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Effects of Mg substitution on the structural and magnetic properties of Co0.5Ni(0.5-x)MgxFe2O4 nanoparticle ferrites 被引量:1

Effects of Mg substitution on the structural and magnetic properties of Co_(0.5)Ni_(0.5-x)Mg_xFe_2O_4 nanoparticle ferrites
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摘要 In this study, nanocrystalline Co-Ni-Mg ferrite powders with composition Coo.5Nio.5-xMgxFe2O4 are successfully synthesized by the co-precipitation method. A systematic investigation on the structural, morphological and magnetic properties of un-doped and Mg-doped Co-Ni ferrite nanoparticles is carried out. The prepared samples are characterized using x-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), and vibrating sample magnetometry (VSM). The XRD analyses of the synthesized samples confirm the formation of single-phase cubic spinel structures with crystallite sizes in a range of - 32 nm to - 36 nm. The lat- tice constant increases with increasing Mg content. FESEM images show that the synthesized samples are homogeneous with a uniformly distributed grain. The results of IR spectroscopy analysis indicate the formation of functional groups of spinel ferrite in the co-precipitation process. By increasing Mg2- substitution, room temperature magnetic measurement shows that maximum magnetization and coercivity increase from - 57.35 emu/g to - 61.49 emu/g and - 603.26 Oe to 684.11 Oe (l Oe = 79.5775 A.m-l), respectively. The higher values of magnetization Ms and Mr suggest that the opti- mum composition is Co0.5Ni0.4Mg0.1Fe204 that can be applied to high-density recording media and microwave devices. In this study, nanocrystalline Co-Ni-Mg ferrite powders with composition Coo.5Nio.5-xMgxFe2O4 are successfully synthesized by the co-precipitation method. A systematic investigation on the structural, morphological and magnetic properties of un-doped and Mg-doped Co-Ni ferrite nanoparticles is carried out. The prepared samples are characterized using x-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), and vibrating sample magnetometry (VSM). The XRD analyses of the synthesized samples confirm the formation of single-phase cubic spinel structures with crystallite sizes in a range of - 32 nm to - 36 nm. The lat- tice constant increases with increasing Mg content. FESEM images show that the synthesized samples are homogeneous with a uniformly distributed grain. The results of IR spectroscopy analysis indicate the formation of functional groups of spinel ferrite in the co-precipitation process. By increasing Mg2- substitution, room temperature magnetic measurement shows that maximum magnetization and coercivity increase from - 57.35 emu/g to - 61.49 emu/g and - 603.26 Oe to 684.11 Oe (l Oe = 79.5775 A.m-l), respectively. The higher values of magnetization Ms and Mr suggest that the opti- mum composition is Co0.5Ni0.4Mg0.1Fe204 that can be applied to high-density recording media and microwave devices.
出处 《Chinese Physics B》 SCIE EI CAS CSCD 2016年第4期358-364,共7页 中国物理B(英文版)
基金 supported by the Ibnu Sina Institute for Scientific and Industrial Research,Physics Department of Universiti Teknologi Malaysia and the Ministry of Education Malaysia(Grant Nos.Q.J130000.2526.04H65)
关键词 CO-PRECIPITATION magnetic materials spinel ferrite magnetic properties co-precipitation magnetic materials spinel ferrite magnetic properties
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  • 1Sepelak V, Baabe D, Mienert D, Schultze D, Krumeich F, Litterst F J and Becker K D 2003 J. Magn. Magn. Mater. 257 377.
  • 2Ramana C V, Kolekar Y D, Kamala Bharathi K, Sinha B and Ghosh K 2013 J. Appl. Phys. 114 183907.
  • 3Karanjkar M M, Tarwal N L, Vaigankar A S and Patil P S 2013 Ceram. Int. 39 1757.
  • 4Tan M, Koseoglu Y, Alan F and Senturk E 2011 J. Alloys Compd. 509 9399.
  • 5Patange S, Shirsath S E, Jangam Lohar G K, Jadhav S S and Jadhav K 2011 J. Appl. Phys. 109 053909.
  • 6Islam M U, Abbas T, Niazi S B, Ahmad Z, Sabeen S and Chaudhry M A 2004 Solid State Commun. 130 353.
  • 7He X M, Yan S M, Li Z W, Zhang X, Song X Y, Qiao W, Zhong W and Du Y W 2015 Chin. Phys. B 24 127502.
  • 8Ati A A, Othaman Z and Samavati A 2013 J. Mol. Struct. 1052 177.
  • 9Li L Z, Tu X Q, Wang R and Peng L 2015 J. Magn. Magn. Mater. 381 328.
  • 10Joshi S, Kumar S M, Chhoker S, Srivastava G, Jewariya M and Singh V N 2014 J. Mol. Struct. 1076 55.

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