High performance air electrode for solid oxide regenerative fuel cells fabricated by infiltration of nano-catalysts
A high performance air electrode fabricated by infiltration of highly active nano-catalysts into a porous scaffold is demonstrated for high-temperature solid oxide regenerative fuel cells (SORFCs). The nitrate precursor solution for Sm0.5Sr0.5CoO3 (SSC) catalyst is impregnated into a porous La0.6Sr0...
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Veröffentlicht in: | Journal of power sources 2014-03, Vol.250, p.15-20 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A high performance air electrode fabricated by infiltration of highly active nano-catalysts into a porous scaffold is demonstrated for high-temperature solid oxide regenerative fuel cells (SORFCs). The nitrate precursor solution for Sm0.5Sr0.5CoO3 (SSC) catalyst is impregnated into a porous La0.6Sr0.4Co0.2Fe0.8O3 (LSCF)–gadolinia-doped ceria (GDC) composite backbone, and extremely fine SSC nano-particles are uniformly synthesized by in-situ crystallization at the initial stage of SORFC operation via homogeneous nucleation induced by urea decomposition. The SSC nano-catalysts are in the size range of 40–80 nm and stable against coarsening upon the SORFC operation at 750 °C. The electrochemical performance is significantly improved by incorporation of SSC nano-catalysts in both power generation and hydrogen production modes. Systematic analysis on the impedance spectra reveals that the surface modification of the air electrode with nano-catalysts remarkably accelerates the chemical surface exchange reactions for both O2 reduction and O2− oxidation, which are the major limiting processes for SORFC performance.
•High performance air electrode is fabricated by nano-catalyst infiltration.•Homogeneous nano-catalysts are formed by urea decomposition.•Surface chemical exchange is accelerated by nano-catalysts.•Performance is improved for power generation and hydrogen production.•Nano-catalysts are stable against coarsening at high temperatures. |
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ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2013.10.123 |