Abstract Microemulsion based approach for nanospheres assembly into anisotropic nanostructures of NiMnO <ce:inf loc='post'>3</ce:inf> and their magnetic properties
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Microemulsion based approach for nanospheres assembly into anisotropic nanostructures of NiMnO 3 and their magnetic properties

机译:基于微乳液的纳米球组件中的纳米球纳米结构的方法 3 及其磁性特性

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AbstractThe present study focuses on synthesis of anisotropic nanostructures of nickel manganese oxide (NiMnO3) obtained by thermal decomposition of nanocrystalline nickel manganese oxalate precursor, Ni0.5Mn0.5(C2O4)·2H2O which crystallized as nanorods. The synthesis of the oxalate precursor has been carried out via microemulsion-mediated process with cationic and non-ionic surfactants. The microemulsion led to reverse micelles, and the film flexibility of the micelle in presence of non-ionic surfactant (Tergitol) was reduced by increasing the chain length of the co-surfactant (1-butanol, 1-hexanol and 1-octanol) which led to the increase in reaction rate and hence increase in the aspect ratio of the nickel manganese oxalate by up to four times. However, in the presence of cationic surfactant, highly uniform nickel manganese oxalate nanorods were obtained. Further, the decomposition of the oxalate precursor was optimized to maintain the anisotropy of the rods of ternary metal oxide (NiMnO3). An electron microscopy study showed that the rods were made up of an assembly of ultrafine nanospheres. The NiMnO3nanostructures were all ferrimagnetic with Curie temperature ranging between 437 and 467K showing increasing saturation magnetization with increase in aspect ratio of the nanorods.
机译:<![cdata [ 抽象 本研究侧重于合成镍锰氧化镍的各向异性纳米结构(nimno 3 )通过纳米晶镍锰锰酸盐前体的热分解,Ni 0.5 MN 0.5 (C 2 O 4 )·2h 2 O作为纳米棒结晶。通过阳离子和非离子表面活性剂的微乳液介导的方法进行了草酸盐前体的合成。通过增加共表面活性剂(1-丁醇,1-己醇和1-辛醇)的链条减少导致反应速率的增加,因此镍锰的纵横比增加了4次。然而,在存在阳离子表面活性剂的存在下,获得高度均匀的镍锰纳米镍。此外,优化了草酸盐前体的分解,以维持三元金属氧化物棒的各向异性(Nimno 3 )。电子显微镜研究表明,杆由超细纳米球的组装组成。 nimno 3 纳米结构都是居里温度的居里温度范围437和467k,显示纳米棒的纵横比的增加,饱和磁化强度增加。

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