Influence of Cu2+, Ni2+, and Zn2+ Ions Doping on the Structure, Morphology, and Magnetic Properties of Co-Ferrite Embedded in SiO2 Matrix Obtained by an Innovative Sol-Gel Route

This paper presents the synthesis of metal doped Co ferrites, M0.2Co0.8Fe2O4 (M = Cu2+, Ni2+, and Zn2+) embedded in SiO2 matrix by an innovative sol-gel route. The structural and morphological characterization provided information about the crystalline phases, crystallite size, and the shape of the prepared ferrites. The thermal study depicted the thermal decomposition and stability of the obtained ferrites. X-ray diffraction indicated nanocrystalline ferrites with spinel structure and the lack of crystalline phase impurities, while Fourier transform infrared spectroscopy revealed the presence of functional groups in precursors and ferrite powders. The lattice parameters showed a gradual increase indicating a uniform distribution of divalent metal ions in the Co ferrite lattice. The crystallite size, magnetic moment, super-exchange and deflection of magnetic domain were influenced by the dopant metal ion. The room temperature magnetization indicated a ferromagnetic behavior of the ferrites annealed at 1000 °C and a superparamagnetic behavior of the ferrites annealed at 700 °C

Dependence of Structural, Morphological and Magnetic Properties of Manganese Ferrite on Ni-Mn Substitution

This paper presents the influence of Mn2+ substitution by Ni2+ on the structural, morphological and magnetic properties of Mn1−xNixFe2O4@SiO2 (x = 0, 0.25, 0.50, 0.75, 1.00) nanocomposites (NCs) obtained by a modified sol-gel method. The Fourier transform infrared spectra confirm the formation of a SiO2 matrix and ferrite, while the X-ray diffraction patterns show the presence of poorly crystalline ferrite at low annealing temperatures and highly crystalline mixed cubic spinel ferrite accompanied by secondary phases at high annealing temperatures. The lattice parameters gradually decrease, while the crystallite size, volume, and X-ray density of Mn1−xNixFe2O4@SiO2 NCs increase with increasing Ni content and follow Vegard’s law. The saturation magnetization, remanent magnetization, squareness, magnetic moment per formula unit, and anisotropy constant increase, while the coercivity decreases with increasing Ni content. These parameters are larger for the samples with the same chemical formula, annealed at higher temperatures. The NCs with high Ni content show superparamagnetic-like behavior, while the NCs with high Mn content display paramagnetic behavior

Effect of Ca2+ doping and annealing temperature on the structure, morphology and magnetic behavior of CaxCo1-xFe2O4/SiO2 nanocomposites

Co-doped ferrites are promising functional materials for many practical applications and their physical properties can be tailored by changing their composition. This study assesses the structure, morphology and magnetic properties of CaxCo1-xFe2O4/SiO2 (x = 0.0–0.5) nanocomposites (NCs) obtained by sol–gel method and annealed at different temperatures (400, 800 and 1200 °C). The effect of Ca2+ doping on the properties of nano-structured Ca-Co ferrite embedded in the SiO2 matrix was investigated by thermogravimetry and differential thermal analysis, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy, Brunauer-Emmett-Teller surface area, inductively coupled plasma optical emission spectrometry, atomic force microscopy (AFM) and magnetic measurements. The thermal analysis showed the formation of metal succinates up to 200 °C and of ferrite above 280 °C. The presence of poorly crystalline ferrite accompanied by silicates at low annealing temperatures and of highly crystalline ferrite accompanied by SiO2 and Ca silicates at high annealing temperatures was identified by XRD. The increased Ca2+ doping led to a decrease in the structural parameters estimated by XRD and the surface area. The AFM images revealed that the NCs have a crystalline core covered by a layer of amorphous SiO2. The hysteresis loop shape indicated the superparamagnetic-like and ferromagnetic behavior of the obtained NCs. The magnetic properties improved with the increase in annealing temperature and depended on the particle size and dopant content. The NCs with low Ca2+ content annealed at 800 °C still show appreciable hysteresis, but doping with high Ca2+ contents drastically affects the magnetic properties

Influence of SiO2 Embedding on the Structure, Morphology, Thermal, and Magnetic Properties of Co0.4Zn0.4Ni0.2Fe2O4 Particles

(Co0.4Zn0.4Ni0.2Fe2O4)α(SiO2)(100−α) samples obtained by embedding Co0.4Zn0.4Ni0.2Fe2O4 nanoparticles in SiO2 in various proportions were synthesized by sol-gel process and characterized using thermal analysis, Fourier-transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy, inductively coupled plasma optical emission spectrometry, and magnetic measurements. Poorly crystalline Co–Zn–Ni ferrite at low annealing temperatures (500 °C) and highly crystalline Co–Zn–Ni ferrite together with traces of crystalline Fe2SiO4 (800 °C) and SiO2 (tridymite and cristobalite) (1200 °C) were obtained. At 1200 °C, large spherical particles with size increasing with the ferrite content (36–120 nm) were obtained. Specific surface area increased with the SiO2 content and decreased with the annealing temperature above 500 °C. Magnetic properties were enhanced with the increase in ferrite content and annealing temperature

Influence of SiO₂ Embedding on the Structure, Morphology, Thermal, and Magnetic Properties of Co_0.4Zn_0.4Ni_0.2Fe₂O₄ Particles

(Co0.4Zn0.4Ni0.2Fe2O4)α(SiO2)(100−α) samples obtained by embedding Co0.4Zn0.4Ni0.2Fe2O4 nanoparticles in SiO2 in various proportions were synthesized by sol-gel process and characterized using thermal analysis, Fourier-transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy, inductively coupled plasma optical emission spectrometry, and magnetic measurements. Poorly crystalline Co–Zn–Ni ferrite at low annealing temperatures (500 °C) and highly crystalline Co–Zn–Ni ferrite together with traces of crystalline Fe2SiO4 (800 °C) and SiO2 (tridymite and cristobalite) (1200 °C) were obtained. At 1200 °C, large spherical particles with size increasing with the ferrite content (36–120 nm) were obtained. Specific surface area increased with the SiO2 content and decreased with the annealing temperature above 500 °C. Magnetic properties were enhanced with the increase in ferrite content and annealing temperature

Sol-Gel Synthesis, Structure, Morphology and Magnetic Properties of Ni0.6Mn0.4Fe2O4 Nanoparticles Embedded in SiO2 Matrix

The structure, morphology and magnetic properties of (Ni0.6Mn0.4Fe2O4)α(SiO2)100−α (α = 0–100%) nanocomposites (NCs) produced by sol-gel synthesis were investigated using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), atomic force microscopy (AFM) and vibrating sample magnetometry (VSM). At low calcination temperatures (300 °C), poorly crystallized Ni0.6Mn0.4Fe2O4, while at high calcination temperatures, well-crystallized Ni0.6Mn0.4Fe2O4 was obtained along with α-Fe2O3, quartz, cristobalite or iron silicate secondary phase, depending on the Ni0.6Mn0.4Fe2O4 content in the NCs. The average crystallite size increases from 2.6 to 74.5 nm with the increase of calcination temperature and ferrite content embedded in the SiO2 matrix. The saturation magnetization (Ms) enhances from 2.5 to 80.5 emu/g, the remanent magnetization (MR) from 0.68 to 12.6 emu/g and the coercive field (HC) from 126 to 260 Oe with increasing of Ni0.6Mn0.4Fe2O4 content in the NCs. The SiO2 matrix has a diamagnetic behavior with a minor ferromagnetic fraction, Ni0.6Mn0.4Fe2O4 embedded in SiO2 matrix displays superparamagnetic behavior, while unembedded Ni0.6Mn0.4Fe2O4 has a high-quality ferromagnetic behavior

Magnetic and Magnetocaloric Properties of Nano- and Polycrystalline Manganites La_(0.7−x)Eu_xBa_0.3MnO₃

Here, we report synthesis and investigations of bulk and nano-sized La(0.7−x)EuxBa0.3MnO3 (x ≤ 0.4) compounds. The study presents a comparison between the structural and magnetic properties of the nano- and polycrystalline manganites La(0.7−x)EuxBa0.3MnO3, which are potential magnetocaloric materials to be used in domestic magnetic refrigeration close to room temperature. The parent compound, La0.7Ba0.3MnO3, has Curie temperature TC = 340 K. The magnetocaloric effect is at its maximum around TC. To reduce this temperature below 300 K, we partially replaced the La ions with Eu ions. A solid-state reaction was used to prepare bulk polycrystalline materials, and a sol-gel method was used for the nanoparticles. X-ray diffraction was used for the structural characterization of the compounds. Transmission electron spectroscopy (TEM) evidenced nanoparticle sizes in the range of 40–80 nm. Iodometry and inductively coupled plasma optical emission spectrometry (ICP-OES) was used to investigate the oxygen content of the studied compounds. Critical exponents were calculated for all samples, with bulk samples being governed by tricritical mean field model and nanocrystalline samples governed by the 3D Heisenberg model. The bulk sample with x = 0.05 shows room temperature phase transition TC = 297 K, which decreases with increasing x for the other samples. All nano-sized compounds show lower TC values compared to the same bulk samples. The magnetocaloric effect in bulk samples revealed a greater magnetic entropy change in a relatively narrow temperature range, while nanoparticles show lower values, but in a temperature range several times larger. The relative cooling power for bulk and nano-sized samples exhibit approximately equal values for the same substitution level, and this fact can substantially contribute to applications in magnetic refrigeration near room temperature. By combining the magnetic properties of the nano- and polycrystalline manganites, better magnetocaloric materials can be obtained

Magnetic Properties and Magnetocaloric Effect of Polycrystalline and Nano-Manganites Pr_0.65Sr_(0.35−x)Ca_xMnO₃ (x ≤ 0.3)

Here we report investigations of bulk and nano-sized Pr0.65Sr(0.35−x)CaxMnO3 compounds (x ≤ 0.3). Solid-state reaction was implemented for polycrystalline compounds and a modified sol–gel method was used for nanocrystalline compounds. X-ray diffraction disclosed diminishing cell volume with increasing Ca substitution in Pbnm space group for all samples. Optical microscopy was used for bulk surface morphology and transmission electron microscopy was utilized for nano-sized samples. Iodometric titration showed oxygen deficiency for bulk compounds and oxygen excess for nano-sized particles. Measurements of resistivity of bulk samples revealed features at temperatures associated with grain boundary condition and with ferromagnetic (FM)/paramagnetic (PM) transition. All samples exhibited negative magnetoresistivity. Magnetic critical behavior analysis suggested the polycrystalline samples are governed by a tricritical mean field model while nanocrystalline samples are governed by a mean field model. Curie temperatures values lower with increasing Ca substitution from 295 K for the parent compound to 201 K for x = 0.2. Bulk compounds exhibit high entropy change, with the highest value of 9.21 J/kgK for x = 0.2. Magnetocaloric effect and the possibility of tuning the Curie temperature by Ca substitution of Sr make the investigated bulk polycrystalline compounds promising for application in magnetic refrigeration. Nano-sized samples possess wider effective entropy change temperature (ΔTfwhm) and lower entropy changes of around 4 J/kgK which, however, puts in doubt their straightforward potential for applications as magnetocaloric materials