Fatma A. Ibrahim , Ishfaq Ahmad , Mohamed S. Hamdy , Gideon F.B. Solre , Sana Ullah Asif
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引用次数: 0
摘要
这项工作展示了对取代了 Ho3+ 的 Ca-Cu 六铁氧体纳米晶体的结构和磁性能进行探索的系统性尝试。通过溶胶-凝胶自燃技术合成了 Ca0.5Cu0.5Fe12-xHoxO19 (x = 0.00, 0.05, 0.10, 0.15, 0.20) M 型六价铁氧体。XRD 光谱用于评估晶相和取代基引起的晶粒变化。晶格参数 "a "和 "c "的范围分别为 (5.887-5.898) Å 和 (23.184-23.195) Å。试样的形态表明,晶粒的分布与 Ho 取代物一致。根据振动样品磁力计(VSM)回路的测定,样品的矫顽力从 2.85 kOe 微增至 3.15 kOe,而饱和磁化率则从 26.41 emu/g 增至 30.13 emu/g。讨论还包括各向异性场 (Ha)、各向异性参数 (B)、磁晶各向异性常数 (K) 和单位公式磁矩 mB(µB) 的变化及其对主要磁性参数的影响。
Insights into the structure and magnetic characteristics of Ho substituted Ca-Cu based Ca0.5Cu0.5Fe12-xHoxO19 hexaferrites nanoparticles
This work demonstrates a systematic attempt to explore the structure and magnetic properties of Ho3+ substituted Ca-Cu hexaferrite nanocrystals. Ca0.5Cu0.5Fe12-xHoxO19 (x = 0.00, 0.05, 0.10, 0.15, 0.20) M−type hexaferrites are synthesized via sol–gel auto combustion technique. XRD spectra is used to evaluate the phase, and substituent-induced modifications of crystallites. The lattice parameters ‘a’ and ‘c’ lies in the range (5.887–5.898) Å and (23.184–23.195) Å. The size of crystallites ranges from 55.73 to 59.41 nm. The specimen’s morphology indicates the consistent distribution of grains with Ho substitution. The coercivity of samples increased slightly from 2.85 to 3.15 kOe, as determined by vibrating sample magnetometer (VSM) loops, whereas saturation magnetization increased from 26.41 to 30.13 emu/g. The discussion also encompasses variations in anisotropy field (Ha), anisotropy parameter (B), magneto-crystalline anisotropic constant (K), and magnetic moment per formula unit mB(µB) and their effect on main magnetic parameters.
期刊介绍:
Launched in January 1998, Inorganic Chemistry Communications is an international journal dedicated to the rapid publication of short communications in the major areas of inorganic, organometallic and supramolecular chemistry. Topics include synthetic and reaction chemistry, kinetics and mechanisms of reactions, bioinorganic chemistry, photochemistry and the use of metal and organometallic compounds in stoichiometric and catalytic synthesis or organic compounds.