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Synthesis and detection the oxidization of Co cores of Co@SiO2 core-shell nanoparticles by in situ XRD and EXAFS

机译:原位XRD和EXAFS合成和检测Co @ SiO2核壳纳米粒子Co核的氧化。

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摘要

In this paper, the Co@SiO2 core-shell nanoparticles were prepared by the sol-gel method. The oxidization of Co core nanoparticles was studied by the synchrotron radiation-based techniques including in situ X-ray diffraction (XRD) and X-ray absorption fine structure (XAFS) up to 800°C in air and N2 protection conditions, respectively. It was found that the oxidization of Co cores is undergoing three steps regardless of being in air or in N2 protection condition. In the first step ranging from room temperature to 200°C, the Co cores were dominated by Co0 state as well as small amount of Co2+ ions. When temperature was above 300°C, the interface between Co cores and SiO2 shells was gradually oxidized into Co2+, and the CoO layer was observed. As the temperature increasing to 800°C, the Co cores were oxidized to Co3O4 or Co3O4/CoO. Nevertheless, the oxidization kinetics of Co cores is different for the Co@SiO2 in air and N2 gas conditions. Generally, the O2 in the air could get through the SiO2 shells easily onto the Co core surface and induce the oxidization of the Co cores due to the mesoporous nature of the SiO2 shells. However, in N2 gas condition, the O atoms can only be from the SiO2 shells, so the diffusion effect of O atoms in the interface between Co core and SiO2 shell plays a key role.
机译:本文采用溶胶-凝胶法制备了Co @ SiO2核壳纳米粒子。通过基于同步辐射的技术研究了Co核纳米颗粒的氧化,该技术包括分别在空气和N2保护条件下分别在800°C下进行原位X射线衍射(XRD)和X射线吸收精细结构(XAFS)。已经发现,无论在空气中还是在N 2保护条件下,Co核的氧化都经历三个步骤。在从室温到200°C的第一步中,Co核以Co 0 状态以及少量的Co 2 + 离子为主。当温度高于300℃时,Co核与SiO2壳之间的界面逐渐被氧化为Co 2 + ,并观察到CoO层。随着温度升高到800°C,Co核被氧化成Co3O4或Co3O4 / CoO。然而,在空气和氮气条件下,Co @ SiO2的Co核的氧化动力学是不同的。通常,由于SiO 2壳的中孔性质,空气中的O 2可以容易地穿过SiO 2壳到达Co芯表面并引起Co芯的氧化。但是,在氮气条件下,O原子只能来自SiO2壳,因此O原子在Co核与SiO2壳之间的界面中的扩散作用起着关键作用。

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