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Preparation of Supported Gold Nanoparticles by a Modified Incipient Wetness Impregnation Method

机译:改进的初湿含浸法制备负载型金纳米粒子

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摘要

In this work, we show that if the mere procedure of impregnation of oxide supports with chloroauric acid, which is well-known to lead to large gold particles, is followed by a step of washing with ammonia, small gold particles (3-4 nm) can be obtained after a treatment of calcination at 300 °C on any type of oxide supports (alumina, titania, silica). Moreover, gold leaching is very limited during the washing step, and a large range of gold loadings (0.7-3.5 wt %) can be achieved. Elemental analysis, Raman spectroscopy, and temperature programmed desorption under argon show that this ammonia posttreatment results in the removal of chloride ligands from the coordination sphere of Au(III) precursor and their replacement by ammine ligands, leading to an ammino-hydroxo or an ammino-hydroxo-aquo gold complex and not to gold hydroxide. The Au/TiO2 catalysts prepared with this modified procedure of impregnation are almost as active as those prepared by deposition-precipitation with urea in the CO oxidation reaction performed at room temperature.
机译:在这项工作中,我们表明,如果仅用众所周知的会导致大金颗粒的氯金酸浸渍氧化物载体的步骤,接着是用氨水洗涤的步骤,则小金颗粒(3-4 nm可在任何类型的氧化物载体(氧化铝,二氧化钛,二氧化硅)上于300°C煅烧处理后获得)。而且,在洗涤步骤中金的浸出非常有限,并且可以实现大范围的金负载量(0.7-3.5重量%)。元素分析,拉曼光谱和氩气下的程序升温脱附表明,这种氨气后处理导致从Au(III)前驱体的配位域中除去氯离子配体,并被氨基配体取代,从而生成氨基羟基或氨基。 -羟基水合金,而不是氢氧化金。用这种改进的浸渍方法制备的Au / TiO2催化剂的活性几乎与在室温下进行的CO氧化反应中用尿素的沉积沉淀法制备的那些一样。

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