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U2 - 10.1039/d4ta08181a
DO - 10.1039/d4ta08181a
M3 - Article
AN - SCOPUS:85216739086
SN - 2050-7488
VL - 13
SP - 6620
EP - 6630
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 9
ER -