期刊
CHEMISTRY OF MATERIALS
卷 20, 期 20, 页码 6567-6576出版社
AMER CHEMICAL SOC
DOI: 10.1021/cm801534a
关键词
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资金
- Department of Energy (DOE) Office of Basic Energy Sciences (BES) [DE FG02-05ER15725]
- National Science Foundation [DMR05-20415]
Metastable YFeO3 with the hexagonal YAlO3 Structure was obtained by a sol-gel process at 700 degrees C, using metal nitrate precursors with pH control and the appropriate citric acid to nitrate ratio. Under similar conditions, YFe1-xPdxO3-delta (0 < x <= 0.1) compositions were also prepared. The substitution of Fe by Pd stabilizes the YAlO3 structure at higher temperatures. The crystal structures of YFe1-xPdxO3-delta (0 <= x <= 0.1) were refined by Rietveld analysis of X-ray and neutron powder diffraction data. The parent hexagonal YFeO3 (x = 0) crystallizes in the space group P6(3)/mmc with a = 3.5099(3) angstrom and c = 11.759(2) angstrom. The redox-driven mobility of Pd to integrate into the oxide host as ions and to dissociate from it as fcc-Pd nanoparticles was monitored by a combination of X-ray diffraction and X-ray photoelectron spectroscopy. Pd nanoparticles in the reduced samples were 2 detected by scanning backscattered electron microscopy and transmission electron microscopy. The Pd+-containing materials showed significant low-temperature (near 100 degrees C) catalytic activity for CO oxidation, comparable to that of highly dispersed PdO/Al2O3, despite their relatively low surface areas.
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