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  • 标题:A comprehensive investigation of direct ammonia-fueled thin-film solid-oxide fuel cells: Performance, limitation, and prospects
  • 本地全文:下载
  • 作者:Seongkook Oh ; Min Jun Oh ; Jongsup Hong
  • 期刊名称:iScience
  • 印刷版ISSN:2589-0042
  • 出版年度:2022
  • 卷号:25
  • 期号:9
  • 页码:1-18
  • DOI:10.1016/j.isci.2022.105009
  • 语种:English
  • 出版社:Elsevier
  • 摘要:SummaryAmmonia is a promising carbon-free hydrogen carrier. Owing to their nickel-rich anodes and high operating temperatures, solid oxide fuel cells (SOFCs) can directly utilize NH3fuel—direct-ammonia SOFCs (DA-SOFCs). Lowering the operating temperature can diversify application areas of DA-SOFCs. We tested direct-ammonia operation using two types of thin-film SOFCs (TF-SOFCs) under 500 to 650°C and compared these with a conventional SOFC. The TF-SOFC with a nickel oxide gadolinium-doped ceria anode achieved a peak power density of 1330 mW cm−2(NH3fuel under 650°C), which is the best performance reported to date. However, the performance difference between the NH3and H2operations was significant. Electrochemical impedance analyses, ammonia conversion quantification, and two-dimensional multi-physics modeling suggested that reduced ammonia conversion at low temperatures is the main cause of the performance gap. A comparative study with previously reported DA-SOFCs clarified that incorporating a more active ammonia decomposition catalyst will further improve low-temperature DA-SOFCs.Graphical abstractDisplay OmittedHighlights•Thin-film SOFCs and a commercial SOFC are tested for direct-ammonia and H2operation•Record-high performance for direct-ammonia operation achieved with thin-film SOFC•2D multi-physics modeling explained the performance gap between NH3and H2fuel•NH3decomposition activity and gas transport are the main causes of the performance gapChemistry; Electrochemistry; Electrochemical energy conversion; Engineering; Materials science
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