4.6 Article

Enhanced oxygen reduction kinetics of IT-SOFC cathode with PrBaCo2O5+δ/Gd0.1Ce1.9O2-δ coherent interface

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 10, 期 7, 页码 3495-3505

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta09615j

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资金

  1. National Key R&D Program of China [2018YFB1502202, 2018YFB0905600]
  2. National Natural Science Foundation of China [51634003, 52074023]

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The article reports the successful synthesis of a dual-phase cathode material with remarkable oxygen reduction reaction activity and low polarization resistance. The coherent interface structure formed between the two phases is beneficial to alleviate lattice thermal expansion and guide oxygen transport. The results demonstrate the promising application of this dual-phase composite material in intermediate/low-temperature solid oxide fuel cells.
One challenge facing the development of high-performance cathodes for solid oxide fuel cells is the slow oxygen reduction kinetics. Here, we report a dual-phase cathode material, double perovskite structure PrBaCo2O5+delta (PBC) and fluorite structure Gd0.1Ce0.9O2-delta (GDC), successfully synthesized using a one-pot method, with remarkable oxygen reduction reaction activity and low polarization resistance under IT-SOFC service conditions. The coherent interface structure is formed between PBC and GDC particles, which is beneficial to alleviate the lattice thermal expansion. The introduction of the cubic GDC phase can guide the oxygen transport among PBC particles with different orientations. When measured in a symmetrical cell configuration in the air at 600 degrees C, PBC-10 wt% GDC electrode shows an area-specific resistance of 0.394 omega cm(2), which is about 78% lower than that of bare PBC electrode under the same situations. The charge transfer process on the electrode surface is the rate-limiting step based on the dependence of polarization resistance at different oxygen partial pressures, where the impedance analysis technique, the distribution of relaxation times (DRT), is devoted to describing the complex electrode reaction processes. The GDC introduction significantly decreases the charge transfer resistance of the PBC-GDC composite cathode. The maximum power density of lab-scale electrolyte-supported cell with PBC-10 wt% GDC cathode reaches 1302, 938, 549 and 235 mW cm(-2) at 850, 750, 650 and 550 degrees C, respectively. Our results demonstrate that such dual-phase composites PBC-GDC produced in one step can be considered a promising cathode material for intermediate/low-temperature solid oxide fuel cells.

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