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Magnetic and conducting Fe3O34-polypyrrole nanoparticles with core-shell structure

机译:具有核-壳结构的磁性和导电Fe3O34-聚吡咯纳米颗粒

摘要

Magnetic and conducting Fe3O4-polypyrrole nanoparticles with core-shell structure were prepared in the presence of Fe3O4 magnetic fluid in aqueous solution containing sodium dodecylbenzene-sulfonate (NaDS) as a surfactant and dopant. Both the conductivity and magnetization of the composites depend strongly on the Fe3O4 content and the doping degree. With increase of Fe3O4 content in the composite, the conductivity at room temperature decreases, but the saturated magnetization and coercive force increase. Transmission electron microscopy (TEM) images of Fe3O4 and Fe3O4-polypyrrole particles show almost spherical particles with diameters ranging from 20 to 30 and 30 to 40 nm, respectively. The thermal stability of Fe3O4-polypyrrole composites is higher than that of pure polypyrrole. Studies of IR, UV-visible and X-ray photoelectron spectroscopy (XPS) spectra suggest that the increased thermal stability may be due to interactions between Fe3O4 particles and polypyrrole backbone.
机译:在含有十二烷基苯磺酸钠(NaDS)作为表面活性剂和掺杂剂的水溶液中,在Fe3O4磁性流体存在下,制备了具有核-壳结构的磁性和导电Fe3O4-聚吡咯纳米颗粒。复合材料的电导率和磁化强度都强烈依赖于Fe3O4的含量和掺杂程度。随着复合物中Fe3O4含量的增加,室温下的电导率降低,但饱和磁化强度和矫顽力增加。 Fe3O4和Fe3O4-聚吡咯颗粒的透射电子显微镜(TEM)图像显示了直径分别为20至30和30至40 nm的几乎球形的颗粒。 Fe3O4-聚吡咯复合材料的热稳定性高于纯聚吡咯。红外,紫外可见光和X射线光电子能谱(XPS)光谱的研究表明,增加的热稳定性可能是由于Fe3O4颗粒与聚吡咯骨架之间的相互作用。

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