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Chemical design of magnetic nanocomposites based on layered double hydroxides

机译:基于层状双氢氧化物的磁性纳米复合材料的化学设计

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Chemical modification of anion-substituted layered double hydroxides (LDHs) was used for the preparation of anisotropic magnetic nanocomposites. The method combines the simplicity of chemical methods and the possibility to prepare two-, one-, or zero-dimensional nanoparticles in oxide/hydroxide matrices. An LDH structure consists of positively charged hydroxide layers bonded with negatively charged anions, which occupy the interlayer space. During chemical reactions of anions in the interlayer space, reaction zone is spatially constrained by the hydroxide layers, giving rise to the conditions similar to those in two-dimensional nanoreactors, such as Langmuir–Blodgett films and self-assembling monolayers. Here we used LDH precursors for the preparation of the Fe- and Ni-based nanocomposites. The precursors were obtained by intercalation of ethylenediaminetetraacetate (edta) complexes of Fe(III) or Ni(II) into the Mg–Al LDH. Substituted LDHs were reduced by H2 to give metal nanoparticles entrapped into the inert Mg–Al oxide matrix. Reduction of anion-substituted LDHs with different content of anionic complexes (and ratio Mg/Al in matrix) occurs at a relatively low temperature (~600 ℃) and results in the formation of metal nanoparticles with different morphology and sizes. The formation of anisotropic metal nanoparticles in the former case is believed to be due to the spatial constraints of the reaction zone and their formation occurs simultaneously with buckling of hydroxide layers.
机译:阴离子取代的层状双氢氧化物(LDHs)的化学改性用于制备各向异性磁性纳米复合材料。该方法结合了化学方法的简单性和在氧化物/氢氧化物基质中制备二维,一维或零维纳米粒子的可能性。 LDH结构由与带负电的阴离子键合的带正电的氢氧化物层组成,该阴离子占据层间空间。在层间空间中阴离子的化学反应过程中,反应区在空间上受到氢氧化物层的约束,从而产生了类似于二维纳米反应器(如Langmuir-Blodgett膜和自组装单层)的条件。在这里,我们使用LDH前体制备铁和镍基纳米复合材料。前体是通过将Fe(III)或Ni(II)的乙二胺四乙酸(edta)配合物插入Mg-Al LDH中获得的。取代的LDH被H2还原,得到包裹在惰性Mg-Al氧化物基质中的金属纳米颗粒。具有不同阴离子配合物含量(和基质中Mg / Al之比)的阴离子取代的LDH的还原在相对较低的温度(〜600℃)下发生,并导致形成具有不同形态和尺寸的金属纳米粒子。在前一种情况下,各向异性金属纳米颗粒的形成被认为是由于反应区的空间限制,并且它们的形成与氢氧化物层的屈曲同时发生。

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