Role of vanadium ions substitution on spinel MnCo2O4 towards enhanced electrocatalytic activity for hydrogen generation.

Improving efficient electrocatalysts (ECs) for hydrogen generation through water splitting is of significant interest in tackling the upcoming energy crisis. Sustainable hydrogen generation is the primary prerequisite to realizing the future hydrogen economy. This work examines the electrocatalytic activity of hydrothermally prepared vanadium doped MnCo spinel oxide microspheres (MC), MnVxCo2-xO4 (Vx-MnCo MC, where x ≤ 0.4) in the HER (hydrogen evolution reaction) process. Magnetization measurements demonstrated a paramagnetic (at high temperatures) to a ferrimagnetic (at low temperatures) transition below the Curie temperature (Tc) in all the samples. The magnetization is found to intensify with the rising vanadium content of MCs. The optimized catalyst Vx-MnCo MCs (x = 0.3) outperformed other prepared ECs with a Tafel slope of 84 mV/dec, a low onset potential of 78.9 mV, and a low overpotential of 85.9 mV at a current density of 10 mA/cm2, respectively. The significantly improved HER performance of hydrothermally synthesized Vx-MnCo MCs (x = 0.3) is principally attributable to many exposed active sites, accelerated electron transport at the EC/electrolyte interface, and remarkable electron spectroscopy for chemical analysis (ECSA) value was found ~ 11.4 cm2. Moreover, the Vx-MnCo MCs (x = 0.3) electrode exhibited outstanding electrocatalytic stability after exposure to 1000 cyclic voltametric cycles and 36 h of chronoamperometric testing. Our results suggest a feasible route for developing earth-abundant transition metal oxide-based EC as a superior electrode for future water electrolysis applications.

Effect of temperature and glass content on crystalline phases in porcelain sintered with recovered automotive glass.

In the pursuit of sustainable porcelain production, this research examines the potential of using recovered automotive glass as a substitute for traditional feldspar, specifically feldspar imported from Spain. Porcelain samples were sintered at different temperatures and with varied proportions of automotive glass. The crystalline phases formed post-sintering were determined through X-ray diffraction and quantified by dissolving the porcelain in concentrated hydrofluoric acid. Results revealed that the inclusion of automotive glass, owing to its dissolved oxide content, accelerated the porcelain melting process and led to an increase in the vitreous phase. Notably, anorthite phases became dominant and mullite formation was evident at 1100 °C, stabilizing in samples G00 and G10, and then increasing at 1200 °C due to the emergence of secondary mullite. This secondary mullite forms from the residual silica after the primary mullite formation and the aluminium in the feldspars, which is about 17 %. For samples G20 and G30, only primary mullite was observed due to the decreased aluminium content resultant from feldspar replacement by glass. These findings underscore the viability of automotive glass in porcelain production, providing a sustainable and effective alternative to feldspar.

Features of structure, magnetic state and electrodynamic performance of SrFe12-xInxO19.

Indium-substituted strontium hexaferrites were prepared by the conventional solid-phase reaction method. Neutron diffraction patterns were obtained at room temperature and analyzed using the Rietveld methods. A linear dependence of the unit cell parameters is found. In3+ cations are located mainly in octahedral positions of 4fVI and 12 k. The average crystallite size varies within 0.84-0.65 µm. With increasing substitution, the TC Curie temperature decreases monotonically down to ~ 520 K. ZFC and FC measurements showed a frustrated state. Upon substitution, the average and maximum sizes of ferrimagnetic clusters change in the opposite direction. The Mr remanent magnetization decreases down to ~ 20.2 emu/g at room temperature. The Ms spontaneous magnetization and the keff effective magnetocrystalline anisotropy constant are determined. With increasing substitution, the maximum of the ε/ real part of permittivity decreases in magnitude from ~ 3.3 to ~ 1.9 and shifts towards low frequencies from ~ 45.5 GHz to ~ 37.4 GHz. The maximum of the tg(α) dielectric loss tangent decreases from ~ 1.0 to ~ 0.7 and shifts towards low frequencies from ~ 40.6 GHz to ~ 37.3 GHz. The low-frequency maximum of the µ/ real part of permeability decreases from ~ 1.8 to ~ 0.9 and slightly shifts towards high frequencies up to ~ 34.7 GHz. The maximum of the tg(δ) magnetic loss tangent decreases from ~ 0.7 to ~ 0.5 and shifts slightly towards low frequencies from ~ 40.5 GHz to ~ 37.7 GHz. The discussion of microwave properties is based on the saturation magnetization, natural ferromagnetic resonance and dielectric polarization types.

Synthesis of Ni0.5Co0.5-xCdxFe1.78Nd0.02O4 (x ≤ 0.25) nanofibers by using electrospinning technique induce anti-cancer and anti-bacterial activities.

Here we report the electrospinning synthesis of Cd-substituted Ni-Co ferrite Ni0.5Co0.5-xCdxFe1.78Nd0.02O4 (x ≤ 0.25) nanofiber (NFs) with a very low concentration of Nd as a dopant. The structure and surface morphology of the Ni0.5Co0.5-xCdxFe1.78Nd0.02O4 (x ≤ 0.25) NFs were analyzed by X-ray powder pattern (XRD), transmission and scanning electron microscopes (TEM) along with Energy-dispersive X-ray (EDX). We have examined the biological applications of the Ni0.5Co0.5-xCdxFe1.78Nd0.02O4 (x ≤ 0.25) NFs on both cancerous cells and bacterial cells. We have found that Ni0.5Co0.5-xCdxFe1.78Nd0.02O4 (x ≤ 0.25) NFs produced inhibitory action on the human colorectal carcinoma cells (HEK-293) and also showed inhibitory action on the bacterial strains (S. aureus and E. coli) respectively. Finally, this is the first report on the synthesis of Cd- substituted Co-Ni ferrite nanofibers using electrospinning technique exhibiting anti-cancer and anti-bacterial activities.Communicated by Ramaswamy H. Sarma.

Exploring the influence of varying pH on structural, electro-optical, magnetic and photo-Fenton properties of mesoporous ZnFe2O4 nanocrystals.

An economically viable and superficial technique was indorsed to yield ZnFe2O4 nanocrystals in the system to investigate the impact of pH variation on the optical, structural, electrical, and magnetic properties of as-prepared nanocrystals. The as-synthesized ZnFe2O4 nanocrystals were premeditated with the application protracted to degradation of Methylene blue organic dye. The results specify that the pH plays the utmost decisive facet in photo-Fenton recital. From XRD (X-Ray diffraction) analyses, it was confirmed that as-synthesized nanocrystals belong to a cubic Fd3m crystal phase. The crystallite size was also determined by the Scherrer formula and it was noticed that as the pH rises the crystallite size also increased. FT-IR (Fourier Transform Infrared) analysis depicts two absorption peaks âˆ¼ 500 and ∼600 cm-1 that represents tetrahedral (Td) and octahedral (Oh) sites. Using TEM (Transmission Electron Microscopy), the morphology was observed to be spherical particles with some agglomeration. Photoluminescence and UV-visible spectral studies were performed to investigate the optical properties. The bandgap energy was seen to decrease as the pH increased. Using BET analysis, the surface area for the as-synthesized samples was found to decrease on increasing the pH. The reaction results showed that the ZnFe2O4 has good photocatalytic activity, which can be attributed to high surface area and pore volume, and large pore size. The ZnFe2O4 produced by the co-precipitation route exhibited promising photocatalytic activity for the removal of textile dye, reaching nearly 99.2% of decolorization at 100 min. Therefore, ZnFe2O4 particles rapidly prepared by the co-precipitation route have the potential for use in treatment of textile wastewater by the heterogeneous photo-Fenton process. With the help of VSM analysis, the coercivity and other magnetic properties were determined for the as-synthesized nanocrystal with plays a significant role in photocatalytic recyclability, which intends to premediate that the prepared nanocrystals can be used in industrial persistence.

Synthesis of Dy-Y co-substituted manganese­zinc spinel nanoferrites induced anti-bacterial and anti-cancer activities: Comparison between sonochemical and sol-gel auto-combustion methods.

This study described the beneficial properties of ultrasonic irradiation approach to synthesize the spinel-type Dy-Y co-substituted Mn-Zn nanospinel ferrites (NSFs). We have used two different approaches like citrate sol-gel combustion and ultrasonic irradiation routes to produced series of Mn0.5Zn0.5Fe2-2x(DyxYx)O4 (0.0 ≤ x ≤ 0.05) NSFs (DyY-MnZn NSFs). The structure and morphology of NSFs X-was examined by using XRD, EDX, SEM and TEM methods. We have found that spinel ferrites and hematite phase in DyY-MnZn NSFs produced by citrate sol-gel, while DyY-MnZn NSFs created by ultrasonic irradiation contain a pure phase of spinel ferrite. TEM analysis revealed the spherical nanoparticles with fairly uniform size. We have also analyzed the biological applications of DyY-MnZn NSFs prepared by both methods (ultrasonication and sol-gel) by examining their anti-cancer and anti-bacterial (Escherichia coli and Staphylococcus aureu) activities. We have found that both methods produced inhibitory actions on colon cancer cells (HCT-116) and bacterial cells, whereas, no inhibitory action was observed when examined on normal and non-cancerous cells (HEK-293).

Synthesis and biological characterization of Mn0.5Zn0.5EuxDyxFe1.8-2xO4 nanoparticles by sonochemical approach.

Metallic nanoparticles (NPs) possess unique properties which makes them attractive candidates for various applications especially in field of experimental medicine and drug delivery. Many approaches were developed to synthesize divers and customized metallic NPs that can be useful in many areas such as, experimental medicine, drug design, drug delivery, electrical and electronic engineering, electrochemical sensors, and biochemical sensors. Among different metallic nanoparticles, manganese (Mn) NPs are the most prominent materials, in the present study, we have synthetized unique Mn0.5Zn0.5DyxEuxFe1.8-2xO4 NPs by using ultrasonication method (x ≤ 0.1). The structure, and surface morphology of Mn0.5Zn0.5DyxEuxFe1.8-2xO4 NPs was characterized by XRD, SEM, TEM and EDX methods. We have examined the biological effects of Mn0.5Zn0.5DyxEuxFe1.8-2xO4 NPs on both normal (HEK-293) and cancerous (HCT-116) cells. We have found that the treatment of Mn0.5Zn0.5DyxEuxFe1.8-2xO4 NPs post 48 h, showed significant decline in cancer cells population as revealed by MTT assay. The IC50 value of Mn0.5Zn0.5DyxEuxFe1.8-2xO4 NPs was ranged between (2.35 µg/mL to 2.33 µg/mL). To check the specificity of the actions, we found that the treatment of Mn0.5Zn0.5DyxEuxFe1.8-2xO4 NPs did not produce any effects on the normal cells, which suggest that Mn0.5Zn0.5DyxEuxFe1.8-2xO4 NPs selectively targeted the cancerous cells. The anti-bacterial properties of Mn0.5Zn0.5DyxEuxFe1.8-2xO4 NPs were also evaluated by MIC and MBC assays. We suggest that Mn0.5Zn0.5DyxEuxFe1.8-2xO4 NPs produced by sonochemical method possess potential anti-cancer and anti-bacterial capabilities.

Peculiarities of the microwave properties of hard-soft functional composites SrTb0.01Tm0.01Fe11.98O19-AFe2O4 (A = Co, Ni, Zn, Cu, or Mn).

Herein, we investigated the correlation between the chemical composition, microstructure, and microwave properties of composites based on lightly Tb/Tm-doped Sr-hexaferrites (SrTb0.01Tm0.01Fe11.98O19) and spinel ferrites (AFe2O4, A = Co, Ni, Zn, Cu, or Mn), which were fabricated by a one-pot citrate sol-gel method. Powder XRD patterns of products confirmed the presence of pure hexaferrite and spinel phases. Microstructural analysis was performed based on SEM images. The average grain size for each phase in the prepared composites was calculated. Comprehensive investigations of dielectric properties (real (ε') and imaginary parts (ε'') of permittivity, dielectric loss tangent (tan(δ)), and AC conductivity) were performed in the 1-3 × 106 Hz frequency range at 20-120 °C. Frequency dependency of microwave properties were investigated using the coaxial method in frequency range of 2-18 GHz. The non-linear behavior of the main microwave properties with a change in composition may be due to the influence of the soft magnetic phase. It was found that Mn- and Ni-spinel ferrites achieved the strongest electromagnetic absorption. This may be due to differences in the structures of the electron shell and the radii of the A-site ions in the spinel phase. It was discovered that the ionic polarization transformed into the dipole polarization.

A study on the spectral, microstructural, and magnetic properties of Eu-Nd double-substituted Ba0.5Sr0.5Fe12O19 hexaferrites synthesized by an ultrasonic-assisted approach.

In this study, an examination on the spectral, microstructural, and magnetic characteristics of Eu-Nd double-substituted Ba0.5Sr0.5Fe12O19 hexaferrites (Ba0.5Sr0.5NdxEuxFe12-2xO19 (x = 0.00-0.05) HFs) fabricated by an ultrasonic-assisted approach has been presented. An UZ SONOPULS HD 2070 ultrasonic homogenizer with frequency of 20 kHz and power of 70 W was used. The chemical bonding, structure and the morphology of the products were evaluated by Fourier-Transform Infrared (FT-IR) Spectroscopy, XRD (X-ray diffraction), scanning and transmission electron microscopy and techniques. The textural properties of the prepared nanomaterials were examined by using the Brunauer-Emmett-Teller (BET) method. The magnetic properties were studied using a vibrating sample magnetometer (VSM) at room temperature (RT) and low temperature 10 K. The magnitudes of various magnetic parameters including Ms (saturation magnetization), Mr (remanence) and Hc (coercivity) were estimated and evaluated. The M-H loops revealed the hard ferrimagnetic nature for all products at both temperatures. The Ms and Mr values showed a decreasing tendency with increasing degree of Eu3+ and Nd3+ substitutions whereas Hc values displayed an increasing trend. At RT, Ms, Mr and Hc values lie in the ranges of 63.0-68.8 emu·g-1, 24.6-39.2 emu·g-1 and 2252.4-2782.1 Oe, respectively. At 10 K, the values of Ms, Mr and Hc lie between 87.5-97.1 emu·g-1, 33.5-40.1 emu·g-1 and 2060.6-2417.2 Oe, respectively. The observed magnetic properties make the prepared products promising candidates to be applied in the recording media.

Sonochemical synthesis of Dy3+ substituted Mn0.5Zn0.5Fe2-xO4 nanoparticles: Structural, magnetic and optical characterizations.

Mn0.5Zn0.5DyxFe2-xO4 (x ≤ 0.03) nanoparticles (NPs) were fabricated by using Ultrasonic irradiation using UZ SONOPULS HD 2070 ultrasonic homogenizer (frequency of 20 kHz and power of 70 W). Structural and morphological analyses were performed via XRD (X-ray powder diffractometer), TEM (Transmission electron microscopy) and SEM (Scanning electron microscopy). XRD presented the formation of Mn-Zn ferrite with average crystal size in 11 to 18 nm range. Direct optical energy band gaps (Eg) were specified applying diffuse reflectance investigations. Eg values are in a small band range of 1.61-1.67 eV. Low (10 K) and room temperature VSM data were recorded applying ±90 kOe external magnetic field. All samples exhibit superparamagnetic properties at RT. Magnetization parameters significantly increase due to coordination of Dy3+ rare earth ions. Magnetic moment per molecule (nB) increases from 0.952 µB to 1.137 µB and from 2.312 µB to 2.547 µB at RT and at 10 K data respectively. 10 K coercivity (Hc) values decrease from 260 Oe to 43 Oe. All samples have squareness ratios (SQR) of 0.231-0.400 range assigning the multi-domain structure at 10 K. ZFC-FC magnetization curves that were registered for two selected samples exhibit a divergence and a sharp drop below their Tpeak positions. This event is typically correlated to the collective freezing of system and spin-glass-like phase. Real part AC susceptibility data slightly shift toward high temperature regions with increasing frequencies. Critical Slowing Down (CSD) model explained the spin dynamics of interacting NPs consistently with literature and proved the spin-glass behavior of samples at low temperatures.

Ni0.4Cu0.2Zn0.4TbxFe2-xO4 nanospinel ferrites: Ultrasonic synthesis and physical properties.

The Fe3+ ions were replace with Tb3+ ions as highly paramagnetic rare earth element within the structure of Ni0.4Cu0.2Zn0.4Fe2O4 nano-spinel ferrites (NSFs). The structural, magnetic, spectroscopic and optic properties have been studied in details. All products have been synthesized via ultrasonic approach via Qsonica ultrasonic homogenizer, frequency: 20 kHz and power: 70 W for 60 min. No annealing or calcination process was applied for any product. The microstructural analysis of products has been done via X-ray powder diffractometry (XRD) which presented the cubic spinel structure with nanosized distribution of all. The cubic morphology of all products were confirmed by both HR-TEM and FE-SEM. Optical band gap (Eg) values were assessed by applying %DR (percent diffuse reflectance) analysis and Kubelka-Munk theory. The Tauc schemes showed that Eg values are in a narrow range (1.87-1.98 eV). The quadrupole splitting, line width, hyperfine magnetic field, isomer shift values and cation distribution have been determined from 57Fe Mossbauer analysis. The magnetic properties of various nanoparticles have been obtained from VSM (vibration sample magnetometer) measurements at 10 and 300 K (RT). The magnetic results revealed superparamagnetic and soft ferromagnetic traits at 10 and 300 K, respectively. Ms (saturation magnetization) and Mr (remanence) initially increase with increasing Tb3+ substituting level up to x = 0.06 then diminish for further x values. Hc (coercivity) shows an opposite variation tendency of Ms and Mr. The observed magnetic traits are deeply discussed in relation with the structure, morphology, magnetic moments and cation distributions.

Structural, magnetic, optical properties and cation distribution of nanosized Co0.7Zn0.3TmxFe2-xO4 (0.0 ≤ x ≤ 0.04) spinel ferrites synthesized by ultrasonic irradiation.

This study expressed the influence of Tm substitution on the structural, optical and magnetic properties of Co-Zn spinel ferrites (Co0.7Zn0.3TmxFe2-xO4 (0.0 ≤ x ≤ 0.04)). The different compositions were synthesized by sonochemical method using Qsonica ultrasonic homogenizer, frequency: 20 kHz and power: 70 W for 60 min. XRD patterns proved the presence of single-phase spinel ferrites with crystallites size in the 8-10 nm range. Cation distribution approved the occupancy of octahedral (B) site by Tm. The morphology and the elements stoichiometry are obtainable through FE-SEM, EDX and elemental mapping. Optical band gap (Eg) values were estimated via DR % (percent diffuse reflectance) investigations and Kubelka-Munk theory. Tauc plots revealed that direct Eg values are ranging between 1.49 and 1.68 eV. The analyses of magnetization versus magnetic field, M(H), were performed. The following magnetic parameters like saturation magnetization Ms, squareness ratio (SQR = Mr/Ms), magnetic moment nB, coercivity Hc and remanence Mr have been evaluated. M(H) curves revealed the superparamagnetic (SP) at RT and ferromagnetic property at 10 K. It was showed that the Tm3+ substitutions significantly affect the magnetic properties of host spinel ferrites. An increasing trend in the Ms, Mr, Hc, and nB values was noticed for lower Tm3+ substitution content.

Sonochemical synthesis and physical properties of Co0.3Ni0.5Mn0.2EuxFe2-xO4 nano-spinel ferrites.

Nanoparticles (NPs) of composition Co0.3Ni0.5Mn0.2EuxFe2-xO4, where 0.00 ≤ x ≤ 0.10 (hereafter called CNMEuF) were synthesized by sonochemical approach using UZ SONOPULS HD 2070 ultrasonic homogenizer (frequency of 20 kHz and power of 70 W). As-synthesized samples were characterized thoroughly to determine the effects of europium ions (Eu3+) substitution on their structure, morphology and magnetic traits. Structural analyses of the synthesized NPs confirmed their high purity and crystalline cubic phases. Percent diffuse reflectance (%DR) data and Kubelka-Munk theory were exploited to evaluate the optical band gap energies of the studied CNMEuF NPs. Values of optical band gap energies obtained from the Tauc plots were observed in the range of 1.47-1.58 eV. The hysteresis loops (at room temperature and 10 K) of synthesized NPs were analyzed to determine their magnetic properties. These NPs disclosed superparamagnetic and hard ferrimagnetic character at room temperature and 10 K, respectively. With exception, the sample with x = 0.10 revealed soft ferrimagnetic behavior at 10 K. Eu3+ doping was shown to have significant influence on the structure and magnetic attributes of the proposed CNMEuF NPs. Values of various magnetic parameters of proposed compositions were reduced with the increase in Eu3+ dopant contents.

Sonochemical synthesis of Eu3+ substituted CoFe2O4 nanoparticles and their structural, optical and magnetic properties.

Magnetic, optic and microstructural properties of ultrasonically synthesized CoEuxFe2-xO4 (x ≤ 0.1) nanoferrites (NFs) have been examined in this study. After sonochemical synthesis, XRD and FT-IR analyses confirmed the purity, the structure (cubic spinel structure and Fd3m space group) and the spectral properties of the spinel ferrite samples. The spherical morphology and chemical compositions of the products were observed via transmission and scanning electron microscopes along with EDX and elemental mapping. Percent diffuse reflectance (%DR) was used for optical investigation. Optical band gaps (Eg) were estimated utilizing Kubelka-Munk theory and Tauc equation. Eg values are in a narrow band of 1.34 to 1.44 eV. The magnetic parameters like Ms (saturation magnetization), SQR = Mr/Ms (squareness ratio), nB (magnetic moment), Hc (coercivity) and Mr (remanence) have been evaluated by analyzing measurements of magnetization versus magnetic field performed at room (RT; T = 300 K) and low (T = 10 K) temperatures. It is showed that the different produced CoEuxFe2-xO4 (0.00 ≤ x ≤ 0.10) nanospinel ferrites present superparamagnetic (SPM) nature at RT. At low temperature, the various produced CoEuxFe2-xO4 (x ≤ 0.08) nanospinel ferrites display ferrimagnetic (FM) nature. With exception, the x = 0.10 sample exhibit SPM behavior at T = 10 K. It is noticed that the Eu3+ substitutions alter in a significant way on the magnetic data. A decreasing trend in the Ms, Mr and nB values was noted with Eu3+ substitutions.

The Conductivity and Dielectric Properties of Neobium Substituted Sr-Hexaferrites.

The Nb3+ ion substituted Sr hexaferrites (SrNbxFe12-xO19 (x = 0.00-0.08) hexaferrites (HFs)) were fabricated via a citrate-assisted sol-gel approach. X-ray powder diffractometer analysis affirmed the pureness of all products. The crystallite sizes of the products which were estimated from Scherrer equation were in the 36-40 nm range. The chemical component of the samples was proved by Energy-dispersive X-ray spectroscopy (EDX) and Elemental mapping. The hexagonal morphology of all products was confirmed by Field Emission Scanning Electron Microscopy (FE-SEM). The electrical conduction mechanisms and dielectric properties of a variety of Nb3+ions-substituted SrNbxFe12-xO19 HFs were investigated by a complex impedance system. Dielectric parameters such as conductivity, dielectric constant, dielectric loss, dielectric tangent loss and complex modulus, were studied at temperatures up to 120 °C in a frequency range varying from 1.0 Hz to 3.0 MHz for several Nb ratios. The frequency dependence of the conductivity was found to comply with the power law with diverse exponents at all frequencies studied here. Subsequently, incremental tendencies in dc conductivity with temperature indicate that the substituted Sr-HFs leads to a semiconductor-semimetal like behavior. This could be attributable to a feature of conduction mechanism which is based on the tunneling processes. Additionally, the dielectric dispersion pattern was also explained by Maxwell-Wagner polarization in accordance with the Koop's phenomenological theory.

Magnetic Attributes of NiFe2O4 Nanoparticles: Influence of Dysprosium Ions (Dy3+) Substitution.

This paper reports the influence of dysprosium ion (Dy3+) substitution on the structural and magnetic properties of NiDyxFe2-xO4 (0.0 ≤ x ≤ 0.1) nanoparticles (NPs) prepared using a hydrothermal method. The structure and morphology of the as-synthesized NPs were characterized via X-ray diffraction (XRD), scanning and transmission electron microscope (SEM, and TEM) analyses. 57Fe Mössbauer spectra were recorded to determine the Dy3+ content dependent variation in the line width, isomer shift, quadrupole splitting, and hyperfine magnetic fields. Furthermore, the magnetic properties of the prepared NPs were also investigated by zero-field cooled (ZFC) and field cooled (FC) magnetizations and AC susceptibility measurements. The MZFC (T) results showed a blocking temperature (TB). Below TB, the products behave as ferromagnetic (FM) and act superparamagnetic (SPM) above TB. The MFC (T) curves indicated the existence of super-spin glass (SSG) behavior below Ts (spin-glass freezing temperature). The AC susceptibility measurements confirmed the existence of the two transition temperatures (i.e., TB and Ts). Numerous models, e.g., Neel-Arrhenius (N-A), Vogel-Fulcher (V-F), and critical slowing down (CSD), were used to investigate the dynamics of the systems. It was found that the Dy substitution enhanced the magnetic interactions.

Exploration of catalytic and cytotoxicity activities of CaxMgxNi1-2xFe2O4 nanoparticles.

The CaxMgxNi1-2xFe2O4 (x ≤ 0.05) nanoparticles (NPs) have been synthesized hydrothermally. The XRD analyses confirmed the purity of all products and their spherical morphology and compositions were explained by SEM, TEM, EDX and Elemental mapping analyses. Results confirmed the composition of CaxMgxNi1-2xFe2O4. The surface area of them was determined by BET analysis. Results indicated that when x is increased surface area of CaxMgxNi1-2xFe2O4 is decreased as compare with x = 0.0, however, at high composition (x = 0.05), surface area is increased. Catalytic activity of CaxMgxNi1-2xFe2O4 (x ≤ 0.05) NPs was studied for the reduction of 4-nitrophenol as a model compound. Reaction was monitored by UV-spectrophotometer at room temperature and at different times. Among different compositions of CaxMgxNi1-2xFe2O4, it was noticed that x = 0.04 exhibited more activity for the reduction of 4-nitrophenol and x = 0.03 was observed least active. Results suggested that CaxMgxNi1-2xFe2O4 could be useful material for catalytic applications. Cytotoxicity activity of CaxMgxNi1-2xFe2O4 (x ≤ 0.05) NPs against HCT116 (Human colon cancer cell line) cell line and MCF-7 (breast cancer cell line) was evaluated by using MTT assay. It was observed that CaxMgxNi1-2xFe2O4 (x ≤ 0.05) NPs exhibited less cytotoxicity. Due to less cytotoxicity, CaxMgxNi1-2xFe2O4 may also be useful in the field of biomedical applications.

Structural, magnetic, optical properties and cation distribution of nanosized Ni0.3Cu0.3Zn0.4TmxFe2-xO4 (0.0 ≤ x ≤ 0.10) spinel ferrites synthesized by ultrasound irradiation.

In this study, Tm3+ ion substituted NiCuZn nanospinel ferrites, Ni0.3Cu0.3Zn0.4TmxFe2-xO4 (0.0 ≤ x ≤ 0.10), have been synthesized sonochemically. The structural, spectroscopic, morphological, optic and magnetic investigation of the samples were done by X-ray powder diffractometry (XRD), Fourier transform infrared spectrophotometry (FT-IR), UV-Vis diffused reflectance (%DR) spectrophotometry, transmission and scanning electron microscopies (TEM and SEM) along with EDX, Vibrating sample magnetometry (VSM), respectively. The purity of prepared products were confirmed via XRD, FT-IR, EDX and elemental mapping analyses. The analyses of magnetization versus M(H) (applied magnetic field) were performed at 300 and 10 K. The following magnetic parameters like Ms (saturation magnetization), SQR = Mr/Ms (squareness ratio), nB(magnetic moment), Hc (coercivity) and Mr (remanence) have been discussed. M(H) loops revealed superparamagnetic property at RT and soft ferromagnetic nature at 10 K. It is showed that the Tm3+ substitutions significantly affect the magnetizations data. A decreasing trend in the Ms, Hc, Mr, and nB values was detected with Tm3+ substitution.

Structural, optical and magnetic properties of Tm3+ substituted cobalt spinel ferrites synthesized via sonochemical approach.

Co-Tm nano-spinel ferrite with chemical formula CoTmxFe2-xO4 (0.0 ≤ x ≤ 0.08) NPs were prepared via sonochemical approach. X-ray powder diffraction patterns, microscopic images (SEM and TEM) and infrared spectra proved the formation of Co spinel ferrite. The effect of Tm3+ substituted on spinal structure was evaluated by lattice parameters, tetrahedral and octahedral bond length and cationic distribution. The band gap energy (Eg) of samples were estimated by performing UV-Vis percent diffuse reflectance (% DR) and applying the Kubelka-Munk theory. Eg values are in an interval between 1.33 eV and 1.64 eV. The analyses of magnetization were performed at room (300 K; RT) and low (10 K) temperatures. Different magnetic parameters including coercivity Hc, saturation magnetization Ms, remanence Mr, squareness ratio (SQR = Mr/Ms) and magnetic moment nB were deduced and discussed. The results showed superparamagnetic (SPM) nature at RT for x = 0.00 and 0.02 samples. However, the other products exhibit ferromagnetic (FM) nature. At 10 K, all synthesized NPs display FM behavior. An amazing increase in the magnitudes of Ms, Mr and Hc was observed at 10 K in comparison to RT, which is principally due to the reduced thermal fluctuations of magnetic moments at lower temperatures. The Tm3+ substitution affects considerably the magnetizations data. An enhancement in the Ms, Mr, and nB was detected on increasing the Tm3+ concentration. The SQR values at RT are found to be smaller than 0.5 postulating a single domain nature with uniaxial anisotropy for all produced ferrites. However, SQRs are in the range 0.66-0.76 at 10 K, suggesting the multi magnetic domain at low temperature, except the x = 0.02 product where the SQR = 0.47 indicating the single magnetic domain. The obtained magnetic results were investigated deeply with relation to structural and microstructural properties.

Impact of La3+ and Y3+ ion substitutions on structural, magnetic and microwave properties of Ni0.3Cu0.3Zn0.4Fe2O4 nanospinel ferrites synthesized via sonochemical route.

In the current study, Ni0.4Cu0.2Zn0.4La x Y x Fe2-x O4 (x = 0.00 - 0.10) nanospinel ferrites (NSFs) were fabricated via an ultrasonic irradiation route. The creation of single phase of spinel nanoferrites (NSFs) was investigated by X-ray powder diffractometry (XRD) and selected area diffraction pattern (SAED). The cubic morphology of all samples was confirmed by scanning and transmission electron microscopies (SEM and TEM) respectively. The UV-Vis investigations provided the direct optical energy band gap values in a narrow photon energy interval of 1.87-1.92 eV. The 57Fe Mössbauer spectroscopy analysis explained that the hyperfine magnetic fields of Octahedral (Oh) and Tetrahedral (Td) sites decreased with substitution. The paramagnetic properties of NPs decrease with increase of content of doped ions. Investigations of magnetic properties reveal a superparamagnetic nature at 300 K and soft ferromagnetic trait at 10 K. The M s (saturation magnetization) and M r (remanence) decrease and the H c (coercivity) increases slightly with La3+ and Y3+ substitution. The observed magnetic traits are deeply discussed in relation with the morphology, structure, magnetic moments and cation distributions. The microwave characterization of the prepared NSFs showed that, dissipation (i.e., absorption) of incoming microwave energy occurs at a single frequency, for each sample, lying between 7 and 10.5 GHz. The reflection losses (RL) at these frequencies range from -30 to -40 dB and the mechanism of which is explained in the framework of dipolar relaxation and spin rotation. The best microwave properties were obtained with a LaY concentration of x = 0.08 having an RL of -40 dB @ 10.5 GHz and an absorption bandwidth of 8.4 GHz @ -10 dB. With these high values of RL and absorbing bandwidth, LaY doped NiCuZn NSF products would be promising candidates for radar absorbing materials in the X-band.