Theoretical investigation of H2 oxidation on the Sr 2Fe1.5Mo0.5O6 (001) perovskite surface under anodic solid oxide fuel cell conditions

Suwit Suthirakun, Salai Cheettu Ammal, Ana B. Muñoz-García, Guoliang Xiao, Fanglin Chen, Hans Conrad Zur Loye, Emily A. Carter, Andreas Heyden

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72 Scopus citations


Periodic density functional theory (DFT) calculations and microkinetic modeling are used to investigate the electrochemical oxidation of H2 fuel on the (001) surface of Sr2Fe1.5Mo 0.5O6 (SFMO) perovskite under anodic solid oxide fuel cell conditions. Three surface models with different Fe/Mo ratios in the topmost layer-identified by ab initio thermodynamic analysis-are used to investigate the H2 oxidation mechanism. A microkinetic analysis that considers the effects of anode bias potential suggests that a higher Mo concentration in the surface increases the activity of the surface toward H2 oxidation. At operating voltage and anodic SOFC conditions, the model predicts that water desorption is rate-controlling and that stabilizing the oxygen vacancy structure increases the overall rate for H2 oxidation. Although we find that Mo plays a crucial role in improving catalytic activity of SFMO, under fuel cell operating conditions, the Mo content in the surface layer tends to be very low. On the basis of these results and in agreement with previous experimental observations, a strategy for improving the overall electrochemical performance of SFMO is increasing the Mo content or adding small amounts of an active transition metal, such as Ni, to the surface to lower the oxygen vacancy formation energy of the SFMO surface.

Original languageEnglish (US)
Pages (from-to)8374-8386
Number of pages13
JournalJournal of the American Chemical Society
Issue number23
StatePublished - Jun 11 2014

All Science Journal Classification (ASJC) codes

  • General Chemistry
  • Biochemistry
  • Catalysis
  • Colloid and Surface Chemistry


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