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Magnetic and photocatalytic properties of nanocrystalline ZnMn_2O_4

机译:纳米ZnMn_2O_4的磁性和光催化性能

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The present study describes the synthesis of ZnMn_2O_4 nanoparticles with the spinel structure. These oxide nanoparticles are obtained from the decomposition of metal oxalate precursors synthesized by (a) the reverse micellar and (b) the coprecipitation methods. Our studies reveal that the shape, size and morphology of precursors and oxides vary significantly with the method of synthesis. The oxalate precursors prepared from the reverse micellar synthesis method were in the form of rods (micron size), whereas the coprecipitation method led to spherical nanoparticles of size, 40-50 nm. Decomposition of oxalate precursors at low temperature (approx 450 deg C) yielded phase pure ZnMn_2O_4 nanoparticles. The size of the nanoparticles of ZnMn_2O_4 obtained from reverse micellar method is relatively much smaller (20-30 nm) as compared to those made by the co-precipitation (40-50 nm) method. Magnetic studies of nanocrystalline ZnMn_2O_4 confirm antiferro-magnetic ordering in the broad range of approx 150 K. The photocatalytic activity of ZnMn_2O_4 nanoparticles was evaluated using photo-oxidation of methyl orange dye under UV illumination and compared with nanocrystalline TiO_2.
机译:本研究描述了具有尖晶石结构的ZnMn_2O_4纳米粒子的合成。这些氧化物纳米颗粒是通过(a)反胶束和(b)共沉淀法合成的草酸金属前体的分解获得的。我们的研究表明,前体和氧化物的形状,大小和形态随合成方法的不同而有很大差异。用逆胶束合成法制得的草酸酯前体为棒状(微米级),而共沉淀法制得的球形纳米颗粒尺寸为40-50 nm。草酸盐前体在低温下(约450摄氏度)分解产生相纯的ZnMn_2O_4纳米颗粒。与通过共沉淀法(40-50nm)制备的那些相比,通过逆胶束法获得的ZnMn_2O_4的纳米颗粒的尺寸相对小得多(20-30nm)。对纳米晶ZnMn_2O_4的磁性研究证实了大约150 K的宽泛范围内的反铁磁有序性。使用甲基橙染料在紫外光下的光氧化作用评估ZnMn_2O_4纳米颗粒的光催化活性,并将其与纳米晶TiO_2进行比较。

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