Wang Haocong, Zhu Wanfeng, Xu Lanlan, Gong Jian, Li Wenjia, Liu Xiaojuan
Collaborative Innovation Center of Suzhou Nano Science and Technology, College of Energy, Soochow University, Suzhou 215006, China.
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, P. R. China.
ACS Appl Mater Interfaces. 2024 Jul 10;16(27):34988-34996. doi: 10.1021/acsami.4c05284. Epub 2024 Jun 26.
The high performance of intermediate-to-low temperature solid oxide fuel cells (ILT-SOFCs) closely depends on the catalytic activity of the cathode material. However, most high-activity perovskite cathodes are rich in Sr and will arise from Sr segregation during the long-term working, resulting in the decay of activity and stability. Herein, by regulating the calcined way and temperature, a type of self-assembled nanocomposite perovskite cathode is developed, the stoichiometric SrCoFeScO (SCFSc) powder self-separates into a cubic phase (3̅, Sc-rich) and a tetragonal phase (4/, Sc-fewer). Meanwhile, a single cubic phase is prepared with the same formula via calcining the SCFSc pellet. It is found that the nanocomposite cathode shows better oxygen reduction reaction catalytic activity than single cubic SCFSc, caused by lower impedance of oxygen surface exchange and bulk diffusion. Particularly, the nanocomposite SCFSc cathode with the self-assembled heterointerfaces mitigates the Sr segregation and shows a peak power density of 1.17 W cm at 700 °C and excellent stability for ∼101 h at 600 °C. This work provides a strategy for the development of nanocomposite cathodes to mitigate cation segregation and improve catalytic activity and stability.
中低温固体氧化物燃料电池(ILT - SOFCs)的高性能紧密依赖于阴极材料的催化活性。然而,大多数高活性钙钛矿阴极富含Sr,在长期工作过程中会出现Sr偏析,导致活性和稳定性下降。在此,通过调节煅烧方式和温度,开发了一种自组装纳米复合钙钛矿阴极,化学计量比的SrCoFeScO(SCFSc)粉末自分离为立方相(3̅,富Sc)和四方相(4/,贫Sc)。同时,通过煅烧SCFSc颗粒以相同配方制备了单一立方相。研究发现,纳米复合阴极表现出比单一立方SCFSc更好的氧还原反应催化活性,这是由于氧表面交换和体扩散的阻抗较低所致。特别地,具有自组装异质界面的纳米复合SCFSc阴极减轻了Sr偏析,在700°C时显示出1.17 W cm的峰值功率密度,并在600°C下具有约101小时的优异稳定性。这项工作为开发纳米复合阴极以减轻阳离子偏析、提高催化活性和稳定性提供了一种策略。