阴极
电化学
氧化物
兴奋剂
钙钛矿(结构)
电导率
极化(电化学)
材料科学
化学工程
价(化学)
无机化学
纳米技术
化学
电极
光电子学
结晶学
物理化学
冶金
工程类
有机化学
作者
Shuting Li,Yuanyuan Liu,Changkun Cai,Ke Xue,Liuzhen Bian,Shengli An
标识
DOI:10.1016/j.jpowsour.2023.233932
摘要
The development of cathode with high oxygen reduction reaction (ORR) activity is crucial for intermediate-temperature solid oxide fuel cells (IT-SOFCs). SrCoO3-δ oxides, a mixed ion-electron conductivity (MIEC), are promising cathode materials. However, pure SrCoO3-δ exhibits a hexagonal or rhombohedral structure with poor electrical properties, limiting its application in IT-SOFCs. In this work, high-valence Ce4+ is doped at the A-site of SrCoO3-δ perovskite to improve the phase structural stability and electrochemical activity of SrCoO3-δ. The findings reveal that Ce4+ doping in small amounts significantly advances the conductivity and ORR activity due to enhanced structural stability. Among the series of samples, Sr0.95Ce0.05Co3-δ (SCC005) presents the best electrochemical performance. Moreover, the addition of Ce0.8Gd0.2O2-δ (GDC) further reduces polarization resistance by about ∼7 times. The peak power density of 1.3 W cm−2 is obtained at 750 °C for the SCC05-30%GDC cathode. The results indicate that A-site Ce doping is a promising strategy to enhance the ORR activity of SrCoO3-δ oxides.
科研通智能强力驱动
Strongly Powered by AbleSci AI