Abstract:In the present study, spinel structure CoFe2O4 nanoparticles were successfully synthesized by the sol‐gel auto‐combustion technique. The effect of apple cider vinegar (ACV) addition as an organic biocompatible agent on the size, morphology, and magnetic properties of CoFe2O4 nanoparticles was investigated in detail. The phase evolution, particle size, and lattice parameter changes of the synthesized phase have been estimated by using Rietveld structure refinement analysis of X‐ray powder diffraction data. Also… Show more
“…Changes in the curve are thought to be due to the sintering temperature which has exceeded its temperature (520℃) [7] thereby reducing Mr and HC; the change was due to the transition from a single domain to multi-domain [14]. The transition change was caused by the critical diameter of CoFe2O4 that was 40 nm according to Figure 7, and thus, after passing the critical diameter, the coercivity was reduced [24,25].…”
Cobalt ferrite or CoFe2O4 has unique physical and magnetic properties depend on its synthesis method. The application of cobalt ferrite as nanomedicine material become more interesting, however analysis on physical and magnetic properties based on synthesis method have not been discussed. The cobalt ferrite in this research was synthesised using two different methods: the sol-gel with duration sintering variations of 500℃, 800℃, and 1100℃ and unsintered sonochemical. The phase identification analysis and crystal size used XRD and morphology analysis used SEM, the functional group bond analysis used FTIR, and magnetic property analysis used VSM. The smallest crystal size from the XRD result was 13.25 nm with 57.04% crystallinity. The morphology from the synthesized cobalt ferrite was mostly agglomerated. The FTIR showed functional group vibration at 601-636 cm -1 that signified the spinel structure of the cobalt ferrite. There was a change of hysteresis loop curve from hard magnetic to soft magnetic, and there was a sample with a paramagnetic curve.
“…Changes in the curve are thought to be due to the sintering temperature which has exceeded its temperature (520℃) [7] thereby reducing Mr and HC; the change was due to the transition from a single domain to multi-domain [14]. The transition change was caused by the critical diameter of CoFe2O4 that was 40 nm according to Figure 7, and thus, after passing the critical diameter, the coercivity was reduced [24,25].…”
Cobalt ferrite or CoFe2O4 has unique physical and magnetic properties depend on its synthesis method. The application of cobalt ferrite as nanomedicine material become more interesting, however analysis on physical and magnetic properties based on synthesis method have not been discussed. The cobalt ferrite in this research was synthesised using two different methods: the sol-gel with duration sintering variations of 500℃, 800℃, and 1100℃ and unsintered sonochemical. The phase identification analysis and crystal size used XRD and morphology analysis used SEM, the functional group bond analysis used FTIR, and magnetic property analysis used VSM. The smallest crystal size from the XRD result was 13.25 nm with 57.04% crystallinity. The morphology from the synthesized cobalt ferrite was mostly agglomerated. The FTIR showed functional group vibration at 601-636 cm -1 that signified the spinel structure of the cobalt ferrite. There was a change of hysteresis loop curve from hard magnetic to soft magnetic, and there was a sample with a paramagnetic curve.
“…The spinel ferrites have a cubic unit cell containing 56 atoms, where 32 of them are oxygen anions, and the other 24 atoms are metallic cations of which only eight occupy tetrahedral sites (A-site) while the other 16 atoms occupy octahedral sites (B-site) [ 12 , 13 ]. Among spinel ferrite nanoparticles, pure cobalt ferrite and its substituted compounds have attracted the considerable attention of numerous researchers in recent decades due to the reliable saturation magnetization ( M s ) [ 14 ], moderate magnetocrystalline anisotropy ( K ) [ 15 , 16 ], high coercivity ( H c ) [ 17 ], high Curie temperature ( T c ) [ 18 ], and thermal stability [ 19 , 20 ]. It is accepted that the chemical, electrical, and magnetic properties of cobalt ferrite nanoparticles are dependent on the chemical composition, cation distribution in the two sub-lattices of A- and B-sites, morphology, surface properties, and preparation method [ 21 , 22 , 23 , 24 ].…”
In recent years, cobalt ferrite has attracted considerable attention due to its unique physical properties. The present study aimed to produce cobalt ferrite magnetic nanoparticles doped with zinc and vanadium using the sol-gel auto-combustion method. For this purpose, Co1-xZnxFe2-yVyO4 (where x = 0.0, 0.1, 0.2, 0.5 and y = 0.00, 0.05, 0.15, 0.25) precursors were calcined at 800 °C for 3h. The prepared samples were characterized with the X-ray diffraction (XRD) method in combination with Rietveld structure refinement, field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR), and vibrating sample magnetometery (VSM). The XRD patterns confirmed the formation of crystalline spinel structure for all samples. However, the diffraction peaks of hematite and iron vanadium oxide phases were observed in the patterns of some doped samples. The average crystallite size for all the synthesized samples was found to be in the range of ~45–24 nm, implying that it decreased by simultaneously doping cobalt ferrite with Zn and V. The FT-IR spectrum confirmed the formation of the spinal structure of ferrite through the observed vibrational bands assigned to the tetrahedral (υ2) and octahedral (υ1) interstitial complexes in the spinel structure. The FE-SEM images showed that morphology, average grain size, and agglomeration of the synthesized powders were affected by doping, which was due to the interactions of the magnetic surface of nanoparticles. The VSM curves demonstrated that saturation magnetization and coercivity values changed in the range of 30–83 emu/g and from 27–913 Oe, respectively. These changes occurred due to the alteration in cation distribution in the spinel structure. This can be attributed to the change in superexchange interactions between magnetic ions by co-substitution of Zn and V ions in Cobalt ferrite and the changes in magnetocrystalline anisotropy.
“…Magnetic nanomaterials have attracted lots of attention during the recent past thanks to their wide range of application in various industries and biomedical premises 1‐6 . As an illustration, magnetic materials have been utilized in the batteries, electrical display, molecular electrical parts, nonlinear optical materials, sensors, electromagnetic shielding materials, and microwave absorption agent, etc M‐type hexaferrites (AFe 12 O 19 ) are a group of complex oxide materials, where A is most often Ba or Sr The structure of M hexaferrites (BaFe 12 O 19 ) consists of R and S blocks.…”
In this study, magnesium‐zirconium–substituted M‐type barium hexaferrites BaFe12‐2xMg+xZrxO19 (BFMZO, 0.25 ≤ x ≤ 1.5) nanoparticles were successfully synthesized by sol‐gel autocombustion technique. On one hand, the effects of Mg‐Zr substitution concentration on the magnetic features of doped magnetic nanoparticles were investigated which showed that increasing the doping concentration causes the saturation magnetization to decrease. On the other hand, the influence of the different layer thicknesses (2, 3, and 4 mm) of BFMZO on the microwave absorption was investigated in X‐band frequencies (8‐12 GHz). Absorption results showed that increasing the film thickness from 2 to 3 mm causes microwave absorption to increase. Moreover, the morphological study reveals that aggregation percentage decreased when the substitution concentration increased. Therefore, size, magnetic, and absorption properties are tunable by substitution concentration.
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