scholarly journals Synthesis of SrFe12O19 by sol-gel method and its morphology and magnetic properties

2016 ◽  
Vol 19 (3) ◽  
pp. 5-10
Author(s):  
Quynh Anh Bao Le ◽  
Vu Hoang Nguyen ◽  
Hoang Thi Thuy Tran ◽  
Ha Ky Phuong Huynh

In this research, strontium hexa-ferrite nanoparticles (SrFe12O19) were synthesized by sol-gel method. The crystal structure, morphology and magnetic properties of nanoparticles were investigated using X-ray Diffraction (XRD), Scanning Electron Microscope (SEM) and Vibrating Sample Magnetometer (VSM). The XRD patterns confirmed the formation of single phase M-type hexagonal crystal structure for powders which was calcined above 700oC. The product shows the magnetization of 66 emu/g, which is consistent with pure hexa-ferrite obtained by other methods, and the magnetic coercivity of 6,145 kOe higher than expected for this hexa-ferrite. The powder morphology is composed of aggregates of hexagonal particles with an average particles size of above 100nm.

2021 ◽  
Author(s):  
Yanchun Zhang ◽  
Aimin Sun ◽  
Liqiong Shao ◽  
Zhaxi Suonan

Abstract In the present work, nanocrystalline Sb3+ ions doped Ni0.2Ba0.1Co0.7Fe2−xSbxO4 (0 ≦ x ≦ 0.1, step by 0.025) ferrites were prepared via sol-gel method. The spinel-phase structure of samples can be confirmed by X-ray diffraction (XRD) patterns. The composition and structure were further studied by fourier transform infrared spectroscopy (FTIR). There were two typical characteristic bands ν1 and ν2 related to the stretching vibrations in spinel ferrite in FTIR spectra. Energy dispersive spectrometer (EDS) analyzed the elements of samples. It indicated that the elements of Ni, Ba, Co, Fe, O and Sb existed in the samples. Vibrating sample magnetometer was used to characterize magnetic properties. The saturation magnetization decreased from 57.65 emu/g to 44.50 emu/g with the increasing Sb3+ ions content, which is attributed to Fe3+ ions replaced by the Sb3+ ions. Remanent magnetization and coercivity first decreased and then increased slightly.


2013 ◽  
Vol 789 ◽  
pp. 87-92 ◽  
Author(s):  
Dwita Suastiyanti ◽  
Bambang Soegijono ◽  
M. Hikam

The formation of barium hexaferrite, BaFe12O19 single phase with nanosize crystalline is very important to get the best performance especially magnetic properties. The samples were prepared by sol gel method in citric acid-metal nitrates system. Hence the mole ratios of Ba2+/Fe3+ were varied at 1:12 and 1:11.5 with pH of 7 in all cases using ammonia solution. The solution was then heated at 80-90°C for 3 to 4 hours. Then it was kept on a pre-heated oven at 150°C. The samples were then heat treated at 450°C for 24 hours. Sintering process was done at 850°C and 1000°C for 10 hours.Crystallite size was calculated by X-Ray Diffraction (XRD) peaks using scherrer formula. To confirm the formation of a single phase, XRD analyses were done by comparing the sample patterns with standard pattern. The peak shifting of pattern could be seen from XRD pattern using rocking curves at extreme certain 2θ. It was used MPS Magnet Physik EP3 Permagraph L to know magnetic characteristics. This method can produce BaFe12O19 nanosize powder, 22-34 nm for crystallite size and 55.59-78.58 nm for particle size. A little diference in nanosize affects the peak shifting of XRD pattern significantly but shows a little difference in magnetic properties especially for samples at 850°C and 1000°C with mole ratio of 1:12 respectively. The well crystalline powder is formed at mole ratio of 1:11.5 at 850°C since it has the finest particle (55.59 nm) and crystalline (21 nm), the highest remanent magnetization (0.161 T) and the lowest intrinsic coersive (275.8 kA/m). It is also fitting exactly to the standard diffraction pattern with the highest value of best Figure of Merit (FoM), 90%. XRD peak position of this sample is almost same with XRD peak position of another sample with sinter temperature 1000°C at same mole ratio.


2012 ◽  
Vol 545 ◽  
pp. 275-278 ◽  
Author(s):  
Lili Widarti Zainuddin ◽  
Norlida Kamarulzaman

A ceramics sample of LiTaO3 was prepared using a sol-gel method. The sample is annealed at 750 °C for 48 hours. X-ray diffraction analysis indicate the formation of single phase, rhombohedral structure. An ac impedance study was used to analyse the conductivity of LiTaO3 at room temperature and at various temperatures.


2011 ◽  
Vol 268-270 ◽  
pp. 356-359 ◽  
Author(s):  
Wen Song Lin ◽  
C. H. Wen ◽  
Liang He

Mn, Fe doped ZnO powders (Zn0.95-xMnxFe0.05O2, x≤0.05) were synthesized by an ameliorated sol-gel method, using Zn(CH3COO)2, Mn(CH3COO)2and FeCl2as the raw materials, with the addition of vitamin C as a kind of chemical reducer. The resulting powder was subsequently compacted under pressure of 10 MPa at the temperature of 873K in vacuum. The crystal structure and magnetic properties of Zn0.95-xMnxFe0.05O2powder and bulk samples have been investigated by X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). X-ray photoelectron spectroscopy (XPS) was used to study chemical valence of manganese, iron and zinc in the samples. The x-ray diffraction (XRD) results showed that Zn0.95-xMnxFe0.05O (x≤0.05) samples were single phase with the ZnO-like wurtzite structure. No secondary phase was found in the XRD spectrum. X-ray photoelectron spectroscopy (XPS) showed that Fe and Mn existed in Zn0.95-xMnxFe0.05O2samples in Fe2+and Mn2+states. The results of VSM experiment proved the room temperature ferromagnetic properties (RTFP) of Mn, Fe co-doped ZnO samples.


Author(s):  
T. Pikula ◽  
T. Szumiata ◽  
K. Siedliska ◽  
V. I. Mitsiuk ◽  
R. Panek ◽  
...  

AbstractIn this work, BiFeO3 powders were synthesized by a sol–gel method. The influence of annealing temperature on the structure and magnetic properties of the samples has been discussed. X-ray diffraction studies showed that the purest phase was formed in the temperature range of 400 °C to 550 °C and the samples annealed at a temperature below 550 °C were of nanocrystalline character. Mössbauer spectroscopy and magnetization measurements were used as complementary methods to investigate the magnetic state of the samples. In particular, the appearance of weak ferromagnetic properties, significant growth of magnetization, and spin-glass-like behavior were observed along with the drop of average grain size. Mössbauer spectra were fitted by the model assuming cycloidal modulation of spins arrangement and properties of the spin cycloid were determined and analyzed. Most importantly, it was proved that the spin cycloid does not disappear even in the case of the samples with a particle size well below the cycloid modulation period λ = 62 nm. Furthermore, the cycloid becomes more anharmonic as the grain size decreases. The possible origination of weak ferromagnetism of the nanocrystalline samples has also been discussed.


2018 ◽  
Vol 735 ◽  
pp. 945-949 ◽  
Author(s):  
Shuai Zheng ◽  
Jiangying Wang ◽  
Jingji Zhang ◽  
Hongliang Ge ◽  
Zhi Chen ◽  
...  

2011 ◽  
Vol 197-198 ◽  
pp. 926-930
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Chen Zhi Jiang

FeVO4photocatalysts were synthesized via a surfactant-assisted sol-gel method and characterized with X-ray diffraction (XRD), scanning electron microsoope (SEM)and specific surface area (BET). The photocatalytic activity was evaluated by photocatalytic degradation of methyl orange (MO) solution under visible light. The XRD patterns of no-surfactant-assisted, PEG-assisted, CTAB-assisted and SDS-assisted FeVO4, indicate that diffraction peaks can be well indexed as triclinc FeVO4. And the crystalline sizes of samples were evaluated as 113, 69, 66, 76 nm for FVO, FVO-PEG, FVO-CATB and FVO-SDS respectively.The addition of surfactant woul greatly affect the morphology of FeVO4photocatalysts, which can lead to different photocatalytic activities between them. In the experimental conditions used, the PEG-assisted FeVO4product had a much higher photocatalytic activity (the photodegradation rate was about 77% or so in 14h) than the other three products.


2014 ◽  
Vol 13 (1) ◽  
pp. 1
Author(s):  
Tanti Haryati ◽  
Novita Andarini ◽  
Mellisa Ika Febrianti

The incorporation of TiO and ZnO material as a composite, to increase the activity of the catalyst. Synthesis of ZnO-TiO2 thin layer made using a sol-gel method with a variation of PEG as a solvent. The purpose of this research was to investigate the structure and morphology of ZnO-TiO2 thin layer on the variation of PEG as a solvent by sol-gel method . Preparation of ZnO sol of the precursor , while the TiO2 sol synthesized by dissolving the anatase TiO2 structure into polyethilen glycol . Sol of ZnO and TiO2 sol do sol mixing to form ZnO–TiO2 after it coated on a glass substrate and then calcined . Products were then characterized by X-ray diffraction to determine the crystal structure and SEM to determine its morphology . The test results show the crystal structure by XRD based difaktogram intensity , the greater the molecular weight of the PEG peak intensity of ZnO-TiO2 showed the lower. While based on morphological examination , it can be seen that the larger molecular weight PEG , ZnO - TiO2 granular greater.


2021 ◽  
Author(s):  
V Maphiri ◽  
L Melato ◽  
Mhlongo ◽  
TT Hlatshwayo ◽  
TE Motaung ◽  
...  

Abstract Un-doped and ZnAlxO(1.5x + 1):0.1% Tb3+ (ZAOT) nano-powders were synthesized via citrate sol-gel method. The Alx moles were varied in the range of 0.25 ≤ x ≤ 5.0. The X-ray powder diffraction (XRD) data revealed that for the x < 1.5, the prepared samples crystal structure consists of mixed phases of the cubic ZnAl2O4 and hexagonal ZnO phases, while for the x ≥ 1.5 the structure consists of single phase of cubic ZnAl2O4. This was confirmed by the Raman and Fourier-Transform Infrared (FTIR) vibrational spectroscopy. Scanning electron microscopy (SEM) showed that varying Alx moles influences the morphology while Transmission electron microscopy (TEM) shows the dual morphology at x < 1.5. The photoluminescence (PL) revealed intense and distinct emissions attributed to both the host and Tb3+ transitions. The emission intensity highly depends on the Alx moles. The International Commission on Illumination (CIE) colour chromaticity showed that the emission colour could be tuned by varying the Alx moles.


2021 ◽  
Vol 21 (4) ◽  
pp. 2604-2612
Author(s):  
Dang Duc Dung ◽  
Nguyen The Hung

A new solid solution, (1−x)Bi0.5Na0.5TiO3+xBaCoO3−δ materials, was fabricated using the sol–gel method. X-ray diffraction showed that the crystal structure of the compound exhibited rhombohedral symmetry and is similar to the crystal structures of host Bi0.5Na0.5TiO3 materials. Distortions in the structures and reduction in the optical band gaps of the Bi0.5Na0.5TiO3 materials were possibly due to the random incorporation of Ba and Co cations into host lattice materials. The magnetic properties of the Bi0.5Na0.5TiO3 materials were tuned by controlling the concentrations of BaCoO3−δ as the solid solution. We expect that our work will provide valuable information on current methods for integrating ferromagnetic properties into lead-free ferroelectric materials for the development of multiferroic materials.


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