<p>The present study investigates the effect of Y<sup>3+</sup> and Cr<sup>3+</sup> co-doping on the crystal structure, vibrational, elastic, morphological and magnetic properties of CoFe<sub>2−x</sub>Y<sub>x/2</sub>Cr<sub>x/2</sub>O<sub>4</sub> (x = 0.00, 0.02, 0.04, 0.06, 0.08, 0.10.) nanoparticles synthesized via cost-effective sol-gel auto-combustion method ensuring high purity. The nanoparticles were synthesized in nano-sized dimension using sol-gel auto-combustion method. All the synthesized nanoparticles show single phase nature associated with cubic spinel structure which was well supported by Rietveld analysis. The Rietveld refinements exhibited a better goodness of fit (χ<sup>2</sup>) between 2.54 and 2.64. The lattice constant decreases from 8.387 Å to 8.380 Å on doping Y<sup>3+</sup> and Cr<sup>3+</sup> ions. The crystallite size obtained from Scherrer’s equation is in the range of 23&#xa0;nm to 18&#xa0;nm. Cation distribution obtained from XRD method and Rietveld method suggests occupancy of Y<sup>3+</sup>, Cr<sup>3+</sup>, Co<sup>2+</sup> ions at octahedral [B] site while Fe<sup>3+</sup> ions get distributed over tetrahedral (A) and octahedral [B] sites. FTIR spectra show the absorption bands near 400&#xa0;cm<sup>− 1</sup> to 550&#xa0;cm<sup>− 1</sup> characterizing the spinel nature. The vibrational and mechanical properties like Debye temperature, stiffness constant, Young’s modulus, bulk modulus, modulus of rigidity increases marginally on doping of Y<sup>3+</sup> and Cr<sup>3+</sup> ions. Raman spectra characterizes the formation of spinel ferrite structure. The surface morphology was viewed through Scanning Electron Microscopy (SEM) technique which show dense morphology with grain size in the range of 21&#xa0;nm to 25&#xa0;nm. The saturation magnetization (Ms) linked with the A-B superexchange interaction decreased with Y<sup>3+</sup> and Cr<sup>3+</sup> ions. The coercivity (Hc) initially increases and then decreases with Y<sup>3+</sup> and Cr<sup>3+</sup> ions within the doping level of x = 0.00 to 0.10.</p>

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Influence of Y3+ and Cr3+ Co-doping on the Structural, Vibrational, Elastic, Morphology and Magnetic Properties of Cobalt Ferrite Nanoparticles

  • Sudarshan Gawali,
  • Yogesh P. Ubale,
  • Subhash M. wani,
  • Smita More,
  • K. M. Jadhav

摘要

The present study investigates the effect of Y3+ and Cr3+ co-doping on the crystal structure, vibrational, elastic, morphological and magnetic properties of CoFe2−xYx/2Crx/2O4 (x = 0.00, 0.02, 0.04, 0.06, 0.08, 0.10.) nanoparticles synthesized via cost-effective sol-gel auto-combustion method ensuring high purity. The nanoparticles were synthesized in nano-sized dimension using sol-gel auto-combustion method. All the synthesized nanoparticles show single phase nature associated with cubic spinel structure which was well supported by Rietveld analysis. The Rietveld refinements exhibited a better goodness of fit (χ2) between 2.54 and 2.64. The lattice constant decreases from 8.387 Å to 8.380 Å on doping Y3+ and Cr3+ ions. The crystallite size obtained from Scherrer’s equation is in the range of 23 nm to 18 nm. Cation distribution obtained from XRD method and Rietveld method suggests occupancy of Y3+, Cr3+, Co2+ ions at octahedral [B] site while Fe3+ ions get distributed over tetrahedral (A) and octahedral [B] sites. FTIR spectra show the absorption bands near 400 cm− 1 to 550 cm− 1 characterizing the spinel nature. The vibrational and mechanical properties like Debye temperature, stiffness constant, Young’s modulus, bulk modulus, modulus of rigidity increases marginally on doping of Y3+ and Cr3+ ions. Raman spectra characterizes the formation of spinel ferrite structure. The surface morphology was viewed through Scanning Electron Microscopy (SEM) technique which show dense morphology with grain size in the range of 21 nm to 25 nm. The saturation magnetization (Ms) linked with the A-B superexchange interaction decreased with Y3+ and Cr3+ ions. The coercivity (Hc) initially increases and then decreases with Y3+ and Cr3+ ions within the doping level of x = 0.00 to 0.10.