Epitaxial Growth of (110) KnbO3 Films on (100) MgO Substrates via Sol-Gel Processing

1994 ◽  
Vol 341 ◽  
Author(s):  
Garo J. Derderian ◽  
James D. Barrie ◽  
Kenneth A. Aitchison ◽  
Martha L. Mecartney

AbstractEpitaxial, single phase (110) KnbO3 films were grown on (100) MgO substrates using a sol-gel process employing ethoxide precursors in methanol. The degree of epitaxy was dependent on both the annealing temperature and the amount of potassium in the film. Excess potassium in the sol-gel solution (K/Nb = 1.2) was necessary to produce single phase films. An amorphous or polycrystalline MgO interfacial layer was observed in some films, postulated to have developed after nucleation of KnbO3 and due to a highly defective surface layer.

1999 ◽  
Vol 606 ◽  
Author(s):  
Keishi Nishio ◽  
Jirawat Thongrueng ◽  
Yuichi Watanabe ◽  
Toshio Tsuchiya

AbstructWe succeeded in the preparation of strontium-barium niobate (Sr0.3Ba0.7Nb2O6 : SBN30)that have a tetragonal tungsten bronze type structure thin films on SrTiO3 (100), STO, or La doped SrTiO3 (100), LSTO, single crystal substrates by a spin coating process. LSTO substrate can be used for electrode. A homogeneous coating solution was prepared with Sr and Ba acetates and Nb(OEt)5 as raw materials, and acetic acid and diethylene glycol monomethyl ether as solvents. The coating thin films were sintered at temperature from 700 to 1000°C for 10 min in air. It was confirmed that the thin films on STO substrate sintered above 700°C were in the epitaxial growth because the 16 diffraction spots were observed on the pole figure using (121) reflection. The <130> and <310> direction of the thin film on STO were oriented with the c-axis in parallel to the substrate surface. However, the diffraction spots of thin film on LSTO substrate sintered at 700°C were corresponds to the expected pattern for (110).


2012 ◽  
Vol 501 ◽  
pp. 236-241 ◽  
Author(s):  
Ftema W. Aldbea ◽  
Noor Bahyah Ibrahim ◽  
Mustafa Hj. Abdullah ◽  
Ramadan E. Shaiboub

Thin films nanoparticles TbxY3-xFe5O12 (x=0.0, 1.0, 2.0) were prepared by the sol-gel process followed by annealing process at various annealing temperatures of 700° C, 800° C and 900° C in air for 2 h. The results obtained from X-ray diffractometer (XRD) show that the films annealed below 900°C exhibit peaks of garnet mixed with small amounts of YFeO3 and Fe2O3. Pure garnet phase has been detected in the films annealed at 900°C. Before annealing the films show amorphous structures. The particles sizes measurement using the field emission scanning electron microscope (FE-SEM) showed that the particles sizes increased as the annealing temperature increased. The magnetic properties were measured at room temperature using the vibrating sample magnetometer (VSM). The saturation magnetization (Ms) of the films also increased with the annealing temperature. However, different behavior of coercivity (Hc) has been observed as the annealing temperature was increased.


2011 ◽  
Vol 197-198 ◽  
pp. 1781-1784
Author(s):  
Hua Wang ◽  
Jian Li ◽  
Ji Wen Xu ◽  
Ling Yang ◽  
Shang Ju Zhou

Intergrowth-superlattice-structured SrBi4Ti4O15–Bi4Ti3O12(SBT–BIT) films prepared on p-Si substrates by sol-gel processing. Synthesized SBT–BIT films exhibit good ferroelectric properties. As the annealing temperature increases from 600°C to 700°C, the remanent polarization Prof SBT–BIT films increases, while the coercive electric field Ecdecreases. SBT–BIT films annealed at 700°C have a Prvalue of 18.9µC/cm2which is higher than that of SBT (16.8µC/cm2) and BIT (14.6µC/cm2), and have the lowest Ecof 142 kV/cm which is almost the same as that of SBT and BIT. The C-V curves of Ag/SBT-BIT/p-Si heterostructures show the clockwise hysteresis loops which reveal the memory effect due to the polarization. The memory window in C-V curve of Ag/SBT-BIT/p-Si is larger than that of Ag/SBT/p-Si heterostructure or Ag/BIT/p-Si heterostructure.


1990 ◽  
Vol 5 (5) ◽  
pp. 1095-1103 ◽  
Author(s):  
Ann M. Kazakos ◽  
Sridhar Komarneni ◽  
Rustum Roy

Three series of cordierite powders were prepared by the sol-gel route: a single phase (monophasic) gel prepared from alkoxides, a nominally triphasic nanocomposite gel made with two nanosized powders and one solution phase, and a truly compositionally triphasic nanocomposite gel prepared from three nanosized powders. Crystalline α-cordierite seeds were also incorporated with the gels and their effectiveness as nucleating agents was investigated and found to lower the crystallization temperature of α-cordierite by 125–150°C. The densification behavior of powder compacts was examined and alterations made to the heat treatment until optimum conditions were found. The truly triphasic compact sintered at 1300°C for 2 h resulted in 100% of theoretical density whereas the nominally triphasic and monophasis pellets densified to 96% and 80%, respectively. The enhanced densification achieved with powder compacct prepared for triphasic nanocomposite gels is due to part to the excess free energy of the three components.


2013 ◽  
Vol 859 ◽  
pp. 361-364 ◽  
Author(s):  
Jing Wang ◽  
Du Shu Huang ◽  
Wei Liu ◽  
Qing Shan Pan ◽  
Yong Min

Degradation properties of phenol using nano-TiO2 as photocatalyst in aqueous solution were investigated. The effect of annealing temperature and ionic modification on the degradation was studied. The results showed that, 500 °C annealed TiO2 was better than 700 °C annealed. Photocatalyst nano-TiO2 material doped with Fe3+ was prepared quickly by sol-gel process and was used as photocatalyst to degrade phenol solution of 100mg/L under UV irradiation for 3 hours. UV spectrophotometer testing was made and found that two peaks at 210 nm and 270 nm were significantly become low, indicating that the phenol has been degraded. The phenol degradation rate was 94.18%.


1996 ◽  
Vol 431 ◽  
Author(s):  
C. K. Narula

AbstractThe high cost of materials prepared by sol-gel processing and the loss of useful surface properties at elevated temperature has prevented the application of sol-gel processed materials in automotive exhaust reduction catalyst formulations. In this report, we briefly describe the important developments needed in the next generation automotive catalysts and the role of sol-gel processed materials. We will also discuss the application of heterometallic alkoxides as sol-gel precursors to achieve the molecular distribution of lanthanides and alkaline earths in alumina matrices needed for the stabilization of alumina based materials at elevated temperatures.


2014 ◽  
Vol 975 ◽  
pp. 268-273
Author(s):  
Bruna da Costa Andrade ◽  
Marcelo Andrade Macedo

Sr1-xGdxCo2Fe16O27-δ, (x = 0.05–0.20) was prepared via the proteic sol-gel process. Single-phase W-type hexaferrite doped with gadolinium was synthesized. The ferrite shows ferrimagnetic behavior with high saturation magnetization, low coercive field, low remnant magnetization, and a resistivity greater than 107 Ω·cm. The substitution of Sr2+ for Gd3+ improved the magnetoelectric properties of the ferrite owing to the increase in the concentration of Fe2+ and improvement of electron conduction.


2000 ◽  
Vol 14 (22n23) ◽  
pp. 801-808 ◽  
Author(s):  
M. RAJENDRAN ◽  
M. GHANASHYAM KRISHNA ◽  
A. K. BHATTACHARYA

A novel all-inorganic aqueous sol–gel process has been developed to fabricate LaFeO3 thin films by dip-coating. Stable, positively charged colloidal sol particles of hydrous lanthanum ferrite with an average particle size (Z av ) of 7 nm were prepared and coated onto quartz plates under controlled conditions. The sols have been characterized using photon correlation spectroscopy (PCS) for Z av and size distribution. The redispersible gel was characterized by thermogravimetric and differential thermal analysis (TG-DTA) and also by isothermal heating followed by X-ray diffraction to identify the reaction sequence to form LaFeO 3. The sol–gel films as deposited were X-ray amorphous on heating up to 500°C, partially crystalline at 600°C, fully crystalline and single phase at 650°C and above. These films were continuous, polycrystalline, single phase, had uniform thickness in the range between 180 to 1000 nm, depending on deposition conditions, and showed about 80% optical transmittance. The optical band gap varied from 2.7 to 3.3 eV as a function of the annealing temperature. The refractive index increased with increase in annealing temperature from 1.55 at 500°C to 1.86 at 800°C.


2011 ◽  
Vol 412 ◽  
pp. 271-274
Author(s):  
Ying Li ◽  
Qiang Xu ◽  
Ling Dai

In order to prepare ultrafine La3NbO7 powder, a potential material for thermal barrier coatings, the calcination process of La3NbO7 was studied in this paper.The precursor of La3NbO7 was synthesized by using a citric acid complex method. A calcination process had been systematically investigated. The reaction temperature was determined by differential scanning calorimetry (DSC). The phase composition of powders was characterized by X-ray diffraction (XRD), and the morphology was obtained by scanning electron microscope (SEM). The results revealed that the single-phase La3NbO7 powder could be successfully prepared while the calcination temperature exceeded 800°C and a better morphology could be maintained at 800°C for 4 hours. Considering all above, an optimum calcination scheme was adopted at 800°C for 4 hours. The as-prepared La3NbO7 powders had a grain size of about 50nm and an average particle size of about 300nm.


2016 ◽  
Vol 16 (4) ◽  
pp. 3914-3920 ◽  
Author(s):  
G. Z Li ◽  
F. H Liu ◽  
Z. S Chu ◽  
D. M Wu ◽  
L. B Yang ◽  
...  

SiO2@Y2MoO6:Eu3+ core–shell phosphors were prepared by the sol–gel process. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectra (EDS), transmission electron microscopy (TEM), photoluminescence (PL) spectra as well as kinetic decays were used to characterize the resulting SiO2@Y2MoO6:Eu3+ core–shell phosphors. The XRD results demonstrated that the Y2MoO6:Eu3+ layers on the SiO2 spheres crystallized after being annealed at 700 °C and the crystallinity increased with raising the annealing temperature. The obtained core–shell phosphors have spherical shape with narrow size distribution (average size ca. 640 nm), non-agglomeration, and smooth surface. The thickness of the Y2MoO6:Eu3+ shells on the SiO2 cores could be easily tailored by varying the number of deposition cycles (70 nm for four deposition cycles). The Eu3+ shows a strong PL emission (dominated by 5D0–7F2 red emission at 614 nm) under the excitation of 347 nm UV light. The PL intensity of Eu3+ increases with increasing the annealing temperature and the number of coating cycles.


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