4.7 Article

Co-electrolysis of H2O-CO2 in a solid oxide electrolysis cell with symmetrical La0.4Sr0.6Co0.2Fe0.7 Nb0.1O3-δ electrode

期刊

JOURNAL OF ELECTROANALYTICAL CHEMISTRY
卷 836, 期 -, 页码 107-111

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jelechem.2019.01.064

关键词

La0.4Sr0.6Co0.2Fe0.7Nb0.1O3-delta; Co-electrolysis; Solid oxide electrolysis cell

资金

  1. National Key R&D Program of China [2017YFB0601904]
  2. Beijing Municipal Science and Technology Commission Project [Z181100005118008]
  3. Yueqi Young Scholar Project (CUMTB)

向作者/读者索取更多资源

The addition of H2O can improve the conversion rate of CO(2 )electrolysis and facilitate the direct production of hydrocarbon fuels, thereby having a wide range of potential applications. An electrolyte-supported symmetrical solid oxide electrolysis cell (SOEC) has been fabricated by using 8% Y2O3 stabilized ZrO2 as electrolyte, Gd0.1Ce0.3O2-delta as buffer layer and novel perovskite La0.4Sr0.6Co0.2Fe0.7Nb0.1O3-delta (LSCFN) material as the symmetrical electrodes. The results reveal that 15% steam can promote CO2 conversion and it significantly reduces polarization resistance of the cell. The current density can reach up to 0.638 A.cm (-2) @1.3 V and 850 degrees C with the composition of 75% CO2-15% H2O-10% H-2(.) The outstanding stability of the cell performance has been demonstrated under different current densities up to 0.5 A.cm(-2) and operating durations up to 110 h at 0.4 A.cm(-2). Overall, LSCFN is a highly-efficient and extremely-stable electrode material for symmetrical SOEC application.

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