Structural, Magnetic, Optical, and MEM Studies on Co-precipitated X 0.4Zn 0.6Fe 2O4 (X = Co, Mn) Nanoferrite Particles

被引:4
|
作者
Kannan, Y. B. [1 ]
Saravanan, R. [2 ,3 ]
Srinivasan, N. [4 ,5 ]
Praveena, K. [6 ,8 ]
Sadhana, K. [7 ,9 ]
机构
[1] Arumugam Pillai Seethai Ammal Coll, Dept Phys, Tiruppattur 630211, India
[2] Madura Coll, Res Ctr, Madurai 625011, Tamil Nadu, India
[3] Madura Coll, PG Dept Phys, Madurai 625011, Tamil Nadu, India
[4] Thiagarajar Coll, Res Ctr, Madurai 625009, Tamil Nadu, India
[5] Thiagarajar Coll, PG Dept Phys, Madurai 625009, Tamil Nadu, India
[6] Univ Hyderabad, Sch Phys, Hyderabad 500046, Andhra Pradesh, India
[7] Indian Inst Sci, Mat Res Ctr, Bangalore 560012, Karnataka, India
[8] Natl Taiwan Normal Univ, Dept Phys, Taipei 1167, Taiwan
[9] Osmania Univ, Univ Coll Sci, Dept Phys, Hyderabad 500004, Andhra Pradesh, India
关键词
XRD; Cation distribution; Maximum entropy method; Magnetic and optical properties; FERRITE NANOPARTICLES; ELECTRICAL-PROPERTIES; CATION DISTRIBUTION; ZN; AC; MICROSTRUCTURE; DEPENDENCE; SIZE;
D O I
10.1007/s10948-017-4081-x
中图分类号
O59 [应用物理学];
学科分类号
摘要
Cobalt and manganese-substituted zinc ferrite X0.4Zn0.6Fe2O4 (X = Co, Mn) nanoparticles have been synthesized by co-precipitation method and characterized for structural, morphology, and magnetic properties by X-ray diffraction (XRD), scanning electron microscopy (SEM), and vibrating sample magnetometry (VSM). The Rietveld refinement method is employed to refine the XRD powder data, and the structural parameters are calculated from the refinement. Substitution of cobalt and manganese causes the lattice parameter to decrease. Particle size, measured from XRD, lies in the nanometer regime. A low saturation magnetization value is obtained in both samples, and the presence of non-collinear spin arrangement is found at octahedral sites. The maximum entropy method (MEM) is employed to study the strength of the bond between the atoms at tetrahedral and octahedral sites in the unit cell of ferrites. Optical band gap energy of the samples is determined by using UV-VIS techniques.
引用
收藏
页码:2673 / 2682
页数:10
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