Zinc Ferrite Nanoparticles Research Articles

Autocombustion Route Derived Zinc Ferrite Nanoparticles as Chemiresistive Sensor for Detection of Alcohol Vapors.

Prolonged exposure to alcohol vapors can have detrimental effects on human health, potentially leading to eye irritation, dizziness, and in some cases, damage to the nervous system. The present article aims to provide a comprehensive understanding on the synthesis and characterization of zinc ferrite (ZnFe2O4) nanoparticles, as well as their interactions with a range of alcohol vapors, including methanol, ethanol, n-propanol, and isopropanol. These alcohols differ in their molecular weight, boiling points, diffusivity, and other properties. The study reveals the semiconducting ZnFe2O4 nanoparticulate sensor's capability for reversible, repeatable, and sensitive detection of alcohol vapors. The sensor exhibits the highest response to ethanol within operating temperature range (225-300 °C). An attempt is made to establish a correlation between the properties of the target analytes and the observed sensing signals. Additionally, the response conductance transients of ZnFe2O4 under the exposure to the studied alcohol vapors are modeled based on the Langmuir-Hinshelwood adsorption mechanism. The characteristic time constants obtained from this modeling are justified with respect to the properties of the analytes.

Combined effect of gallic acid and zinc ferrite nanoparticles on wheat growth and yield under salinity stress

Salinity stress significantly impacts crops, disrupting their water balance and nutrient uptake, reducing growth, yield, and overall plant health. High salinity in soil can adversely affect plants by disrupting their water balance. Excessive salt levels can lead to dehydration, hinder nutrient absorption, and damage plant cells, ultimately impairing growth and reducing crop yields. Gallic acid (GA) and zinc ferrite (ZnFNP) can effectively overcome this problem. GA can promote root growth, boost photosynthesis, and help plants absorb nutrients efficiently. However, their combined application as an amendment against drought still needs scientific justification. Zinc ferrite nanoparticles possess many beneficial properties for soil remediation and medical applications. That’s why the current study used a combination of GA and ZnFNP as amendments to wheat. There were 4 treatments, i.e., 0, 10 µM GA, 15 μM GA, and 20 µM GA, without and with 5 μM ZnFNP applied in 4 replications following a completely randomized design. Results exhibited that 20 µM GA + 5 μM ZnFNP caused significant improvement in wheat shoot length (28.62%), shoot fresh weight (16.52%), shoot dry weight (11.38%), root length (3.64%), root fresh weight (14.72%), and root dry weight (9.71%) in contrast to the control. Significant enrichment in wheat chlorophyll a (19.76%), chlorophyll b (25.16%), total chlorophyll (21.35%), photosynthetic rate (12.72%), transpiration rate (10.09%), and stomatal conductance (15.25%) over the control validate the potential of 20 µM GA + 5 μM ZnFNP. Furthermore, improvement in N, P, and K concentration in grain and shoot verified the effective functioning of 20 µM GA + 5 μM ZnFNP compared to control. In conclusion, 20 µM GA + 5 μM ZnFNP can potentially improve the growth, chlorophyll contents and gas exchange attributes of wheat cultivated in salinity stress. More investigations are suggested to declare 20 µM GA + 5 μM ZnFNP as the best amendment for alleviating salinity stress in different cereal crops.

Efficient removal of crystal violet dye from water using zinc ferrite-polyaniline nanocomposites.

Nanomaterials are widely employed in wastewater treatment, among which nanoferrites and their composites hold significant prominence. This study adopts a green approach to synthesize zinc ferrite nanoparticles, subsequently integrating them with polyaniline (PANI) to fabricate the ZnFe2O4-PANI nanocomposite. Characterization of the prepared ZnFe2O4-PANI nanocomposite was conducted using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopic (SEM) techniques. Using Scherrer's equation, the crystallite size of the synthesized zinc ferrite nanoparticles was found to be 17.67nm. SEM micrographs of the ZnFe2O4-PANI nanocomposite revealed that in situ polymerization of ZnFe2O4 with polyaniline transforms the amorphous surface morphology of the polymer into a homogeneous nanoparticle structure. The adsorption of crystal violet (CV) dye onto the surface of the ZnFe2O4-PANI nanocomposite depends on pH, adsorbent dosage, temperature, concentration levels and duration. The Langmuir adsorption model fitted the data well, indicating adherence to a pseudo-second-order kinetic pattern. Thermodynamic values ΔG°, ΔH° and ΔS° indicated that the adsorption process occurred spontaneously. Advantages and disadvantages of the technique have also been highlighted. Mechanism of adsorption is discussed. From the obtained results, it is evident that the ZnFe2O4-PANI nanocomposite holds promise as a sorbent for the removal of dye from wastewater.

Boosting highly effective photocatalytic activity through g-C3N4 coupled Al doped zinc ferrite nanoparticles: Maximizing dye degradation kinetics

Photocatalysts have gotten much attention because of the growing need to protect the environment, and metal-doped zinc ferrite heterojunctions are an exciting system to look into. The current study involves synthesizing aluminum-doped zinc ferrite (Al@ZF) nanoparticles (NPs) and nanocomposites of Al@ZF with S@g-C3N4 via a hydrothermal method and then evaluating their photocatalytic activity. Al@ZF NPs were prepared by varying the percentage of aluminum (0.5, 1, 3, 5, 7 and 9 wt %). Photocatalytic measurements were carried out employing methylene blue (MB) as the model dye. The Al@ZF NPs with 1 % concentration showed the best photocatalytic capability among all of them. Correspondingly, the S@g-C3N4/Al@ZF nanocomposites (NCs) were made by varying the percentage of S@g-C3N4 (10, 30, 50 and 70 wt %) with the 1 % Al@ZF NPs. Then, photocatalytic working measurements of the S@g-C3N4/Al@ZF NCs proved that the 50 % S@g-C3N4/Al@ZF NC showed the highest photocatalytic activity and completely degraded MB within 150 min of light irradiation. To verify the morphological structure of these artificial nanoparticles and nanocomposites, several analytical techniques including XRD, SEM, TEM, BET, FTIR, and XPS were used. The produced photocatalyst's quick degradation kinetics and simplicity in separation may provide new opportunities for the oxidation of persistent organic pollutants. To our best knowledge, no prior report has been made on the synthesized nanocomposite. The proposed modification of Al@ZF using 50 % S@g-C3N4 is effective, less expensive, non-toxic, and highly efficient for scalable wastewater treatment applications.

Correction to Effect of Chitosan on the Microstructural Properties of Zinc Ferrite Nanoparticles

Correction to Effect of Chitosan on the Microstructural Properties of Zinc Ferrite Nanoparticles

Cubic structured core/shell NiFe2O4@ZnFe2O4 nanocomposite: Structural, morphological and magnetic properties

Double ferrite nanocomposites with NiF2O4 as the core and ZnFe2O4 as the shell, were synthesised through combination of co-precipitation and hydrothermal methods. This two-step process resulted in formation of a cubic structured core of around 100 nm and a shell of zinc ferrite nanoparticles which are below 10 nm in size. The core/shell structures were characterised using various techniques such as XRD, Raman, TEM/EDS and VSM. In addition, Ni leaching out of these structures was tested in the ultra-pure water and saline solution. These analyses demonstrated that the shell of zinc ferrites effectively prevents Ni leaching from the core keeping the concentration of nickel well below the level usually found in drinking water. These core/shell nanocomposites exhibit a ferrimagnetic behaviour.

MOFs-Based Magnetic Nanozyme to Boost Cascade ROS Accumulation for Augmented Tumor Ferroptosis.

The emerging cell death modality of ferroptosis has garnered increasing attention for antitumor treatment but still suffers from low therapeutic efficacy. A metal-organic frameworks (MOFs)-based magnetic nanozyme (PZFH) comprising porphyrin-based Zr-MOF (PCN) on zinc ferrite (ZF) nanoparticles modified with hyaluronic acid, delivering excellent magnetophotonic response for efficient ferroptosis, is reported here. PZFH shows multienzyme-like cascade activity encompassing a photon-triggered oxidase-like catalysis to generate O2 -, which is converted to H2O2 by superoxide dismutase-like activity and subsequent ·OH by magneto-promoted peroxidase (POD) behavior. Newly formed Fe─N coordination and increased Fe2+/Fe3+ levels in the PZFH contribute to the enhanced POD activity, which is further enhanced by accelerated surface electron transfer when exposure to alternated magnetic field. Accumulation of lipid peroxides is eventually accomplished through the conversion of ·OH radicals and singlet oxygen (1O2) produced through laser irradiation. When combined with the depletion of inhibition of glutathione and glutathione peroxidase 4, PZFH exhibits significantly enhanced ferroptosis in tumor-bearing mice, offering insights into nanomedicine for ferroptosis and holding great promise in clinical antitumor therapies.

Immobilized lipase enzyme on green synthesized magnetic nanoparticles using Psidium guava leaves for dye degradation and antimicrobial activities.

Zinc ferrite nanoparticles (ZnF NPs) were synthesized by a green method using Psidium guava Leaves extract and characterized via structural and optical properties. The surface of ZnF NPs was stabilized with citric acid (CA) by a direct addition method to obtain (ZnF-CA NPs), and then lipase (LP) enzyme was immobilized on ZnF-CA NPs to obtain a modified ZnF-CA-LP nanocomposite (NCs). The prepared sample's photocatalytic activity against Methylene blue dye (MB) was determined. The antioxidant activity of ZnF-CA-LP NCs was measured using 1,1-diphenyl-2-picryl hydrazyl (DPPH) as a source of free radicals. In addition, the antibacterial and antibiofilm capabilities of these substances were investigated by testing them against gram-positive Staphylococcus aureus (S. aureus ATCC 25923) and gram-negative Escherichia coli (E. coli ATCC 25922) bacterial strains. The synthesized ZnF NPs were discovered to be situated at the core of the material, as determined by XRD, HRTEM, and SEM investigations, while the CA and lipase enzymes were coated in this core. The ZnF-CA-LP NCs crystallite size was around 35.0nm at the (311) plane. Results obtained suggested that 0.01g of ZnF-CA-LP NCs achieved 96.0% removal of 5.0ppm of MB at pH 9.0. In-vitro zone of inhibition (ZOI) and minimum inhibitory concentration (MIC) results verified that ZnF-CA-LP NCs exhibited its encouraged antimicrobial activity against S. aureus and E. coli (20.0 ± 0.512, and 27.0 ± 0.651mm ZOI, respectively) & (1.25, and 0.625μg/ml MIC, respectively). ZnF-CA-LP NPs showed antibiofilm percentage against S. aureus (88.4%) and E. coli (96.6%). Hence, ZnF-CA-LP NCs are promising for potential applications in environmental and biomedical uses.

Synthesis, characterization and application of rare earth (Lu3+) doped zinc ferrites in carbon monoxide gas sensing and supercapacitors

The novel rare earth (Lu) doped zinc ferrite nanoparticles, synthesized via a solution combustion approach, exhibit exceptional sensitivity to carbon monoxide (C.O.), a capability studied for the first time. The successful detection of C.O. by these nanoparticles underscores their potential as efficient gas sensors. Structural and morphological characterization confirmed the creation of single-phase zinc ferrite nanoparticles, utilizing various standard and advanced modern probes.To assess the gas sensing capabilities, the nanoparticles were exposed to carbon monoxide gas, revealing an outstanding gas response of 80 % at 300 °C, with a response against 20,000 parts per million by volume (PPMv) of carbon monoxide. These results indicate the promising applicability of Lu-doped zinc ferrite nanoparticles in C.O. gas sensing applications.Furthermore, the supercapacitance performance of the synthesized nanoparticles was investigated. Electrodes fabricated from Lu-doped zinc ferrite nanoparticles (Lu 0, 0.3, 0.5, and 0.7) were examined in a 3 M K.O.H. electrolyte using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (E.I.S.). The electrochemical properties of all nanoparticles exhibited good Faradaic behaviour, with the Lu 0.7 electrode achieving a high specific capacitance of 280 F/g at a current density of 0.25 A/g. This highlights the prominent electrochemical stability and potential applications of Lu-doped zinc ferrite nanoparticles in energy storage devices.Overall, the comprehensive investigation of the gas sensing and super capacitance performance of Lu-doped zinc ferrite nanoparticles demonstrates their versatility and potential for various technological applications, including gas sensing and energy storage. These findings pave the way for further research and development in utilizing rare earth-doped ferrite nanoparticles for advanced functional materials.

Influence of Zirconium substitution on electrical properties of Nickel-Zinc Ferrites

The Zirconium substituted Nickel Zinc Ferrite nano particles with chemical composition of Ni(0.5-x)Zn(0.5-x)ZrxFe2O4, where the value of x varies from 0 to 0.2, have been synthesized by the sol-gel auto combustion method, using high purity nitrates and fuelling agent citric acid. The structural property was studies from X-ray diffraction spectra. The crystallite size decreases with increase in Zirconium substitution. The electrical property of the same was investigated by studying the dielectric constant, and AC conductivity. There are fluctuations in these properties with variation in Zirconium substitution in Ni-Zn Ferrite.

Tailoring Zinc Ferrite Nanoparticle Surface Coating for Macrophage-Affinity Magnetic Resonance Imaging of Atherosclerosis.

Atherosclerosis is a chronic inflammatory disease characterized by the formation of atherosclerotic plaques, while macrophages as key players in plaque progression and destabilization are promising targets for atherosclerotic plaque imaging. Contrast-enhanced magnetic resonance imaging (CE-MRI) has emerged as a powerful noninvasive imaging technique for the evaluation of atherosclerotic plaques within arterial walls. However, the visualization of macrophages within atherosclerotic plaques presents considerable challenges due to the intricate pathophysiology of the disease and the dynamic behavior of these cells. Biocompatible ferrite nanoparticles with diverse surface ligands possess the potential to exhibit distinct relaxivity and cellular affinity, enabling improved imaging capabilities for macrophages in atherosclerosis. In this work, we report macrophage-affinity nanoparticles for magnetic resonance imaging (MRI) of atherosclerosis via tailoring nanoparticle surface coating. The ultrasmall zinc ferrite nanoparticles (Zn0.4Fe2.6O4) as T1 contrast agents were synthesized and modified with dopamine, 3,4-dihydroxyhydrocinnamic acid, and phosphorylated polyethylene glycol to adjust their surface charges to be positively, negatively, and neutrally charged, respectively. In vitro MRI evaluation shows that the T1 relaxivity for different surface charged Zn0.4Fe2.6O4 nanoparticles was three higher than that of the clinically used Gd-DTPA. Furthermore, in vivo atherosclerotic plaque MR imaging indicates that positively charged Zn0.4Fe2.6O4 showed superior MRI efficacy on carotid atherosclerosis than the other two, which is ascribed to high affinity to macrophages of positively charged nanoparticles. This work provides improved diagnostic capability and a better understanding of the molecular imaging of atherosclerosis.

Poly O-toluidine-coated acetic acid modified eggshell-chitosan with ZnFe2O4 nanoparticles as a new and promising sorbent nanocomposite for rapid removal of toxic dyes such as Brilliant Green and Acid Red from the aquatic environment

The conversion of organic waste into valuable commodities is essential for safeguarding the environment and promoting the sustainable development of the economy. This investigation centres on the production of Zinc ferrite nanoparticles (ZnF NPs), modified eggshells (MES) impregnated with chitosan (CS) and coated with poly ortho-toluidine P(OT) nanocomposites (NCs). This synthesis involves a quaternary composition denoted as P(OT)/MES/CS/ZnF NCs, achieved through chemical polymerization techniques. The resulting NCs were characterized and applied for the removal of Brilliant Green (B.GR) and Acid Red (A.RE). Four distinct compositions, namely pure P(OT), binary P(OT)/MES, ternary P(OT)/MES/CS, and quaternary P(OT)/MES/CS/ZnF NCs, were synthesized. The outcomes revealed that the quaternary P(OT)/MES/CS/ZnF NCs exhibited the highest adsorption capacities for B.GR and A.RE at)27.03 and 142.8 mg−1(, respectively. The findings revealed that the most favorable parameters for the removal of A.RE were attained at a pH of 2, using 15 mg of P(OT)/MES/CS/ZnF NCs at a concentration of 25 mg/L for a duration of 120 min. On the other hand, when it comes to removing B.GR, the best results were shown while using 15 mg of P(OT)/MES/CS/ZnF NCs at a concentration of 5 mg/L for 120 min, specifically at a pH of 6. The greatest real wastewater removal efficiencies for A.RE dye and B.GR dye, respectively, were found to be 99.5% and 97.6% under these operating circumstances. These optimal quaternary NCs demonstrated the ability to be regenerated four times without significantly compromising their adsorption properties and exhibited a remarkable capacity to remove 96–98% of dyes from real polluted water. Through the use of regression data and a pseudo-second-order model, the adsorption kinetics were explained, with R2 values of 0.994 for A.RE and 0.993 for B.GR, respectively. Thermodynamic parameters of dye adsorption by the NCs affirmed the fact that adsorption occurs spontaneous and have endothermic nature. This study underscores an effective synthesis approach applicable for large-scale production of new adsorbents for water treatment purposes.

Highly nanocrystalline Mg doped ZnFe2O4 powders for rapid and simultaneous adsorption of Lead, Copper, and Cadmium heavy metals ions in synthetic / sea waters

This research aims to investigate the effect of Mg doping on individual and simultaneous adsorption of Pb+2, Cu+2, and Cd+2 heavy metals in aqueous solution and in seawater samples, by Zinc ferrite nanoparticles. The Mg-doped Zinc ferrite nanoparticles are synthesized successfully by the sol-gel route and varying Mg concentrations. TEM, XRD, FTIR, Raman, and XPS characterizations confirm the cubic spinel structure of Zinc ferrite with a semi-spherical shaped nanosized particles (10-15nm) irrespective of Mg doping content. The BET surface area manifests a significant increase within Mg doping (39.3 m2/g) compared with the pure zinc ferrite (28.4 m2/g). Accordingly, Mg-doped Zinc ferrite powders demonstrate considerable adsorption capacities for Pb+2 (143.5mg/g), Cu+2 (117mg/g), and Cd+2 (77mg/g) within 2h under optimized experimental conditions. The prepared nanopowders exhibit high selectivity towards Pb+2 in simultaneous adsorption in aqueous solutions (85mg/g) and real seawater samples. Nonetheless, the selectivity of Pb+2 ions drops dramatically to 25mg/g within real seawater samples due to the strong ionic strength of high-salinity seawater. This study provides insights into the importance of doped spinel ferrite nanoparticles in highly efficient, rapid, and simultaneous adsorption of heavy metals. Besides, it reveals the challenge of performing the adsorption process in real seawater.

Probing temperature-dependent magnetism in cobalt and zinc ferrites: A study through bulk and atomic-level magnetic measurements for spintronics

Spinel ferrites (MFe2O4) are integral to various industries, particularly spintronics, which utilizes the intrinsic spin of electrons as well as the electronic charge to develop devices that dictate spin-based transport, advancing new memory, logic applications, and improving magnetic storage technologies. These materials are valued for their exceptional optical, magnetic and electrical properties, and their easily tunable shape and size. This flexibility of spinel ferrites and their connection to the material’s magnetic behavior can be investigated by studying a range of spinel ferrite structures. In this study, the magnetic behaviors of cobalt ferrite (CFO) and zinc ferrite (ZFO) nanoparticles were examined using a vibrating sample magnetometer (VSM, bulk magnetometry) and X-ray Magnetic Circular Dichroism (XMCD, atomic magnetometry). The Rietveld refinement of XRD data supported single phase spinel structure, while X-ray Absorption Spectroscopy (XAS), particularly through the Co L-edge XANES analysis, detected both Co2+ and Co3+ ions in CFO, suggesting significant ferromagnetic behavior due to octahedral site occupation. In contrast, ZFO exhibited antiferromagnetic character, with Zn2+ ions in tetrahedral sites, and canted antiferromagnetism manifesting as a hysteresis loop below 300 K, potentially related to lattice distortions or strain. At the atomic scale, XMCD analysis, along with sum rules, estimated the average magnetic moments for cobalt and zinc ferrites to be 3.045 ± 0.1 (1.448 ± 0.1) and 0.657 ± 0.1 (2.12 ± 0.1) μB at temperatures of 300 K (90 K), respectively. However, VSM-based bulk measurements indicated magnetic moments of 2.566 (2.288) and 0.281 × 10−3 (0.6503 × 10−3) μB for CFO and ZFO, respectively, at the same temperatures. The observed variation between bulk and atomic-scale magnetic moments points to complex interstitial interactions within the spinel ferrite’s sublattices. This discrepancy between the atomic-scale and bulk magnetic moments suggests intricate interstitial interactions within the spinel ferrite’s sublattices. These insights into the structural and magnetic intricacies of spinel ferrite nanoparticles enhance our understanding, facilitating the design of cutting-edge spintronic devices.

Zinc Ferrite Nanoparticle Coatings on Austenitic Alloy Steel.

The phase transition of austenitic stainless steel of commercial label CL20ES and zinc ferrite nanoparticles was studied in an oxidative atmosphere of dry air to develop a low-cost, effective technique for covering-layer fabrication. CL20ES powder and zinc ferrite powder were mechanically mixed. This mixture was studied in an atmosphere of dry air at different annealing temperatures from room temperature to 900 °C. The employed characterization techniques are X-ray powder diffraction, Mössbauer spectroscopy in the transmission geometry, and scanning electron microscopy with elemental mapping. The fabricated layers were also characterized by surface-specific techniques such as conversion electron Mössbauer spectroscopy and grazing incidence X-ray powder diffraction. The analyzed powder mixture shows resistance against oxidation in dry air and high temperatures. These results were employed to produce zinc ferrite covering layers on 3D-printed cylinders of CL20ES. The results show a predisposition of zinc ferrite to be recrystallized at temperatures above 350 °C without the production of corrosive substances on steel. The zinc ferrite layers were analyzed by an ultrasonic hardness tester as well, which proved the hardness enhancement.

Impedance characterization of hydrothermally synthesized nickel zinc ferrite nanoparticles for electronic application

This study comprehensively investigates the structural, morphological, dielectric, and conductivity properties of Ni0.5Zn0.5Fe2O4 nanoparticles synthesized through a hydrothermal method, focusing on their suitability for technological applications. The nanoparticles exhibited a cubic structure with an average grain size of approximately 19 nm. The dielectric properties were analyzed with respect to frequency and temperature, showcasing behaviors consistent with Maxwell-Wagner and Koop's theories. The dielectric plane plots, corresponding to the impedance circuit in the Smith Chart, were found to align with the Davidson-Cole relaxation model. Moreover, the conductivity properties adhered to the Jonscher Power law, resembling conductive properties akin to semiconductors in accordance with the band theory. Notably, the s parameter, indicative of the DC conduction mechanism, displayed temperature-dependent variations, suggesting compatibility with the small polar and correlated hopping barrier conduction models. The thermal activation energies of the Ni0.5Zn0.5Fe2O4 nanoparticles at 102, 103, 104, 105, and 106 rad/s frequencies have been recorded at 0.115, 0.141, 0.157, 0.133 and 0.121 eV, respectively. The experimental results strongly suggest that Ni0.5Zn0.5Fe2O4 nanoparticles hold promise as an inspiring material for electronic circuit applications.

Optical, conductivity, dielectric, and magnetic properties of polymer nanocomposite based on PAM/cs matrix and ZnFe2O4 NPs for use in magneto-electronic and energy storage capacitor devices

In this study, a cast synthesis approach was used to create flexible nanocomposite films made of polyacrylamide (PAM), chitosan (Cs), and zinc ferrite nanoparticles (ZnFe2O4 NPs). XRD analysis was used to examine the composite structure. They demonstrated the effective interaction between ZnFe2O4 NPs and PAM/Cs blend. As the concentration of nanomaterial in the host polymer matrix grew, it was observed that the PAM/Cs matrix's direct and indirect energy band gaps decreased while its absorbance of ultraviolet–visible radiations increased. The nanocomposite's AC conductivity was significantly higher than that of the blend, and 2.5 wt percent of the nanocomposite showed the highest electrical conductivity. It was observed that as frequency raised, the ε′ and ε″ declined though the concentration of nanoparticles enhanced these characteristics. Because of the high dielectric permittivity of ZnFe2O4, the values of ε′ and ε″ raised as ZnFe2O4 were higher. The outcome of the vibrating sample magnetometer (VSM) demonstrated the ferromagnetic property of the produced nanocomposites. Furthermore, the VSM study shows that as the nanoparticles content increases, the PAM/Cs/ZnFe2O4 nanocomposites' Ms, Hc, and Mr also increase. These PAM/Cs/ZnFe2O4 films were shown by the experimental results to be promising candidates for bandgap-regulated materials, electromagnetic interference shielders, frequency tunable nanodielectric, and flexible dielectric substrates for future microelectronic, optoelectronic technologies, and capacitive energy storage.

ZnFe2O4@SiO2@L-Lisin@Cr-EDTA coordination polymer: A novel, green, magnetic, reusable, and versatile nanocatalyst for the oxidation of sulphides

In this research, the design, and synthesis of ZnFe2O4@SiO2@L-Lisin@Cr-EDTA coordination polymer magnetic nanoparticles as a novel, recyclable, and heterogeneous catalyst was developed. EDTA with four carboxylic groups as an outstanding chelating agent was utilized for the preparation of the Cr-EDTA metal-organic framework (Cr-EDTA coordination polymer). In the next step, by immobilizing the synthesized Cr-EDTA coordination polymer on the surface of the Zinc ferrite nanoparticles, ZnFe2O4@SiO2@L-Lisin@Cr-EDTA coordination polymer was synthesized. The magnetic nanocatalyst (ZnFe2O4@SiO2@L-Lisin@Cr-EDTA coordination polymer) was characterized by using various methods such as BET, FTIR, SEM, XRD, EDX, TGA, VSM, and Map analysis. Also, the oxidation of sulfides to sulfoxide was efficiently performed using the ZnFe2O4@SiO2@L-Lisin@Cr-EDTA coordination polymer catalytic system. The synthesized catalyst can be reused for five periods without loss of catalytic activity.

Aptamer-Modified Zinc Ferrite Nanoparticles for Autophagy-Mediated Chemotherapy and MR Imaging of Ovarian Cancer

Aptamer-Modified Zinc Ferrite Nanoparticles for Autophagy-Mediated Chemotherapy and MR Imaging of Ovarian Cancer

Structural, Optical, Electrical, and Magnetic Characterization of PC/PEO Blend Incorporated with ZnFe2O4 Nanoparticles

In this study, zinc ferrite nanoparticles (ZnFe2O4 NPs) were incorporated into a polycarbonate/polyethylene oxide (PC/PEO) blend using the casting method. The resulting blends were subjected to comprehensive analysis using various techniques. X‐ray diffraction (XRD) analysis revealed that the presence of ZnFe2O4 nanoparticles had a significant impact on the crystal structure of the PC/PEO blend, leading to a reduction in crystallinity. Fourier‐transform infrared (FT‐IR) measurements further confirmed the uniform distribution and compatibility of PC and PEO as polymer components, as well as their compatibility with the blend containing ZnFe2O4 NPs. The optical properties of the PC/PEO blend, including band gap and Urbach energy, were quantified using the Kubelka–Munk method. The incorporation of ZnFe2O4 NPs resulted in the formation of sub‐band states between the valence and conduction bands, leading to a decrease in the band gap values. Field emission scanning electron microscopy (FESEM) analysis revealed a noticeable modification in the surface roughness, with the addition of ZnFe2O4 NPs resulting in a smoother surface texture. The electrical properties of the blends, including dielectric constant, dielectric loss, and AC conductivity, were measured. The addition of ZnFe2O4 NPs increased the dielectric constant (ε′) at lower frequencies, while it remained relatively stable at higher frequencies due to the localized charge carriers within the polymer blend. The higher values of ε’ observed at lower frequencies can be attributed to the movement of ions, which contributes to enhanced ionic conductivity. The magnetic properties of the blends were evaluated, demonstrating an increase in magnetic saturation upon the addition of ZnFe2O4 NPs. These findings provide valuable insights into the structural, optical, electrical, and magnetic characteristics of PC/PEO blends incorporated with ZnFe2O4 nanoparticles, thereby highlighting their potential for a wide range of technological applications.