水热合成法制备微纳米MnO2晶体不同形貌的电磁特性

Different crystal structure evolvement and the electromagnetic properties of nano-Manganese Dioxide

  • 摘要: 本文采用水热合成法,以(NH4)2S2O8作氧化剂,以MnSO4为锰源,在不同水热反应时间下制备了不同晶体结构和形貌的二氧化锰。利用X射线粉末衍射(XRD),扫描电子显微镜(SEM)和透射电子显微镜(TEM)对产物进行成分、晶型和形貌进行分析,并通过电磁参数的测试对产物的电磁特性以及电磁波损耗机制进行讨论。结果表明,水热反应时间由1h逐渐增加到48h后,二氧化锰晶体结构由纯γ型逐渐转变为纯β型,中间产物为γ、α和β的混合体,二氧化锰的形貌也由球状经团絮状后逐渐转变为直径约为5-10nm纳米线状。复介电常数随反应时间增加而增加,复磁导率却正好相反,由此最后分析了二氧化锰的电磁波损耗机制。

     

    Abstract: MnO2 with different morphology and crystal structure were prepared via a low-temperature hydrothermal method in stainless-steel autoclave at 120℃ and different dwell time, which (NH42S2O8 is oxidizing agent and MnSO4 is Mn source. The products were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscope (TEM), and the electromagnetic properties and microwave loss mechanism of as-obtained MnO2 were firstly reported. The results show that the dwell times play a crucial role in the phase purity, the crystal structure, the morphology and the electromagnetic properties of the products. The as-prepared MnO2 transformed gradually from γ-MnO2 to α-MnO2 and β-MnO2 and became finally a pure tetragonal phase of β-MnO2, and the morphology changed also from microspheres with flocculus on the surface into dispersive nanorods with the increase of the dwell times from 1h to 48h. The real and imaginary parts of the complex permittivity of as-prepared MnO2 increased orderly with rising dwell times, and the complex magnetic permeability were on the contrary. Lastly, the microwave loss mechanism of as-obtained MnO2 was analysed.

     

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