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论文类型：期刊论文

发表时间：2010-10-07

发表刊物：JOURNAL OF PHYSICAL CHEMISTRY C

收录刊物：SCIE、EI、Scopus

卷号：114

期号：39

页面范围：16525-16533

ISSN号：1932-7447

摘要：Interstitial silicide-modified nickel, with high selectivity in some hydrogenation reactions, had been produced by dissolving silicon atoms into the nickel lattices. The metallic nickel was obtained by reducing the as-prepared high surface area NiO, followed by modification of the bulk nickel through silification of silane/H(2) at relatively low temperature and atmospheric pressure. The as-prepared materials were characterized by X-ray diffraction, magnetic measurements, X-ray photoelectron spectroscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, and temperature-programmed reduction. The results show nickel suicide formation involves the following sequence as a function of increasing temperature: Ni (cubic) -> Ni(2)Si (orthorhombic) -> NiSi (orthorhombic) -> NiSi(2) (cubic). The insertion of Si atoms into the interstitial sites between Ni atoms resulted in a significant change in the unit cell lattice of nickel. All of the silicide-modified nickel materials were ferromagnetic at room temperature, and saturation magnetization values drastically decreased when Si is present. Silicide-modified nickel develops a thin silicon oxide layer during exposure to air, which can be removed by H(2)-temperature programmed reduction. The as-prepared bulk silicide-modified nickel showed above 92% styrene selectivity in the hydrogenation of phenylacetylene under 0.41 MPa H(2) and at 50 degrees C for 5 h. In addition, only low conversions were obtained for styrene hydrogenation under the same hydrogen pressure and temperature for 50 min. These results indicate that these novel silicide-modified nickels are promising catalysts for the selective hydrogenation of unsaturated hydrocarbons.