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Pd2+/Pd0 redox cycling in hexagonal YMn(0.5)Fe(0.5)O3: implications for catalysis by PGM-substituted complex oxides
Joshua A Kurzman1, Jun Li, Thomas D Schladt
1Department of Chemistry and Biochemistry, Materials Research Laboratory, University of California, Santa Barbara, California 93106, USA.
Inorganic Chemistry
|August 2, 2011
Summary
This study investigated palladium (Pd) redox cycling in complex oxides for catalysis. While Pd cycled, the material showed limited tolerance, forming PdO and not improving CO oxidation catalysis.
Area of Science:
- Solid-state chemistry
- Materials science
- Catalysis
Background:
- Complex oxides can exhibit redox cycling of platinum group metals (PGMs) like palladium (Pd).
- Pd-substituted complex oxides can reversibly extrude metallic Pd and reincorporate Pd(2+) ions.
Purpose of the Study:
- To synthesize and characterize YMn(0.5)Fe(0.5-x)Pd(x)O(3-δ) complex oxides.
- To investigate the redox cycling behavior of Pd within these complex oxides.
- To evaluate the catalytic performance for CO oxidation.
Main Methods:
- Sol-gel synthesis at 800 °C.
- High-resolution synchrotron X-ray powder diffraction for structural refinement.
- Synchrotron X-ray diffraction and EXAFS studies for redox cycling monitoring.
- Testing catalytic activity for CO oxidation.
Main Results:
- YMn(0.5)Fe(0.5-x)Pd(x)O(3-δ) compounds were successfully synthesized and characterized.
- The materials showed modest tolerance to redox cycling, forming stable PdO.
- Catalytic performance for CO oxidation was comparable to previously studied materials and finely dispersed PdO.
- No significant catalytic improvement was observed with increasing Pd substitution.
Conclusions:
- The hexagonal YMnO(3) structure does not efficiently facilitate oxygen transport for improved catalysis.
- Solid-state chemistry and structural factors influence PGM redox cycling efficacy and catalytic performance in complex oxides.
- Limited redox cycling tolerance and lack of enhanced catalytic activity were observed in these specific Pd-substituted complex oxides.
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