Preparation and magnetic properties of nano size nickel ferrite particles using hydrothermal method
© Nejati et al 2012
Received: 17 December 2011
Accepted: 30 March 2012
Published: 30 March 2012
Nickel ferrite, a kind of soft magnetic materials is one of the most attracting class of materials due to its interesting and important properties and has many technical applications, such as in catalysis, sensors and so on. In this paper the synthesis of NiFe2O4 nanoparticles by the hydrothermal method is reported and the inhibition of surfactant (Glycerol or Sodium dodecyl sulfate) on the particles growth is investigated.
For investigation of the inhibition effect of surfactant on NiFe2O4 particles growth, the samples were prepared in presence of Glycerol and Sodium dodecyl sulfate. The X-ray powder diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometer (VSM) and inductively coupled plasma atomic emission spectrometer (ICP-AES) techniques were used to characterize the samples.
The results of XRD and ICP-AES show that the products were pure NiFe2O4 and also nanoparticles grow with increasing the temperature, while surfactant prevents the particle growth under the same condition. The average particle size was determined from the Scherrer's equation and TEM micrographs and found to be in the range of 50-60 nm that decreased up to 10-15 nm in presence of surfactant. The FT-IR results show two absorption bands near to 603 and 490 cm-1 for the tetrahedral and octahedral sites respectively. Furthermore, the saturated magnetization and coercivity of NiFe2O4 nanoparticles were in the range of 39.60 emu/g and 15.67 Qe that decreased for samples prepared in presence of surfactant. As well as, the nanoparticles exhibited a superparamagnetic behavior at room temperature.
Nanosized nickel ferrite particles were synthesized with and without surfactant assisted hydrothermal methods. The results show that with increasing of temperature, the crystallinity of nanoparticles is increased. In the presence of surfactants, the crystallinity of NiFe2O4 nanoparticles decreased in comparison with surfactant- free prepared samples. All of the nickel ferrite nanoparticles were superparamagnetic at room temperature.
Nanosized spinel ferrite particles, a kind of soft magnetic materials with structural formula of MFe2O4 (M = divalent metal ion, e.g. Mn, Mg, Zn, Ni, Co, Cu, etc.), are one of the most attracting class of materials due to their interesting and important properties such as low melting point, high specific heating, large expansion coefficient, low saturation magnetic moment and low magnetic transition temperature, etc.[1, 2]. Because of these properties, the spinel ferrites have many technical applications, such as in photoelectric devices  catalysis , sensors , nano devices , microwave devices [7, 8] and magnetic pigments .
Remarkable electrical and magnetic properties of ferrites depend upon the nature of the ions, their charges and their distribution among tetrahedral (A) and octahedral (B) sites . Nickel ferrite is one of the versatile and technologically important soft ferrite materials because of its typical ferromagnetic properties, low conductivity and thus lower eddy current losses, high electrochemical stability, catalytic behavior, abundance in nature, etc. This ferrite is an inverse spinel in which eight units of NiFe2O4 go into a unit cell of the spinel structure. Half of the ferric ions preferentially fill the tetrahedral sites (A-sites) and the others occupy the octahedral sites (B-sites) . Thus the compound can be represented by the formula (Fe3+) A [Ni2+Fe3+]BO42- . The synthesis of spinel ferrite nanoparticles has been intensively studied in the recent years and the principal role of the preparation conditions on the morphological and structural features of the ferrites is discussed [13–16]. Large-scale applications of ferrites with small particles and tailoring of specific properties have prompted the development of widely used chemical methods, including hydrothermal , sonochemical reactions , sol-gel methods, microwave plasma , co-precipitation , microemulsion methods , citrate precursor techniques  and mechanical alloying  for the fabrication of stoichiometric and chemically pure spinel ferrite nanoparticles. The hydrothermal route is one of the most commonly used techniques owing to its economics and high degree of compositional control. In addition, the hydrothermal synthesis does not require extremely high-processing temperature or sophisticated processing. For example, ferrites can be prepared via the hydrothermal route at a temperature of ~150°C, whereas the solid state method requires a temperature of 800°C .
In this work, nano crystalline nickel ferrite, NiFe2O4, was successfully prepared via reaction between metal chlorides in ethylacetate solution with and without surfactant assisted processes. Investigations on the particle size, morphology and magnetic properties of inverse spinel nickel ferrite in at different conditions are carried out by the XRD, FT-IR, TEM, ICP-AES and VSM techniques.
Results and discussion
The samples (a) and (b) that prepared without surfactant at 45 and 80°C, consisted of amorphous solids which have not been detected by XRD technique. This may be related to the formation of amorphous state of nickel, iron oxides and or NiFe2O4 nanoparticles. Weak diffraction peaks in the samples (c) and (d), prepared without surfactant at 100 and 130°C, were attributed to the effect of increasing of temperature on the improvement of crystalline properties of amorphous nickel ferrite and also the conversion of some Ni and Fe oxides to produce nickel ferrite crystallites. Increasing of temperature up to 150°C led to the formation of well crystalline nickel ferrite (sample e). As Figure 2 shows, in the presence of surfactants (glycerol and sodium dodecyl sulfate) at 150°C in samples (f) and (g), crystallinity of NiFe2O4 nanoparticles was decreased in comparison with surfactant- free prepared samples .
The crystallite size (D) of the NiFe2O4 present in the samples (c-g)
Table 1 shows that with increase in the temperature from 100°C to 150°C in samples (c-e), the average size of NiFe2O4 nanoparticles also increases that can be attributed to the temperature assists crystal growth and/or the redistribution of cations among octahedral and tetrahedral sites . Additionally, Figure 2 shows that in the presence of surfactant about samples (f and g), diffraction peak (311) is broad and therefore smaller NiFe2O4 nanoparticles are formed. This fact may be due to the role of surfactants in the decrease of the agglomeration of particles . From the ICP-AES result, the atomic ratio of Ni- Fe is 0.49, which is close to that of NiFe2O4.
Morphology and microstructure
The observed values of saturation magnetization and the coercivity of NiFe2O4 nanoparticles
It is obvious from Table 2 that: (a) the values of saturation magnetization for NiFe2O4 nanoparticles are significantly lower than the multidomain bulk particles (55 emu/g). Smit and Wijn have reported Ms equal to 50 emu/g for bulk nickel ferrite particles . Nathani and Misra have measured Ms equal to 25 emu/g for NiFe2O4 nanoparticles with size 8 nm . (b) The amounts of Ms and Hc for samples (g and f) are equal to 34.45-35.10 emu/g and 0.60-0.64Oe respectively, which increase to 39.60 emu/g and 15.67 Qe for sample (e). In fact, the magnetic behavior of nickel ferrite nanoparticles is very sensitive to the crystallinity and particle size. The increase in saturation magnetization was most likely attributed to the increasing of crystallinity and particle size of the samples  and can be explained on the basis of changes in exchange interactions between tetrahedral and octahedral sub-lattices. In case of nickel ferrite, any configuration of Ni2+ and Fe3+ ions in both octahedral and tetrahedral sites, tends to increase the net magnetization per formula unit . On the other hand, variation of coercivity with particle size can be explained on the basis of domain structure, critical diameter, strains, magneto crystalline anisotropy and shape anisotropy of crystal . Therefore the magnetic behavior of nano-size nickel ferrites can be a collective effect of these interactions .
Nanosized nickel ferrite particles were synthesized with and without surfactant assisted hydrothermal methods. The FT-IR spectra showed two characteristic metal oxygen vibrational bands. The average particle size of samples was in the range of 12-53 nm, as revealed by XRD and TEM techniques. The temperature rise up to 150°C led to the increasing of crystallinity of nanoparticles. In the presence of surfactants, the crystallinity of NiFe2O4 nanoparticles decreased in comparison with surfactant- free prepared samples. All of the nickel ferrite nanoparticles were superparamagnetic at room temperature. The saturation magnetization and coercivity values were found to be low, which attributed to the various parameters such as crystallinity and particle size. The saturation magnetization and coercivity were reduced with decreasing of crystallinity and particle size of nanoparticles.
NiCl2.6H2O, FeCl3.6H2O, NaOH, Triethyl amine, Ethyl acetate, Glycerol and Sodium dodecyl sulfate were purchased from Merck chemical company and were used as received without further purification. The deionized water used in all experiments, had a conductivity of less than 10-6 Scm-1.
A 0.4 M (25 mL) solution of iron chloride (FeCl3.6H2O) and a 0.2 M (25 mL) solution of nickel chloride (NiCl2.6H2O) in double distilled deionized water were mixed with vigorous stirring. 5 M triethyl amine in ethylacetate solution was used to adjust the pH at 10. The mixture was heated at different temperatures (45, 80, 100, 130 and 150°C) for 18 h. Hydrothermal synthesis at 100, 130 and 150°C, were carried out in a Teflon-lined autoclave reactor. The black precipitate was filtered off, washed with deionized water and dried in a vacuum oven at 70°C for 3 h. Also we prepared NiFe2O4 nanoparticles via surfactant assisted process. 0.078 M of surfactant (Glycerol or Sodium dodecyl sulfate) was dissolved in 35 mL deionized water and was added to the solution of salts under vigorous stirring. Adjustment of pH and other processes were performed as above at 150°C.
Infrared spectra were recorded in the range of 400-4000 cm-1 with a Bruker vector 22 FT-IR spectrometer from samples in KBr pellets. The structural characterization was performed using Brucker AXS (model D8 Advance) X-ray powder diffractometer (Cu Kα radiation source, λ = 0.154 nm) with the Bragg angle ranging from 10-70° generated at 40 kV and 35 mA at room temperature. Transmission electron microscopy (TEM) analysis was performed using Cambridge, stereo scan 360, 1990, 100 kV accelerating voltage. The magnetic measurements were carried out at room temperature by using a vibrating sample magnetometer, model VSM, BHV-55, Riken Japan with a magnetic field up to 8 kQe. Inductively coupled plasma atomic emission spectrometer (ICP-AES) was carried out on a Thermo Fisher Scientific ICP-IRIS Advantage.
The author thanks the Payame Noor University, Tabriz center for the financial support of project.
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