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Synthesis of FePtAu Nanoparticles in High-Boiling-Point Solvents

机译:高沸点溶剂中FePtAu纳米粒子的合成

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Partially ordered FePtAu nanoparticles with size around 8 nm were prepared by the simultaneous decomposition of iron pentacarbonyl and reduction of gold acetate and platinum acetylacetonate. The high boiling point chemical, hexadecylamine, was used as a solvent, and 1-adamantanecarboxylic acid was used as a stabilizer. The final temperature was controlled between 300 ℃-360 ℃ during synthesis, where disordered FePt particles could be partially transformed into the ordered Llo phase. A nonmagnetic mechanical stirrer was used in order to avoid agglomeration of the fct-FePt particles during synthesis. XRD patterns of as-made samples showed weak super-lattice peaks, indicating partial chemical ordering of the FePtAu particles. The coercivities of partially transformed as-made particles vary from a few hundred oersteds to a few thousand oersteds, depending on the concentration of gold additive and the temperature of synthesis. Dynamic coercivity measurements yield thermal stability factors and switching volumes that are slightly higher than would be expected for noninteracting particles.
机译:通过同时分解五羰基铁,还原乙酸金和乙酰丙酮铂,制备了尺寸约8 nm的部分有序的FePtAu纳米粒子。高沸点化学品十六烷基胺用作溶剂,而1-金刚烷羧酸用作稳定剂。在合成过程中,最终温度控制在300℃-360℃之间,其中无序的FePt颗粒可以部分转化为有序的Llo相。为了避免合成过程中fct-FePt颗粒的团聚,使用了非磁性机械搅拌器。制成样品的XRD图谱显示弱的超晶格峰,表明FePtAu颗粒的部分化学有序。根据金添加剂的浓度和合成温度的不同,部分转变后的成品粒子的矫顽力从几百奥斯特到几千奥斯特不等。动态矫顽力测量得出的热稳定性因子和转换量比非相互作用颗粒的预期值稍高。

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