Ammonia gas sensing and magnetic permeability of enhanced surface area and high porosity lanthanum substituted Co–Zn nano ferrites

This work reports magnetic permeability and ammonia gas sensing characteristics of La³⁺ substituted Co–Zn nano ferrites possessing chemical formula Co_0.7Zn_0.3La_xFe_2-2xO₄ (x = 0–0.1) synthesized by a sol-gel route. Refinement of X-ray diffraction (XRD) patterns of the ferrite powders by the Rietveld technique has revealed the creation of single-phase spinel structure. The tenancy of constituent cations at tetrahedral/octahedral sites was obtained from the refinement of XRD. The crystallite sizes calculated from the W–H method vary from 20 to 24 nm. The scanning electron microscope (SEM) profiles of the ferrite samples were analyzed for the morphological details. The energy dispersive X-ray analysis (EDAX) patterns of the samples were obtained to test the elemental purity of the ferrites within their stoichiometry. The transmission electron microscope (TEM) image of the ferrite (x = 0.1) exhibits the spherical and oval shaped particles with a mean size of 20 nm. Fourier transform infra-red (FTIR) spectra were analyzed to confirm the superseding of La³⁺ cations at octahedral sites. The Brunauer-Emmett-Teller (BET) analysis of nitrogen adsorption-desorption isotherms of the ferrites was performed to investigate the porous structure and to determine the surface area of the nanocrystalline ferrites. The oxidation states of the constituent ions were confirmed by means of X-ray photoelectron spectroscopy (XPS). The complex permeability as a function of frequency was studied to explore the effects of structural parameters on the magnetic behaviour of the ferrites. Analysis of gas sensing properties of the ferrites have proved that the Co–Zn–La ferrite with controlled La composition can be utilized as an effective ammonia gas sensing material in commercial gas sensors.     

Structural,optical, electrical,dielectric, molecular vibrational and magnetic properties of La3+ doped Mg–Cd–Cu ferrites prepared by Co-precipitation technique

Ferrites are among the most frequently investigated materials mainly due to interesting and practically different properties. Therefore, easily and cost-effective lanthanum doped Mg_0.5Cd_0.25Cu_0.25Fe_2-xLa_xO₄ (x = 0.0, 0.0125, 0.025, 0.0375 and 0.05) ferrites were synthesized by a co-precipitation route, a comprehensive characterisation of their structural, optical, electric, dielectric, molecular vibrational, and magnetic properties were carried out. X-ray diffraction analysis confirmed the formation of a cubic spinel structure. Variations in frequency bands were also observed with amplification in optical band gap energy (2.95 – 3.38 eV) due to La³⁺ ions insertion. The electric resistivity had opposite trends at low and high temperatures with increasing La³⁺ content. The Curie temperature, activation energy, and drift mobility were also determined to have values consistent with the semiconducting behavior of the soft ferrites. The saturation magnetization (M_S) has a maximum value 49.385 emu/g with remanent magnetization (M_r) was 34.928 emu/g and coercivity 661.4 Oe for La³⁺ concentration x = 0.05. The minimum dielectric loss was observed for La³⁺ concentration x = 0.025. Moreover, the resistivity (ρ) has a maximum value of 7.95 × 10⁴ Ω cm for La³⁺ concentration x = 0.025. The calculated frequency range of La³⁺ doped Mg–Cd–Cu ferrites was detected in the microwave range (3.36 – 10.80 GHz), suggesting the potential application of the materials in longitudinal recording media and microwave absorbance.     

Influence of rare-earth La3+ ion doping on microstructural,magnetic and dielectric properties of Mg0.5Ni0.5Fe2-xLaxO4 (0 ≤ x ≤ 0.1) ferrite nanoparticles

A series of La³⁺ ion doped magnesium nickel ferrites, Mg_0.5Ni_0.5Fe_2-xLa_xO₄ (0 ≤ x ≤ 0.1) having a cubic spinel structure were prepared by the co-precipitation method. Various characterization techniques, including X-ray diffractometer (XRD), high resolution transmission electron microscopy (HR-TEM), electron spin resonance (ESR) and vibrating sample magnetometer (VSM) were used to investigate structural and magnetic properties. The average crystallite size decreases and lattice parameter increases with La³⁺ ion doping and lie in the range of 12–7 nm and 8.347–8.361 Å respectively. Analysis of ESR spectra reveals that, g-value with La³⁺ ion addition decreases from 2.57 to 2.12. The saturation magnetization and the coercivity decrease with increasing rare-earth content. Magnetic-hysteresis (M − H) loop shifts from a ferromagnetic to a superparamagnetic nature with La³⁺ ion addition. The dielectric study was carried out in the frequency range of 1 KHz to 4000 KHz and temperature ranging 30 °C–350 °C using the impedance analyzer. The dielectric constant decreases with increasing frequency and the La³⁺ ion concentration. The dielectric loss of the sample increases with increasing temperature. The magnetic properties of the synthesized nanoparticles make them a potential material for stable ferrofluid application and the low tangent loss value makes these material a potential candidate for frequency-based applications.     

Tailoring the structural,magnetic and dielectric properties of Ni-Zn-CdFe2O4 spinel ferrites by the substitution of lanthanum ions

In this paper, we have tailored the structural, magnetic and dielectric properties of Ni_0.5Zn_0.3Cd_0.2Fe_2-yLa_yO₄ (y?=?0.0–0.21) nano-structured spinel ferrites by the substitution of La³⁺ ions. The investigated samples were synthesized by Sol-gel auto-combustion method and were characterized using XRD, SEM, VSM, FTIR and dielectric measurements. Single phase nanostructure formation of synthesized material was confirmed by XRD analysis. The effect of La³⁺ ions on crystallite size, grain size, lattice constant and bulk densities was calculated and it was found that lattice constant first increased upto concentration y?=?0.105 then decreased with further substitution of dopant ions. FTIR results for all synthesized samples demonstrated two absorption bands at υ₁ =?540.8?cm^?1 and υ₂ =?490.8?cm^?1 corresponds to tetrahedral and octahedral sites of spinel structure respectively. With the increase in La³⁺ ions concentration, saturation magnetization and remanence both found to be decreased down to lowest M_s value of 34.1?emu/g which is not yet reported in the literature according to best of our knowledge. Dielectric results showed that by decreasing frequency, both dielectric loss and dielectric constant decreases. AC conductivity has two regions, at low frequency region ac conductivity increases while at high frequency region, it decreases with increasing frequency. The measured results for all synthesized nano-ferrites suggested that synthesized nanoferrites are recommended for high frequency and microwave absorbing applications.     

Effect of substitution of La3+ on structural and electrical properties of Sr(Fe0.5Nb0.5)O3 ceramic

In this work, we have mainly reported the effect of lanthanum substitution on structural, dielectric, impedance and transport properties of strontium iron niobate (i.e., Sr_1-xLa_x(Fe_0.5Nb_0.5)_1-x/4O₃ (x = 0, 0.05, 0.1, 0.15, 0.2)). The materials were synthesized using standard ceramic technology. The preliminary structural analysis was done by using the room temperature X-ray diffraction data. The samples of higher concentrations (x = 0.15 and x = 0.20) show the development of an additional phase (i.e., LaNbO₄ and Sr₃La₄O₉). Studies of frequency and temperature dependence of dielectric parameters exhibit an anomaly and relaxor behavior in the compounds. The electrical impedance and modulus analysis of frequency and temperature-dependent data show the contributions of grains and grain boundaries in the resistive and capacitive properties of the compounds. The study of transport properties of AC conductivity has provided the conduction and relaxation mechanism. The substitution of La³⁺ has significantly changed the dielectric constant, tangent loss, and transport properties of the material.     

Effect of isovalent substitution of La3+ in Ca-doped LaNbO4 on the thermal and electrical properties

The effect of the equimolar substitution of lanthanum in Ca-doped LaNbO₄ on the functionality of (La_0.5Ln_0.5)_0.99Сa_0.01NbO_4–δ (where Ln?=?La, Nd and Sm) is investigated in the present work. Highly dense, single-phase and of microstructurally quality ceramic samples are synthesized, using a solid state reaction method. The relation between Ln³⁺ ionic radii with thermal and electrical properties is successfully revealed. It is found that the partial substitution with other lanthanides can be considered as a promising tool to suppress thermal expansion differences between low- and high-temperature modifications of lanthanum niobates; however, at the same time, the ionic conductivity decreases, which requires searching the trade-off for the optimal composition identification.     

Erbium substituted nickel–cobalt spinel ferrite nanoparticles: Tailoring the structural,magnetic and electrical parameters

In this article, we have reported an effective, rapid as well as economical Er³⁺ substituted Ni_0.4Co_0.6Fe₂O₄ ferrite nanoparticles synthesized via surfactant-assisted co-precipitation route. The synthesized nanoparticles were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), dielectric properties, current-voltage (I–V) measurements, and vibrating sample magnetometry (VSM). XRD and FTIR confirmed the face-centered (FCC) spinel structure of all compositions of the synthesized spinel ferrite nanoparticles. The deviations in the lattice constant granted with the variation in size of the guest (Er³⁺) and host (Fe³⁺) cations. These ferrites were also subjected for electrical, magnetic and dielectric investigations. I–V measurements showed that resistivity values decreased from 6.20 × 10⁷ Ω cm to 0.03 × 10⁷ Ω cm with the increased Er³⁺ contents. Saturation magnetization increased from 35.99 to 39.95 emu/g. This high value of saturation magnetization suggested the possible utilization of such ferrites for practical applications such as microwave and recording devices fabrication. Interestingly, the magnetic and dielectric properties of nickel-cobalt ferrite nanoparticles showed ample improvement upon Er³⁺ substitution. The results clearly indicate the potential of Er⁺³ substituted spinel ferrite particles in various advanced technological devices fabrication.     

Preparation and properties of sol–gel synthesized Mg-substituted Ni2Y hexagonal ferrites

A series of single phased Y-type hexagonal ferrites Sr₂Ni_2?xMg_xFe₁₂O₂₂ (x=0.0, 0.1, 0.2, 0.3, 0.4, 0.5) were synthesized by the sol–gel auto combustion method. The effects on structural, magnetic and electrical properties have been investigated by substituting Mg²⁺ at Ni²⁺ sites. The X-ray diffraction (XRD) patterns confirm single phase Y-type hexaferrite and various parameters such as lattice constants, cell volume, X-ray density, bulk density and porosity have been calculated from XRD data. The Fourier transform infrared (FTIR) spectra show the characteristics absorption ferrite peaks of the sintered sample. The microstructure was studied by scanning electron microscopy (SEM). All the ferrites show a hexagonal platelet-like shape which is a most suitable shape for microwave absorption. The dielectric constant followed the Maxwell–Wagner interfacial polarization and relaxation peaks were observed in the dielectric loss properties. The room temperature dc electrical resistivity and activation energy were found to decrease for samples x=0.1, 0.2 and increase for the rest of samples hence making these materials suitable for multilayer chip inductors (MLCIs). A soft magnetic behavior was revealed by M–H loops. Saturation magnetization (M_s), retentivity (M_r), coercivity (H_c) and magnetic moment (n_B) were found to decrease as the Mg²⁺ contents increased.     

Y3+ composition and particle size influenced magnetic and dielectric properties of nanocrystalline Ni0.5Cu0.5YxFe2-xO4 ferrites

The rare earth Yttrium (Y³⁺) doped Ni–Cu nanoferrites (NCY ferrites) with chemical formulation, Ni_0.5Cu_0.5Y_xFe_2-xO₄ (x = 0–0.125) were prepared successfully by the sol gel route. The X-ray diffraction (XRD) of NCY ferrites revealed that a single phase of cubic spinel is created within the synthesized ferrites. The crystallite sizes obtained by XRD pattern are in the range of 51–84 nm, in good agreement with those obtained by transmission electron microscopy (TEM) and field emission scanning electron microscopy (FSEM). The calculated lattice parameter of NCY ferrite unit cells initially decreases up to x = 0.1 and increase afterwards for x = 0.125. From FESEM and TEM micrographs, surface morphology and microstructure of NCY nanoferrites were studied. The energy dispersive X-ray spectroscopy (EDS) patterns have confirmed the stoichiometric presence of Ni, Cu, Y, O and Fe, those were used to prepare the samples. The variations in the magnetic properties with Y³⁺ compositions were investigated by obtaining the hysteresis loops of NCY ferrites. The magnetic hopping lengths L_A and L_B were calculated from XRD. The saturation magnetization, Bohr magneton number, coercivity and retentivity of the ferrites were influenced by the structural parameters like crystallite size and lattice strain. The frequency variation of dielectric constant and loss tangent exhibit space charge polarization as a phenomenon governing the dielectric behavior of the ferrites.     

High-performance inductive couplers based on novel Ce3+ and Co2+ ions co-doped Ni-Zn ferrites

High-performance inductive couplers require Ni-Zn ferrites of high saturation magnetization, Curie temperature, permeability and application frequency. However, for inductive couplers some of these properties run against each other in one ferrite. To balance these requirements, in this work, novel Ni-Zn ferrite ceramics co-doped by Ce³⁺ and Co²⁺ ions with chemical formula Ni_0.4Zn_0.5Co_0.1Ce_xFe_2-xO₄ (x = 0–0.06) were designed and fabricated by a molten salt method. For the acquired ferrites, both Ce³⁺ and Co²⁺ ions could come into the lattices. The initially doped Co²⁺ ions would cause a slightly decreased grain size and dramatically reduced the specimen densification, but the further added Ce³⁺ ions could effectively inhibit the density reduction, while the grain size continues to dwindle. The additional Ce³⁺ ions would generate a foreign CeO₂ phase in the acquired specimens. The sole doping of Co²⁺ ions would aggrandize the saturation magnetization of ferrites, but the introduction of Ce³⁺ ions would cause its decrease. However, with an appropriate doping level, the Ce³⁺ and Co²⁺ ions co-doped ferrites could preserve a relatively high saturation magnetization, while the Curie temperature and cut-off frequency of the ferrites are dramatically augmented, although the permeability would be somewhat reduced. The as-acquired ferrites were simulated to apply in inductive couplers, revealing that the devices manufactured by the Ni_0.4Zn_0.5Co_0.1Ce_xFe_2-xO₄ ferrites had significantly high maximum operating frequency, compared with that of the one manufactured by pure Ni_0.5Zn_0.5Fe₂O₄ ferrite.     

The influence of ZrO2 additive on sintering and microstructure of lithium and lithium-titanium-zinc ferrites

The effect of ZrO₂ addition (0–3?wt%) on sintering and microstructure of lithium and lithium-titanium-zinc ferrites was studied. The Vickers hardness and dc electrical resistivity were investigated and discussed in correlation with the structural properties. Ferrite powders with the chemical compositions of LiFe₅O₈ and Li_0.65Fe_1.6Ti_0.5Zn_0.2Mn_0.05O₄ were prepared by the conventional ceramic technique. The synthesized ferrites were doped with various amount of ZrO₂ and then were sintered at 1050?°C for 2?h. Dilatometric studies showed that the zirconia addition affects the densification process of ferrite ceramics so that the shrinkage rate of pressed ferrite powders during their heating decreased with an increase in ZrO₂ content. The bulk density of the sintered ferrites varied slightly as the concentration of the additive was increased from 0 to 2?wt%, while the density of ferrite doped with 3?wt% ZrO₂ significantly decreased. X-ray diffraction and scanning electron microscopy analyses showed that the lattice parameter of ferrites increases and their average grain size decreases as the additive content grows. It was established that small amounts of ZrO₂ additive (up to 2?wt%) improve significantly the hardness and the electrical resistivity of ferrites.     

Electrical conductivity of La1−xCaxFeO3−δ solid solutions

La_1−xCa_xFeO_3−δ solid solutions (x=0, 0.1, 0.2, 0.3, 0.4, 0.5 and 0.6) were investigated. The samples were prepared by the polymerizable complex route and characterized by X-ray diffraction and complex impedance spectroscopy techniques. Results reveal the formation of a single perovskite phase for the La_1−xCa_xFeO_3−δ (0≤x≤0.5) compositions. However, the La_0.4Ca_0.6FeO_3−δ sample is a mixture of many phases: perovskite, calcium ferrite and iron oxide. The unsubstituted lanthanum ferrite oxide, as well as the substituted samples, exhibits an orthorhombic symmetry. The direct current conductivity analyses reveal a typical negative temperature coefficient of the resistance behaviour for all the samples. The incorporation of calcium into the lanthanum ferrite lattice results in a significant improvement of the direct current conductivity. In fact, La_0.8Ca_0.2FeO_3−δ oxide shows the optimal conduction value. For all the studied compositions, a change in the activation energy is highlighted around 440 °C. This behaviour is attributed to the antiferromagnetic to paramagnetic transition of lanthanum ferrite. As for the alternating current conductivity, it obeys the Jonsher's power law. The correlated barrier hopping model is proposed to describe the transport mechanism in the studied matrix.     

Effect of Zn substitution on the structural and magnetic properties of nanocrystalline NiFe2O4 ferrites

Nanocrystalline Ni_1?xZn_xFe₂O₄ (where, x = 0.0, 0.2, 0.4, 0.6, 0.8 & 1) samples were synthesized through solution combustion technique using oxylyl de-hydrazide (ODH) as a fuel and the effect of dopant and its concentration on the structural and magnetic properties was investigated. As-prepared samples were characterized using different characterization techniques such as, XRD, SEM-EDS, TEM and Raman spectroscopy for their phase-purity, crystallinity, surface morphology and elemental composition; also magnetic properties were investigated through EPR, Mossbauer spectroscopy and vibrating sample magnetometer (VSM). Rietveld fitted XRD and Raman studies confirm the formation of cubic spinel structured ferrites and substitution of Zn ion at Ni site without formation of impurity phases. No other structural changes were observed and the structure remains in cubic phase with increase of Zn concentration. SEM and TEM micrographs reveal that the particles are agglomerated and the particles size were found in the nano range. Also good stoichiometric composition was observed in all the compositions of Zn substituted Ni ferrite samples. Magnetic measurements (VSM) reveal that pure Ni ferrites exhibits soft magnetic behaviour. Further the ferromagnetic behaviour suppressed with the substitution of diamagnetic Zn ion and with increase of its concentration in Ni ferrites, which was further evidenced in the Mossbauer spectroscopic results. At room temperature, electronic paramagnetic resonance spectra exhibits a broad resonance signal with Lande's g factor varies from 2.23 to 1.95 with increase in Zn content, which is attributed to spin exchange interactions between Fe³⁺, Ni²⁺ and Zn²⁺ ions also asymmetric EPR spectra was observed. The investigated results show that, Zn substitution has greater impact on the magnetic properties of Ni ferrites due to the diamagnetic nature of Zn, which inturn alters the cationic distribution and the exchange interactions between Ni-Fe and Fe-Fe.     

Optimization of structural,electrical, and magnetic properties of ytterbium substituted W-type hexaferrite for multi-layer chip inductors

The rare earth (Yb³⁺) substituted W-type hexagonal ferrites with composition CaPb_2-xYb_xFe₁₆O₂₇ (x = 0.0, 0.5, 1.0, 1.5, 2.0) were synthesized by a facile and cost-effective sol-gel auto combustion method with post heat treatment. The synthesized hexagonal ferrites were characterized by a variety of analytical techniques, and an impedance analyzer was used to investigate the effects of Ytterbium on structural, magnetic, spectral and dielectric properties. The relationship between their impedance, structure and dielectric properties was investigated. The X-ray diffraction patterns verify the presence of single-phase W-type hexagonal ferrites. Physical properties such as D_bulk (bulk density), D_xrd (X-ray density), and P (porosity) of the CaPb_2-xYb_xFe₁₆O₂₇ W-type hexagonal ferrites were calculated. The bulk density of all the samples was decreased, and X-ray intensity was increased with the Ytterbium replacement in the W-type hexaferrite. By adding Yb³⁺ ions, the lattice parameters, cell volume and X-ray density were reduced due to the substitution of ytterbium with smaller ionic radii compared to the lead ion with large ionic radii. The AC-conductivity was increased from (1.523 × 10^?5 to 6.699 × 10^?5) Ωcm^?1. The dielectric constant and tangent loss was found to decrease substantially. The magnetic properties were found to enhance by the substitution of Yb³⁺. The low coercivity value of Yb³⁺ substituted W-type hexagonal ferrites are suitable for magnetic recording media operated at a high-frequency regime. The enhancement of electrical, dielectric and magnetic characteristics suggests these materials as promising for multi-layer chip inductors (MLCIs) circuit applications.     

The influence of Nd substitution in Ni–Zn ferrites for the improved microwave absorption properties

Nanocrystalline Ni–Zn ferrites with different neodymium contents (Ni_0.5Zn_0.5Nd_xFe_2-xO₄) were synthesized by sol-gel route combined with self-propagating combustion (SPC) method. The presence of surface functional groups, crystal structure and morphology of the samples were studied by FT-IR, XRD and SEM. The results show that the prepared samples are composed of spinel phase under the condition of low neodymium content, like the pure Ni–Zn ferrite. While neodymium oxide appears after the content of Nd³⁺ exceeds a certain limit (x > 0.04) and there exist two phases in the ferrite. The results of vibrating sample magnetometer (VSM) and vector network analyzer (VNA) show that adjusting the content of Nd is significant in improving the dielectric properties and microwave absorption capacity of the materials, specifically at low frequencies. When x < 0.04, the enhancement of dielectric loss ability of spinel ferrites by doping Nd³⁺ is the dominant factor affecting microwave absorption ability of samples. The secondary phase Nd₂O₃ hardly appears under this condition, thus the weakening effect of Nd³⁺ addition on magnetic loss ability is not obvious. When x = 0.04, the optimal absorption peak of the material reaches −20.8 dB at 4.4 GHz with a thickness of 8.5 mm and the effective absorption bandwidth (R_L < −10 dB) was 3.2 GHz. On the contrary, when x > 0.04, the magnetic loss ability decreases rapidly (e.g., Ms decreases from 82.47 emu/g to 59.77 emu/g). Meanwhile, the dielectric loss increases slowly and the microwave absorption capacity decreases.     

Comparative behaviour of various oxides in the electrochemical reactions of oxygen evolution and reduction in alkaline medium

The electrochemical behaviour of ferrites having the composition La_1-xSr_xFeO_3-y in the oxygen reaction has been studied. The catalytic activity of these compounds was compared with that of copper manganite Cu_1.4Mn_1.6O₄ and that of lanthanum strontium cobaltite La_0.5Sr_0.5CoO₃ as well as with that of surface oxides developed on nickel and its alloys. It was shown that in the evolution of oxygen, nickel and its alloys (NiBe-NiCo₂) are the least polarizable materials.In the reduction of oxygen, it was shown that all the mixed oxides undergo reduction at the same time as the reduction of oxygen. For the ferrites, the catalytic activity for oxygen reduction is related to the fraction of vacancies existing in the compound.     

Effect of magnesium ferrite doping with lanthanide ions on dark-, visible- and UV-driven methylene blue degradation on heterogeneous Fenton-like catalysts

The catalytic behavior of magnesium ferrites doped with lanthanide ions (La³⁺, Ce³⁺, Sm³⁺, Gd³⁺, and Dy³⁺) on Methylene Blue (MB) degradation using Fenton process was studied. A slow increase in cubic Fd3m crystalline structure parameters and increase in crystallite size of doped samples magnesium ferrites were observed. A dramatic decrease in catalytic activity of catalysts obtained at 600 °C as compared to catalysts obtained at 300 °C was explicitly observed and this was grossly attributed to the elimination of surface hydroxyl groups as ascertained by FT-IR analysis. The initial magnesium ferrite demonstrated the highest catalytic activity under dark- (kˈ 0.0555 min⁻¹) and visible-light (kˈ 0.1029 min⁻¹) conditions. Catalytic efficiency of the lanthanides doped catalysts under UV-irradiation in accordance with the maximum appearance rate constant kˈ decreased in the following order Ce³⁺ > Dy³⁺ > La³⁺ ≈ MgFe₂O₄ > Sm³⁺ > Gd³⁺. The most active ferrites provided up to 99% of MB degradation in 60 and 20 min for visible- and UV-driven Fenton processes. Findings obtained from this study were observed to be competitive with other heterogeneous Fenton catalysts.     

Study of strontium ferrites substituted by lanthanum on the structural and magnetic properties

M-type strontium ferrites, Sr_0.8La_0.2Fe₁₂O₁₉ have been synthesized by conventional ceramic process. The effects of lanthanum addition and sintering temperature on microstructures and magnetic properties of SrFe₁₂O₁₉ and Sr_0.8La_0.2Fe₁₂O₁₉ samples were investigated. Microstructural analysis of the SrFe₁₂O₁₉ and Sr_0.8La_0.2Fe₁₂O₁₉ specimens, sintered at different temperatures revealed that average grain sizes of SrFe₁₂O₁₉ ferrites were larger than that of Sr_0.8La_0.2Fe₁₂O₁₉ ferrite and increased with increasing sintering temperature. The X-ray diffraction (XRD) results confirmed the strontium hexagonal ferrite phase of SrFe₁₂O₁₉ and Sr_0.8La_0.2Fe₁₂O₁₉ compounds. A maximum coercivity value of 4850 Oe and maximum saturation magnetization value of 102 emu/g were obtained for the SrFe₁₂O₁₉ ferrite sintered at 1150 °C and for the SrFe₁₂O₁₉ and Sr_0.8La_0.2Fe₁₂O₁₉ ferrites sintered at 1300 °C, respectively. The remanence (Mr) of Sr_0.8La_0.2Fe₁₂O₁₉ sample sintered at 1200 °C possesses the maximum value of 60 emu/g.     

Morphological Study of Lanthanum-Doped Nano Spinel Ferrite via Normal Micelles Method

Lanthanum-doped nano spinel ferrite compounds were synthesized via normal micelles method, characterized by means of TGA/DSC curves to know calcination temperature and stoichiometry of elements confirmed by EDAX. X-ray diffraction shows well defined cubic spinel structure with secondary phase of ortho ferrite LaFeO₃. Lattice parameter exhibited gradual increases with increasing in La³⁺ ion concentrations due to the larger ionic radii of La³⁺ ions replace Fe³⁺ ions. FT-IR spectra recorded in the range of 4000–400 cm^?1 to detect vibrational bands. Surface morphology analyzed by SEM, The particle size analyzed by Dynamic Light Scattering, full width half maxima of 311 peak obtained from XRD and TEM analysis, reveals that fine particle nature with little agglomeration and average particle size determined in the range of few nano meters.