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|Title:||Sr1−xCaxMoO3–Gd0.2Ce0.8O1.9 as the anode in solid oxide fuel cells : effects of Mo precipitation||Authors:||Xiao, Peng
|Keywords:||DRNTU::Engineering::Chemical engineering||Issue Date:||2013||Source:||Xiao, P., Ge, X., Liu, Z., Wang, J.-Y., & Wang, X. (2014). Sr1−xCaxMoO3–Gd0.2Ce0.8O1.9 as the anode in solid oxide fuel cells: Effects of Mo precipitation. Journal of Alloys and Compounds, 587, 326-331.||Series/Report no.:||Journal of alloys and compounds||Abstract:||Calcium is incorporated into strontium molybdate to form Sr1-xCaxMoO3 as an electronic conductor for solid oxide fuel cells (SOFCs). Metallic molybdenum was observed with the increasing content of Ca substitution for Sr in Sr1-xCaxMoO3. Rietveld refinement reveals the phase transition from cubic to tetragonal perovskite structure, which implies its decreased thermodynamic stability under reducing conditions with increasing content of Ca. X-ray diffraction (XRD) and differential scanning calorimetry-thermo-gravimetric analysis (DSC-TGA) further prove that this Mo ex-solution is reversible. The electrochemical performances of Sr1-xCaxMoO3 towards H2 and CH4 oxidation at 800 ºC are examined. The performance is improved in H2 atmosphere with the introduction of Ca, 330 mW cm-2 of Sr0.5Ca0.5MoO3–Gd0.2Ce0.8O1.9 (GDC) vs. 280 mW cm-2 of SrMoO3–GDC, which can be ascribed to the segregated Mo as the additional catalyst. However, carbon deposition is observed after exposure to CH4 at 800 ºC for both Sr0.7Ca0.3MoO3‒GDC and Sr0.5Ca0.5MoO3‒GDC, in contrast to the absence of carbon on SrMoO3‒GDC.||URI:||https://hdl.handle.net/10356/103914
|ISSN:||0925-8388||DOI:||10.1016/j.jallcom.2013.10.187||Rights:||© 2013 Elsevier B.V. This is the author created version of a work that has been peer reviewed and accepted for publication by Journal of Alloys and Compounds, Elsevier B.V. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [DOI:http://dx.doi.org/10.1016/j.jallcom.2013.10.187].||Fulltext Permission:||open||Fulltext Availability:||With Fulltext|
|Appears in Collections:||SCBE Journal Articles|
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