In Situ and Simultaneous Observation of Palladium Redox and Oxygen Storage/Release in Pd/Sr-Fe-O Perovskite Catalysts Using Dispersive XAFS

  • Kimura Masao
    Advanced Technology Research Laboratories, Nippon Steel Corporation
  • Niwa Yasuhiro
    Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization (KEK)
  • Uemura Kenichi
    Advanced Technology Research Laboratories, Nippon Steel Corporation
  • Nagai Toru
    Advanced Technology Research Laboratories, Nippon Steel Corporation
  • Inada Yasuhiro
    Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization (KEK)
  • Nomura Masaharu
    Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization (KEK)

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タイトル別名
  • <i>In Situ</i> and Simultaneous Observation of Palladium Redox and Oxygen Storage/Release in Pd/Sr–Fe–O Perovskite Catalysts Using Dispersive XAFS
  • <i>In Situ</i> and Simultaneous Observation of Palladium Redox and Oxygen Storage/Release in Pd/Sr&ndash;Fe&ndash;O Perovskite Catalysts Using Dispersive XAFS

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抄録

We have succeeded in in situ and simultaneously observing the redox reaction of palladium and the oxygen storage/release process in a newly developed palladium-promoted Sr–Fe–O (Pd/Sr–Fe–O) catalyst during redox-gas cycles using dispersive X-ray absorption fine structure (XAFS) analysis at 673 K with a time resolution of less than 20 ms. The Pd/Sr–Fe–O catalyst, which exhibits high performance for automotive emission control, has a unique “multi-phase-domain” structure, where a single grain is composed of nano-sized domains of three phases: SrFeO3−δ, Sr4Fe6O13−δ and SrFe12O19−δ. In situ observation has shown a strong correlation between the redox of the palladium and the oxygen storage/release in the Pd/Sr–Fe–O catalyst, and the correlation factors differ between the reduction and oxidation reactions. The oxide phases exhibit a type of “oxygen buffer” effect in the oxidation cycle and delay the formation of Pd–O, resulting in the high performance of the catalyst.

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