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Synthesis of Size and Shape-Controlled Co Nanoparticles from Cobalt Acetate by Thermal Decomposition

机译:热分解法从乙酸钴合成尺寸和形状可控的钴纳米粒子

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Monodisperse cobalt nanoparticles with relatively high coercivities were synthesized by thermal decomposition of cobalt acetate for the application of ultra-high density magnetic recording media. For thermal decomposition, cobalt carbonyl, Co2(CO)8, has often been used as a precursor to generate the nanoparticles. However, this cobalt carbonyl is strongly toxic and relatively expensive. To avoid these disadvantages, we synthesized Co nanoparticles by thermal decomposition of cobalt acetate tetrahydrate, Co(CH3COO)2·4H2O. The cobalt nanoparticles with various morphologies were synthesized in a high boiling point solvent trioctylamine (TOA). First, Co nanoparticles were prepared using various protecting agents consisting of oleic acid, oleylamine, trioctylphosphine (TOP), and polyvinylpyrrolidone (PVP) in the absence of reducing agents. These Co nanoparticles had average particle sizes of 13.9~21.3 nm, clear face-centered cubic crystalline structure and their coercivity was measured to be 342.0 Oe. The PVP was very effective in controlling the particle growth while hindering agglomeration between the particles. When 1,2-dodecanediol as a reducing agent was added to the reactant, the particle size was decreased down to 10 nm. However, in the case of without TOP, triangular prism-shaped nanoparticles were prepared with the average size of about 86.0 nm and its coercivity is 478.5 Oe. XRD pattern of the prism-like cobalt particles corresponded to a hexagonal close-packed crystalline phase. PVP was effective in controlling particle growth while hindering agglomeration between the particles at high temperature. These as-prepared Co nanoparticles with a moderate coercivity can be used in the application of patterned media.
机译:通过乙酸钴的热分解合成了具有较高矫顽力的单分散钴纳米颗粒,用于超高密度磁记录介质的应用。对于热分解,羰基钴Co2(CO)8通常被用作生成纳米颗粒的前体。但是,这种羰基钴有剧毒并且相对昂贵。为避免这些缺点,我们通过热分解四水合醋酸钴Co(CH3COO)2·4H2O合成了Co纳米粒子。在高沸点溶剂三辛胺(TOA)中合成了具有各种形态的钴纳米颗粒。首先,在不存在还原剂的情况下,使用由油酸,油胺,三辛基膦(TOP)和聚乙烯吡咯烷酮(PVP)组成的各种保护剂制备Co纳米颗粒。这些Co纳米粒子的平均粒径为13.9〜21.3 nm,具有清晰的面心立方晶体结构,矫顽力为342.0 Oe。 PVP在控制颗粒生长的同时非常有效地阻止了颗粒之间的团聚。当将1,2-十二烷二醇作为还原剂添加到反应物中时,粒径减小至10nm。然而,在没有TOP的情况下,制备了具有约86.0nm的平均尺寸并且其矫顽力为478.5Oe的三棱柱形纳米颗粒。棱柱状钴颗粒的XRD图谱对应于六方密堆积的结晶相。 PVP在控制颗粒生长的同时有效地阻止了高温下颗粒之间的团聚。这些制备的具有中等矫顽力的Co纳米颗粒可用于图案化介质的应用。

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