Effect of surfactants (PVB/EDTA/CTAB) assisted sol-gel synthesis on structural,magnetic and dielectric properties of NiFe2O4 nanoparticles

Nanocrystalline NiFe₂O₄ was synthesized by sol-gel route using various surfactants such as PVP, EDTA and CTAB. The effect of different surfactants on structure, magnetic and dielectric properties of the NiFe₂O₄ nanoparticles (NPs) were investigated. The prepared samples were inspected by XRD, HRSEM, and TEM. Powder XRD studies confirmed the realization of single crystalline cubic structure of the NiFe₂O₄ nanoferrites. The addition of surfactants significantly modified the crystallite size of the final products. Dielectric features of NiFe₂O₄ NPs were slightly modified with different surfactants. The magnetic results revealed an enormous decrease in coercivity and a moderate reduction in the saturation magnetization when EDTA and CTAB were used as compared to PVP. The present results declare that the adding of various surfactants in the sample preparation controls the size of NiFe₂O₄ NPs and thus noticeably influences the magnetic parameters.     

Synthesis and characterization of monodisperse NiFe2O4 nanoparticles

Narrow size distribution nickel ferrite nanoparticles with average particle size of around 6 nm has been synthesized via rapid thermo-decomposition method in the presence of oleylamine in solution which acted as neutralizing, stabilizing and reducing agent OAm coated NiFe₂O₄ NPs. X-ray powder diffraction (XRD), Fourier Transform Infrared Spectra (FT-IR), Thermal Gravimetric Analysis (TGA), Scanning Electron Microscopy (SEM), Transmission electron microscopy (TEM), Vibrating Simple Magnetometer (VSM) and also Mössbauer Spectroscopy were used for structural, morphological, spectroscopic and magnetic characterization of the product. The XRD analysis revealed the formation of single phase nickel ferrite with Fd-3m space group. Both FT-IR and TGA analyses confirmed the formation of desired nanocomposite. FT-IR analysis also showed characteristic IR absorption bands of the spinel nickel ferrite phase and oleylamine. TEM and SEM analysis showed that product have almost spherical structural morphology. TEM images showed that NiFe₂O₄ nanoparticles have narrow size distribution and Energy Dispersive X-ray (EDX) analysis confirmed the presence of metal ions in the required stoichiometric ratio. Superparamagnetic property of the product was confirmed by VSM. From ⁵⁷Fe Mössbauer spectroscopy data, the variation in line width, isomer shift, quadrupole splitting and hyperfine magnetic field values have been determined. The Mössbauer spectra for OAm coated NiFe₂O₄ NPs. is consisting of one paramagnetic central doublets and one magnetic Zeeman sextet. Finally, the synthetic procedure can be extended to the preparation of high quality metal or alloy nanoparticles.     

Magnetic resonance of the NiFe2O4 nanoparticles in the gigahertz range

We report an adjustable magnetic resonance frequency from 1.45 to 2.54 GHz for NiFe₂O₄ nanoparticles which were prepared by a sol–gel process. X-ray diffraction and scanning electron microscopy results indicate that the samples are polycrystalline nanoparticles, and the size of the particles increases obviously with the thermal treatment temperature. The consequence of the surface composition suggests that the oxygen defects are present in the nanoparticle surface, and this surface magnetic state can show a strong surface anisotropy. With decreasing size of the particle, the surface magnetic effect is predominant, resulting in an increase of resonance frequency for NiFe₂O₄ nanoparticles. This finding provides a new route for NiFe₂O₄ materials that can be used in the gigahertz range.     

Effect of TiN content on properties of NiFe2O4-based ceramic inert anode for aluminum electrolysis

NiFe₂O₄-based ceramic inert anodes for aluminum electrolysis doped with various TiN nanoparticles were prepared by a two-step cold-pressing sintering process to investigate how TiN affected the sintering behavior and properties of the composites. The differential scanning calorimetry-thermogravimetry (DSC-TG), X-ray diffraction (XRD), and microstructure analysis results indicated that the Ti and N were evenly distributed in the NiFe₂O₄ matrix to form a solid solution. The maximum linear shrinkage and linear shrinkage rate were enhanced with the increase of TiN nanoparticles contents, and the sintering activation energy of initial stage was lowered from 382.63 to 279.58 kJ mol⁻¹ with the TiN nanoparticles additive range from 0 to 9 wt%. When the content of TiN nanoparticles was 7 wt%, the relative density, bending strength, and elastic modulus reached their maximum values of 97.24%, 73.88 MPa, and 3.77 GPa, respectively, whereas the minimum static corrosion rate of NiFe₂O₄-based ceramic of 0.00114 g cm⁻² h⁻¹ was obtained, mainly attributed to the relatively dense and stable microstructure. The electrical conductivity of NiFe₂O₄-based ceramics presented a clear ascending trend with increasing TiN nanoparticles content and elevated temperature, attributed to the increased concentration and migration rate of carrier.     

NiFe<Subscript>2</Subscript>O<Subscript>4</Subscript>@SiO<Subscript>2</Subscript> Nanoparticles Stabilized by Porous Silica Shells

Abstract  

NiFe₂O₄ nanoparticles stabilized by porous silica shells (NiFe₂O₄@SiO₂) were prepared using a one-pot synthesis and characterized for their physical and chemical stability in severe environments, representative of those encountered in industrial catalytic reactors. The SiO₂ shell is porous, allowing transport of gases to and from the metal core. The shell also stabilizes NiFe₂O₄ at the nanoparticle surface: NiFe₂O₄@SiO₂ annealed at temperatures through 973 K displays evidence of surface Ni, as verified by H₂ TPD analyses. At 1,173 K, hematite forms at the surface of the metallic cores of the NiFe₂O₄@SiO₂ nanoparticles and surface Ni is no longer observed. Without the silica shell, however, even mild reduction (at 773 K) can draw Fe to the surface and eliminate surface Ni sites.     

Histidine-Assisted Synthesis and Cellular Compatibility of Magnetic Cobalt Oxide Nanoparticles at Room Temperature

Magnetic nanoparticles (NPs) of cobalt oxide (Co₃O₄) with the diameter of 20–40 nm have been prepared by a simple liquid deposition method in the Histidine (His) assistance at room temperature. Ethanol plays an important role in the preparation of cobalt oxide NPs with a polycrystalline structure. The growth mechanism for Co₃O₄ cube particles has been preliminarily explained. The hysteresis loop of NPs reveals their good magnetic property indicating that they can be used in hyperthermia, cell separation etc. These applications need the magnetic particles with cytocompatible properties. The analysis of IR spectrum, TG curve and HRTEM image indicated that cobalt oxide particles was conjugated with the His molecules. Escherichia coli (E. coli) and L929 cells tests suggest a good cellular compatibility at a concentration of less than 0.25 mg/mL, indicating that the prepared Co₃O₄ NPs have a potential for several biomedical applications.     

Effects of morphology on the electrochemical performance of NiFe2O4 nanoparticles with battery-type behavior

We report the synthesis of NiFe₂O₄ nanoparticles by the complexation EDTA-citrate method under acidic (pH = 3) and basic (pH = 9) conditions. The structural, optical, vibrational, magnetic, and electrochemical properties were studied. The samples have crystallite sizes of 21 nm (pH 3) and 73 nm (pH 9), with rounded particles and layered structures. The ⁵⁷Fe Mössbauer spectra at 12 K showed that both samples had an inverse spinel cation distribution. At 5 K, the sample prepared at pH 9 showed saturation magnetizations of about 50 emu/g. Raman spectra showed typical bands of NiFe₂O₄ phase. The materials were tested as electrodes under alkaline condition. The cyclic voltammetry and charge-discharge experiments indicated a battery-type behavior, with maximun capacities of 65 and 5 C/g (at specific currents of 3 and 10 A/g) for samples prepared at pH 9 and 3, respectively. This work offers a route for obtaining NiFe₂O₄ nanoparticles with different morphologies and sizes tuned by the synthesis conditions.     

NiFe2O4/SiO2 nanostructures as a potential electrode material for high rated supercapacitors

Engineered materials are crucial for the higher efficiency of supercapacitors. Current work presents roughly shaped spherical NiFe₂O₄ nanoparticles dispersed in the SiO₂ matrix NiFe₂O₄/SiO₂ as a newfangled electrode material for supercapacitors with remarkable performance. Designing the NiFe₂O₄/SiO₂ nanostructure with a sol-gel method followed by the Stober method to grow silica has instigated NiFe₂O₄/SiO₂ as dynamic material with higher electrochemical activity. Physicochemical aspects of NiFe₂O₄/SiO₂ nanostructures are evaluated using Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, and transmission electron microscopy analysis. The electrochemical activity is evaluated by cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) representing the comparable efficiency and reversibility of the electrode materials. The prepared electrode shows a capacitance of 925 F/g (154.1 mAh/g or 555 C/g) at 1 A/g, with 95.5% capacitance retention after 5000 cycles at 20 mA/cm². The improved electrochemical performance of the NiFe₂O₄/SiO₂ electrode can be subjected to prompt diffusion process provided by NiFe₂O₄/SiO₂ and enhanced redox reactions owing to the high surface area. The mentioned features decrease the total impedance of the electrodes as suggested by electrochemical impedance spectroscopy (EIS).     

Bimagnetic hard/soft and soft/hard ferrite nanocomposites: Structural,magnetic and hyperthermia properties

Recent studies show that the chemical composition and shape of magnetic nanoparticles (NPs) play an important role in their properties. In particular, the bimagnetic NPs display useful and in many cases, more interesting properties than single-phase NPs. In this work, we prepared Fe₃O₄ and CoFe₂O₄ cube-like NPs and bimagnetic hard/soft (CoFe₂O₄/Fe₃O₄) and soft/hard (Fe₃O₄/CoFe₂O₄) nanocomposites (core/coating) using a facile and eco-friendly co-precipitation method that allows the synthesis of the cube-like NPs at temperatures near room temperature. The phase purity and the crystallinity of the NPs with a spinel structure were confirmed by the X-ray diffraction and infrared spectra techniques. Transmission electron microscopy (TEM) images revealed that the NPs have a cubic-like shape with an average dimension of 20 nm. Energy dispersive X-ray analysis, Mössbauer spectroscopy and SQUID magnetic measurements indicated the co-existence of Fe₃O₄ and CoFe₂O₄ phases in nanocomposites. In addition, the hysteresis loops exhibited a single-phase behavior in the nanocomposites that indicates there is a good exchange-coupling interaction between the hard and soft magnetic phases. The CoFe₂O₄/Fe₃O₄ nanocomposites presented a larger saturation magnetization than the CoFe₂O₄ NPs that is effective for their use in magnetic hyperthermia. Finally, we studied the hyperthermia properties of samples in an alternating magnetic field with a frequency of 276 kHz and field amplitude of 13.9 kA/m. Our results showed that magnetic hyperthermia efficiency simultaneously depends on the composition of samples along with magnetic anisotropy and saturation magnetization.     

Sol–gel mediated surface modification of nanocrystalline NiFe2O4 spinel powders with amorphous SiO2

Surface modification of nanocrystalline NiFe₂O₄ spinel particles with amorphous SiO₂ by the sol–gel process at 350 °C was demonstrated. Amorphous phase of the SiO₂ layer was evaluated by X-ray diffraction technique. Structural coordination of the pristine and SiO₂ coated NiFe₂O₄ particles as investigated by employing FTIR analysis. Thickness of the SiO₂ layer was investigated through transmission electron microscopy and it was identified to be ～10–23 nm over nanocrystalline NiFe₂O₄ particles. The magnetic behavior of pristine and surface modified NiFe₂O₄ particles were investigated using vibrating sample magnetometer (VSM). Magnetic studies showed the retention of magnetic property of surface modified NiFe₂O₄ particles with the reduced saturation magnetization and coercivity compared to the pristine NiFe₂O₄ particles, which is respectively due to the lower fraction of the magnetic component and the formation of interfacial structure.     

Polypyrrole/NiFe2O4 composites with improved hexavalent chromium removal from aqueous solution

Polypyrrole/NiFe₂O₄ (PPy/NiFe₂O₄) composites were prepared by ultrasonic oxidative polymerization in the presence of NiFe₂O₄ nanoparticles (NPs). The nanostructure of PPy/NiFe₂O₄ was confirmed by the X‐ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), and vibrating sample magnetometer (VSM) examinations. The adsorption of Cr(VI) onto the PPy/NiFe₂O₄ composite was lowly pH dependent and the adsorption kinetics followed the Pseudo‐second‐order model. The Langmuir isothermal model well described the adsorption isotherm data and the maximum adsorption capacity increased with the increase of temperature. The maximum adsorption capacity of the PPy/NiFe₂O₄ for Cr(VI) ions was up to 50 mg/g at pH 2.0. The excellent adsorption characteristic of PPy/NiFe₂O₄ composite will render it a highly efficient and economically viable adsorbent for Cr(VI) ions removal. POLYM. COMPOS., 38:2779–2787, 2017. © 2015 Society of Plastics Engineers     

Synthesis and rheological characterization of nano-magnetorheological fluid using inverse spinel ferrite (NiFe2O4)

In recent years, the utilization of nanoparticles for nano-magnetorheological fluid (NMRF) synthesis is gaining popularity in automotive applications. From this perspective, the nickel ferrite (NiFe₂O₄) nanoparticles were prepared by gel burning method and characterized using the X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy-energy dispersive X-ray analysis (FESEM-EDX), and vibration sample magnetometer (VSM). The XRD and FTIR results showed the phase formation and characteristic metal–oxygen M–O vibrations. The FESEM images showed quasi-spherical crystallites with considerable agglomeration. The magnetic properties measured showed the ferromagnetic nature of NiFe₂O₄. The nanosized NiFe₂O₄ was used for NMRF preparation and characterization.     

Improved magnetic and electromagnetic absorption properties of xSrFe12O19/(1−x)NiFe2O4 composites

xSrFe₁₂O₁₉/(1−x)NiFe₂O₄ composites (0 ≤ x ≤ 1.0) were synthesized by using a conventional solid-state synthetic route. The results show that magnetic hysteresis loops of the xSrFe₁₂O₁₉/(1−x)NiFe₂O₄ composites are similar to those of individual component ferrites, except for the 0.1SrFe₁₂O₁₉/0.9NiFe₂O₄ and 0.3SrFe₁₂O₁₉/0.7NiFe₂O₄, suggesting that the hard/soft magnetic phases are well exchange-coupled. The saturation magnetization, coercivity, and remanent magnetization of the xSrFe₁₂O₁₉/(1−x)NiFe₂O₄ composites are increased with increasing content of SrFe₁₂O₁₉, with maximal values of 42.1 Am² kg⁻¹, 78.7 kA m⁻¹, 17.2 Am² kg⁻¹, respectively, as the content x is about 0.5. They are higher than those of the individual components, implying that interface coupling is present in the magnetic composites. The coercivity and remanent magnetization of the composites are increased initially with increasing sintering temperature and then show a downward tendency. For the component SrFe₁₂O₁₉ and NiFe₂O₄, the minimum reflection losses are −12.5 dB and −18.3 dB at match thicknesses of 2.5 mm and 2 mm, respectively. Compared with those of the component SrFe₁₂O₁₉ and NiFe₂O₄, the microwave absorption performances of the xSrFe₁₂O₁₉/(1−x)NiFe₂O₄ composites are improved remarkably, especially for the samples of x = 0.3 and x = 0.9. The minimum reflection losses values of the 0.3SrFe₁₂O₁₉/0.7NiFe₂O₄ composite are −31.6 dB (12.7 GHz) and −20.2 dB (13 GHz), while those of the 0.9SrFe₁₂O₁₉/0.1NiFe₂O₄ composites are −23.7 dB (16.3 GHz) and −33.5 dB (15.8 GHz), as the matching thicknesses are 2.5 mm and 2 mm, respectively. Therefore, the xSrFe₁₂O₁₉/(1−x)NiFe₂O₄ composites could be used as potential microwave absorption materials.     

A self‐repairing cermet anode: Preparation and corrosion behavior of (Cu–Ni–Fe)/NiFe2O4 cermet with synergistic action

In this paper, the cermet (Cu–Ni–Fe)/(NiFe₂O₄–10NiO) anodes were prepared through the powder metallurgy method, followed by being evaluated in the bench scale (200 A) electrolysis tests for more than 1000 hour. The results showed that the as‐prepared anodes exhibited excellent corrosion resistance with corrosion rate less than 0.99 cm/a, which satisfied the requirements of the aluminum industry. The analysis results were confirmed by SEM, EDS, and XRD. The results showed that the outstanding corrosion resistance of the anodes relied on a continuous and dense NiFe₂O₄ film formed on the surface of the anode material, which protected the inner structure of anode material during electrolysis. Finally, a model based on the synergistic action between the metal phase and the ceramic phase was built to illustrate the forming mechanism of the NiFe₂O₄ passivating film.     

Synthesis of magnetically separable core–shell structured Ni<Subscript>x</Subscript>Fe<Subscript>1−x</Subscript>Fe<Subscript>2</Subscript>O<Subscript>4</Subscript>@TiO<Subscript>2</Subscript> nanoparticles photocatalysts for the degradation of organic dyes

In this paper, the core–shell structured NiFe₂O₄@TiO₂ nanoparticles and nanochains as photocatalysts were successfully prepared through hydrothermal and hydrolysis method. The as-prepared core–shell structure was composed of a magnetic NiFe₂O₄ core and photocatalytic titanium oxide coating shell. SEM and TEM images characterized the morphology of NiFe₂O₄@TiO₂ nanoparticles. Moreover, the results of XRD patterns proved that the TiO₂ coating shell consisted of anatase. The VSM measurements showed that the saturation magnetization values of NiFe₂O₄ and NiFe₂O₄@TiO₂ nanoparticles was 65 and 53 emu/g, respectively. The photocatalyst of NiFe₂O₄@TiO₂ nanoparticles exhibited the outstanding recyclable performance for RhB. And, the photo_degradation ration of maintained 69 % after the photocatalyst experienced ten photocatalysis experiments, which is better than that of Fe₃O₄@TiO₂ photocatalysts.     

Preparation,characterization and electromagnetic properties of polyaniline/carbon nanotubes/nickel ferrite nanocomposites

New electromagnetic nanocomposites were prepared from polyaniline (PANI)/oxidized single‐walled carbon nanotubes (OxSWCNTs)/NiFe₂O₄ by in situ polymerization of aniline using hexanoic acid as a soft template. OxSWCNT and NiFe₂O₄ were prepared first so as to be used in the formulation of PANI composites. Transmission electron microscope (TEM) results revealed the formation of PANI nanoparticles of 60 nm diameter, OxSWCNT of 24 nm, and NiFe₂O₄ of 54 nm. Also, TEM image of the ternary composite indicated agglomerative coating of PANI appearing as a gray shells and black core of NiFe₂O₄ with widening the diameter of OxSWCNT to be around 66 nm. Dc conductivity was measured as a function of temperature. Magnetic susceptibility was measured as a function of temperature and magnetic field intensity. All samples revealed NiFe₂O₄‐dependent ferromagnetism. The activation energies for dc conductivity suggest that the conductivity is owing to hopping conduction mechanism. A synergistic effect between NiFe₂O₄ and PANI/OxSWCNT is observed. POLYM. COMPOS.,, 2012. © 2012 Society of Plastics Engineers     

Effect of Mg doping on magnetic,and dielectric properties of NiCr2O4 nanoparticles

The structural, magnetic, and dielectric properties of spinel Magnesium (Mg) doped Nickel chromite (NiCr₂O₄) nanoparticles (NPs) have been studied in detail. The X-ray powder diffraction exhibited normal spinel phase formation of Mg_xNi_1-xCr₂O₄ (x = 0, 0.2, 0.4, 0.6, and 1) NPs with a maximum average crystallite size of about 44 nm for x = 0.2 composition. The FTIR spectra of these NPs revealed the characteristic Ni–O and Mg–O and Cr–O bands around 639 cm^?1 and 497 cm^?1, respectively which confirmed the spinel structure. Temperature-dependent zero field cooled and field cooled graphs of NiCr₂O₄ NPs showed phase changes from ferrimagnetic to paramagnetic state at 86 K, while MgCr₂O₄ NPs showed antiferromagnetic (AFM) transition at Neel temperature (T_N) at 15 K due to corner-sharing of Cr³⁺ ions at a tetrahedral lattice site resulting in a highly magnetic frustrated structure. The field dependent magnetization (M ? H) loops of Mg_xNi_1-xCr₂O₄ NPs confirmed the competing AFM interactions and ferrimagnetic interactions resulting in a sharp decreased saturation magnetization with Mg doping. Dielectric constant, dielectric loss, and ac conductivity of these NPs showed size-dependent variation and depicted maximum value at x = 0.2 Mg concentration. In summary, the magnetic and dielectric properties of Mg doped NiCr₂O₄ NPs were modified by variations in the average crystallite size and magnetic exchange interactions, which may be suitable for different technological applications.     

Study on performance of magnetic fluorescent nanoparticles as gene carrier and location in pig kidney cells

We evaluated the performance of green fluorescent magnetic Fe₃O₄ nanoparticles (NPs) as gene carrier and location in pig kidney cells. When the mass ratio of NPs to green fluorescent protein plasmid DNA reached 1:16 or above, DNA molecules can be combined completely with NPs, which indicates that the NPs have good ability to bind negative DNA. Atomic force microscopy (AFM) experiments were carried out to investigate the binding mechanism between NPs and DNA. AFM images show that individual DNA strands come off of larger pieces of netlike agglomerations and several spherical nanoparticles are attached to each individual DNA strand and interact with each other. The pig kidney cells were labelled with membrane-specific red fluorescent dye 1,1^′-dioctadecyl-3,3,3^′,3^′-tetramethylindocarbocyanine perchlorate and nucleus-specific blue fluorescent dye 4^′,6-diamidino-2-phenylindole dihydrochloride. We found that green fluorescent nanoparticles can past the cell membrane and spread throughout the interior of the cell. The NPs seem to locate more frequently in the cytoplasm than in the nucleus.     

Synthesis and Characterization of Multiwall-Carbon Nanotubes Decorated with Nickel Ferrite Hybrid

Acid functionalized multiwall carbon nanotube, (MWCNT)-COOH/nickel ferrite (NiFe₂O₄), magnetic hybrids were synthesized by a co-precipitation method. X-ray diffraction, Fourier transform infrared spectrometry, thermal gravimetry, transmission electron microscopy, vibrating sample magnetometry and Impedance Spectroscopy were used to characterize the physical and electrical properties of the MWCNT-COOH/NiFe₂O₄ hybrid. NiFe₂O₄ NPs are stably attached to the surface of via carboxyl groups (COOH). The magnetic saturation value of the product was found as 8 emu/g. A tunneling conduction mechanism was believed to occur in the hybrid. The real modules (M′) of the product illustrate power law variation with a power exponent of approximately unity. These magnetic MWCNT-COOH/NiFe₂O₄ hybrids exhibit a promising prospective in the application of bio-nanoscience and technology.     

Magnetic resonance imaging of glioma with novel APTS-coated superparamagnetic iron oxide nanoparticles

We report in vitro and in vivo magnetic resonance (MR) imaging of C6 glioma cells with a novel acetylated 3-aminopropyltrimethoxysilane (APTS)-coated iron oxide nanoparticles (Fe₃O₄ NPs). In the present study, APTS-coated Fe₃O₄ NPs were formed via a one-step hydrothermal approach and then chemically modified with acetic anhydride to generate surface charge-neutralized NPs. Prussian blue staining and transmission electron microscopy (TEM) data showed that acetylated APTS-coated Fe₃O₄ NPs can be taken up by cells. Combined morphological observation, cell viability, and flow cytometric analysis of the cell cycle indicated that the acetylated APTS-coated Fe₃O₄ NPs did not significantly affect cell morphology, viability, or cell cycle, indicating their good biocompatibility. Finally, the acetylated APTS-coated Fe₃O₄ nanoparticles were used in magnetic resonance imaging of C6 glioma. Our results showed that the developed acetylated APTS-coated Fe₃O₄ NPs can be used as an effective labeling agent to detect C6 glioma cells in vitro and in vivo for MR imaging. The results from the present study indicate that the developed acetylated APTS-coated Fe₃O₄ NPs have a potential application in MR imaging.