阳极
催化作用
电解质
氢
陶瓷
氨
阴极
直接乙醇燃料电池
氧化物
分解
材料科学
氮氧化物
碳纤维
化学工程
无机化学
化学
冶金
质子交换膜燃料电池
电极
工程类
有机化学
复合材料
复合数
物理化学
燃烧
作者
Jiwon Yun,Grace Xiong,Seungchan Kim,Dylan Bardgett,Sihyuk Choi,Sossina M. Haile
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-10-24
卷期号:9 (11): 5520-5528
被引量:7
标识
DOI:10.1021/acsenergylett.4c02263
摘要
Ammonia has received considerable attention as a promising carbon-free hydrogen carrier. At temperatures above 400 °C, NH3 is thermodynamically unstable with respect to decomposition into nitrogen and hydrogen and is, thus, suitable for direct use in solid oxide fuel cells (SOFCs) without external reforming. However, poor catalytic activity for ammonia decomposition at the moderate temperatures of protonic ceramic fuel cell (PCFC) operation has resulted in low fuel cell power output relative to operation on hydrogen and likely contributes to reported cell degradation. Here we prepared cells based on a thermodynamically robust electrolyte, a high activity cathode, and an anode with a distinctive structure to overcome challenges of poor activity and stability. The cells delivered peak power densities of 0.59 and 0.44 W cm–2 under H2 and NH3, respectively, at 500 °C, excellent stability over a period of 200 h, and no detectable NOx in the anode exhaust gas.
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