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Synthesis of water dispersed Fe_3O_4@ZnO Composite Nanoparticles by the Polyol Method

机译:多元醇法合成水分散Fe_3O_4 @ ZnO复合纳米粒子

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Water-soluble Fe_3O_4@ZnO composite nanoparticles (NPs) were synthesized using a polyol route. The effects of the addition of the ZnO phase were evaluated by varying the Zn/Fe molar ratio in the 0.25-1.00 range as a function of the reaction time. X-ray diffractometry confirmed the formation of the magnetite and ZnO phases and suggested the possible formation of a composite structure. Also, using this method, pure magnetite and ZnO NPs were synthesized. The average crystallite sizes were estimated to 6.3 ± 0.3 nm and 8.6 ± 0.6 nm for magnetite and ZnO NPs, respectively. The samples were examined using transmission electron microscopy. Fourier transform infrared spectra indicated the presence of adsorbed species onto the solids surface, which may explain the good stability of the materials in water. Photoluminescence measurements at room temperature for pure ZnO nanoparticles exhibited the characteristic excitonic emission around 395 nm. Vibrating Sample Magnetometer measurements at room temperature evidenced the superparamagnetic behavior of magnetite nanocrystals, with a saturation magnetization of 60emu/g. The maximum magnetization ranged from 28 to 54emu/g for the composite NPs. Moessbauer spectroscopy measurements at room temperature showed evidence of evolving Fe-sites associated to superparamagnetic particles, as reflected on the coexistence of prominent doublet peaks and very weak sextet peaks.
机译:使用多元醇路线合成了水溶性Fe_3O_4 @ ZnO复合纳米颗粒(NPs)。通过将Zn / Fe摩尔比在0.25-1.00范围内变化作为反应时间的函数来评估添加ZnO相的效果。 X射线衍射法证实了磁铁矿和ZnO相的形成,并暗示可能形成复合结构。同样,使用这种方法,可以合成纯磁铁矿和ZnO NP。磁铁矿和ZnO NP的平均微晶尺寸估计分别为6.3±0.3 nm和8.6±0.6 nm。使用透射电子显微镜检查样品。傅立叶变换红外光谱表明固体表面上存在吸附物质,这可以解释该物质在水中的良好稳定性。室温下对纯ZnO纳米颗粒的光致发光测量显示出约395 nm的特征激子发射。室温下振动样​​品磁力计的测量证明了磁铁矿纳米晶体的超顺磁行为,饱和磁化强度为60emu / g。复合NP的最大磁化强度为28-54emu / g。室温下的Moessbauer光谱测量表明,与超顺磁性粒子相关的Fe位置不断演化的证据,反映在突出的二重峰和非常弱的六重峰的共存上。

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