Synthesis and characterization of Ni-Zn ferrite nanoparticles

Nickel zinc ferrite nanoparticles Ni_xZn_1−xFe₂O₄ (x=0.1, 0.3, 0.5) have been synthesized by a chemical co-precipitation method. The samples were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, electron paramagnetic resonance, dc magnetization and ac susceptibility measurements. The X-ray diffraction patterns confirm the synthesis of single crystalline Ni_xZn_1−xFe₂O₄ nanoparticles. The lattice parameter decreases with increase in Ni content resulting in a reduction in lattice strain. Similarly crystallite size increases with the concentration of Ni. The magnetic measurements show the superparamagnetic nature of the samples for x=0.1 and 0.3 whereas for x=0.5 the material is ferromagnetic. The saturation magnetization is 23.95 emu/g and increases with increase in Ni content. The superparamagnetic nature of the samples is supported by the EPR and ac susceptibility measurement studies. The blocking temperature increases with Ni concentration. The increase in blocking temperature is explained by the redistribution of the cations on tetrahedral (A) and octahedral (B) sites.     

Structural characterization and magnetic properties of superparamagnetic zinc ferrite nanoparticles synthesized by the coprecipitation method

Single phase zinc ferrite (ZnFe₂O₄) nanoparticles have been prepared by the coprecipitation method without any subsequent calcination. The effects of precipitation temperature in the range 20–80 °C on the structural and the magnetic properties of zinc ferrite nanoparticles were investigated. The crystallite size, microstructure and magnetic properties of the prepared nanoparticles were studied using X-ray diffraction (XRD), Fourier transmission infrared spectrum, transmission electron microscope (TEM), energy dispersive X-ray spectrometer and vibrating sample magnetometer. The XRD results showed that the coprecipitated nanoparticles were single phase zinc ferrite with mixture of normal and inverse spinel structures. Furthermore, ZnFe₂O₄ nanoparticles have the crystallite size in the range 5–10 nm, as confirmed by TEM. The magnetic measurements exhibited that the zinc ferrite nanoparticles synthesized at 40 °C were superparamagnetic with the maximum magnetization of 7.3 emu/g at 10 kOe.     

Synthesis of cobalt ferrite nano-particles and their magnetic characterization

Cobalt ferrite nano-particles (CoFe₂O₄) were synthesized by the co-precipitation method with ammonium hydroxide as an alkaline solution. The reactions were carried out at different temperatures between 20 and 80 °C. The nano-particles have been investigated by magnetic measurements, X-ray powder diffraction and transmission electron microscopy. The average crystallite size of the synthesized samples was between 11 and 45 nm, which was found to be dependent on both pH value of the reaction and annealing temperatures. However, lattice parameters, interplane spacing and grain size were controlled by varying the annealing temperature. Magnetic characterization of the nano-samples were carried out using a vibrating sample magnetometer at room temperature. The saturation magnetization was computed and found to lie between 5 and 67 emu/g depending on the particle size of the studied sample. The coercivity was found to exhibit non-monotonic behavior with the particle size. Such behavior can be accounted for by the combination between surface anisotropy and thermal energies. The ratio of remanence magnetization to saturation magnetization was found to exhibit almost linear dependence on the particle size.     

Synthesis and characterization of carboxymethyl dextran-coated Mn/Zn ferrite for biomedical applications

Previous studies have shown that magnetic nanoparticles possess great potential for various in vivo applications such as magnetic resonance imaging contrast enhancement, tissue repair, cancer treatment agents, and controlled drug delivery. Many of these applications require that magnetic nanoparticles be colloidally stable in biological media. The goal of this study was to obtain a magnetic fluid produced by the colloidal suspension of manganese/zinc ferrite (MZF) nanoparticles that could be stably dispersed in aqueous solution throughout the range of physiological pH and ionic strength. These superparamagnetic nanoparticles were stabilized through steric repulsion by coating with biologically compatible carboxymethyl dextran (CMDx). Samples of the resultant magnetic fluid were analyzed using Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), X-ray diffraction (XRD), zeta potential measurements, dynamic light scattering, transmission electron microscopy (TEM), and SQUID magnetometry. Results show that we obtained superparamagnetic metal-oxide crystals with composition of Mn_0.24Zn_0.76Fe₂O₄. Cell viability measurements show the material is non-toxic to MCF-7 and CaCo-2 cell lines at concentrations of up to 7.5 mg/mL of particle fraction for contact time of up to 48 h.     

Ionic magnetic fluid based on cobalt ferrite nanoparticles: Influence of hydrothermal treatment on the nanoparticle size

Magnetic fluid based on cobalt ferrite nanoparticles was obtained using a hydrothermal treatment added to the Massart procedure. This treatment increases the average size of the nanoparticles from 11.9 to 18.7 nm and also improves the dispersity and crystallinity of the cobalt ferrite particles. The nanoparticles obtained after the hydrothermal treatment were dispersed in aqueous solvent by the classical procedure for ionic magnetic fluids. The ferrofluid thus obtained is stable at pH 7 and may be useful for hyperthermia applications.     

Synthesis and characterization of lithium ferrite by oxalate precursor route

Nanocrystalline lithium ferrite (LiFe₅O₈) powders have been synthesized by oxalate precursor route. The effects of Fe³⁺/Li⁺ mole ratio, and annealing temperature on the formation, crystalline size, morphology and magnetic properties were systematically studied. The Fe³⁺/Li⁺ mole ratio was controlled from 5 to 3.33 while the annealing temperature was controlled from 600 to 1100 °C. The resultant powders were investigated by differential thermal analyzer (DTA), X-ray diffractometer (XRD), scanning electron microscopy (SEM) and vibrating sample magnetometer (VSM). DTA results showed that LiFe₅O₈ phase started to form at around 520 °C. XRD indicated that LiFe₅O₈ phase always contained α-Fe₂O₃ impurity and the hematite phase formation increased by increasing the annealing temperature ?850 °C for different Fe³⁺/Li⁺ mole ratios 5, 4.55 and 3.85. Moreover, lithium ferrite phase was formed with high conversion percentage at critical annealing temperature 750–800 °C. Single well crystalline LiFe₅O₈ phase was obtained at Fe³⁺/Li⁺ mole ratio 3.33 and annealing temperatures from 800 to 1000 °C. Maximum saturation magnetization (68.7 emu/g) was achieved for the formed lithium ferrite phase at Fe³⁺/Li⁺ mole ratio 3.33 and annealing temperature 1000 °C.     

Structure and magnetic properties of nanocrystalline cobalt ferrite powders synthesized using organic acid precursor method

Nanocrystalline octahedra of cobalt ferrite CoFe₂O₄ powders were synthesized using the organic acid precursor route. The effect of the calcination temperature, Fe³⁺/Co²⁺ molar ratio, calcination time and type of organic acid (oxalic, benzoic and tartaric acids) on the formation, crystallite size, microstructure and magnetic properties was studied systematically. The Fe³⁺/Co²⁺ molar ratio was varied from 2 to 1.739 while the annealing temperature was controlled from 400 to 1000 °C for various periods from 0.5 to 2 h. The resulting powders were investigated using X-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and vibrating sample magnetometer (VSM). XRD results indicate that a well crystallized, single spinel cobalt ferrite phase was formed for the precursors annealed at 600-800 °C for 2 h, using oxalic and tartaric acids as precursors for Fe³⁺/Co²⁺ molar ratio 1.818. The crystallite size of as-formed powders was in the range of 38.0-92.6 nm at different operating conditions. The calcination temperature and Fe³⁺/Co²⁺ molar ratio have a significant effect on the microstructure of the produced cobalt ferrite. The microstructure of the produced powders was found to be octahedra-shaped. The crystalline, pure cobalt ferrite powders with magnetic properties having a maximum saturation magnetization (76.1 emu/g) was achieved for the single phase at Fe³⁺/Co²⁺ molar ratio 1.818 and annealing temperature of 600 °C for 2 h using tartaric acid precursor.     

Heat treatment effects on microstructure and magnetic properties of Mn-Zn ferrite powders

Mn-Zn ferrite powders (Mn_0.5Zn_0.5Fe₂O₄) were prepared by the nitrate-citrate auto-combustion method and subsequently annealed in air or argon. The effects of heat treatment temperature on crystalline phases formation, microstructure and magnetic properties of Mn-Zn ferrite were investigated by X-ray diffraction, thermogravimetric and differential thermal analysis, scanning electron microscopy and vibrating sample magnetometer. Ferrites decomposed to Fe₂O₃ and Mn₂O₃ after annealing above 550 °C in air, and had poor magnetic properties. However, Fe₂O₃ and Mn₂O₃ were dissolved after ferrites annealing above 1100 °C. Moreover, the 1200 °C annealed sample showed pure ferrite phase, larger saturation magnetization (M_s=48.15 emu g⁻¹) and lower coercivity (H_c=51 Oe) compared with the auto-combusted ferrite powder (M_s=44.32 emu g⁻¹, H_c=70 Oe). The 600 °C air annealed sample had the largest saturation magnetization (M_s=56.37 emu g⁻¹) and the lowest coercivity (H_c=32 Oe) due to the presence of pure ferrite spinel phase, its microstructure and crystalline size.     

Preparation and characterization of ZnSn-substituted barium ferrite thin films

The preparation of ZnSn-substituted barium ferrite films by sputtering deposition was studied. The as-sputtered films were amorphous, and annealing at a minimum of 750 °C was required to crystallize the films, based on the X-ray diffraction analysis and the magnetic measurements. Scanning electron microscopy combined with energy-dispersive X-ray spectroscopic microanalysis confirmed that the films were single phase with the composition BaZn_xSn_xFe_12−2xO₁₉, x=0.2−0.3, and their thicknesses were 0.4-1.0 μm when annealed at 750-900 °C. Atomic and magnetic force microscopy studies showed no significant grain growth upon annealing and that the films consisted of single-domain grains forming interaction-cluster-type domains. The natural ferromagnetic resonance frequency was determined at around 4 GHz, together with substantial magnetic losses that make these films promising candidates for microwave absorbers.     

Synthesis and magnetic properties of Mn–Zn ferrite nanoparticles

Mn–Zn ferrite nanoparticles (Mn_1−xZn_xFe₂O₄) are synthesized by a hydrothermal precipitation approach using metal sulfate solution and aqueous ammonia. The analysis methods of XRPD, TEM, TGA, and VSM are used to characterize the magnetic nanoparticles. Through the characterization of the precipitated nanoparticles, the effects of the reacting component proportions and preparation techniques on the Curie temperature, the magnetization, and the size distribution of Mn–Zn ferrite nanoparticles are discussed. Furthermore, the Mn–Zn ferrite nanoparticles are used to prepare ferrofluid. Variation of the magnetic properties of the ferrite nanoparticles with the composition content x of Zn and the magnetic moment of the nanoparticles are discussed.     

The role of copper ions on the structural and magnetic characteristics of MgZn ferrite nanoparticles and thin films

In this study Cu_xMg_0.5−xZn_0.5Fe₂O₄ (x=0-0.5) nanoparticles and thin films were prepared by sol-gel processing. The morphologies of nanoparticles were observed by transmission electron microscope (TEM). The Mössbauer spectroscopy (MS) was employed to determine the site preference of the constitutive elements. Magnetic dynamics of the nanoparticles was studied by the measurement of AC magnetic susceptibility versus temperature at different frequencies. The phenomenological Néel-Brown and Vogel-Fulcher models were employed to distinguish between interacting or non-interacting system. Results exhibited that there is strong interaction between fine particles. X-ray diffraction (XRD) patterns of the thin films indicate the formation of single-phase cubic spinel structure. Atomic force microscope (AFM) was employed to evaluate the surface morphologies of the prepared thin films. Vibrating sample magnetometer (VSM) was employed to probe magnetic properties of samples. It was found that with an increase in the amount of copper, the saturation of magnetization and initial permeability increase.     

The effect of cation distribution on magnetization of ZnFe2O4 nanoparticles

In this work zinc ferrite (ZnFe₂O₄) nanoparticles have been prepared by sol-gel method in two different media, one acidic and another one basic and then annealed at different temperatures from 350 to 800 °C. XRD investigations show that both samples have a single phase spinel structure. Mean crystallite sizes of the samples were calculated, using Scherrer’s formula, which are 13 and 16 nm for the samples prepared in acidic and basic media, respectively. The variation of cation distribution in the samples was estimated by the ratio of (2 2 0) and (2 2 2) intensity diffraction peaks and the results show that as-prepared nanoparticles have different ionic distributions in comparison with that of bulk zinc ferrite. Also the results show that by increasing annealing temperature the ionic distribution of the zinc ferrite nanoparticles tends to that of bulk sample. The magnetic properties of the samples were studied by VSM and the results show that zinc ferrite nanoparticles have a ferrimagnetic behavior. Also the morphology of the powders was examined by TEM.     

镍锰铁氧体纳米线阵列的制备与表征

采用真空负压灌注技术, 结合溶胶-凝胶法在多孔氧化铝模板的纳米孔洞中成功制备了平均直径为80 nm左右的Ni_{1- x}Mn_xFe₂O₄(x=0, 0.25, 0.5, 0.75) 纳米线阵列. XRD结果显示所制备的纳米线阵列为立方尖晶石结构, SEM和TEM的结果表明纳米线是由大量不同晶体取向的亚微晶粒联接组成. 磁测量结果显示, 随着Mn掺杂浓度的增加, 饱和磁化强度先增加而后减小, 这种变化与离子在尖晶石结构中的替代、占位变化有关. 相比于块体材料的NiFe₂O₄, 由于非线性磁结构比例的增加, 导致了线体NiFe₂O₄的饱和磁化强度降低.     

Hydrothermal synthesis and magnetic properties of gadolinium-doped CoFe2O4 nanoparticles

CoFe_2−xGd_xO₄ (x=0-0.25) nanoparticles were synthesized via a simple hydrothermal process at 200 °C for 16 h without the assistance of surfactant. The as-synthesized powders were characterized by X-ray diffraction, transmission electron microscopy, and a vibrating sample magnetometer. The X-ray diffraction results showed that the as-synthesized powders were in the pure phase with a doping amount of ≤0.25, and the peaks could be readily indexed to the cubic spinel cobalt ferrite. Transmission electron microscopy and high resolution transmission electron microscopy observations revealed that the gadolinium-doped cobalt ferrite nanoparticles were single crystal, roughly spherical, uniformly distributed, and not highly agglomerated. The room temperature magnetic field versus magnetization measurements confirmed a strong influence of gadolinium doping on the saturation magnetization and coercivity due to large lattice distortion and grain growth of small particles.     

Preparation of magnesium ferrite nanoparticles by ultrasonic wave-assisted aqueous solution ball milling

Magnesium ferrite, MgFe₂O₄ nanoparticles with high saturation magnetization were successfully synthesized using ultrasonic wave-assisted ball milling. In this study, the raw materials were 4MgCO₃·Mg(OH)₂·5H₂O and Fe₂O₃ powders and the grinding media was stainless steel ball. The average particle diameter of the product MgFe₂O₄ powders was 20 nm and the saturation magnetization of them reached 54.8 emu/g. The different results of aqueous solution ball milling with and without ultrasonic wave revealed that it was the coupling effect of ultrasonic wave and mechanical force that played an important role during the synthesis of MgFe₂O₄. In addition, the effect of the frequency of the ultrasonic wave on the ball milling process was investigated.     

Impact of sonochemical synthesis condition on the structural and physical properties of MnFe2O4 spinel ferrite nanoparticles

Herein, we report sonochemical synthesis of MnFe₂O₄ spinel ferrite nanoparticles using UZ SONOPULS HD 2070 Ultrasonic homogenizer (frequency: 20 kHz and power: 70 W). The sonication time and percentage amplitude of ultrasonic power input cause appreciable changes in the structural, cation distribution and physical properties of MnFe₂O₄ nanoparticles. The average crystallite size of synthesized MnFe₂O₄ nanoparticles was increased with increase of sonication time and percentage amplitude of ultrasonic power input. The occupational formula by X-ray photoelectron spectroscopy for prepared spinel ferrite nanoparticles was (Mn_0.29Fe_0.42)[Mn_0.71Fe_1.58]O₄ and (Mn_0.28Fe_0.54) [Mn_0.72Fe_1.46]O₄ at sonication time 20 min and 80 min, respectively. The value of the saturation magnetization was increased from 1.9 emu/g to 52.5 emu/g with increase of sonication time 20 min to 80 min at constant 50% amplitude of ultrasonic power input, whereas, it was increased from 30.2 emu/g to 59.4 emu/g with increase of the percentage amplitude of ultrasonic power input at constant sonication time 60 min. The highest value of dielectric constant (ε′) was 499 at 1 kHz for nanoparticles at sonication time 20 min, whereas, ac conductivity was 368 × 10⁻⁹ S/cm at 1 kHz for spinel ferrite nanoparticles at sonication time 20 min. The demonstrated controllable physical characteristics over sonication time and percentage amplitude of ultrasonic power input are a key step to design spinel ferrite material of desired properties for specific application. The investigation of microwave operating frequency suggest that these prepared spinel ferrite nanoparticles are potential candidate for fabrication of devices at high frequency applications.     

Synthesis and magnetic properties of the size-controlled Mn-Zn ferrite nanoparticles by oxidation method

Size-controlled Mn_0.67Zn_0.33Fe₂O₄ nanoparticles in the wide range from 80 to 20 nm have been synthesized, for the first time, using the oxidation method. It has been demonstrated that the particle size can be tailor-made by varying the concentration of the oxidant. The magnetization of the 80 nm particles was 49 A m² kg⁻¹ compared to 34 A m² kg⁻¹ for the 20 nm particles. The Curie temperatures for all the samples are found to be within 630±5 K suggesting that there is no size-dependent cation distribution. The critical particle size for the superparamagnetic limit is found to be about 25 nm. The effective magnetic anisotropy constant is experimentally determined to be 7.78 kJ m⁻³ for the 25 nm particles, which is about an order of magnitude higher than that of the bulk ferrite.     

Preparation and characterization of complex ferrite nanoparticles by a polymer-pyrolysis route

The polymer-pyrolysis route used in this work was to synthesize the copolymeric precursor of the mixed metallic ions and then to pyrolyze the precursor into complex spinel ferrite nanoparticles. Thermogravimetric analysis (TGA) showed that the complex ferrite nanoparticles could be obtained by calcination of their precursors at 500°C. The structures, elemental analyses and particle morphology of the as-calcined products were characterized by powder X-ray diffraction (XRD), ICP-AES, transmission electron microscope (TEM) and electron diffraction (ED) pattern. The results revealed that the as-calcined powders were complex spinel ferrites and the size of those nanoparticles ranged from 10 to 20 nm. Magnetic measurements were carried out at room temperature using a vibrating sample magnetometer (VSM). The saturation magnetization of the Mn–Zn ferrites was related to the molar ratio of Mn to Zn and increased with the increase of Mn. The complex Co–Mn–Zn ferrite nanoparticles showed a high magnetization of 58 emu/g at the applied field of 10 kOe and a low coercivity of 30 Oe, which indicated that this materials exhibited characteristics of soft ferromagnetism.