scholarly journals Electric Properties of NaTaO3 Obtained by Hydrothermal Method

2015 ◽  
Vol 58 (1) ◽  
pp. 48-55
Author(s):  
Dan Malaescu ◽  
Ioan Grozescu ◽  
Paula Sfirloaga ◽  
Paulina Vlazan ◽  
Catalin N. Marin
Keyword(s):  
Hydrothermal Method ◽  
Complex Impedance ◽  
Imaginary Component ◽  
Relaxation Processes ◽  
X Ray Diffraction ◽  
Real Component ◽  
Perovskite Materials ◽  
Two Samples ◽  
Electron Microscopy Analysis ◽  
In Series

Abstract Two samples of NaTaO3 perovskite materials were prepared by the standard hydrothermal method at the same reaction temperature (600 °C) but with different sintering times: 6 hours for sample S1 and 12 hours for sample S2.Using X-ray diffraction (XRD), it shows that samples S1 and S2 are mixtures of Na-Ta oxides (Ta2O5 and the prevailing phase NaTaO3). The scanning electron microscopy analysis (SEM), shows that the grains are connected each other in agglomerated clusters of size about few hundred nanometers.The frequency (f) dependencies of complex impedance, Z(f) = Z’(f) - i Z’’(f) of the samples, over the frequency range 20 Hz - 2 MHz, at room temperature are presented. The real component Z’ of the complex impedance decreases with increasing frequency and the imaginary component Z’’ has two maximum corresponding to two relaxation processes.The results obtained from the complex impedance spectroscopy, Z’’(Z’) showed the appearance of two semicircles, corresponding to grain and grain boundary mechanism. Experimental results have been fitted with two parallel RC equivalent circuits connected in series and the parameters R and C have been evaluated.

Preparation of Fibrous CaO Sorbent by Hydrothermal Method

2012 ◽  
Vol 534 ◽  
pp. 86-88
Author(s):  
Shi Mei Yang ◽  
Shao Yun Shan ◽  
Qing Ming Jia ◽  
Ting Wei Hu ◽  
Li Hong Jiang ◽  
...  
Keyword(s):  
Hydrothermal Method ◽  
Absorption Capacity ◽  
Co2 Absorption ◽  
X Ray Diffraction ◽  
Absorption Properties ◽  
Hydrothermal Temperature ◽  
Crystal Forms ◽  
Electron Microscopy Analysis ◽  
Calcium Source ◽  
Microscopy Analysis

Using urea and calcium chloride as precipitator and calcium source, fibrous CaCO3 precursors were prepared using hydrothermal method, then fibrous CaO sorbent was obtained by calcination. The influence of hydrothermal temperature on CO2 absorption properties was discussed. X-ray diffraction analysis showed that pure CaCO3 phase with aragonite and calcite crystal forms was obtained. Scanning electron microscopy analysis showed that the resultant CaO sorbent presented a fibrous microstructure, which inherited the morphologies of CaCO3. The absorption capacity of the resultant CaO sorbent reached 59.86%, being 76% of theoretical absorption capacity. In addition, compared with the CaO sorbent from analytical pure CaCO3, the obtained fibrous CaO-sorbent have the better cyclic absorption properties.

scholarly journals Complex Impedance of Manganese Ferrite Powders Obtained by Two Different Methods

2015 ◽  
Vol 58 (1) ◽  
pp. 14-26 ◽  
Author(s):  
I. Mălăescu ◽  
Antoanetta Lungu ◽  
C. N. Marin ◽  
Paulina Vlăzan ◽  
Paula Sfirloagă
Keyword(s):  
Complex Impedance ◽  
Compositional Analysis ◽  
Grain Morphology ◽  
Relaxation Mechanism ◽  
Relaxation Processes ◽  
Ferrite Powder ◽  
Manganese Ferrite ◽  
Electrical Equivalent Circuit ◽  
Capacitive Properties ◽  
Two Samples

Abstract Two samples of manganese ferrite powder were obtained by the calcination method (sample A) and hydrothermal method (sample B). The crystal structure of the samples has been determined using X-ray diffraction analysis (XRD). The results shown that the sample A has three phases (FeMnO3, Mn2O3 and Fe2O3) and the prevailing phase is FeMnO3 with perovskite structure and the sample B has only a single phase (MnFe2O4). The grain morphology was analyzed by scanning electron microscopy (SEM) and the compositional analysis was done by energy dispersive spectroscopy (EDAX). Measurements of the frequency (f) and temperature (T) dependent complex impedance, Z(f, T) = Z’(f, T) - i Z’’(f, T) of the samples over the frequency range 20 Hz - 2 MHz, at various temperature values from 300C to 1100C are presented. From these measurements, we have shown that the temperature dependence of the relaxation time is of Arhenius type, which suggests that the conduction process is thermally activated. The values obtained for the activation energy Ea, are: 16meV (sample A) and 147.65meV (sample B). Applying complex impedance spectroscopy technique, the obtained results shows the shape of a single semicircle at each temperature over the measurement range, meaning that the electrical process obeys to a single relaxation mechanism. The impedance and related parameters of the electrical equivalent circuit depend on the temperature and the microstructure of samples. The resistive and capacitive properties of the investigated samples are dominated with the conduction and relaxation processes associated with the grain boundaries mechanism..

scholarly journals Simultaneous Multi-Bragg Peak Coherent X-ray Diffraction Imaging

Crystals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 312
Author(s):  
Florian Lauraux ◽  
Stéphane Labat ◽  
Sarah Yehya ◽  
Marie-Ingrid Richard ◽  
Steven J. Leake ◽  
...  
Keyword(s):  
Bragg Reflection ◽  
Volume Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Crystal Substrate ◽  
In Series ◽  
Diffraction Imaging ◽  
Diffraction Patterns ◽  
Lattice Planes ◽  
Oriented Parallel

The simultaneous measurement of two Bragg reflections by Bragg coherent X-ray diffraction is demonstrated on a twinned Au crystal, which was prepared by the solid-state dewetting of a 30 nm thin gold film on a sapphire substrate. The crystal was oriented on a goniometer so that two lattice planes fulfill the Bragg condition at the same time. The Au 111 and Au 200 Bragg peaks were measured simultaneously by scanning the energy of the incident X-ray beam and recording the diffraction patterns with two two-dimensional detectors. While the former Bragg reflection is not sensitive to the twin boundary, which is oriented parallel to the crystal–substrate interface, the latter reflection is only sensitive to one part of the crystal. The volume ratio between the two parts of the twinned crystal is about 1:9, which is also confirmed by Laue microdiffraction of the same crystal. The parallel measurement of multiple Bragg reflections is essential for future in situ and operando studies, which are so far limited to either a single Bragg reflection or several in series, to facilitate the precise monitoring of both the strain field and defects during the application of external stimuli.

scholarly journals Impedance Spectroscopic Study of Nickel Sulfide Nanostructures Deposited by Aerosol Assisted Chemical Vapor Deposition Technique

Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1105
Author(s):  
Sadia Iram ◽  
Azhar Mahmood ◽  
Muhammad Fahad Ehsan ◽  
Asad Mumtaz ◽  
Manzar Sohail ◽  
...  
Keyword(s):  
Chemical Vapor Deposition ◽  
Vapor Deposition ◽  
Nickel Sulfide ◽  
Variable Temperature ◽  
Complex Impedance ◽  
Equivalent Circuit Model ◽  
Chemical Vapor ◽  
Relaxation Processes ◽  
Impedance Plot ◽  
Vapor Deposition Technique

This research aims to synthesize the Bis(di-isobutyldithiophosphinato) nickel (II) complex [Ni(iBu2PS2)] to be employed as a substrate for the deposition of nickel sulfide nanostructures, and to investigate its dielectric and impedance characteristics for applications in the electronic industry. Various analytical tools including elemental analysis, mass spectrometry, IR, and TGA were also used to further confirm the successful synthesis of the precursor. NiS nanostructures were grown on the glass substrates by employing an aerosol assisted chemical vapor deposition (AACVD) technique via successful decomposition of the synthesized complex under variable temperature conditions. XRD, SEM, TEM, and EDX methods were well applied to examine resultant nanostructures. Dielectric studies of NiS were carried out at room temperature within the 100 Hz to 5 MHz frequency range. Maxwell-Wagner model gave a complete explanation of the variation of dielectric properties along with frequency. The reason behind high dielectric constant values at low frequency was further endorsed by Koops phenomenological model. The efficient translational hopping and futile reorientation vibration caused the overdue exceptional drift of ac conductivity (σac) along with the rise in frequency. Two relaxation processes caused by grains and grain boundaries were identified from the fitting of a complex impedance plot with an equivalent circuit model (Rg Cg) (Rgb Qgb Cgb). Asymmetry and depression in the semicircle having center present lower than the impedance real axis gave solid justification of dielectric behavior that is non-Debye in nature.

PIEZOELECTRIC PROPERTIES OF PZT FILMS PREPARED BY HYDROTHERMAL METHOD

2006 ◽  
Vol 20 (25n27) ◽  
pp. 3805-3810 ◽  
Author(s):  
NOBUYOSHI FUJIWARA ◽  
KAZUHIRO KUSUKAWA ◽  
KHAIRUNISAK ABDUL RAZAK ◽  
WEI GAO
Keyword(s):  
Hydrothermal Method ◽  
Lead Zirconate Titanate ◽  
Piezoelectric Properties ◽  
Compressive Loading ◽  
Pure Titanium ◽  
Lead Zirconate ◽  
Loading Frequency ◽  
X Ray Diffraction ◽  
Pzt Films ◽  
Transverse Effect

Lead zirconate titanate (PZT) thin films of 5 μm thick were produced by a hydrothermal method on pure titanium substrates. ZrOCl 2-8 H 2 O , Pb ( NO 3)2 and TiO 2 were used as precursors and KOH as a promoter. The hydrothermal synthesis of PZT includes nucleation and crystal growth processes at 120°C or 140°C. The crystallization states were investigated by using scanning electron microscopy and X-Ray diffraction. Piezoelectric properties were evaluated from unimorph cantilever type actuators made of the films. The relationships between the deflection of the actuator due to piezoelectric transverse effect and applied electric field in the direction of thickness of the films showed good linearity. The output voltage from the films under cyclic compressive loading increased with increasing loading frequency, and is saturated at 10 Hz. The PZT films produced by the present methods are satisfactory as a smart material, and are better than the films produced using TiCl 4 as Ti precursor.

Cetyltrimethylammonium bromide- and ethylene glycol-assisted preparation of mono-dispersed indium oxide nanoparticles using hydrothermal method

2014 ◽  
Vol 68 (8) ◽  
Author(s):  
Selvakumar Dhanasingh ◽  
Dharmaraj Nallasamy ◽  
Saravanan Padmanapan ◽  
Vinod Padaki
Keyword(s):  
Ethylene Glycol ◽  
Hydrothermal Method ◽  
Indium Oxide ◽  
Cetyltrimethylammonium Bromide ◽  
Oxide Nanoparticles ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
Diffraction Patterns

AbstractThe influence of cetyltrimethylammonium bromide and ethylene glycol on the size and dispersion of indium oxide nanoparticles prepared under hydrothermal conditions was investigated. The precursor compound, indium hydroxide, obtained by the hydrothermal method in the absence as well as the presence of cetyltrimethylammonium bromide, was converted to indium oxide by sintering at 400°C. The formation of nanoscale indium oxide upon sintering was ascertained by the characteristic infrared adsorption bands and X-ray diffraction patterns of indium oxide. Transmission electron microscopy and band gap values confirmed that the cetyltrimethylammonium bromide facilitated the formation of indium oxide nanoparticles smaller in size and narrower in distribution than those prepared without the assistance of cetyltrimethylammonium bromide.

Phase Formation in FeOx-SiO2-Cu2O-ZnO-FeS System during Melts Crystallization

2010 ◽  
Vol 297-301 ◽  
pp. 602-607
Author(s):  
Evgeny N. Selivanov ◽  
R.I. Gulyaeva ◽  
N.I. Selmenskich
Keyword(s):  
Cooling Rate ◽  
Phase Formation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Two Samples ◽  
And Calorimetry

The phase formation in oxide-sulphidic systems was studied with the use of X-ray diffraction, mineralography, combined thermogravimetry and calorimetry, in addition to Х-ray spectral microanalysis. The purpose of this work was to estimate the effect of cooling rate of melts in FeOx-SiO2-Cu2O-ZnO-FeS systems on structure and content of the resulting phases. Test subjects were two samples having following compositions (wt. %): I - 40.5 Fe, 2.41 S, 0.87 Cu, 3.87 Zn, 32.1 SiO2 and II - 40.7 Fe, 3.05 S, 8.55 Cu, 4.1 Zn and 19.5 SiO2. Cooling rate of the melts was changed from 0.3 up to 900оС/s.

Preparation of NiO Microspheres by Hydrothermal Method and its Electrochemical Capacitive Properties

2015 ◽  
Vol 814 ◽  
pp. 81-85 ◽  
Author(s):  
Qian Qian Li ◽  
Run Hua Fan ◽  
Ke Lan Yan ◽  
Kai Sun ◽  
Xu Ai Wang ◽  
...  
Keyword(s):  
Hydrothermal Method ◽  
Electrochemical Impedance ◽  
Specific Capacity ◽  
Rate Capability ◽  
Average Diameter ◽  
Three Dimensions ◽  
Electrochemical Characteristics ◽  
X Ray Diffraction ◽  
High Specific Capacity ◽  
Capacitive Properties

The precursor Ni (OH)2 was synthesized by a simple hydrothermal method with hexamethylenetetramine ((CH2)6N4) as precipitant and template, and then NiO was gained after calcination. The phase and morphology of the synthesized product were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM), and the electrochemical capacitive characterization was performed using cyclic voltammetry (CV), chronopotentiometry and electrochemical impedance spectroscopy (EIS) in a 6mol/L KOH aqueous solution electrolyte. The result shows that spherical NiO without impurity was synthesized, the average diameter of the spheres is 5 um and these spheres were constructed by the interactive arrangement of many nanoflakes in three dimensions. This kind of NiO shows the typical electrochemical characteristics of pseudo capacitance with high specific capacity and excellent rate capability. The specific capacity can reach 515F/g at the current density of 1A/g

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