4.8 Article

Highly Active and Durable Air Electrodes for Reversible Protonic Ceramic Electrochemical Cells Enabled by an Efficient Bifunctional Catalyst

期刊

ADVANCED ENERGY MATERIALS
卷 12, 期 12, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202103783

关键词

air electrodes; bifunctional catalysts; protonic ceramic electrochemical cells; solid oxide cells; water electrolysis

资金

  1. U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy (EERE) Hydrogen and Fuel Cell RD Program [DE-EE0008439]
  2. National Natural Science Foundation of China [52102212, 51972043]
  3. Foundation of Yangtze Delta Region Institute (Huzhou) of University of Electronic Science and Technology of China, China [U03210010, U03210028]
  4. China Scholarship Council (CSC)

向作者/读者索取更多资源

The electrocatalytic activity and stability of a conventional air electrode for protonic ceramic electrochemical cells are greatly enhanced by a multiphase catalyst coating, leading to improved performance in high steam concentration environments.
The commercialization of reversible protonic ceramic electrochemical cells is hindered by the lack of highly active and durable air electrodes exposed to high concentration of steam under operating conditions. Here, findings that dramatically enhance the electrocatalytic activity and stability of a conventional (La0.6Sr0.4)(0.95)Co0.2Fe0.8O3-delta (LSCF) air electrode by a multiphase catalyst coating composed of a conformal Pr1-xBaxCoO3-delta thin film and exsolved BaCoO3-delta nanoparticles, are reported. At 600 degrees C, the catalyst coating decreases the polarization resistance of the LSCF air electrode by a factor of 25 (from 1.09 to 0.043 omega cm(2)) in air and the degradation rate by two orders of magnitude (from 1.0 x 10(-2) to 1.8 x 10(-4) omega cm(2) h(-1) in humidified air with 30 vol% H2O). Further, a single cell with the catalyst-coated LSCF air electrode at 600 degrees C demonstrates a high peak power density of 1.04 W cm(-2) in the fuel cell mode and a high current density of 1.82 A cm(-2) at 1.3 V in the electrolysis mode. The significantly enhanced performance of the LSCF air electrode is attributed mainly to the high rate of surface oxygen exchange, fast surface proton diffusion, and the rapid H2O and O-2 dissociation on the catalysts.

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