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Thermally driven self-assembly of nanomicelles: A facile route to functional monodisperse mesoporous colloidal nanocomposites of inorganic nature and mesoscale size

机译:纳米胶束的热驱动自组装:制备具有无机性质和中尺度尺寸的功能性单分散介孔胶态纳米复合材料的便捷途径

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Thermally driven self-assembly of nanomicelles can be a feasible route to produce monodisperse porous colloidal nanocomposites of inorganic nature and sizes around the mesoscale (below 100 nm). Success relies on extending the lifetime of intermediate droplets (size below about 100 nm) that are obtained under particular conditions. Herein, the conditions for the long-term stabilization of these unique templates are studied and a model proposed to produce monodisperse porous colloidal nanocomposites. As an example of the potential applications of this methodology, functional colloidal nanocomposites with a high loading of the doping material (30 mol%) are obtained. In particular, superparamagnetic nanomagnets of metallic nature encapsulated in porous oxide colloidal matrixes of mesoscale size that easily respond to an external magnetic field are prepared and characterized in terms of structure and textural and magnetic properties.
机译:纳米胶束的热驱动自组装可能是生产无机性质和尺寸在中尺度(低于100 nm)附近的单分散多孔胶体纳米复合材料的可行途径。成功取决于延长在特定条件下获得的中间液滴(尺寸小于约100 nm)的寿命。在此,研究了这些独特模板的长期稳定条件,并提出了一种制备单分散多孔胶体纳米复合材料的模型。作为该方法的潜在应用的实例,获得了具有高负载掺杂材料(30mol%)的功能性胶体纳米复合材料。特别地,制备了金属性质的超顺磁性纳米磁体,其封装在容易响应外部磁场的中尺度尺寸的多孔氧化物胶体基质中,并根据结构,结构和磁性能进行表征。

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