LAUSR

The broad and large-scale application of solid oxide fuel cells (SOFCs) technology hinges significantly on the development of highly active and robust electrode materials. Here, Ni-free anode materials decorated with metal nanoparticles are synthesized by in situ reduction of Fe-doping Sr2CoMo1-xFexO6-δ (x = 0, 0.05, 0.1) double perovskite oxides under a reducing condition at 850 °C. The exsolved nanoparticles from the Sr2CoMo0.95Fe0.05O6-δ (SCMF0.05) lattice are Co-Fe alloy with rich multiple-twinned defects, significantly enhancing the catalytic activity of the SCMF0.05 anode toward the oxidation of H2 and CH4. The electrolyte-supported single cell with the reuduced SCMF0.05 anode reaches peak power densities as high as 992.9 and 652.3 mW cm-2 in H2 and CH4 at 850 °C, respectively, while maintaining superior stability (∼50 h at 700 °C). The reduced SCMF0.05 anode also demonstrates excellent coking resistance in CH4, which can be attributed to the increased oxygen vacancies due to Fe doping and the effective catalysis of multiple-twinned Co-Fe alloy nanoparticles for reforming of CH4 to H2 and CO. The findings in this work may provide a new insight for the design of highly active and durable anode catalysts in SOFCs.