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磁赤铁矿纳米颗粒的快速合成与表征

Rapid synthesis and characterization of maghemite nanoparticles.

作者信息

Tural Bilsen, Ozenbaş Macit, Atalay Selçuk, Volkan Mürvet

机构信息

Department of Chemistry, Middle East Technical University, 06531-Ankara, Turkey.

出版信息

J Nanosci Nanotechnol. 2008 Feb;8(2):861-6. doi: 10.1166/jnn.2008.b269.

Abstract

Fe2O3-SiO2 nanocomposites were prepared by a sol-gel method using various evaporation surface to volume (S/V) ratios ranging from 0.03 to 0.2. The Fe2O3-SiO2 sols were gelated at various temperatures ranging from 50 degrees C to 70 degrees C, and subsequently they were calcined in air at 400 degrees C for 4 hours. The structure and the magnetic properties of the prepared Fe203-SiO2 nanocomposites were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), differential thermal analysis (DTA), and vibrating sample magnetometer (VSM) measurements. The gelation temperature of the Fe2O3-SiO2 sols influenced strongly the particle size and crystallinity of the maghemite nanoparticles. It was observed that the particle size of maghemite nanoparticles increased with the increasing of the gelation temperature of the sols, which may be due to the agglomeration of the maghemite particles at elevated temperatures inside the microporosity of the silica matrix during the gelation process, and the subsequent calcination of these gels at 400 degrees C resulted in the formation of large size iron oxide particles. Magnetization studies at temperatures of 10, 195, and 300 K showed superparamagnetic behavior for all the nanocomposites prepared using the evaporation surface to volume ratio (S/V) of 0.1, 0.2, 0.09, and 0.08. The saturation magnetization, Ms, values measured at 10 K were 5.5, 8.5, and 9.5 emu/g, for the samples gelated at 50, 60, and 70 degrees C, respectively. At the gelation temperature of 70 degrees C, gamma-Fe2O3 crystalline superparamagnetic nanoparticles with the particle size of 9 +/- 2 nm were formed in 12 hours for the samples prepared at the S/V ratio of 0.2.

摘要

采用溶胶 - 凝胶法,利用各种蒸发表面积与体积(S/V)比在0.03至0.2范围内制备了Fe2O3 - SiO2纳米复合材料。Fe2O3 - SiO2溶胶在50℃至70℃的不同温度下凝胶化,随后在空气中于400℃煅烧4小时。使用X射线衍射(XRD)、透射电子显微镜(TEM)、差热分析(DTA)和振动样品磁强计(VSM)测量对制备的Fe2O3 - SiO2纳米复合材料的结构和磁性进行了表征。Fe2O3 - SiO2溶胶的凝胶化温度强烈影响了磁赤铁矿纳米颗粒的粒径和结晶度。观察到磁赤铁矿纳米颗粒的粒径随着溶胶凝胶化温度的升高而增大,这可能是由于在凝胶化过程中,磁赤铁矿颗粒在二氧化硅基质的微孔内高温下发生团聚,并且随后在400℃对这些凝胶进行煅烧导致形成了大尺寸的氧化铁颗粒。在10K、195K和300K温度下的磁化研究表明,对于所有使用蒸发表面积与体积比(S/V)为0.1、0.2、0.09和0.08制备的纳米复合材料均表现出超顺磁性行为。对于在50℃、60℃和70℃凝胶化的样品,在10K下测量的饱和磁化强度Ms值分别为5.5、8.5和9.5emu/g。在凝胶化温度为70℃时,对于以S/V比0.2制备的样品,在12小时内形成了粒径为9±2nm的γ - Fe2O3晶体超顺磁性纳米颗粒。

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