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首页> 外文期刊>RSC Advances >Magnetic, X-ray and Mossbauer studies on magnetite/maghemite core-shell nanostructures fabricated through an aqueous route
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Magnetic, X-ray and Mossbauer studies on magnetite/maghemite core-shell nanostructures fabricated through an aqueous route

机译:磁性,X射线和Mossbauer研究通过水法制备的磁铁矿/磁赤铁矿核壳纳米结构

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摘要

Uniform 6-13 nm sized 0D superparamagnetic Fe3O4 nanocrystals were synthesized by an aqueous 'co-precipitation method' under a N-2 atmosphere as a function of temperature to understand the growth kinetics. The crystal phases, surface charge, size, morphology and magnetic characteristics of as-synthesized nanocrystals were characterized by XRD, Raman spectroscopy, FTIR, TG-DTA, BET surface area, dynamic light scattering along with zeta potential, HR-TEM, EDAX, vibrating sample magnetometry and Mossbauer spectroscopy. TEM investigation revealed highly crystalline spherical magnetite particles in the 8.2-12.5 nm size range. The kinetically controlled as-grown nanoparticles were found to possess a preferential (311) orientation of the cubic phase, with a highest magnetic susceptibility of similar to 57 emu g(-1). The Williamson-Hall technique was employed to evaluate the mean crystallite size and microstrain involved in the as-synthesized nanocrystals from the X-ray peak broadening. In addition to FTIR and Raman spectra, Rietveld structural refinement of XRD confirms the magnetite phase with 5-20% maghemite in the sample. VSM and Mossbauer spectral data allowed us to fit the magnetite/maghemite content to a core-shell model where the shell is 0.2-0.3 nm thick maghemite over a magnetite core. The activation energy of <10 kJ mol(-1) calculated from an Arrhenius plot for the complex process of nucleation and growth by diffusion during synthesis shows the significance of the precipitation temperature in the size controlled fabrication processes of nanocrystals. Brunauer-Emmett-Teller (BET) results reveal a mesoporous structure and a large surface area of 124 m(2) g(-1). Magnetic measurement shows that the particles are ferromagnetic at room temperature with zero remanence and zero coercivity. This method produced highly crystalline and dispersed 0D magnetite nanocrystals suitable for biological applications in imaging and drug delivery.
机译:通过水“共沉淀法”在N-2气氛下根据温度合成6-13 nm尺寸的均匀0D超顺磁性Fe3O4纳米晶体,以了解其生长动力学。通过XRD,拉曼光谱,FTIR,TG-DTA,BET表面积,动态光散射以及Zeta电位,HR-TEM,EDAX,X射线衍射,透射电镜等手段对合成后的纳米晶体的晶体相,表面电荷,尺寸,形貌和磁特性进行了表征。振动样品磁力分析和Mossbauer光谱学。 TEM研究表明,高度结晶的球形磁铁矿颗粒尺寸在8.2-12.5 nm之间。发现动力学控制的生长纳米颗粒具有立方相的优先(311)方向,具有最高的磁化率,类似于57 emu g(-1)。 Williamson-Hall技术被用来从X射线峰展宽评估所合成的纳米晶体的平均微晶尺寸和微应变。除FTIR和拉曼光谱外,XRD的Rietveld结构改进还证实了样品中磁铁矿相中磁石含量为5-20%。 VSM和Mossbauer光谱数据使我们能够将磁铁矿/磁赤铁矿的含量拟合到核-壳模型中,该模型的壳层为磁铁矿上0.2-0.3 nm厚的磁赤铁矿。从Arrhenius图计算得出的活化能<10 kJ mol(-1),用于合成过程中通过扩散的成核和生长这一复杂过程,显示出沉淀温度在纳米晶体尺寸控制的制造过程中的重要性。 Brunauer-Emmett-Teller(BET)结果显示了介孔结构和124 m(2)g(-1)的大表面积。磁性测量表明,该颗粒在室温下为铁磁性,剩磁为零,矫顽力为零。该方法产生了高度结晶且分散的0D磁铁矿纳米晶体,适用于成像和药物输送中的生物应用。

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