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Structural and magnetic properties of polymer-stabilized tetragonal Ni nanoparticles

机译:聚合物稳定的四方镍纳米粒子的结构和磁性

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摘要

Ni nanoparticles (Ni-NPs), with diameter (D) ranging 5-30 nm, were synthesized by reducing nickel chloride with NaBH4 in the presence of polymer molecules of poly-vinyl alcohol (PVA) in cold water. Nickel chloride was dispersed in the PVA molecules which stabilized the resulting Ni-NPs. Experiments were carried out with and without PVA to elucidate the effect of PVA molecules on the structural and magnetic properties of Ni-NPs. It was found that both uncoated (uc) and PVA-coated (pc) Ni-NPs exhibit a tetragonal (t) crystal structure, i.e. different from the cubic (fcc) structure of bulk nickel. pc Ni-NPs (paramagnetic in nature) converted to fcc Ni (spherical shape, D 12 nm) on annealing at 573 K in air, exhibiting a saturation magnetization M s = 20.5 emu/g, squareness ratio M r /M s = 0.48 and coercivity H c = 248 Oe, which is higher than the bulk Ni (0.7 Oe). uc Ni-NPs showed little improvement in M s and H c on air annealing. The core-shell structure resulted in a high H c value in stable pc Ni-NPs in air. Electron magnetic resonance revealed exchange interaction between the core and shell, which changes on annealing in air.
机译:在聚乙烯醇(PVA)的聚合物分子存在下,通过NaBH 4 还原氯化镍合成了直径(D)范围为5〜30nm的镍纳米粒子(Ni-NPs)。冷水。氯化镍分散在PVA分子中,从而稳定了生成的Ni-NP。在有和没有PVA的情况下进行了实验,以阐明PVA分子对Ni-NPs的结构和磁性的影响。发现未涂覆的(uc)和PVA涂覆的(pc)Ni-NP均显示出四方(t)晶体结构,即不同于块状镍的立方(fcc)结构。 pc Ni-NPs(本质上为顺磁性)在573 K的空气中退火后转变为fcc Ni(球形,D 12 nm),表现出饱和磁化强度M s = 20.5 emu / g,矩形比M r / M s = 0.48,矫顽力H c = 248 Oe,高于整体Ni(0.7 Oe)。 uc Ni-NPs在空气退火中对M s 和H c 的改善很小。核-壳结构导致空气中稳定的pc Ni-NP中的H c 值较高。电子磁共振揭示了核与壳之间的交换相互作用,该相互作用在空气中退火时发生变化。

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  • 来源
    《Philosophical Magazine》 |2010年第11期|p.1401-1414|共14页
  • 作者单位

    a Department of Physics and Meteorology, Indian Institute of Technology, Kharagpur, West Bengal, India b Materials Science Centre, Indian Institute of Technology, Kharagpur 721302, West Bengal, India;

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