Enhancement of the magnetic and optical properties of Ni0.5Zn0.5Fe2O4 nanoparticles by ruthenium doping

The characterization of Nanosized Ni 0.5 Zn 0.5 Ru x Fe 2− x O 4 (0.00 ≤  x  ≤ 0.015), prepared by the wet chemical coprecipitation method, is reported in the current investigation. X-ray powder diffraction (XRD) analysis has confirmed the formation of a single phased spinel cubic structure. While t...

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Veröffentlicht in:Applied physics. A, Materials science & processing Materials science & processing, 2022-05, Vol.128 (5), Article 409
Hauptverfasser: Basma, H., Al Boukhari, J., Abd Al Nabi, M., Aridi, A., Sayed Hassan, R., Naoufal, D., Roumie, M., Awad, R.
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container_title Applied physics. A, Materials science & processing
container_volume 128
creator Basma, H.
Al Boukhari, J.
Abd Al Nabi, M.
Aridi, A.
Sayed Hassan, R.
Naoufal, D.
Roumie, M.
Awad, R.
description The characterization of Nanosized Ni 0.5 Zn 0.5 Ru x Fe 2− x O 4 (0.00 ≤  x  ≤ 0.015), prepared by the wet chemical coprecipitation method, is reported in the current investigation. X-ray powder diffraction (XRD) analysis has confirmed the formation of a single phased spinel cubic structure. While transmission electron microscopy (TEM) studies have shown an increase in the particle size for high content of Ru 3+ doping. The elemental composition of all samples was investigated using energy dispersive x-ray (EDX) measurements. The results showed a reciprocal relation between the Fe 3+ and Ru 3+ contents, suggesting the successful substitution of Ru 3+ in Fe 3+ sites. UV–Vis spectroscopy studies, via Urbach energy analysis, proposed a perturbation in the band structure of Ni 0.5 Zn 0.5 Fe 2 O 4 induced by Ru 3+ substitution, affecting both the direct and indirect bandgap energies. Excitation wavelength-dependent photoluminescence (PL) studies, presented for the first time, have shown a strong dependence of the emission spectra on both the excitation wavelength and Ru 3+ doping. The PL analysis suggests the utilization of Ni 0.5 Zn 0.5 Ru x Fe 2− x O 4 as a candidate for photocatalytic applications. Furthermore, VSM studies, have shown a transition from superparamagnetic to soft ferromagnetic for Ru 3+ doped samples. The saturation magnetization, coercivity, and effective anisotropy were enhanced as a result of Ru 3+ doping. Finally, photocatalysis experiments have shown an enhancement of the degradation rate of nitrobenzene for the sample with x  = 0.0125 with the ability of magnetic recycling, in agreement with the PL and VSM studies.
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X-ray powder diffraction (XRD) analysis has confirmed the formation of a single phased spinel cubic structure. While transmission electron microscopy (TEM) studies have shown an increase in the particle size for high content of Ru 3+ doping. The elemental composition of all samples was investigated using energy dispersive x-ray (EDX) measurements. The results showed a reciprocal relation between the Fe 3+ and Ru 3+ contents, suggesting the successful substitution of Ru 3+ in Fe 3+ sites. UV–Vis spectroscopy studies, via Urbach energy analysis, proposed a perturbation in the band structure of Ni 0.5 Zn 0.5 Fe 2 O 4 induced by Ru 3+ substitution, affecting both the direct and indirect bandgap energies. Excitation wavelength-dependent photoluminescence (PL) studies, presented for the first time, have shown a strong dependence of the emission spectra on both the excitation wavelength and Ru 3+ doping. 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A, Materials science &amp; processing</title><addtitle>Appl. Phys. A</addtitle><description>The characterization of Nanosized Ni 0.5 Zn 0.5 Ru x Fe 2− x O 4 (0.00 ≤  x  ≤ 0.015), prepared by the wet chemical coprecipitation method, is reported in the current investigation. X-ray powder diffraction (XRD) analysis has confirmed the formation of a single phased spinel cubic structure. While transmission electron microscopy (TEM) studies have shown an increase in the particle size for high content of Ru 3+ doping. The elemental composition of all samples was investigated using energy dispersive x-ray (EDX) measurements. The results showed a reciprocal relation between the Fe 3+ and Ru 3+ contents, suggesting the successful substitution of Ru 3+ in Fe 3+ sites. UV–Vis spectroscopy studies, via Urbach energy analysis, proposed a perturbation in the band structure of Ni 0.5 Zn 0.5 Fe 2 O 4 induced by Ru 3+ substitution, affecting both the direct and indirect bandgap energies. Excitation wavelength-dependent photoluminescence (PL) studies, presented for the first time, have shown a strong dependence of the emission spectra on both the excitation wavelength and Ru 3+ doping. The PL analysis suggests the utilization of Ni 0.5 Zn 0.5 Ru x Fe 2− x O 4 as a candidate for photocatalytic applications. Furthermore, VSM studies, have shown a transition from superparamagnetic to soft ferromagnetic for Ru 3+ doped samples. The saturation magnetization, coercivity, and effective anisotropy were enhanced as a result of Ru 3+ doping. 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X-ray powder diffraction (XRD) analysis has confirmed the formation of a single phased spinel cubic structure. While transmission electron microscopy (TEM) studies have shown an increase in the particle size for high content of Ru 3+ doping. The elemental composition of all samples was investigated using energy dispersive x-ray (EDX) measurements. The results showed a reciprocal relation between the Fe 3+ and Ru 3+ contents, suggesting the successful substitution of Ru 3+ in Fe 3+ sites. UV–Vis spectroscopy studies, via Urbach energy analysis, proposed a perturbation in the band structure of Ni 0.5 Zn 0.5 Fe 2 O 4 induced by Ru 3+ substitution, affecting both the direct and indirect bandgap energies. Excitation wavelength-dependent photoluminescence (PL) studies, presented for the first time, have shown a strong dependence of the emission spectra on both the excitation wavelength and Ru 3+ doping. The PL analysis suggests the utilization of Ni 0.5 Zn 0.5 Ru x Fe 2− x O 4 as a candidate for photocatalytic applications. Furthermore, VSM studies, have shown a transition from superparamagnetic to soft ferromagnetic for Ru 3+ doped samples. The saturation magnetization, coercivity, and effective anisotropy were enhanced as a result of Ru 3+ doping. Finally, photocatalysis experiments have shown an enhancement of the degradation rate of nitrobenzene for the sample with x  = 0.0125 with the ability of magnetic recycling, in agreement with the PL and VSM studies.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00339-022-05552-7</doi><orcidid>https://orcid.org/0000-0002-0060-5259</orcidid></addata></record>
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subjects Anisotropy
Applied physics
Characterization and Evaluation of Materials
Coercivity
Condensed Matter Physics
Doping
Emission spectra
Excitation
Ferromagnetism
Machines
Magnetic properties
Magnetic saturation
Manufacturing
Materials science
Nanoparticles
Nanotechnology
Nitrobenzene
Optical and Electronic Materials
Optical properties
Perturbation
Photocatalysis
Photoluminescence
Physics
Physics and Astronomy
Processes
Ruthenium
Spectrum analysis
Substitutes
Surfaces and Interfaces
Thin Films
X ray powder diffraction
title Enhancement of the magnetic and optical properties of Ni0.5Zn0.5Fe2O4 nanoparticles by ruthenium doping
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