Enhanced stability of ammonia-fed protonic ceramic fuel cells via infiltration of Co-Fe catalyst

被引:0
作者
Tao, Haoliang [1 ,2 ]
Tang, Wenqiang [1 ]
Zhao, Xueyan [1 ]
Zhu, Liangzhu [1 ,3 ]
机构
[1] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Zhejiang Key Lab Adv Fuel Cells & Electrolyzers Te, Ningbo 315201, Zhejiang, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Hubei Univ Automot Technol, Coll Mat Sci & Engn, Shiyan 442002, Hubei, Peoples R China
关键词
Protonic ceramic fuel cells; Ammonia; Co-Fe catalyst; Cell stability; FREE HYDROGEN-PRODUCTION; ON-SITE GENERATION; POWER-GENERATION; DECOMPOSITION; NANOPARTICLES; PERFORMANCE; METHANE; OXIDES; ANODE;
D O I
10.1016/j.ijhydene.2025.03.312
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, Co-Fe catalysts of different molar ratios are infiltrated into protonic ceramic fuel cell (PCFC) to improve the efficiency of ammonia cracking and cell stability. The degradation rate at 600 degrees C decreases by as high as 88 % under a current density of 625 mA cm-2, proving the effectiveness of infiltrating Co-Fe catalysts. The postmortem analysis indicates that the infiltrated Co-Fe trends to accumulate to Ni particles in the anode and the synergism of Ni, Fe, and Co contributes to the improvement of structure integrity and cell stability in ammonia. We find that the structure evolution corresponding to cell degradation started from the regions near the anode functional layer and the separation of electrolyte grains could be regarded as the failure initiation for NH3-fed PCFC. Both electrochemical stability test and the microstructural observation suggest that a decoration of Co to Fe ratio of 1:1 is more beneficial for NH3-fed PCFC.
引用
收藏
页码:70 / 78
页数:9
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