Atif M, Husnain H Ul, Rehman Atta Ur, Younas U, Rafique T, Khalid W, Ali Z, Nadeem M
Functional Materials Lab, Department of Physics, Air University PAF Complex E-9 Islamabad Pakistan
Department of Physics, The University of Hong Kong Pokfulam Hong Kong.
RSC Adv. 2024 Feb 26;14(10):6883-6895. doi: 10.1039/d3ra06684c. eCollection 2024 Feb 21.
Herein, Ni-Cu co-doped barium hexaferrites (BaFeCuNiO, 0.0 ≤ ≤ 1.0 with an interval of 0.25) were successfully synthesized using a co-precipitation method. The formation of a magnetoplumbite structure with the 6/ space group was confirmed by Rietveld refinement of the obtained X-ray diffraction patterns. Microstructural investigations revealed grains in the shape of hexagonal plates, while co-doping resulted in a variation in the grain sizes of the prepared samples. X-ray photoelectron spectroscopy was performed to determine the valence state of iron in the prepared hexaferrites. Impedance spectroscopy analysis revealed that dielectric permittivity initially decreased with an increase in the co-dopant content up to = 0.5 and then increased by two orders of magnitude for = 1.0. Alternatively, resistive properties showed microstructural resistance values in the range 10-10 Ω, with the highest value obtained for the sample with = 0.5. Furthermore, magnetic measurements indicated that all the prepared samples exhibited ferrimagnetic behaviour. Saturation magnetization and magnetic anisotropy values were found to be the highest for the sample with = 1.0, which also had the lowest coercivity among the prepared samples. Herein, the observed variations in the obtained results can be explained by the variations in grain sizes and the Fe/Fe ratio associated with the preferential occupation of co-dopants at octahedral sites. Based on our findings, the BaFeNiO ( = 1.0) composition appears to be the most promising choice as a microwave absorption material among the prepared samples owing to the coexistence of high dielectric permittivity (>10 at 10 Hz) and saturation magnetization (73 emu g).
在此,采用共沉淀法成功合成了镍铜共掺杂的六方铁酸钡(BaFeCuNiO,0.0≤≤1.0,间隔为0.25)。通过对所得X射线衍射图谱进行Rietveld精修,证实形成了具有6/空间群的磁铅石结构。微观结构研究表明晶粒呈六方板状,而共掺杂导致所制备样品的晶粒尺寸发生变化。进行了X射线光电子能谱分析以确定所制备六方铁氧体中铁的价态。阻抗谱分析表明,介电常数最初随着共掺杂剂含量增加至=0.5而降低,然后对于=1.0增加了两个数量级。另外,电阻特性显示微观结构电阻值在10-10Ω范围内,对于=0.5的样品获得最高值。此外,磁性测量表明所有制备的样品都表现出亚铁磁性行为。发现对于=1.0的样品,饱和磁化强度和磁各向异性值最高,该样品在所制备的样品中也具有最低的矫顽力。在此,所观察到的结果变化可以通过晶粒尺寸的变化以及与共掺杂剂在八面体位置的优先占据相关的Fe/Fe比来解释。基于我们的发现,由于高介电常数(在10Hz时>10)和饱和磁化强度(73emu g)共存,BaFeNiO(=1.0)组成似乎是所制备样品中作为微波吸收材料最有前景的选择。