期刊
JOURNAL OF POWER SOURCES
卷 305, 期 -, 页码 240-248出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpowsour.2015.11.097
关键词
Solid oxide co-electrolysis cell; Perovskite; Molybdenum doped strontium ferrite; Chemical equilibrium co-electrolysis model; Synthesis gas
资金
- Shell's Game-Changer grant [PT53482]
- Fundamental Research Funds for the Central University [2042015kf0043]
- National Natural Science Foundation of China [51502207]
High temperature H2O/CO2 co-electrolysis process is performed on the symmetrical Sr2Fe1.5Mo0.5O6-Sm0.2Ce0.8O1.9(SDC)/La0.8Sr0.2Ga0.87Mg0.13O3 (LSGM)/SFM-SDC cells, which exhibit excellent electrochemical performance with the current density of -734 mAcm(-2) at 13 V and the interfacial polarization resistance of 0.48 Omega cm(2) at 850 degrees C. Enhanced co-electrolysis kinetics are obtained with increasing the operating temperature and applied cell voltage. Synthesis gas of H2O and CO is produced by H2O splitting and reverse water gas shift (RWGS) reaction on the SFM-SDC/LSGM/SFM-SDC co-electrolysis cells. Effects of temperature and electrolysis current on the produced gas fraction are predicted using the chemical equilibrium co-electrolysis model. High CO2 conversion rate and ideal Hy to CO ratio of approximately 2 can be achieved by adjusting appropriate inlet gas fraction, temperature and electrolysis current. The SFM-SDC/LSGM/SFM-SDC cell shows a relative stable cell voltage in the 103-h galvanostatic test. (C) 2015 Elsevier B.V. All rights reserved.
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