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Large Scale Solid-state Synthesis of Catalytically Active Fe3O4@M (M = Au Ag and Au-Ag alloy) Core-shell Nanostructures

机译:催化活性Fe3O4 @ M(M = AuAg和Au-Ag合金)核壳纳米结构的大规模固态合成

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摘要

Solvent-less synthesis of nanostructures is highly significant due to its economical, eco-friendly and industrially viable nature. Here we report a solid state synthetic approach for the fabrication of Fe3O4@M (where M = Au, Ag and Au-Ag alloy) core-shell nanostructures in nearly quantitative yields that involves a simple physical grinding of a metal precursor over Fe3O4 core, followed by calcination. The process involves smooth coating of low melting hybrid organic-inorganic precursor over the Fe3O4 core, which in turn facilitates a continuous shell layer post thermolysis. The obtained core-shell nanostructures are characterized using, XRD, XPS, ED-XRF, FE-SEM and HR-TEM for their phase, chemical state, elemental composition, surface morphology, and shell thickness, respectively. Homogeneous and continuous coating of the metal shell layer over a large area of the sample is ascertained by SAXS and STEM analyses. The synthesized catalysts have been studied for their applicability towards a model catalytic hydrogen generation from NH3BH3 and NaBH4 as hydrogen sources. The catalytic efficacy of the Fe3O4@Ag and Ag rich alloy shell materials are found to be superior to the corresponding Au counterparts. The saturation magnetization studies reveal the potential of the core-shell nanostructured catalysts to be magnetically recoverable and recyclable.
机译:纳米结构的无溶剂合成由于其经济,环保和工业上可行的性质而具有重要意义。在这里,我们报告了一种固态合成方法,用于以接近定量的产率制备Fe3O4 @ M(其中M = AgAu,Ag和Au-Ag合金)核-壳纳米结构,其中包括在Fe3O4核上简单地物理研磨金属前驱体,其次是煅烧。该工艺涉及在Fe3O4核芯上平滑涂覆低熔点的杂化有机-无机前驱体,从而促进热解后的连续壳层。使用XRD,XPS,ED-XRF,FE-SEM和HR-TEM对获得的核-壳纳米结构进行表征,分别涉及其相,化学状态,元素组成,表面形态和壳厚度。通过SAXS和STEM分析确定了在大面积样品上金属壳层的均匀连续涂层。已经研究了合成催化剂对于由NH 3 BH 3和NaBH 4作为氢源产生模型催化氢的适用性。发现富Fe3O4 @ Ag和Ag合金壳材料的催化效果优于相应的Au对应物。饱和磁化研究表明,核-壳纳米结构催化剂具有磁性可回收和可回收的潜力。

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