Journal
JOURNAL OF POWER SOURCES
Volume 516, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.jpowsour.2021.230660
Keywords
SOEC; Ni depletion; Phase-field model; Lattice Boltzmann model; Cell performance
Funding
- National Key Research and Development Program of China, China [2017YFB0601904]
- Research Grant Council, University Grants Committee, Hong Kong SAR, China [PolyU 152064/18E, N_PolyU552/20]
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Through a comprehensive numerical study, it was found that nickel depletion in the fuel electrode of SOEC can lead to nickel phase coarsening, consequently reducing the electrochemical performance of the electrode. Increasing the wettability of the nickel phase can effectively mitigate the reduction of active reaction sites caused by nickel coarsening.
During the long-term operation of solid oxide electrolysis cell (SOEC), the coarsening and depletion of the Ni phase of the electrode are found to decrease the cell performance and limit cell durability. In this study, a comprehensive numerical study is conducted to quantitatively evaluate the degradation process in the fuel electrode of SOEC. The phase-field model is adopted to track the Ni phase migration process and generate the electrode structures with Ni depletion. An electrode model based on the lattice Boltzmann method is then used to evaluate the electrochemical performance of the fuel electrode. It is found that the maximum width of the Ni depletion region can reach 3-4 mu m. The Ni depletion will aggravate the coarsening of the Ni phase. The corresponding electrochemical evaluation also shows that the randomly distributed ionic particles in the porous fuel electrode lengthens the ion transport path and increases the electrode ohmic overpotential. The Ni depletion also increases the activation overpotential loss due to the reduction of the active reaction sites. The severe Ni depletion can increase the total overpotential by up to 52.8% compared to the initial state. Besides, increasing the wettability of the Ni phase can effectively suppress the reduction of active reaction sites due to Ni coarsening.
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