Sovann Khan, Aleksandar Staykov, Junko Matsuda, Maksymilian Kluczny, Kuan-Ting Wu, Kakeru Ninomiya, Maiko Nishibori, Jun Tae Song, Motonori Watanabe, Miki Inada and Tatsumi Ishihara
{"title":"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†","authors":"Sovann Khan, Aleksandar Staykov, Junko Matsuda, Maksymilian Kluczny, Kuan-Ting Wu, Kakeru Ninomiya, Maiko Nishibori, Jun Tae Song, Motonori Watanabe, Miki Inada and Tatsumi Ishihara","doi":"10.1039/D4TA08181A","DOIUrl":null,"url":null,"abstract":"<p >Oxide perovskites, such as SrCoO<small><sub>3</sub></small>, are considered to be promising air electrode catalysts for solid oxide cells. SrCoO<small><sub>3</sub></small> 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 SrCoO<small><sub>3</sub></small> was improved by co-doping of cerium (Ce) and samarium (Sm) at the A site (Sr site) of SrCoO<small><sub>3</sub></small>. 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 LaGaO<small><sub>3</sub></small>-supported cell with Ce–Sm co-doped SrCoO<small><sub>3</sub></small> as an air electrode was 0.62 W cm<small><sup>−2</sup></small> in fuel cell mode, and the current density in steam electrolysis mode at 1.5 V was 0.93 A cm<small><sup>−2</sup></small>. The increased air electrode activity could be assigned to the improvement in the surface active sites and electrical conductivity of SrCoO<small><sub>3</sub></small> by simultaneous substitution of Ce with Sm at the A site.</p>","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":" 9","pages":" 6620-6630"},"PeriodicalIF":9.5000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/ta/d4ta08181a?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ta/d4ta08181a","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
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.
氧化钙钛矿,如SrCoO3,被认为是固体氧化物电池中有前途的空气电极催化剂之一。SrCoO3由非贵重元素组成,对氧还原和析氧反应等多种反应具有活跃的催化活性。然而,这种材料的催化活性是有限的,特别是在降低的温度下。本研究通过在SrCoO3的A位(Sr位)共掺杂铈(Ce)和钐(Sm),获得了提高SrCoO3催化活性的有效方法。虽然从离子大小和配位数的角度来看,Ce被认为是b位掺杂剂,但少量的Ce成功地取代了Sr位,同时也取代了Sm。少量铈(~ 2.5 mol %)在a位上取代后,氧还原和进化活性显著提高。在973 K时,以Ce-Sm共掺杂SrCoO3作为空气电极的lagao3负载电池在燃料电池模式下产生的最大功率密度为0.62 W cm-2,在1.5 V的蒸汽电解模式下产生的电流密度为0.93 A cm-2。通过在A位同时用Sm取代Ce,提高了SrCoO3的表面活性位点和电导率,从而提高了空气电极活性。
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.