期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 112, 期 7, 页码 2244-2247出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp711880e
关键词
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High-temperature-stable Au@SnO2 core/shell supported catalyst was prepared by a simple intermetallics-based dry-oxidation approach in which the size of the core can be controlled easily by varying the size of the pre-made Au seeds. The change of their structure was investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). In the as-prepared supported catalysts, An particles with a mean size of ca. 15 nm were highly encapsulated by the SnO2, shell. Moreover, the Au@SnO2 core/shell supported catalysts showed superior catalytic activity compared to non-encapsulated Au-SnO2. XPS spectra showed that the interactions between the Au catalyst and oxide support in the well-encapsulated Au@SnO2 core/shell nanoparticles are much stronger than those in the non-encapsulated Au-SnO2 nanoparticles, further indicating the synergetic confinement effect in such nanoscaled catalyst/ support core/shell systems.
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