催化作用
材料科学
化学工程
燃料电池
图层(电子)
陶瓷
质子交换膜燃料电池
复合材料
化学
有机化学
工程类
作者
Yuxin Pan,Hua Zhang,Kang Xu,Yucun Zhou,Bote Zhao,Wei Yuan,Kotaro Sasaki,YongMan Choi,Yu Chen,Meilin Liu
标识
DOI:10.1016/j.apcatb.2022.121071
摘要
Nickel-based cermet anode-supported protonic ceramic fuel cells (PCFCs) show great potential for direct utilization of ammonia. However, the insufficient activity of anode and the deterioration of anode activity/durability caused by the undesired interaction between nickel and ammonia greatly limit the application. Here, we report tubular PCFCs embedded with a catalytic iron layer. Such cells show peak power densities of 1.507 W cm -2 and 1.078 W cm -2 at 700 ° C when using H 2 and NH 3 as fuel, respectively, which are the highest tubular PCFC performance so far ever reported. In addition, the stability of cells with the catalyst layer has been dramatically enhanced when compared with that of cells without the catalyst layer. The enhancement of activity and durability is attributed to the catalytic activity of iron for ammonia decomposition, through which the direct contact between nickel and ammonia has been minimized and the anode structure has therefore been protected. • A robust tubular cell has been fabricated via a phase inversion process. • The cell delivers excellent peak power densities of 1.507 W cm -2 on H 2 , and 1.078 W cm -2 on NH 3 at 700 ° C. • The cell durability is greatly enhanced when integrated with a catalytic Fe layer. • A DFT study indicates that the Fe layer can effectively decompose the NH 3 .
科研通智能强力驱动
Strongly Powered by AbleSci AI