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Nanoscale gold intercalated into mesoporous silica as a highly active and robust catalyst

机译:纳米级金作为高活性和强固性催化剂嵌入介孔二氧化硅中

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Stable gold/mesoporous silica nanocomposites (with Au nanoparticles intercalated in the walls of mesoporous silica) were successfully synthesized by the hydrothermal method and applied as catalysts. A challenging issue associated with intercalation and the use of coordinating agents is the effect of the coordinating agent on the mesoporous silica structure and periodicity. This investigation is targeted at elaborating the effect of the coordinating agent on the resulting mesoporous structure. The amount of Au coordinating agent bis[3-(triethoxysilyl)propyl]-tetrasulfide (TESPTS) was systematically altered to synthesize a range of materials with varying Au loadings and morphologies. These materials were characterized by N _2 adsorption-desorption, x-ray diffraction, transmission electron microscopy and UV-visible spectroscopy. The structures of the catalysts were found to range from mesoporous to vesical- and foam-like upon varying the TESPTS/polymer template (P123) ratio. Additionally, the sizes of Au nanoparticles increased by increasing the amount of TESPTS. The catalytic properties of the resulting materials were examined using oxidation of benzyl alcohol and reduction of 4-nitrophenol as probe reactions. The intercalated systems demonstrated high activity and more importantly were robust and readily reusable. This approach to imparting stability to nanoscale materials may be much more broadly applicable and expand the types of environments in which they can be utilized.
机译:通过水热法成功地合成了稳定的金/介孔二氧化硅纳米复合材料(金纳米粒子插入介孔二氧化硅壁中)并用作催化剂。与插层和配位剂的使用有关的挑战性问题是配位剂对介孔二氧化硅结构和周期性的影响。这项研究的目的是阐述配位剂对所得介孔结构的影响。系统地改变了Au配位剂双[3-(三乙氧基甲硅烷基)丙基]-四硫化物(TESPTS)的数量,以合成一系列具有不同Au含量和形态的材料。这些材料通过N _2吸附-解吸,x射线衍射,透射电子显微镜和紫外可见光谱进行表征。当改变TESTPS /聚合物模板(P123)的比例时,发现催化剂的结构范围从中孔到囊状和泡沫状。另外,通过增加TESPTS的量来增加Au纳米颗粒的尺寸。使用苄醇的氧化和4-硝基苯酚的还原作为探针反应来检查所得材料的催化性能。插层式系统显示出高活性,更重要的是,它们坚固且易于重用。这种赋予纳米级材料稳定性的方法可以更广泛地应用,并且扩展了可以利用它们的环境的类型。

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