Enhancing ceramic fuel cells stability via anode lithium content regulation based on anode-assisted in-situ densification of electrolyte technology

Hao Wang, Enyi Hu, Bin Zhu*, Jun Wang, Peter Lund

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

Abstract

The high temperature (>750 °C) operation has always hindered ceramic fuel cells (CFCs) commercialization. This work investigates the effect of lithium content in anode on the performance and stability of low-temperature (< 550 °C) CFCs based on anode-assisted in-situ densification of electrolyte (AASDE) technology. Electrochemical impedance spectroscopy (EIS) analysis reveals that increasing lithium content in the anode results in valley values for ohmic resistance and anode activation resistance while cathode activation resistance decreases. Consequently, CFCs with optimal lithium content in anode exhibit improved performance and stability. Specifically, CFCs using Li0.8Ni0.91Co0.06Al0.03O2 anode achieve maximum power density of 493 mW cm−2 and stable operation for 47 h at current density of 163 mA cm−2 at 500 °C. EIS curves under various atmospheres and concentration cell curve indicate that sodium doped samarium oxide (NDS) electrolyte shows proton conduction based on AASDE technology. High temperature contact angle of 2.6 ° indicates that LiOH can adsorb onto NDS, forming a stable physicochemical system. Based on a stable electrolyte system, the CFCs maintain stable operation for 42 h at 450 °C. This study highlights the potential for low-cost, stable operation of CFCs at low temperatures based on AASDE technology.

Original languageEnglish
Article number134357
JournalFuel
Volume387
DOIs
Publication statusPublished - 1 May 2025
MoE publication typeA1 Journal article-refereed

Keywords

  • Anode-assisted in-situ densification of electrolyte
  • Electrochemical impedance spectroscopy
  • Lithium content of the anode
  • Low-temperature ceramic fuel cells
  • Physiochemical compatibility
  • Stability

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