Table of Contents Author Guidelines Submit a Manuscript
Journal of Nanomaterials
Volume 2014 (2014), Article ID 452468, 7 pages
Research Article

Enhanced Magnetization of Sol-Gel Synthesized Pb-Doped Strontium Hexaferrites Nanocrystallites at Low Temperature

1Department of Physics and Astronomy, College of Science, King Saud University, P.O. Box 800, Riyadh 11421, Saudi Arabia
2Centre of Excellence in Solid State Physics, University of the Punjab, Lahore 54590, Pakistan
3Department of Physics, School of Science and Engineering (SSE), Lahore University of Management Sciences (LUMS), Lahore 54792, Pakistan
4Department of Chemical Engineering, College of Engineering, King Saud University, P.O. Box 800, Riyadh 11421, Saudi Arabia
5Interdisciplinary Research Centre in Biomedical Materials (IRCBM), COMSATS Institute of Information Technology, Defence Road, Off Raiwind Road, Lahore 54600, Pakistan
6Industrial Catalysts Research Chair, King Saud University, Riyadh 11421, Saudi Arabia

Received 24 January 2014; Revised 1 May 2014; Accepted 3 May 2014; Published 27 May 2014

Academic Editor: Debasis Dhak

Copyright © 2014 Shahid M. Ramay et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Effect of Pb doping on the structural and low temperature magnetic properties of (), synthesized by sol-gel autocombustion technique, has been investigated. The powder samples were sintered at 800°C for 2 h in order to develop the stable hexagonal phase, characteristic of the SrFe12O19 structure. The consequences of Pb substitution (at iron sites) on various structural parameters like lattice constants, unit cell volume, crystallite size, and porosity have been discussed. Fourier transform infrared frequency bands were utilized to determine the formation of tetrahedral and octahedral clusters of M-type ferrites. Hexagonal texture of the grains, a characteristic of the hexagonal crystal structure of SrFe12O19, was refined by Pb substitution. The magnetic properties, determined using a vibrating sample magnetometer, revealed that saturation magnetization decreased, while coercivity was increased with the increase of Pb contents. However, the increased squareness ratio and hence the energy product motivate the utilization of these ferrite compositions where hard magnetic characteristics are required. The increased values of saturation magnetization were observed at reduced temperature of 200 K, attributable to the better spin alignments of individual magnetic moments at low temperature.

1. Introduction

M-type hexagonal ferrites belong to immensely valuable class of magnetic materials, with a host of applications ranging from simple permanent magnets used in electric motors to modern day applications, for instance, as radar wave absorbing materials. Owing to its high values of saturation magnetization and coercivity [1], strontium hexaferrite, in particular, is a very important member of this class of magnetic materials, being widely used in telecommunication [2], magnetooptic recording media, microwave devices [3], and electronic industry [4]. Various preparation techniques like coprecipitation process, molten salt method, solid state reaction method [5], double sintering ceramic technique [6], microwave-induced combustion process, sol-gel based synthesis routes [7], and so forth have been adopted by the researchers to refine the astonishing structural and magnetic properties of these ferrites. However, sol-gel based autocombustion route, being easier, energy efficient, and cheaper, has emerged as a novel technique to prepare single phase strontium hexaferrites. The crystal structure of SrFe12O19 is hexagonal which has a great influence on valuable characteristics of these ferrites. One-unit cell of these ferrites is composed of 64 ions that are distributed in such a way that these form two formula units, each having one spinel S-block and one hexagonal R-block [2]. The Fe3+ ions are oriented on five different crystallographic sites in the unit cell. These ions are the major cause of magnetism in these ferrites, resulting in net magnetic moment of 20  per formula unit [8, 9].

Ferrimagnetic strontium hexaferrites are n-type semiconductor with band gap energy of 0.6 eV. Researchers are attempting to improve the intrinsic properties of these ferrites for innovations. For this purpose, introduction of some divalent or trivalent dopant element and optimization of preparation technique play a vital role. Diamagnetic Pb ions, substituted at Fe sites with spin up, could enhance the hard magnetic characteristics of SrFe12O19 when doped stoichiometrically. Hence, it has been understood as a quite suitable dopant choice for these ferrites to improve not only the structural properties but also the magnetic properties [2, 3, 8]. In the present work, we have successfully employed sol-gel based autocombustion technique to prepare the ferrite samples in phase-pure form to investigate the structural and low temperature magnetic properties of Pb-doped strontium hexaferrites for use in devices that work efficiently with high values of coercivity and electrical devices that show minimum energy losses at higher applied frequencies.

2. Experimental

Single phase polycrystalline samples with compositions ( were prepared by a novel sol-gel based autocombustion route. A transparent homogenous solution was obtained by dissolving stoichiometric proportions of analytical grade strontium nitrate (Sigma Aldrich), iron (III) nitrate (Sigma Aldrich), lead (II) nitrate (Sigma Aldrich), and citric acid (Avonchem, UK) in 50 mL of deionized water. The relative molar concentrations of citric acid, used as a fuel, and metal nitrates were in the ratio of 2 : 1. The solution was placed over a hot plate, positioned in a fume hood. The temperature of the hot plate was gradually increased to 90°C. The solution was continuously stirred using a magnetic stirrer at 500 rpm, for about 1 h, until it converted into a soft gel. At that instance, the rotator was stopped and the stirrer was removed from the gel. The temperature of the gel was increased in steps up to 300°C. As the gel was heated at this temperature for about 15 min., it burnt suddenly and vigorously and converted into soft and fluffy powder. The product was grinded to get homogenously mixed powder samples. All the samples were synthesized using the same procedure and sintered at 800°C for 2 h in order to get hexagonal ferrite phases. X-ray diffraction (XRD) was used to investigate the crystal structure of the prepared samples. The thermogravimetric/differential (TG/DTA) analysis was performed using EXSTAR SII TG/DTA 7300 analyzer in order to investigate any weight loss of the samples at high temperatures. The powder samples were then pelletized and surface morphology was analyzed using a JSM-6610 Oxford (with EDX attachment) scanning electron microscope (SEM). Energy dispersive X-ray spectroscopy (EDX) was performed to get quantitative analysis of the samples. The formation of chemical bonds in the desired crystal phase was confirmed by Fourier transform infrared spectroscopy (FTIR). Magnetic behavior of the samples was analyzed using a 14 Tesla Quantum design PPMS (Physical Properties Measurement System).

3. Results and Discussion

Crystal structure of all the prepared samples was determined by X-ray diffraction, following the complete procedure as described by Cullity [10]. Data obtained from the diffractometer was plotted. Positions of the diffracted intensities were noted and corresponding values of sin2θ were evaluated. These values were multiplied by 1/3, 1/4, and 1/7 in order to find a repeated number named “” related to the lattice parameter “” and wavelength () of the incident radiation by the relation . Using this relation, value of “” was evaluated for 200 plane. The relation was used to find a parameter, “” and hence the lattice constant, “,” using the expression . hkl values corresponding to all the diffracted intensities were determined and the patterns were indexed as shown in Figure 1. The indexing of the patterns revealed that crystal structures of all the samples exhibit characteristic hexagonal structure. In addition, the indexed peaks were also matched with the standard data (ICSD-00-033-1340), which confirmed that samples revealing hexagonal structure consisted of M-type strontium hexaferrites. TGA was performed up to 800°C with a heating rate of 20°C/min. to determine any carbon related species that may be present in the samples due to reaction of Sr2+ with CO2 which may be available from the atmosphere and/or from the decomposition of citric acid. Figure 2 shows the %age weight loss for the four samples from room temperature to 800°C. The curves reveal a good stability and do not indicate any significant weight loss. Hence, it is inferred that no carbon related species are present in the prepared samples and sintering of samples at 800°C is sufficient to hinder the formation of SrCO3 enabling the Sr2+ available to stimulate the incorporation of Sr2+ into strontium hexaferrite matrix [11]. Slight increase in the lattice parameters “” and “” was observed that led to a minute increase in the unit cell volume as well. The trend might be attributed to the larger ionic radius of the substituent, Pb2+ (0.98 Å) as compared to the host, Fe3+ (0.49 Å). The crystallite sizes of all the samples evaluated using Scherrer’s relation (, is a constant, is full width at half maximum in radians, and is diffraction angle in degrees) were increased slightly as the Pb concentration was increased in the series. The bulk density () was calculated from the weight and dimensions of the sintered pellets using the relation , where is the mass, is the radius, and is the thickness of the samples. X-ray density () of the samples was calculated using the relation [12], where is the molecular weight of the composition, is Avogadro’s number, and is the lattice constant. The bulk and X-ray densities were used to calculate the porosity . The values of all these structural parameters have been shown in Table 1. The results reveal that porosity of the samples was decreased as the Pb contents were substituted at the Fe sites in the series of the samples. In other words, the grains became more compact and densified with the Pb substitution which could play a significant role in establishing the structural and magnetic properties.

Table 1: Values of lattice constants, their axial ratio, unit cell volume (), crystallite size (), bulk density (), X-ray density (), porosity (), saturation magnetization (), remanence (), , and coercivity () at (, 0.1, 0.2, 0.3, and 0.4).
Figure 1: X-ray diffraction patterns of () sample.
Figure 2: TGA spectra of () samples.

Figure 3 shows the FTIR spectra of all the prepared samples. In ferrites, the spectroscopically active region lies between 400 cm−1 and 800 cm−1 [13]. In our samples, there were sharp and clear peaks at 600 cm−1, 550 cm−1, and 440 cm−1, corresponding to the characteristics peaks of chemical bonds in SrFe12O19 structure [14]. The peak intensity remained almost the same as the amount that Pb dopant was increased by in the series, which indicated that Pb could be successfully substituted in a dilute amount at the Fe sites, without disturbing the stoichiometry of the parent hexagonal SrFe12O19 structure. With the increase in Pb contents, the chemical polarization of the internal bonds could be shared in the form of Fe-O-Pb and Sr-O-Pb chemical bonds, resulting in compact structures as that of SrFe12O19. The peaks at 3421 cm−1 and 1639 cm−1 exhibit the structure and bending bonds of the surface hydrogen group (–OH) earned from the damped environment [15].

Figure 3: FTIR spectra of () samples.

Figure 4 shows the microstructural morphology of the samples obtained using a scanning electron microscope. Figure 4(a) reveals the micrograph of pure SrFe12O19 sample indicating that most of the grains are like platelets having sharp grain boundaries. A close look at this image might provide hindsight of the hexagonal texture of the grains, a characteristic of the hexagonal crystal structure of the SrFe12O19. With the substitution of Pb contents at Fe sites, the microstructural morphology of the grains was further refined until at  Pb contents; well defined hexagonal grains were witnessed which were varying in size ranging from 0.190 to 0.291 μm. The uniform grain sizes and homogeneous contrast throughout the focused area confirm that the sample consists of single phase ferrite composition. The shape and compatibility of grains play a vital role in determining the structural and magnetic properties of ferrites [16]. The platelet-like hexagonal texture of ferrites has been investigated as a potential candidate for use in microwave absorbing coatings [17]. The elemental composition of the constituents elicited from EDX, shown in the inset of Figures 4(a) and 4(d), confirms the stoichiometric ratio of the elements in the prepared samples and the incorporation of Pb at Fe sites. The quantitative data of atomic and percentage composition of elements was in close agreement with the dissolved reactants.

Figure 4: SEM micrographs of () samples.

Figure 5 shows the magnetic-hysteresis (M-H) loops of the prepared samples obtained at 300 K. Magnetic parameters like saturation magnetization (), remanence (), and coercivity () were determined from M-H loops as listed in Table 1. The and values as a function of Pb contents have been plotted in Figure 6. The plots reveal that the substitution of Pb contents at A-site of Fe changes the magnetic properties of the ferrite samples in a remarkable way. The and values of the ferrite samples were decreased from 63.22 to 41.62 emu/g and 33.03 to 23.66 emu/g, respectively, whereas the value was increased from 2360 to 6015 Oe with the increase in the Pb contents. However, the ratio was observed to increase from 0.52 to 0.57 in the series, as the decrease in value is less prominent as the corresponding decrease in the value, making the later samples in the series more effective, as far as energy product is concerned. The value of at is in close agreement with a recently reported value [18]. The crystal structure has been understood as a critical factor which decides the magnetic behavior of the material. The crystal structure of SrFe12O19 has five nonequivalent sublattices with three octahedral (2a, 12k, and 4f), one tetrahedral (4f1), and one trigonal bipyramidal (2b) sites [19]. Among these, three sites (2a, 12k, and 2b) possess upward spin and two sites (4f1 and 4f2) spin downward. Hence, net magnetic moment results due to upward spins. When Pb with a diamagnetic nature is substituted with some of the iron ions, a decrease in the net saturation magnetization is observed which decreases further as the Pb contents are increased up to . This decrease in value could be attributed to the decrease of superexchange interactions among , as the substituted ions prefer to occupy the octahedral 12k site which has upward spin [20], followed by 2a and 4f2 sites [19]. Each Fe3+ ion possesses a magnetic moment of 5 . Therefore, an M-type molecule of SrFe12O19 possesses a magnetic moment of 20.6 . The substitution of a diamagnetic ion at a site with spin up reduces the total magnetic moment of the specimen and hence the values decrease.

Figure 5: M-H loops of () samples at 300 K.
Figure 6: and as a function of Pb contents at Fe sites in at 300 K.

The increase in with the increase in Pb contents may be described on the basis of Stoner-Wohlfarth relation, = 2, where is magnetocrystalline anisotropy and is permittivity of free space (). Hence, a decrease in and an increase in [21] are the possible factors for an increased value of .

Figure 7 shows the M-H loops of the samples at 200 K. The and values of all the samples increased as compared to their corresponding values at 300 K in the series, with the decrease in temperature, as has been plotted in Figure 8 and listed in Table 1, but decreased with the increase of Pb contents in the series. The increase in as a function of Pb contents at 200 K (Figure 7) could also be explained as discussed earlier. The increased values of at 200 K might be described on the basis of Weiss theory of ferromagnetism [22]. According to this theory, at low temperatures, the thermal activation energy of the magnetic ions reduces which in turn helps the magnetic moments to align more easily in the applied field direction. Therefore, an overall increase in the magnetic moment and hence in the is observed. The increased squareness ratio () in this case as well favors the use of these materials for the applications where high energy products are desired.

Figure 7: M-H loops of ( samples at 200 K.
Figure 8: and as a function of Pb contents at Fe sites in at 200 K.

4. Conclusion

In this paper, the influence of Pb doping on the structural and low temperature magnetic behavior of () has been investigated systematically. X-ray diffraction analysis of all the samples revealed the hexagonal phase characteristics of the SrFe12O19 crystal structure. A slight increase in the lattice constants ( and ) and the unit cell volume was attributed to the larger ionic radii of dopant Pb as compared to the host Fe site. The crystallite size was also increased in the series as the Pb contents were increased. The porosity was decreased from 39.53 to 33.04% in the series making the samples more compact to improve the structural and hence the magnetic properties. FTIR spectroscopy confirmed the metal-oxygen bonds formation in the hexagonal structure of the samples. Surface morphology has been described using SEM images and elemental stoichiometric composition has been found using EDX spectroscopy. Saturation magnetization was found to decrease, while coercivity was increased with the increase of Pb contents in the series at 300 K. When temperature was reduced to 200 K, the saturation magnetization of the relevant samples was increased, credited to the preferred individual spin alignments at low temperature. Remanence was also decreased, but the corresponding effect was less prominent as the and consequently the energy product was found to increase, corroborating the use of these ferrite compositions where hard magnetic characteristics are required.

Conflict of Interests

The authors declare that they have no conflict of interests regarding the publication of this paper.


The authors extend their appreciation to the Deanship of Scientific Research at King Saud University for funding the work through the research group project no. RGP-VPP-106.


  1. Y.-P. Fu and C.-H. Lin, “Fe/Sr ratio effect on magnetic properties of strontium ferrite powders synthesized by microwave-induced combustion process,” Journal of Alloys and Compounds, vol. 386, no. 1-2, pp. 222–227, 2005. View at Publisher · View at Google Scholar · View at Scopus
  2. Z. Ullah, S. Atiq, and S. Naseem, “Influence of Pb doping on structural, electrical and magnetic properties of Sr-hexaferrites,” Journal of Alloys and Compounds, vol. 555, pp. 263–267, 2013. View at Google Scholar
  3. I. V. Zavislyak, M. A. Popov, and G. Srinivasan, “A cut-off millimeter wave resonator technique for mapping magnetic parameters in hexagonal ferrites,” Measurement Science and Technology, vol. 20, no. 11, Article ID 115704, 2009. View at Publisher · View at Google Scholar · View at Scopus
  4. S. Hussain and A. Maqsood, “Structural and electrical properties of Pb-doped Sr-hexa ferrites,” Journal of Alloys and Compounds, vol. 466, no. 1-2, pp. 293–298, 2008. View at Publisher · View at Google Scholar · View at Scopus
  5. S.-D. Kim and J.-S. Kim, “Magnetic properties of Sr-ferrites synthesized in molten (NaCl + KCl) flux,” Journal of Magnetism and Magnetic Materials, vol. 307, no. 2, pp. 295–300, 2006. View at Publisher · View at Google Scholar · View at Scopus
  6. S. Hussain and A. Maqsood, “Thermal transport properties of silica added Sr-hexa ferrites as a function of temperature,” Materials Letters, vol. 62, no. 6-7, pp. 1002–1005, 2008. View at Publisher · View at Google Scholar · View at Scopus
  7. L. You, L. Qiao, J. Zheng, M. Jiang, L. Jiang, and J. Sheng, “Magnetic properties of La-Zn substituted Sr-hexaferrites by self-propagation high-temperature synthesis,” Journal of Rare Earths, vol. 26, no. 1, pp. 81–84, 2008. View at Publisher · View at Google Scholar · View at Scopus
  8. M. J. Iqbal and S. Farooq, “Extraordinary role of Ce-Ni elements on the electrical and magnetic properties of Sr-Ba M-type hexaferrites,” Materials Research Bulletin, vol. 44, no. 11, pp. 2050–2055, 2009. View at Publisher · View at Google Scholar · View at Scopus
  9. C. M. Fang, F. Kools, R. Metselaar, G. De With, and R. A. De Groot, “Magnetic and electronic properties of strontium hexaferrite SrFe12O19 from first-principles calculations,” Journal of Physics Condensed Matter, vol. 15, no. 36, pp. 6229–6237, 2003. View at Publisher · View at Google Scholar · View at Scopus
  10. B. D. Cullity, Elements of X-Ray Diffraction, Addison-Wesley, 2nd edition, 1978.
  11. R. M. Garcia, E. R. Ruiz, and E. E. Rams, “Structural characterization of low temperature synthesized SrFe12O19,” Materials Letters, vol. 50, no. 2-3, pp. 183–187, 2001. View at Google Scholar · View at Scopus
  12. J. Smit and H. P. J. Wijn, Ferrites, John Wiley & Sons, New York, NY, USA, 1959.
  13. X. Yang, Q. Li, J. Zhao, B. Li, and Y. Wang, “Preparation and magnetic properties of controllable-morphologies nano-SrFe12O19 particles prepared by sol-gel self-propagation synthesis,” Journal of Alloys and Compounds, vol. 475, no. 1-2, pp. 312–315, 2009. View at Publisher · View at Google Scholar · View at Scopus
  14. T. Xie, L. Xu, and C. Liu, “Synthesis and properties of composite magnetic material SrCoxFe12-xO19 (x = 0-0.3),” Powder Technology, vol. 232, pp. 87–92, 2012. View at Google Scholar
  15. S. Kong, P. Zhang, X. Wen et al., “Influence of surface modification of SrFe12O19 particles with oleic acid on magnetic microsphere preparation,” Particuology, vol. 6, no. 3, pp. 185–190, 2008. View at Publisher · View at Google Scholar · View at Scopus
  16. M. Ahmad, R. Grossinger, M. Kriegisch, F. Kubel, and M. U. Rana, “Characterization of Sr-substituted W-type hexagonal ferrites synthesized by sol-gel autocombustion method,” Journal of Magnetism and Magnetic Materials, vol. 332, pp. 137–145, 2013. View at Google Scholar
  17. J. Xu, H. Zou, H. Li, G. Li, S. Gan, and G. Hong, “Influence of Nd3+ substitution on the microstructure and electromagnetic properties of barium W-type hexaferrite,” Journal of Alloys and Compounds, vol. 490, no. 1-2, pp. 552–556, 2010. View at Publisher · View at Google Scholar · View at Scopus
  18. F. S. Jesus, A. M. Bolarin-Miro, C. A. Cortes-Escobedo, R. Valenzuela, and S. Ammar, “Mechanosynthesis, crystal structure and magnetic characterization of M-type SrFe12O19,” Ceramics International, vol. 40, no. 3, pp. 4033–4038, 2014. View at Google Scholar
  19. S. Singhal, T. Namgyal, J. Singh, K. Chandra, and S. Bansal, “A comparative study on the magnetic properties of MFe12O19 and MAlFe11O19 (M = Sr, Ba and Pb) hexaferrites with different morphologies,” Ceramics International, vol. 37, no. 6, pp. 1833–1837, 2011. View at Publisher · View at Google Scholar · View at Scopus
  20. M. J. Iqbal, M. N. Ashiq, P. Hernandez-Gomez, and J. M. Munoz, “Synthesis, physical, magnetic and electrical properties of Al-Ga substituted co-precipitated nanocrystalline strontium hexaferrite,” Journal of Magnetism and Magnetic Materials, vol. 320, no. 6, pp. 881–886, 2008. View at Publisher · View at Google Scholar · View at Scopus
  21. D. Y. Chen, Y. Y. Meng, D. C. Zeng, Z. W. Liu, H. Y. Yu, and X. C. Zhong, “CTAB-assisted low-temperature synthesis of SrFe12O19 ultrathin hexagonal platelets and its formation mechanism,” Materials Letters, vol. 76, pp. 84–86, 2012. View at Google Scholar
  22. P. Weiss, “L'hypothèse du champ moléculaire et la propriété ferromagnétique,” Journal of Physics, Theory Applications, vol. 6, no. 4, pp. 661–690, 1907. View at Google Scholar