- Research article
- Open Access
Influence of calcination temperature on structural and magnetic properties of nanocomposites formed by Co-ferrite dispersed in sol-gel silica matrix using tetrakis(2-hydroxyethyl) orthosilicate as precursor
© Gharagozlou et al 2011
Received: 24 January 2011
Accepted: 13 April 2011
Published: 13 April 2011
Effects of calcination temperatures varying from 400 to 1000°C on structural and magnetic properties of nanocomposites formed by Co-ferrite dispersed in the sol-gel silica matrix using tetrakis(2-hydroxyethyl) orthosilicate (THEOS) as water-soluble silica precursor have been investigated. Studies carried out using XRD, FT-IR, TEM, STA (TG-DTG-DTA) and VSM techniques. Results indicated that magnetic properties of samples such as superparamagnetism and ferromagnetism showed great dependence on the variation of the crystallinity and particle size caused by the calcination temperature. The crystallization, saturation magnetization Ms and remenant magnetization Mr increased as the calcination temperature increased. But the variation of coercivity Hc was not in accordance with that of Ms and Mr, indicating that Hc is not determined only by the crystallinity and size of CoFe2O4 nanoparticles. TEM images showed spherical nanoparticles dispersed in the silica network with sizes of 10-30 nm. Results showed that the well-established silica network provided nucleation locations for CoFe2O4 nanoparticles to confinement the coarsening and aggregation of nanoparticles. THEOS as silica matrix network provides an ideal nucleation environment to disperse CoFe2O4 nanoparticles and thus to confine them to aggregate and coarsen. By using THEOS as water-soluble silica precursor over the currently used TEOS and TMOS, the organic solvents are not needed owing to the complete solubility of THEOS in water. Synthesized nanocomposites with adjustable particle sizes and controllable magnetic properties make the applicability of Co-ferrite even more versatile.
Magnetic nanocomposites consisting of spinel ferrite nanoparticles in a non magnetic SiO2 matrix exhibit interesting properties arising in size effects and magnetic interactions [1–5]. Among them, CoFe2O4-SiO2 magnetic nanocomposites have high potential for applications as magnetic fluids , drug delivery , and high density information storage  due to remarkable properties of bulk cobalt ferrite (high saturation magnetization and coercivity, strong anisotropy, mechanical hardness and chemical stability) , combined with the magnetic properties characteristic of nanoparticles, which depend strongly on particle shape and size, particle-matrix interactions and degree of dispersion throughout the matrix. Recently, cobalt ferrite nanoparticles were also known to be a photomagnetic material that shows a remarkable light induced coercivity change [10–12].
Based on the above technological challenge and scientific importance, researches such as ceramic method , sol-gel , co-precipitation , solvent evaporation , hydrothermal , combustion , microemulsion  and citrate methods  have been made into various synthesis routes of nanocrystalline ferrites. In the earlier report, cobalt ferrite nanoparticles have been synthesized by the polymeric precursor method . While the nanoparticles obtained usually have a strong tendency to aggregate, this makes it very difficult to exploit their unique physical properties . To reduce the unwanted crystallite coarsening and particles aggregation, attempts have been made to synthesize nanocomposites by embedding ferrite nanoparticles in a suitable matrix . Different matrixes such as resins , polymer films  and silica glasses [26, 27] have been studied. Studies on magnetic nanocomposites of ferrite nanoparticles dispersed in the silica matrix [28, 29] have revealed a behavior different from that of bulk systems.
Among various synthetic routes, sol-gel process has proved to be an efficient method to prepare ultra-fine particles dispersed in different matrices. Through this method, a good control of the sample morphology, texture, structure, and chemical composition can be attained by carefully monitoring the preparation parameters. The size and morphology of the nanoparticles and their properties may be controlled by modifying the composition of the nanocomposites and by thermal treatment conditions . This is the reason why the sol-gel synthesis method has gone an intensive development.
Tetraalkoxysilanes (tetramethoxysilane, TMOS and tetraethoxysilane, TEOS) are common precursors to synthesize silicate. Their hydrolysis in aqueous solutions and further polycondensation reactions cause formation of sol particles of which the cross-linking leads to the self-organization into a porous three-dimensional network in the bulk. In view of the fact that tetraalkoxysilanes are poor-water soluble compounds, methanol or ethanol is generally added to avoid the phase separation [31, 32]. This problem has been countered by the use of polyol silicates possessing improved water solubility  I. Gill and A. Ballesteros, Encapsulation of biologicals within silicate, siloxane, and hybrid sol-gel polymers: an efficient and generic approach. J. Am. Chem. Soc. (1998), pp. 8587-8598. TMOS and TEOS, as shown recently in , can be also exchanged for tetrakis(2-hydroxyethyl) orthosilicate (THEOS). This completely water-soluble precursor forms nanocomposite monolithic material in aqueous solutions in the absence of added alcohol.
In this paper, effects of calcination temperature on structural and magnetic properties of cobalt ferrite nanocomposites in silica matrix prepared by sol-gel method using tetrakis(2-hydroxyethyl) orthosilicate (THEOS) as silica precursor have been reported aiming at tuning the magnetic properties of CoFe2O4 nanoparticles dispersed in a sol gel silica matrix and greatly expanding the range of applications by adjusting the calcination temperature. Also, FT-IR and thermal analysis (TG-DTG-DTA) of the alcogel precursor have been carried out. Therefore, special attention is given to the correlation between the structural and magnetic properties of CoFe2O4 nanoparticles embedded in THEOS as silica precursor for different calcination temperatures.
All the chemicals were of analytical grade and used without any further purification. Nanocomposites of cobalt ferrite dispersed in a silica matrix were prepared by sol-gel process using tetrakis(2-hydroxyethyl) orthosilicate (THEOS) as a water-soluble silica precursor of silica and metallic nitrates as precursors of the ferrite. The THEOS:H2O and Fe:Co molar ratios were controlled at 1:5 and 2:1, respectively. The weight ratio of nanocomposites was 30 wt.% CoFe2O4 in the silica matrix. The sol was prepared by dissolving Fe(NO3)3.9H2O and Co(NO3)2.6H2O in deionized water, followed by the addition of the aqueous solution of THEOS. After vigorous stirring for 1 h, the sol was allowed to gel at room temperature for some days in a partially closed glass vessel. The obtained alcogel was put into an oven for further drying at 110°C for 24 h to obtain the xerogel. The xerogel was calcined at different temperatures varying from 400 to 1000°C for 2 h with a heating rate of 10°C/min in ambient atmosphere.
X-ray diffraction (XRD) patterns were collected using a Philips PNA-analytical diffractometer with CuKα radiation. FT-IR spectra (500-4000 cm-1) were recorded on a Perkin Elmer Spectrum One spectrophotometer with KBr pellets. Thermal analyses (TG-DTG-DTA) including the thermogravimetery (TG), derivative thermogravimetery (DTG) and differential thermal analysis (DTA) were carried out using a Perkin Elmer simultaneous thermal analyzer (STA Pyris Diamond Model) with the heating rate of 5°C/min in flowing air. The TEM images and selected area electron diffraction (SAED) pattern were recorded on a Philips CM 200 FEG transmission electron microscope. Magnetic measurements were carried out at room temperature using a vibrating sample magnetometer (VSM).
Results and Discussion
X-ray diffraction (XRD) analysis
Our results showed that with increasing calcination temperature, the intensity of peaks increases and the diffraction peaks become sharper and narrower. This indicates the enhancement of the crystallinity which originated from the increment of the crystalline volume ratio due to the size enlargement of the nuclei [35, 36]. The full-width at half maximum (FWHM) of the diffraction peaks decreases with increasing calcination temperature discloses that the average crystallite size is becoming bigger correspondingly. The very broad peak at 2θ of around 23° in XRD patterns of all samples was attributed to the characteristic diffraction peak of the amorphous SiO2 matrix.
All of the diffraction peaks confirmed the formation of the pure single-phase cobalt ferrite with the face-centered cubic spinel phase and Fd3 m (2 2 7) space group. No diffraction peaks of impurities were observed in the patterns. It showed that in comparison with the previous report using TEOS as a silica precursor , Co-ferrites with more crystallinity have been successfully synthesized at lower calcination temperatures under current mild experimental conditions.
The increase of the calcination temperature results in sharper peaks with the increased intensity and higher crystallization without changes in the obtained phases.
Crystallite size and magnetic properties of the nanocomposite samples calcined at different temperatures varying from 400 to 1000°C.
Crystallite size (nm)
Coercivity Hc (Oe)
where t is the crystallite size, λ the wavelength of X-ray radiation (CuKα), θ the Bragg angle and β is the full width at half maximum (FWHM) of the most intense diffraction peak (311). The crystallinity and crystallite size increase at higher calcination temperatures, indicating that the silica network plays an important role in restricting the growth and aggregation of Co-ferrite nanoparticles.
In IR spectra of samples calcined at different temperatures varying from 400 to 1000°C, the intensities of the broad bands associated with the absorbed water are drastically weakened. Also, the disappearance of the absorption at 1384 cm-1 could be ascribed to the complete decomposition of the nitrate species after calcination, as confirmed by the thermal analysis. The band at 605 cm-1 assigned to the Si-O-Fe vibration increases in intensity with increasing the calcination temperature, which can be ascribed to the enhanced interactions between CoFe2O4 particles and the silica matrix . The characteristic absorptions for the silica network slightly increased in intensity with increasing calcination temperature. With increasing the calcination temperature the intensity of ≡Si-O-Si≡ absorption band of the SiO4 tetrahedron of the silica network at 1079 cm-1 increases.
Transmission electron microscopy (TEM) analysis
It can be observed that the values of Ms and Mr were increased by increasing the temperature from 400 to 1000°C which arising from spin non-colinearity at the surface of the crystals. The changes in the magnetic properties of the samples can be attributed to the modification of the crystallinity and crystallite sizes dependent on the calcination temperature. The energy of a magnetic particle in the external field is proportional to its particle sizes via the number of molecules in a single magnetic domain. Therefore, the decrease of the Ms values with the decrease of particle sizes can be attributed to surface effects that are the result of finite-size scaling of nanocrystallites .
It can be observed that the Ms and Mr values for samples calcined at different temperatures were increased by increasing the temperature (Figure 5). This type of behavior is entirely consistent with a model of particle growth in the system in such a way that differences in the magnetic parameters are associated with changes in the particle size . The variation of coercivity Hc was not in accordance with that of Ms and Mr, indicating that Hc is not determined only by the size of nanoparticles. Hc values were significantly less than previous reports using TEOS as a silica precursor [37, 40]. Therefore changes in magnetic properties such as superparamagnetism and ferromagnetism of samples can be recognized by the modification of the crystallinity and crystallite sizes dependent on the calcination temperature . The lower Ms values related to the particles with the smaller size could be attributed to the surface distortion due to the interaction of transition metal ions in the spinel lattice with the oxygen atoms, which can reduce  the net magnetic moment in the particle. This effect is particularly prominent for the ultrafine particles due to their large surface to volume ratio. Finite size effects have been reported as being responsible for the reduction of the saturation magnetization of nanoparticles .
It is found that the M-H curves of samples calcined at 400-600°C take on incomplete reversibility, and corresponding Mr values is about 0.01 emu/g, which means that samples are superparamagnetic. When the calcination temperature is up to or above 800°C, typical saturated hysteresis loops can be observed. For samples calcined at 400-600°C, the size of most nanoparticles is smaller than the critical size to remain ferromagnetic; hence they will show superparamagnetic behavior. However, if the calcination temperature is increased until the size of most nanocrystallites exceeds the critical size, there will be noncoherent magnetization change in the nanoparticles themselves, and sample shows ferromagnetic properties. Therefore, we can change the calcination temperature of nanocomposites to achieve ideal magnetic properties and behavior. Calcination temperatures at 400-600°C can be applied if samples used in areas such as ferrofluid technology which CoFe2O4 should be of superparamagnetic.
In summary, the influence of the calcination temperature on the magnetic properties and crystallinity of cobalt ferrite nanocomposites successfully synthesized by sol-gel method using tetrakis(2-hydroxyethyl) orthosilicate (THEOS) have been investigated with the aim of tuning the magnetic properties and greatly expanding the range of applications. The tetrakis(2-hydroxyethyl) orthosilicate as silica matrix network provides an ideal nucleation environment to disperse CoFe2O4 nanoparticles and thus to confine them to aggregate and coarsen. By using THEOS as precursor over the currently used TEOS and TMOS, the organic solvents are not needed owing to the complete solubility of THEOS in water. Particle sizes of the samples increased with the calcination temperature. Our results showed that the magnetic properties of the nanocomposite samples were strongly affected by the calcination temperature as a consequence of the gradual increase in the crystallinity and particle size. The saturation magnetization for all the samples was lower than that of the CoFe2O4 bulk phase owing to the particle sizes obtained. Therefore, size-adjustable and magnetic controllable cobalt ferrite nanoparticles were obtained by embedding CoFe2O4 particles in the amorphous silica network and controlling suitable calcination temperature. The magnetic properties of the synthesized nanocomposites indicate that these materials have good potential for important technological applications, e.g. in ferrofluid technology, bioprocessing and magneto-optical devices.
It would be acknowledged that this work was supported by the National Elite Foundation. We are also grateful to the Institute for Color Science and Technology for their support.
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