The Influence of Cu Subtitution on the Crystal and Morphological Structure of Ca0.9La0.05Bi0.05Mn1-xCuxO3 (x = 0, 0.025, 0.05, 0.075, and 0.1) Manganites

2020 ◽  
Vol 860 ◽  
pp. 112-116
Author(s):  
Bathara Bhisma Arbianto ◽  
Budhy Kurniawan ◽  
Arief Sudarmaji

The sequence of Cu substituted Ca0.9La0.05Bi0.05Mn1-XCuxO3 ( x = 0, 0.025, 0.05, 0.075, and 0.1) manganite has been studied and it has effect in the structure. The samples was synthesized using the citric acid sol-gel method. The samples was sintered at 800 °C for 5 hours. The crystallography and morphological of all samples was investigated using X-Ray Diffractometer (XRD) and Scanning Electron Microscope (SEM). The Rietveld analysis of the powder x-ray diffraction shows that all the samples crystallize in orthorhombic structure with pnma space group symmetry without any impurity phase. The Cu substitution does not change the crystal structure, but it changes the grain size. SEM results showed a valid different morphological structure. The increasing Cu concentration, it made the grain size larger, dispite all the samples had the same treatment.

2008 ◽  
Vol 1122 ◽  
Author(s):  
Gianguido Baldinozzi ◽  
David Simeone ◽  
Dominique Gosset ◽  
Mickael Dollé ◽  
Georgette Petot-Ervas

AbstractWe have synthesized Gd-doped ceria polycrystalline samples (5, 10, 15 %mol), having relative densities exceeding 95% and grain sizes between 30 and 160 nm after axial hot pressing (750 °C, 250 MPa). The samples were prepared by sintering nanopowders obtained by sol-gel chemistry methods having a very narrow size distribution centered at about 16 nm. SEM and X-ray diffraction were performed to characterize the sample microstructures and to assess their structures. We report ionic conductivity measurements using impedance spectroscopy. It is important to investigate the properties of these systems with sub-micrometric grains and as a function of their composition. Therefore, samples having micrometric and nanometric grain sizes (and different Gd content) were studied. Evidence of Gd segregation near the grain boundaries is given and the impact on the ionic conductivity, as a function of the grain size and Gd composition, is discussed and compared to microcrystalline samples.


2013 ◽  
Vol 1 (1) ◽  
pp. 11-14
Author(s):  
N. Sahu ◽  
◽  
R. K. Duchaniya ◽  

The ZnO-CdO nanocomposite was prepared by sol-gel method by using their respective nitrates. It is a simple and low cost method to prepare nanocomposites. The drying temperature and drying period of prepared gel was varied during the synthesis process. The prepared samples were characterized by using scanning electron microscope (SEM), particle size analysis (PSA), X-ray diffraction (XRD) and photoluminescence spectroscopy (PL) to get surface morphology, idea of getting particle of nanosized range so that further characterizations can be done, to study the optical property of synthesized nanocomposite and measure the band gap . The grain size determined by Scherrer’s formula was found to be between 30-50 nm.


2005 ◽  
Vol 20 (10) ◽  
pp. 2676-2681 ◽  
Author(s):  
Maolin Pang ◽  
Xiaoming Liu ◽  
Jun Lin

R2MoO6:Eu3+ (R = Gd, Y, La) phosphors were prepared by the Pechini sol-gel process. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), reflectance spectra, photoluminescence (PL) spectra, and lifetimes were used to characterize the resulting phosphors. The results of XRD indicate that all of the R1.96Eu0.04MoO6 (R = Gd, Y, La) phosphors crystallized completely at 800 °C. Y1.96Eu0.04MoO6 and Gd1.96Eu0.04MoO6 are of isomorphous monoclinic (α) structure, while La1.96Eu0.04MoO6 preferentially adopts the tetragonal (γ) form. FE-SEM study reveals that the samples mainly consist of aggregated particles with an average grain size ranging from 100 to 250 nm. The luminescent properties of R2MoO6:Eu3+ (R = Gd, Y, La) phosphors are largely dependent on their structure, grain size, and powder morphology. The isomorphous Y2MoO6:Eu3+ and Gd2MoO6:Eu3+ phosphors show very similar luminescence properties, which differ greatly from that of the La2MoO6:Eu3+ phosphor.


2012 ◽  
Vol 512-515 ◽  
pp. 147-152
Author(s):  
Shao Peng Zhang ◽  
Xiao Hui Wang ◽  
Long Tu Li

Nanocrystalline lead zirconate titanate (PZT) powders with composition at the morphotropic phase boundary (MPB) were synthesized by a simple aqueous based sol-gel method, using lead nitrate, zirconium nitrate and tetrabutyl titanate as the starting materials. The sol could be easily transformed into gel, firstly heated at 120°C for 10h, then at 180°C for 24h. The thermal decomposition process of the gel was investigated by thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) techniques. The effect of citrate addition amount on the calcining temperature was discussed. The results reveal that pure perovskite phase PZT powders can be obtained at a calcining temperature as low as 600°C. The average grain size of the powders was determined by transmission electron microscope and X-ray diffraction. The influences of calcining temperature and the pH value of the solution on the grain size were investigated. The sintering temperature and electrical properties of the ceramics derived by nano-powders were compared with those prepared by the conventional ceramic processing. The result shows that using the nanopowder, the sintering temperature could be reduced by about 100°C and the ferroelectric properties were enhanced.


2019 ◽  
Vol 290 ◽  
pp. 245-251
Author(s):  
Abdalla Bahboh ◽  
Abdul Halim Shaari ◽  
Hussein Baqiah ◽  
Soo Kien Chen ◽  
Mohd Mustafa Awang Kechik ◽  
...  

The effects of the multiforric BiFO3 nanoparticles addition on the structure and superconducting properties of YBa2Cu3O7–δ (Y123) with different concentrations were systematically investigated using X-ray diffraction (XRD), field emission scanning electron micrograph (FESEM), EDX and four point probe measurement. It was found that the added samples were predominant by Y-123 phase beside small amount of Y-211 and unreacted BiFeO3 secondary phases. Samples with less (wt.%) BFO added YBCO precursor powder preserved the orthorhombic structure similar to the pure YBCO, while samples with higher wt% addition show orthorhombic-to-tetragonal transition tendency. The samples became more porous and their grain size slightly decreased with addition of BiFeO3. The addition of nanoBiFeO3 disturbed the grain growth of Y123, thus resulting in the degradation of superconducting properties of the samples. The superconducting transition temperature (Tc onset) of samples decreased from 92 K for x=0.0 to 44 K for x=10.0 wt. %, which could be attributable to oxygen vacancy disorder.


2020 ◽  
Vol 75 (3) ◽  
pp. 249-256
Author(s):  
Mukhtar Ahmad ◽  
Rizwan Ali ◽  
Atiq ur Rehman ◽  
Akbar Ali ◽  
Ishrat Sultana ◽  
...  

AbstractMultiferroics with chemical formula BiAlxFe1−xO3 (x = 0, 0.1, 0.2, and 0.3) and substituted by Al are synthesised using sol–gel auto-combustion. The materials are sintered at 500 °C for 5 h. In the ongoing study, the crystal structure of BiAlxFe1−xO3 was investigated by X-ray diffraction. After confirming the rhombohedral single-phase crystal structure, various characterisation techniques, such as scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) spectroscopy, elemental mapping images, electrical properties, Fourier transform infrared spectroscopy, and vibrating sample magnetometry (VSM), were used to investigate the synthesised samples. The grain size estimated from SEM images decreased as Al contents increased. Elemental composition was confirmed by EDX spectra. Direct current electrical resistivity increased whereas drift mobility decreased with increasing Al contents. The VSM results of Al-doped BiFeO3 (BFO) demonstrate that BFO crystals with size >60 nm show anti-ferromagnetic behaviour, which is evident in the present study. The increase in Al doping results in an increase in coercivity, as grain size and coercivity are inversely related with each other. This is because of the replacement of Fe3+ by Al3+ ions, which weakens the sub-lattice interactions. It has been observed that BFO materials with such parameters are favourable for ferroelectric random access memories where data can be written electrically and read magnetically.


2008 ◽  
Vol 368-372 ◽  
pp. 378-380
Author(s):  
Xiu Mei Han ◽  
J. Lin ◽  
M. Yu ◽  
C.K. Lin ◽  
Xi Wei Qi ◽  
...  

Spherical SiO2 particles were coated with Ca2Y8(SiO4)6O2:Eu3+ phosphor layers through a sol-gel process. The results of XRD (X-ray diffraction) analysis indicated that the phosphors crystallized completely at 1000oC. AFM study revealed that the average grain size is 500 nm. In Ca2Y8(SiO4)6O2:Eu3+ spherical phosphors , the Eu3+ showed its characteristic red emission at 612 nm(5D0-7F2) upon excitation into its charge transfer band of Eu3+-O2- at 242nm.


Author(s):  
Haiwen Chen ◽  
Shengli Hu ◽  
Ge Zhang ◽  
Zhengming Jiang ◽  
JiaJun Mo ◽  
...  

Multiferroic nanocrystalline Bi[Formula: see text]Sr[Formula: see text]FeO3 ([Formula: see text], 0.05, 0.1) samples were synthesized using the sol–gel method and characterized by powder X-ray diffraction, Mössbauer spectroscopy and SQUID system. The small-angle X-ray diffraction analysis showed that the sample underwent phase transition from rhombohedral to pseudo-cubic structure with the enhancement of Sr content. In addition, impurity peaks gradually diminished, indicating that content of impurities of samples reduced. Furthermore, it can be determined that there is only Fe[Formula: see text] in all the samples and impurity phase that existed in the samples was Bi[Formula: see text]FeO[Formula: see text] by fitting Mössbauer spectra. It is further confirmed that Bi[Formula: see text] Sr[Formula: see text]FeO3 samples were generated by oxygen vacancy equilibrium valence state when Sr[Formula: see text] ions replaced Bi[Formula: see text] ions. The change of quadrupole splitting indicated that a low concentration of Sr[Formula: see text] ions diffused homogeneously in the sample. Magnetization measurement showed that the magnetization of the sample increased gradually with the substitution of Bi[Formula: see text] by nonequivalent Sr[Formula: see text] ions, which can be ascribed to the decrease of grain size and the increase of oxygen vacancy and specific surface in the samples.


2012 ◽  
Vol 05 ◽  
pp. 188-195
Author(s):  
M. Golmohammad ◽  
A. Nemati ◽  
M. A. Faghihi Sani

Ba 0.7 Sr 0.3 TiO 3 was prepared via simple sol-gel method by using titanium tetrabutoxide, barium and strontium carbonates, citric acid and ethylene glycol as starting materials. Simultaneous Thermal Analysis (STA) was used to examine thermal behavior of xerogel. The crystallite size of BST was about 21nm calculated by X-Ray diffraction (XRD) and confirmed by transition electron microscopy (TEM). Using these nanocrystalline powders, BST pellets were prepared and sintered in various temperatures. The grain size effect on electrical properties was studied and found that as the grain size decreased, the dielectric constant decreased too.


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