Sol-gel Auto-combustion Technique Research Articles

Synthesis and dielectric evaluations of Er doped Mg-Mn-Cr ferrites

In this study solgel auto-combustion technique was successfully implanted to synthesized Er-doped soft ferrites with the chemical formula Mg₀.₂Mn₀.₈Cr0.03Fe1.97-xErₓO₄ (MMCE ferrites). The required stoichiometric amounts of the chemicals, along with citric acid as a polymerization mediator, were calculated and used. The electrical and structural properties of Er-substituted Mg-Mn-Cr ferrite were characterized using various techniques. X-ray diffraction analysis confirmed that all samples exhibited a single-phase spinel structure with an Fd-3m space group, with X-ray density, lattice constant, and crystallite size varying based on Er concentration. Fourier Transform Infrared (FTIR) spectroscopy revealed stretching and cation vibrations of other groups in the wave number range of 250 cm⁻¹ to 1500 cm⁻¹. Scanning electron microscope (SEM) images showed that the particles were agglomerated, forming larger, closely packed clusters. DC resistivity measurements indicated that the resistivity of the samples increased significantly, reaching 10¹⁰ Ω·m at the highest La concentration. Currently, rare-earth-substituted ferrite nanoparticles are widely used in high-frequency microwave devices due to their exceptional electrical properties, making ferrites highly valuable.

Study of Pr doped nanocrystalline LiCoO2 cathode material for spintronic and energy storage applications: A theoretical and experimental analysis

In this study, Pr3+ substituted LiCoO2 lithium-rich cathode materials were prepared using the sol-gel auto-combustion technique to enhance cycling performance. LiCo1-xPrxO2 samples having Pr concentrations x = 0.00–0.10 were synthesized. X-ray diffraction (XRD) showed a rhombohedral structure with space group R-3m, further verified by the Rietveld refinement. Field emission scanning electron microscopy (FESEM) revealed the presence of distinct and well-defined submicron-scale grains. FTIR spectroscopy confirmed Co–O stretching bonds within 590–560 cm−1 and revealed peaks at around 560–590, 830–860, and 1320-1480 cm−1, which could be attributed to the electrochemical performance of Pr-doped species. Moreover, EDX spectroscopy confirmed the typical elemental peaks of only Co, Pr, and O, confirming the required phase presence. The cyclic voltammetry showed improved reversibility and stability due to Pr doping. The first-principles computations were performed using the lattice constant extracted from XRD measurements. The pure LiCoO2 with a semiconducting nature became half-metallic due to Pr doping (LiCo0.84Pr0.16O2). The magnetic properties indicate that LiCoO2 and LiCo0.84Pr0.16O2 exhibit positive magnetic order, which shows that these are suitable candidates for spintronic applications. The pure LiCoO2 revealed intercalation voltages of 4.10–2.73V and a theoretical capacity 40–203 mAh/g. Meanwhile, for LiCo0.84Pr0.16O2, the intercalation voltages and theoretical capacity improved to 4.42–2.85 V and 42 to 211 mAh/g, respectively. The combined experimental and theoretical study suggests that Pr-doped LiCoO2 is suitable for spintronic applications and energy applications such as composite cathodes.

Insights into the structure and magnetic characteristics of Ho substituted Ca-Cu based Ca0.5Cu0.5Fe12-xHoxO19 hexaferrites nanoparticles

This work demonstrates a systematic attempt to explore the structure and magnetic properties of Ho3+ substituted Ca-Cu hexaferrite nanocrystals. Ca0.5Cu0.5Fe12-xHoxO19 (x = 0.00, 0.05, 0.10, 0.15, 0.20) M−type hexaferrites are synthesized via sol–gel auto combustion technique. XRD spectra is used to evaluate the phase, and substituent-induced modifications of crystallites. The lattice parameters ‘a’ and ‘c’ lies in the range (5.887–5.898) Å and (23.184–23.195) Å. The size of crystallites ranges from 55.73 to 59.41 nm. The specimen’s morphology indicates the consistent distribution of grains with Ho substitution. The coercivity of samples increased slightly from 2.85 to 3.15 kOe, as determined by vibrating sample magnetometer (VSM) loops, whereas saturation magnetization increased from 26.41 to 30.13 emu/g. The discussion also encompasses variations in anisotropy field (Ha), anisotropy parameter (B), magneto-crystalline anisotropic constant (K), and magnetic moment per formula unit mB(µB) and their effect on main magnetic parameters.

Physical properties of ultrasonic assisted MWCNT/Ni0.5Co0.5Pr0.2Fe1.8O4 nanocomposites for future energy storage applications

The demand for materials with superior magnetic and dielectric properties is critical for the advancement of high-performance electronic and magnetic devices. In response to this need, Ni0.5Co0.5Pr0.2Fe1.8O4 (NiCoPrFeO) nanoparticles were synthesized using the sol–gel auto-combustion technique, known for its simplicity and versatility. To enhance the functional properties of these nanoparticles, multiwalled carbon nanotubes (MWCNTs) were incorporated, recognized for their high electrical conductivity and low density, to create a novel nanocomposite. The structural and physical properties of the prepared NiCoPrFeO/MWCNTs nanocomposites were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), vibrating sample magnetometry (VSM), and Impedance Analysis. XRD confirmed the successful formation of the nanocomposite NiCoPrFeO/MWCNTs. TEM provided detailed insights into particle size to be around 18.553 and the interactions between the nanoparticles and MWCNTs. FTIR spectra indicated the presence of absorption bands ‘ν1′ and ‘ν2′ to be around 545 and 415 cm−1 which is characteristic of the cubic spinel structure. The addition of MWCNTs significantly improved the magnetic properties of the nanocomposite, with higher MWCNT concentrations leading to stronger magnetization, as shown by VSM analysis the values of Mr, Ms and Hc were found between 1.41 to 4.79 emu/g, 16.67 to 24.35 emu/g and 204.29 to 569.77 Oe, respectively. The dielectric properties, including dielectric constant, dielectric loss, loss tangent, and AC conductivity, exhibited notable improvements with increasing MWCNT content across varying frequencies. These results suggest that NiCoPrFeO/MWCNTs nanocomposites could be a promising solution for improving materials used in electronic and magnetic devices, leading to more efficient and advanced technologies.

Annealing-induced changes in Sol-Gel synthesized nano-CoFe2O4: A study of structure, morphology and magnetism

Magnetic nano-sized CoFe₂O₄ spinel ferrites were synthesized using the sol-gel auto-combustion technique, and the impact of annealing temperature on their structural and magnetic properties was systematically studied. Samples were annealed at 500 °C, 700 °C, and 900 °C for 5 hours. XRD analysis confirmed crystallization in the Fd3m space group, with average crystallite sizes ranging from 30 to 34 nm. Structural parameters such as ionic radii, bond lengths, and cation distribution were also calculated, revealing partial inversion with an inversion factor of 0.68. FE-SEM analysis showed uniform morphology and increasing grain size with higher annealing temperatures. EDS confirmed stoichiometric Co and Fe ion content, while FTIR indicated strong metal-oxide bonds characteristic of CoFe₂O₄. Magnetic measurements demonstrated that higher annealing temperatures enhanced saturation magnetization and magnetocrystalline anisotropy while reducing coercivity, highlighting the significant influence of annealing temperature on CoFe₂O₄ nanoparticles' performance.

Impact of Al3+ substitution on structural, Raman, transport electromagnetic properties of LiFe2O4 nanoparticles

Nanocrystalline Li0.5AlxFe2.5-xO4(x = 0.0 to 0.8 in steps, x = 0.2) compounds were prepared using the sol-gel auto-combustion technique. X-ray diffraction (XRD) analysis confirmed the single-phase cubic spinel structure, which showed that the lattice constant changed significantly, especially in the x = 0.6 sample, where it decreased clearly. The crystallite size decreased with increasing Aluminium content, reaching a small value of about 5 nm for the composition x = 0.8 sample. Raman peaks of pure LiFe2O4 were determined in both phases (alpha and beta), while smaller peaks at 198 and 236 cm−1 that related to the alpha phase were distinguished. All peaks diminished in intensity after Al3+ ions were doped to LiFe2O4 except for the peak at 700, where it became predominantly. The bandgap of the samples was deduced and analyzed from Tauc's plot according to UV–Vis spectra. The change in the electronic structure of the Li-Al ferrites, at which the size of the ferrite becomes close to the de Broglie wavelength, results in a band gap for the Al replaced by LiFe2O4 with different electronic configurations. The variation of the fundamental part of the dielectric constant (ε′), loss tangent (tan δ), and AC conductivity with frequency has been discussed with composition. The increase in Al3+ ion content affected the coercive force, as it decreased, while the saturation magnetism increased when adding Aluminium (x = 0.2) and then began to decline gradually.

One-Pot Synthesis and Characterization of Magnetic α-Fe2O3/CuO/CuFe2O4 Nanocomposite for Multifunctional Therapeutic Applications.

This study demonstrates a novel nanostructured drug delivery system utilizing α-Fe2O3/CuO/CuFe2O4 ternary nanocomposite for effective drug transport in sick tissues. Centella Asiatica plant extract was employed to synthesize the Fe2O3/CuO/CuFe2O4 nanocomposite via sol-gel auto combustion technique. The structural and morphological characteristics of the nanocomposite were investigated by XRD, FT-IR, SEM, EDX, and VSM for magnetic properties. The XRD analysis demonstrates the successful synthesis of Fe2O3/CuO/CuFe2O4 nanocomposite with an average crystallite size of 18.393 nm. The antioxidant and antifungal capabilities of this nanocomposite were assessed for its biological activity. A notable inhibitory zone was observed when tested against the Alternaria spp. and Bipolaris sorokiniana fungi. An IC50 value of 109.88 μg/ml was found in the DPPH test, indicating that the nanocomposite exhibited remarkable antioxidant characteristics. Subsequently, metronidazole was encapsulated with a success rate of 55.53 % at pH 1.2, while at pH 7.4 it gained 57.83 %. The drug release of nanocomposite at pH 1.2 after 330 min was 43.41 % and at pH 7.4 after 300 min it was 52.3 %. The results indicate its potential as an excellent candidate for drug delivery. Furthermore, pH was found to be an effective catalyst in the drug loading and release processes.

Synthesis and application of strontium-doped zinc ferrite nanomaterial in humidity sensing

Humidity sensors, being an important component of the Internet of Things (IoT) and artificial intelligence (AI), are currently used in noncontact sensing, electronic skin, respiratory analysis, etc. In this study, the sol-gel auto-combustion technique was used to prepare strontium-doped zinc ferrite (ZnFe2O4) nanomaterials. The synthesized materials have been characterized using Fourier transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), energy dispersive X-ray (EDX), and field emission scanning electron microscopy (FESEM) techniques. The doping of strontium increases the lattice parameter and reduces the crystallite size. The synthesized nanoparticles were used to design a humidity sensor for the first time, and several humidity-sensing properties were investigated. The designed humidity sensor has a response and recovery times of 19 s and 81 s, respectively. It has low humidity hysteresis, excellent repeatability, and a minute ageing effect.A comparison of the present study with previous reports suggests that the developed humidity sensor is promising in terms of recovery, response times, and material.

Designing Tb-doped Mn-Ni-Cu ferrite meta-absorbers for a broad frequency range: Magnetodielectric, physical, reflection loss, and absorptivity characteristics

Developing meta-absorbers with exceptional EM wave absorption, shielding capacity, and superior dissipation performance remains worthwhile in the gigahertz (GHz) range. Electromagnetic pollution has a detrimental impact on the health of living organisms due to the emergence of high-frequency waves from communication devices. The challenges were addressed by preparing, designing, and simulating ferrite-based meta-absorbers. The nanoferrites of Tb-doped Mn-Ni-Cu (Mn0.2Ni0.3Cu0.5TbxFe2-xO4) with different levels of Tb (x = 0.00, 0.025, 0.05, 0.075) were prepared utilizing the sol-gel auto combustion technique. The phase, structural, elastic, and magnetic features of the Tb-doped Mn-Ni-Cu ferrites were examined using XRD, FESEM, FTIR, and VSM techniques, respectively. The MAUD software was utilized to obtain refinement and precise structural characteristics. The force constant, phase, and elastic properties were also assessed. The magnetization and coercivity exhibited a reduction. An assessment was conducted on the performance of field switching and high-frequency response. At high frequencies, the dielectric characteristics, such as complex permeability and permittivity, exhibit greater values, while losses diminish. At a frequency of 4.6 GHz, a reflection loss (RL) of −54.21 dB was measured for x = 0.05, whereas a reflection loss of −54.03 dB was measured for x = 0.075. The meta-absorbers of Tb-doped Mn-Ni-Cu ferrites were designed and simulated. The absorptivity of the Tb-doped Mn-Ni-Cu ferrite substrate material is illustrated. The meta-absorber exhibited three distinct absorption peaks at frequencies of 1.5, 2.5, and 4.5–6 GHz, respectively. The absorptivity of the material likewise rises with an increase in the incidence angle; the material's absorptivity also increases. The TM mode exhibited the highest values at an angle of 60 degrees, while the TE mode displayed the highest values at an angle of 0 degrees. Tb-doped Mn-Ni-Cu ferrites are effective for electromagnetic interference (EMI), multilayer ceramic integrated circuits (MLCIs), shielding, and absorbing high-frequency signals in 5 G applications.

Tailoring the Surface of Sintered Magnesia–Chromia Catalyst with a Sol–Gel Auto-Combustion Technique

Tailoring the Surface of Sintered Magnesia–Chromia Catalyst with a Sol–Gel Auto-Combustion Technique

Tweaking the structural, micro–structural, optical and dielectric properties of anatase titanium dioxide via doping of nitrogen ions

The pure nanostructured anatase titanium dioxide (TiO2) and subsequent nitrogen–doped derivatives (TiO2–xNx; where, x = 0.005, 0.01, 0.05) were synthesized by sol–gel auto–combustion technique. XRD analysis confirms the formation of pure anatase phase of TiO2 up to doping of 1 mol% (x = 0.01) of nitrogen having tetragonal structure with space group of I41/amd whereas an additional monoclinic phase of TiO2–B was observed at 5 mol% of nitrogen doping in TiO2. This sample has smallest crystallite size of ∼4.7 ± 0.2 nm corresponding to TiO2–B phase and ∼12.0 ± 0.1 nm corresponding to anatase phase. XRD also reveals that the crystallite size of all other samples having pure anatase phase ranges between ∼8.7 ± 0.1 nm & 13.9 ± 0.1 nm. The crystalline phase revealed from XRD of all samples was further supported by the Raman analysis. The direct optical band gap of pure TiO2 (∼3.4 eV) was reduced non–monotonically after nitrogen doping in the ranges from ∼2.8 eV (TiO1.95N0.05) to ∼2.0 eV (TiO1.99N0.01). FTIR spectra confirm the metal oxide bond formation, surface adsorption of water molecules and presence of residual hydroxyl group in all crystalline samples. HRTEM analysis validates the coexistence of secondary phase of TiO2–B along with anatase phase of TiO2 in studied highest doped sample (TiO1.95N0.05) including its broader particle size distribution as compared to pure TiO2. The electrical studies reveal that the highest values of dielectric constant and ac conductivity can be realized for pure TiO2 and at 1 mol% (x = 0.01) of nitrogen doping, among all the studied nitrogen doped samples.

Exploring the structural, optical, dielectric and magnetic properties of rare earth samarium doped Ca-Mg based Ca0.5Mg0.5Fe12−xSmxO19 ferrite nanoparticles

The emergence of M-type hexaferrite presents an encouraging alternative to rare earth magnets, due to its economic feasibility and outstanding magnetic properties. This makes it a viable option for applications in the electric automotive and magnetic industry applications. In this study, we utilized a sol–gel auto-combustion technique to synthesize a series of samarium (Sm) doped calcium-magnesium (Ca-Mg) hexaferrite samples having chemical formula Ca0.5Mg0.5Fe12−xSmxO19 (x = 0.00, 0.05, 0.10, 0.15, and 0.20). The XRD analysis confirmed the crystal structure of the synthesized materials, revealing a consistent magneto-plumbite phase across all samples. Scanning electron microscopy (SEM) investigations further confirmed the homogeneous distribution and agglomeration of nanostructures. FTIR analysis identified the presence of two primary absorption bands in Ca-Mg hexaferrites with both bands exhibiting a shift towards lower frequency ranges with increasing doping levels. The dielectric loss (ε″) and dielectric constant (ε′) were higher at lower frequencies but decreased as the frequency increased. Additionally, higher concentrations of samarium resulted in further reductions in both dielectric loss (ε″) and dielectric constant (ε′). Notably, saturation magnetization (Ms) and remanence (Mr) values demonstrated an increasing trend with higher degrees of Sm+3 substitution, while coercivity (Hc) values exhibited relative stability. Our findings indicate that these materials possess promising magnetic parameters falling within the ranges of 31.52–37.77 emu·g−1 for Ms, 18.16–21.53 emu·g−1 for Mr, and 2.088–2.243 kOe for Hc, suggesting their potential utility across diverse applications including permanent magnets used in electric vehicle motors, storage devices, microwave components, and electromagnetic radiation absorbers.

Investigation of structural, optical, and magnetic properties of NiFe2O4 for efficient photocatalytic degradation of organic pollutants through photo fenton reactions

Nowadays, water pollution generated from textile effluents is one of the major problems for the human race and ecology. Hence, development of sustainable strategies to lower the water pollution level has become a burning need. In this regard, the present study focuses on the preparation of nano catalyst NiFe2O4 to catalyze the chemical reactions on industrial organic dyes for their fast cleansing from water. By sol-gel auto-combustion technique, NiFe2O4 nanoparticles were synthesized and exposed to thermal process at temperatures of 400, 600, and 800 °C. Highly crystalline phase with spinel cubic structured NiFe2O4 was formed with a crystal size of 18.71 nm, which was confirmed by XRD analysis. The FTIR spectra showed two fundamental absorption bands in the range 597.80–412.59 cm−1, which are the characteristics of tetrahedral M − O and octahedral M − O bond in NiFe2O4. The surface morphology of calcined NiFe2O4 was investigated by scanning electron microscope (SEM). The nanoparticle size analyzer exhibited that the synthesized NiFe2O4 nanoparticles had an average particle size of ∼ 291.3 nm. Three stage decomposition patterns were observed for NiFe2O4, which was analyzed by a temperature programmed STA. Zeta potential analyzer showed that the synthesized sample S1 and S2 were stable in the dispersion medium. Also, NiFe2O4 exhibited optical band gap energies for direct band transitions within the visible spectrum measured to be 1.43–1.45 eV, rendering them effective as photocatalysts under sunlight. The samples showed magnetic measurements by VSM with saturation magnetization, coercivity, remnant magnetization value of 66.81 emu/g, 4.13 Oe and 12.94 emu/g, respectively. The synthesized photocatalyst, NiFe2O4, at 400 °C, significantly degraded three toxic organic pollutants—Methylene blue, Rhodamine B, and Congo Red—under visible light through ‘Photo-Fenton’ reaction mechanisms. Among the three dyes, Methylene Blue exhibited the highest degradation percentage with a rate constant of 0.0149 min−1 and followed pseudo-first-order kinetic model.

Cr-doped Li-based [formula omitted]-(Beta) type hexaferrites: XRD, FTIR, XPS and dielectric evaluations for high-frequency applications

The rapid growth of electronic technology and communications have led to increase demand for high performance microwave absorbing materials. Ferrites are frequently used to absorb microwaves and protect against electromagnetic contamination. In the present study, β-type hexaferrite samples with different chemical compositions of LiFe11-xCrxO17 (x = 0.0, 0.1, 0.3, and 0.5) have been manufactured through the sol-gel auto-combustion technique. The effect of substituting Cr3+ on its structural, electrical and dielectric characteristics was examined. The XRD evaluation helped to develop a single-phase structure for all samples. The substitution of Cr3+ has changed the structural characteristics. FTIR analysis was used to investigate the vibrational properties of Cr-doped β-type hexaferrite. Two absorption bands in the infrared spectroscopy were used to indicate the tetrahedral and octahedral sites. XPS results revealed the incorporation of every metal ion related to their particular electronic states. The dielectric studies were determined in terms of frequency (1–6 GHz) and every sample behavior was described using the Maxwel-Wagner and Koop theories. Impedance analysis was utilized to study the effects of relaxation time and grain boundaries on the electrical features of the produced nanomaterials. Impedance Cole-Cole plots prove that all samples exhibit non-Debye-type multiple relaxation processes. It was observed that among all the synthesized samples, LiFe10.9Cr0.1O17 has a minimum reflection loss of −37.80 dB at 1.22 GHz. Cr-doped β-type hexaferrite results suggested using and designing hexaferrite-based nanocomposite for high-frequency absorbers in the microwave range.

Structural, dielectric and Magnetic properties of Samarium doped (Ni–Zn) based Spinel Ferrite (Ni0.5Zn0.5SmxFe2-xO4) nanomaterials

Samarium doped Ni-Zn ferrites (Ni0.5Zn0.5SmxFe2-xO4) were synthesized using sol-gel auto-combustion technique with Sm3+ doping concentrations varying as x = 0.00, 0.05, 0.10, 0.15, and 0.20. The prepared nanomaterials were examined using X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), complex impedance spectroscopy (CIS) and vibrating sample magnetometer (VSM). The XRD examination verified the pure FCC spinel phase of all samples with no impurity peak. The FTIR analysis for spinel molecules formation identified two frequency bands at the octa and tetrahedral sites. The TEM analysis confirmed the shape, size and distribution of prepared nanoparticles. The different dielectric properties were analyzed with a frequency range of 1 MHz–3 GHz and the impact of doping was also studied simultaneously. Magnetic nature of prepared materials was investigated at room using the VSM. It is found that the prepared nanomaterials are suitable for high energy storage as well as magnetic applications.

Physical properties of La3+ ion doped Ni[sbnd]Zn based spinel ferrite nanomaterials for technological applications

Spinel ferrite nanoparticles are extensively utilized in various everyday applications due to their exceptional capabilities. They are highly effective and efficient for various applications such as energy storage devices, microwave, electrode design, fuel cells, and recording media. Based on these applications, five samples of lanthanum doped nickel‑zinc spinel ferrite Ni0.5Zn0.5LaxFe2-xO4 nanoparticles were synthesized using the sol-gel auto-combustion technique. The lanthanum concentrations varied as x = 0.00, 0.05, 0.10, 0.15 and 0.20. X-ray diffraction (XRD) analysis revealed the formation of single phase cubic spinel structure of the prepared samples. The crystallite size was determined using the Scherrer formula and the values lies in the range of 9.22 to 20.09 nm. The chemical composition of the prepared samples was confirmed using Fourier transform infrared spectroscopy (FTIR) analysis. Transmission electron microscopy (TEM) confirmed the agglomeration and spherical shape morphology of the nanoparticles with an average particle size of 40 nm. Magnetic properties along with La3+ ion concentrations were investigated using the vibrating sample magnetometer (VSM). The dielectric properties of the prepared samples were carried out using impedance analyzer with an applied frequency ranging from 1 MHz to 3 GHz. Furthermore, the polarization mechanism in the applied frequency range was discussed with relaxation behavior at high frequency. The impact of La3+ concentrations on different parameters such as dielectric constant, impedance, electric modulus, tangent loss, and Ac conductivity were also investigated. The investigation of dielectric parameters. The relaxation mechanism at high frequency provided a significant impact of such type of materials to store energy due lake of hopping between the tetra and octahedral sites by addition of La3+ doping. The prepared samples exhibit excellent magnetic as well dielectric properties which makes suitable for microwave devices and soft magnetic applications.

Synthesis and characterization of cerium doped NiZn nano ferrites as substrate material for multi band MIMO antenna.

In addressing issues related to electromagnetic interference, the demand for ferrite materials with exceptional magnetic and dielectric properties has escalated recently. In this research, sol-gel auto combustion technique prepared Nickel zinc ferrites substituted with cerium, denoted as Ni0.5Zn0.5Ce0.02Fe1.98O4.X-ray diffraction (XRD), Vibrating Sample Magnetometer (VSM), and Field Emissions Scanning Electron Microscope (FESEM) were used to investigate the structure, magnetic properties, and morphology of Cerium doped NiZn Nano ferrites, respectively. The magnetic and dielectric properties of the sample was examined within a frequency range of 2.5-5.5 GHz. Sample exhibits low permittivity (2.2), high permeability (1.4), low dielectric (0.35) and magnetic loss tangent (-0.5) and highest saturation magnetization measuring 30.28 emu/g. A Novel Double-band, 4x4 MIMO window grill-modeled antennas operating on 3.5 GHz and 4.8 GHz frequency bands for 5G smartphones is designed using the CST microwave studio suite. The performance of window grilled 4x4 MIMO antenna model with Cerium doped NiZn nano ferrites as substrate, is investigated and found the return loss of -35 and -32 dB, with the bandwidth of 200MHz, gain (1.89 & 4.38dBi), envelope correlation coefficient (0.00185), channel capacity loss (0.2bps/Hz), and interterminal isolation of (22& 19dB).The results show that the antenna size is reduced with improved bandwidth, higher isolation and better diversity gain performance using Cerium doped NiZn nano ferrite substrate compared to conventional dielectric substrates.

Enhanced room temperature ferromagnetism and versatile optical properties in MgFe2O4 spinel ferrite prepared under different calcination temperatures

This study employs the sol-gel auto combustion technique fueled by diethanolamine (DEA) to synthesize nanocrystalline magnesium ferrite (MgFe2O4) powders. During the study, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–visible diffuse reflectance spectroscopy (UV-DRS), photoluminescence spectroscopy (PL), and vibrating sample magnetometry (VSM) were then used in order to determine how differing calcination temperatures influence the structure, chemical bonding, surface texture, morphology, optical, fluorescence, and magnetic properties of the resulting MgFe2O4 powders. The findings from the XRD and FT-IR analysis indicate that a single-phase spinel structure is formed in each of the MgFe2O4 samples. According to UV-DRS analysis, optimal calcination improved sample reflection levels in comparison to the visible and infrared spectral findings for the as-synthesized sample. The calcined samples exhibited bandgap energy (Eg) ranging from 2.11 eV to 2.14 eV, which was greater than the 2.02 eV of the as-synthesized sample. Examination of the PL spectra in the range of 380–700 nm revealed various light emission bands for the samples, which increased significantly in intensity at higher calcination temperatures. Furthermore, higher calcination temperatures also increased the magnetization of the MgFe2O4 spinel powders, while coercivity dropped significantly.

Sr-doped CuFe2O4 nanoparticles: Exploring structural, magnetic, and blood compatibility characteristics

The aim of this study is to investigate the structural, magnetic, and blood compatibility properties of Sr2+ substituted for Cu2+ in Cu1−xSrxFe2O4 (x = 0.0 to 1 with a 0.25 increment) nanoparticles synthesized via the sol-gel auto-combustion technique. Regardless of the substitution rate, the sol-gel auto-combustion method consistently yields powders with sizes ranging from 20 to 40 nm. The specific surface area of the produced powders is determined as 12 m2/g. X-ray diffraction analysis reveals that CuFe2O4 exhibits a singular phase; however, as the Sr2+ ion substitution increases, the emergence of various secondary phases becomes apparent, with their proportions increasing with the substitution rate. The magnetic characteristics of the synthesized powders exhibit variations in magnetization, correlating with the distribution of cations in the sublattice points. Coercivities are influenced by both anisotropy and secondary phases. Saturation magnetization decreases from 31.3 (CuFe2O4) to 7.6 (SrFe2O4) emu/g with Sr replacement. The lowest observed coercivity is 429.5 Oe in powders prepared with CuFe2O4 composition, while the highest is measured at 583.8 Oe in nanopowders prepared with Cu0.5Sr0.5Fe2O4 composition. Moreover, blood compatibility experiments indicate significantly low hemolysis ratios for Cu1−xSrxFe2O4 nanoparticles. Additionally, all examined samples exhibit an increase in Soret band intensity compared to the negative control test, suggesting potential biocompatibility.

Envisioning the structural and room temperature impedance spectroscopy study of praseodymium modified lanthanum ferrites

Praseodymium-modified lanthanum ferrites with general formula La1-xPrxFeO3 [x = 0.0, 0.1, 0.3, 0.5] were prepared using the sol-gel auto combustion technique. The X-ray diffraction patterns of all samples supported the orthorhombic crystal structure with the Pbnm space group. With increasing Pr concentration, it was discovered that the average crystallite size dropped from 44.29 to 29.83 nm. An LCR metre was used to evaluate the frequency-dependent dielectric characteristics between 100 Hz and 1 MHz at room temperature. A single semicircle on the Nyquist plots highlights the impact of grain resistance on electrical behaviour. The depressed semicircles at intermediate frequencies might be created by the grain boundary effect, while semicircles depressed at high frequencies imply grain conduction. The dielectric behaviour of lanthanum ferrites is explained based on Koop’s theory. The loss factor resulting from domain wall resonance displayed the same dielectric constant dispersion behaviour. At high frequencies, orthoferrites were shown to have lower dielectric losses. This is due to the constrained motion of the domain wall, which suggests that magnetically tunable filters and oscillators are possible practical uses.