Nanosize Effects on Magnetic Properties and Peak Shifting of X-Ray Diffraction Pattern of BaFe12O19 Produced by Sol Gel Method

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.


2016 ◽  
Vol 254 ◽  
pp. 200-206 ◽  
Author(s):  
Catalina Nuțescu Duduman ◽  
María Isabel Barrena Pérez ◽  
José Maria Gómez de Salazar ◽  
Ioan Carcea ◽  
Daniela Lucia Chicet ◽  
...  

Nanostructured SnO2 was prepared based on the sol-gel method used in the preparation of crystalline metal oxides. Sol-gel process can be described as a forming network of oxide polycondensation reaction of a molecular precursor in a liquid. Six experiments were carried out. Morphological structures and chemical composition were examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) after calcination. It is noted that TEM images show that the spheres consist from nanocrystals, quantitative EDS analysis of the chemical composition shows an absence of the chlorine, which is a desired fact. For structural characterization of the material we used X-Ray Diffraction (XRD). The X-ray diffraction pattern for all samples indicates peaks which are agreeable with standard diffraction pattern of SnO2. The particle size of all samples was in the range of 28-92 nm calculated according to Scherrer equation.


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.


2018 ◽  
Vol 8 ◽  
pp. 184798041880064 ◽  
Author(s):  
VM Maphiri ◽  
BF Dejene ◽  
TE Motaung ◽  
TT Hlatshwayo ◽  
OM Ndwandwe ◽  
...  

Mg1.5Al2O4.5: x% Eu3+ (0 ≤ x ≤ 2) nanopowders were successfully synthesized via sol–gel method. The X-ray diffraction (XRD) spectrum revealed that the Mg1.5Al2O4.5: x% Eu3+ matches the single phase of face-centred cubic MgAl2O4. The estimated average crystallite sizes calculated using the XRD spectra were found to be in the order of 4 nm. The estimated crystal size was confirmed by the high-resolution transmission electron microscopy. The energy dispersive X-ray spectroscopy confirmed the presence of all expected elementary composition (Mg, Al, O and Eu). The field emission gun scanning electron microscope showed that varying the Eu3+ concentration influence the morphology of the prepared nanophosphor. The photoluminescence results showed that the host emits the violet colour at around 382 nm, which was attributed to the defects within the band gap ( Eg) of host material. The Eu3+-doped samples showed the emission at around 560, 580, 593, 618, 655 and 704 nm which are, respectively, attributed to the 5D1 → 7F3, 5D0 → 7F0, 5D0 → 7F1, 5D0 → 7F2, 5D0 → 7F3 and 5D0 → 7F4 characteristic transitions in Eu3+. The International Commission on Illumination colour chromaticity showed that the Eu3+ doping influences the emission colour.


2014 ◽  
Vol 664 ◽  
pp. 75-79
Author(s):  
Beh Hoe Guan ◽  
Muhammad Hanif Zahari ◽  
Lee Kean Chuan

This study investigates the influence of calcination temperatures on the magnetic properties of Ni0.5Zn0.5Fe2O4(Ni-Zn) ferrites.Ni-Zn ferrite with the chemical formula Ni0.5Zn0.5Fe2O4was prepared from their respective nitrate salts through the sol-gel method. The resulting ferrites were characterized using X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) and vibrating sample magnetometer (VSM). Single phased Ni0.5Zn0.5Fe2O4 was obtained at all calcination temperatures.FESEM Micrographs reveals an increase in the grain size with the increase of the calcination temperature. Consequently, the magnetic saturation of the samples were found to increase with each increase in the calcination temperature where the highest value obtained is 70.58 emu/g for the samples calcined at 1000°C.


2012 ◽  
Vol 545 ◽  
pp. 143-147
Author(s):  
Annie Maria Mahat ◽  
Kelimah Elong ◽  
Nor Diyana Abdul Aziz ◽  
Mohd Sufri Mastuli ◽  
Norlida Kamarulzaman

Titanium dioxide powders were synthesized via a sol-gel method using titanium nitride as the precursor. The structure and morphology of the synthesized powders were investigated and characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). XRD results indicate that pure single phase titanium dioxide of rutile structure had been obtained. It was also revealed that annealing temperature plays an important role in the formation of single phase titanium dioxide powders. Increasing heat treatments also modified the shape and surface morphology from chunks and rock-like morphology to a mixture of flaky aggregates. Conductivity studies using a.c. impedance technique was used. The conductivity of the sample annealed at 400 °C is 89 % higher than that annealed at 800 °C and attributed to the phase and morphology of the samples.


2013 ◽  
Vol 756 ◽  
pp. 91-98 ◽  
Author(s):  
Ftema W. Aldbea ◽  
Noor Bahyah Ibrahim ◽  
Mustafa Hj. Abdullah

Terbium –substituted yttrium iron garnet (Tb1.5Y1.5Fe5O12) films nanoparticles were successfully prepared by a sol-gel method. The films were deposited on the quartz substrate using spin coating technique. To study effect of annealing temperature, the annealing process was executed at 700, 800 and 900 °C in air for 2 hours. The X-ray diffraction (XRD) proved that the pure phase of garnet structure was detected for the film annealed at 900 °C. The lattice parameter increased with the increment of annealing temperature and the highest value of 12.35 Å was obtained at 900 °C. Field Emission Scanning Electron Microscope (FE-SEM) results showed that the particle size increased from 43nm to 56nm as annealing temperature increased from 700 to 900°C. The film’s thickness also affected by increasing of annealing temperature and become thin at 900 °C due to densification process occurred at high annealing temperature. The elemental compositions of the Tb1.5Y1.5Fe5O12 film were detected using an Energy Dispersive X-raySpectroscopy (EDX). Magnetic properties at room temperature were measured using a Vibrating Sample Magnetometer (VSM).The saturation magnetization Ms increased with the annealingtemperature and showed a high value of 104emu/cm3, but the coercivity Hc of the film was decreased due to the increment of the particle size. Normal 0 21 false false false MS X-NONE X-NONE MicrosoftInternetExplorer4 Terbium –substituted yttrium iron garnet (Tb1.5Y1.5Fe5O12) films nanoparticles were successfully prepared by a sol-gel method. The films were deposited on the quartz substrate using spin coating technique. To study effect of annealing temperature, the annealing process was executed at 700, 800 and 900°C in air for 2 hours. The X-ray diffraction (XRD) proved that the pure phase of garnet structure was detected for the film annealed at 900 °C. The lattice parameter increased with the increment of annealing temperature and the highest value of 12.35 Å was obtained at 900 °C. Field Emission Scanning Electron Microscope (FE-SEM) results showed that the particle size increased from 43nm to 56nm as annealing temperature increased from 700 to 900 °C. The film’s thickness also affected by increasing of annealing temperature and become thin at 900 °C due to densification process occurred at high annealing temperature. The elemental compositions of the Tb1.5Y1.5Fe5O12 film were detected using an Energy Dispersive X-ray Spectroscopy (EDX). Magnetic properties at room temperature were measured using a Vibrating Sample Magnetometer (VSM).The saturation magnetization Ms increased with the annealing temperature and showed a high value of 104emu/cm3, but the coercivity Hc of the film was decreased due to the increment of the particle size. st1\:*{behavior:url(#ieooui) } /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;}


Nanopages ◽  
2019 ◽  
pp. 1-11
Author(s):  
G. M. Taha ◽  
M. N. Rashed ◽  
M. S. El-Sadek ◽  
M. A. Moghazy

Abstract BiFeO3 (BFO) nanopowder was synthesized in a pure form via a sol- gel method based on glycol gel reaction. Effect of drying and preheating temperature on preventing other phases was studied. Many parameters were studied as calcination temperature and time & stirring temperature as well. The prepared powder was characterized by X-Ray Diffraction of powder (XRD) and Transmission Electron Microscope (TEM). High pure BiFeO3 was obtained by preheated process at 400 °C for 0.5 h and calcination at 600 °C for 0.5 h without any impurities compared to dry at110 °C.


2011 ◽  
Vol 399-401 ◽  
pp. 1447-1450
Author(s):  
Zhi Yong Yu ◽  
Han Xing Liu

The layered LiNi1/2Mn1/2O2 cathode materials were synthesized by a sol gel method. The effects of calcination temperature and time on the structural and electrochemical properties of the LiNi1/2Mn1/2O2 were investigated. The prepared samples were characterized by X-ray diffraction (XRD) and electrochemical analysis. The results revealed that the layered LiNi1/2Mn1/2O2 material could be optimal synthesized at temperature of 900°C for 10h. The sample prepared under the above conditions has the highest initial discharge capacity of 151 mAh/g and showed no dramatic capacity fading during 20 cycles between 2.5-4.5V at a current rate of 20mA/g.


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