Performance-enhanced direct ammonia protonic ceramic fuel cells using CeO2-supported Ni and Ru catalyst layer

Xiaoxiao Li, Jiangping Chen, Yunyun Huang*, Huihuang Fang, Chongqi Chen, Fulan Zhong, Li Lin, Yu Luo*, Yuqing Wang, Lilong Jiang

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Ammonia is an exceptional fuel for solid oxide fuel cells (SOFCs), because of the high content of hydrogen and the advantages of carbon neutrality. However, the challenge lies in its unsatisfactory performance at intermediate temperatures (500–600 °C), impeding its advancement. An electrolyte-supported proton-ceramic fuel cell (PCFC) was fabricated employing BaZr0.1Ce0.7Y0.2O3−δ (BZCY) as the electrolyte and Ba0.5Sr0.5Co0.8Fe0.2O3−δ (BSCF) as the cathode. In this study, the performance of PCFC using NH3 as fuel within an operating temperature range of 500–700 °C was improved by adding an M(Ni,Ru)/CeO2 catalyst layer to reconstruct the anode surface. The electrochemical performance of direct ammonia PCFC (DA-PCFC) were improved to different extents. Compared to H2 as fuel, the degradation ratio of peak power densities (PPDs) of Ni/CeO2-loaded PCFC fueled with NH3 decreased at 700–500 °C, with a decrease to 13.3% at 700 °C and 30.7% at 500 °C. The findings indicate that Ru-based catalysts have a greater promise for direct ammonia SOFCs (DA-SOFCs) at operating temperatures below 600 °C. However, the enhancement effect becomes less significant above 600 °C when compared to Ni-based catalysts.

Original languageEnglish
Pages (from-to)875-884
Number of pages10
JournalFrontiers in Energy
Volume18
Issue number6
DOIs
Publication statusPublished - Dec 2024

Keywords

  • ammonia
  • anode
  • M/CeO catalyst layer
  • proton-ceramic fuel cell (PCFC)

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