Solvothermal Preparation and Thermal Phase Change Behaviors of Nanosized Tetragonal-Phase Silver Selenide (Ag2Se)

2013 ◽  
Vol 850-851 ◽  
pp. 128-131 ◽  
Author(s):  
Jun Li Wang ◽  
Hui Feng ◽  
Wei Ling Fan
Keyword(s):  
Transition Temperature ◽  
Phase Change ◽  
Photoelectron Spectroscopy ◽  
Tetragonal Phase ◽  
Room Temperature ◽  
Variable Temperature ◽  
Cubic Phase ◽  
Silver Selenide ◽  
X Ray ◽  
Change Behaviors

Nanocrystalline silver selenide (Ag2Se) with an average diameter of 100 nm were prepared by a facile solvothermal method. X-ray energy dispersive (EDS) spectroscopy and X-ray photoelectron spectroscopy (XPS) studies confirmed that the products were pure Ag2Se. Room-temperature powder X-ray diffraction (XRD) measurements indicated that the as-prepared Ag2Se nanocrystals exhibit a metastable tetragonal polymorphic phase, rather than the common orthorhombic phase at room temperature. The variable-temperature XRD and differential scanning calorimetry (DSC) thermal analysis techniques were used to investigate the phase change behaviors of the tetragonal Ag2Se nanocrystals, and the results showed that the low-temperature tetragonal phase transforms to the high-temperature cubic phase at about 106 °C. This transition temperature is lower by ~30 °C than the orthorhombic-cubic transition temperature (133140 °C) previously reported for Ag2Se. Meanwhile, two exothermic peaks, loaded at 61 and 89 °C, respectively, were detected in the cooling DSC scan for the cubic to tetragonal phase transition, and the reason was discussed.

High-temperature X-ray powder diffraction study of the tetragonal-cubic phase transition in nanocrystalline, compositionally homogeneous ZrO2–CeO2 solid solutions

2008 ◽  
Vol 23 (S1) ◽  
pp. S70-S74 ◽  
Author(s):  
L. M. Acuña ◽  
R. O. Fuentes ◽  
D. G. Lamas ◽  
I. O. Fábregas ◽  
N. E. Walsöe de Reca ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Phase Transition ◽  
High Temperature ◽  
Powder Diffraction ◽  
Solid Solutions ◽  
Tetragonal Phase ◽  
Room Temperature ◽  
Cubic Phase ◽  
X Ray ◽  
First Order

Crystal structure of compositionally homogeneous, nanocrystalline ZrO2–CeO2 solutions was investigated by X-ray powder diffraction as a function of temperature for compositions between 50 and 65 mol % CeO2. ZrO2-50 and 60 mol % CeO2 solid solutions, which exhibit the t′-form of the tetragonal phase at room temperature, transform into the cubic phase in two steps: t′-to-t″ followed by t″-to-cubic. But the ZrO2-65 mol % CeO2, which exhibits the t″-form, transforms directly to the cubic phase. The results suggest that t′-to-t″ transition is of first order, but t″-to-cubic seems to be of second order.

Temperature Dependent Raman Scattering and Dielectric Permittivity Measurements of Pb1−x Srx TiO3 Films

2003 ◽  
Vol 784 ◽  
Author(s):  
V. M. Naik ◽  
M. Smith ◽  
H. Dai ◽  
P. Talagala ◽  
R. Naik ◽  
...  
Keyword(s):  
Phase Transition ◽  
Dielectric Permittivity ◽  
Raman Spectra ◽  
Tetragonal Phase ◽  
Room Temperature ◽  
Cubic Phase ◽  
X Ray Diffraction ◽  
Phonon Modes ◽  
X Ray ◽  
Permittivity Measurements

ABSTRACTPb1-x Srx TiO3 (x = 0 to 1.0) films of thickness ∼ 4 μ m have been prepared on sapphire and Pt substrates by metalorganic decomposition (MOD) method. X-ray diffraction results show that the films are polycrystalline with a perovskite tetragonal phase at room temperature for x < 0.5 and a cubic phase for x > 0.5. Room temperature Raman spectra show a systematic variation of lattice vibrational modes with x. The most notable changes in the Raman spectra with x are the decrease in the splitting of A1(3TO) and E(3TO) modes and the disappearance of E(3TO) mode at x ∼ 0.6. Although the x-ray diffraction peaks for films with x > 0.5 show a cubic phase at room temperature, the Raman spectra show the characteristic phonon modes of a tetragonal phase even at x = 0.7. The dielectric permittivity versus temperature measurements for films with x ≤ 0.7 show a broad dielectric anomaly corresponding to a diffuse ferroelectric to paraelectric phase transition. The phase transition temperature (Tc) values are consistently lower than the corresponding bulk ceramic alloys. Furthermore, Tc are also determined by monitoring the temperature dependence of the splitting between E(3TO) and A1(3TO) phonon modes in the Raman spectra of Pb1-x Srx TiO3 films for x ≤ 0.6. There has been good agreement between the two methods.

Study on CdSe Nanoparticles Synthesized by Chemical Method

2013 ◽  
Vol 665 ◽  
pp. 267-282 ◽  
Author(s):  
M.P. Deshpande ◽  
Nitya Garg ◽  
Sandip V. Bhatt ◽  
Bindiya Soni ◽  
Sunil H. Chaki
Keyword(s):  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Cadmium Acetate ◽  
Cdse Nanoparticles ◽  
Effect Of Temperature ◽  
Longitudinal Optical Phonon ◽  
Cubic Phase ◽  
Phonon Modes ◽  
X Ray ◽  
Wide Range

CdSe is a II-VI group semiconducting material with optimum bulk band gap of 1.74eV. It is a promising material due to its wide range of technological applications in optoelectronics devices. CdSe nanoparticles have been synthesized at different temperatures starting from Room temperature to 80°C using appropriate precursor solutions containing Cadmium acetate, Triethanolamine (TEA), Ammonia and Sodium selenosulphate. The pH of Solution was around 10.50 ± 0.10 during synthesis. We confirmed the elemental analysis by Energy Dispersive X-ray Analysis (EDAX) and X-ray Photoelectron Spectroscopy (XPS) technique. X-Ray Diffraction (XRD) studies shows that the synthesized nanoparticles belonged to cubic phase with crystallite size lying between 2nm-4nm. The effect of temperature on particle size, lattice parameter, density of dislocation and strain were investigated. Blue shift of 103nm to125nm has been observed from optical absorption spectra and raman measurements performed at room temperature using He-Ne laser (632nm, 5mW) showed the presence of longitudinal optical phonon modes. Photoluminescence (PL) studies shows a shift of 30nm when compared with the bulk PL emission peak.

scholarly journals Assessing the importance of cation size in the tetragonal-cubic phase transition in lithium garnet electrolytes.

2021 ◽  
Author(s):  
Mark Stockham ◽  
Alice Griffiths ◽  
Bo Dong ◽  
Peter Slater
Keyword(s):  
Phase Transition ◽  
Transition Temperature ◽  
Cell Volume ◽  
Tetragonal Phase ◽  
Variable Temperature ◽  
Lithium Ion ◽  
Cubic Phase ◽  
Formula Unit ◽  
Electrochemical Window ◽  
Lithium Garnets

Lithium garnets are promising solid-state electrolytes for next generation lithium-ion batteries. These materials have high ionic conductivity, a wide electrochemical window and stability with Li metal. However, lithium garnets have a maximum limit of 7 lithium atoms per formula unit (e.g. La3Zr2Li7O12), before the system transitions from a cubic to a tetragonal phase with poor ionic mobility. This arises from full occupation of the Li sites. Hence, the most conductive lithium garnets have Li between 6-6.55 Li per formula unit, which maintains the cubic symmetry and the disordered Li sub-lattice. The tetragonal phase, however, forms the highly conducting cubic phase at higher temperatures, thought to arise from increased cell volume and entropic stabilisation permitting Li disorder. However, little work has been undertaken in understanding the controlling factors of this phase transition, which could enable enhanced dopant strategies to maintain room temperature cubic garnet at higher Li contents. Here, a series of nine tetragonal garnets were synthesised and analysed via variable temperature XRD to understand the dependence of site substitution on the phase transition temperature. Interestingly the octahedral site cation radius was identified as the key parameter for the transition temperature with larger or smaller dopants altering the transition temperature noticeably. A site substitution was, however, found to make little difference irrespective of significant changes to cell volume.

scholarly journals Synthesis of Magnetic Ferrocene-Containing Polymer with Photothermal Effects for Rapid Degradation of Methylene Blue

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 558
Author(s):  
Wenhui Zhu ◽  
Caiyun Zhang ◽  
Yali Chen ◽  
Qiliang Deng
Keyword(s):  
Methylene Blue ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Degradation Rate ◽  
Model Compound ◽  
Vibrating Sample Magnetometer ◽  
Simulated Sunlight ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir

Photothermal materials are attracting more and more attention. In this research, we synthesized a ferrocene-containing polymer with magnetism and photothermal properties. The resulting polymer was characterized by Fourier-transform infrared (FT-IR), vibrating sample magnetometer (VSM), scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Its photo-thermocatalytic activity was investigated by choosing methylene blue (MB) as a model compound. The degradation percent of MB under an irradiated 808 nm laser reaches 99.5% within 15 min, and the degradation rate is 0.5517 min−1, which is 145 times more than that of room temperature degradation. Under irradiation with simulated sunlight, the degradation rate is 0.0092 min−1, which is approximately 2.5 times more than that of room temperature degradation. The present study may open up a feasible route to degrade organic pollutants.

scholarly journals pH-controlled synthesis of sustainable lauric acid/SiO2 phase change material for scalable thermal energy storage

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shafiq Ishak ◽  
Soumen Mandal ◽  
Han-Seung Lee ◽  
Jitendra Kumar Singh
Keyword(s):  
Electron Microscopy ◽  
Phase Change ◽  
Lauric Acid ◽  
Photoelectron Spectroscopy ◽  
Phase Change Materials ◽  
Precursor Solution ◽  
Thermal Reliability ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Heating And Cooling

AbstractLauric acid (LA) has been recommended as economic, eco-friendly, and commercially viable materials to be used as phase change materials (PCMs). Nevertheless, there is lack of optimized parameters to produce microencapsulated PCMs with good performance. In this study, different amounts of LA have been chosen as core materials while tetraethyl orthosilicate (TEOS) as the precursor solution to form silicon dioxide (SiO2) shell. The pH of precursor solution was kept at 2.5 for all composition of microencapsulated LA. The synthesized microencapsulated LA/SiO2 has been characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), X-Ray photoelectron spectroscopy (XPS), Scanning electron microscopy (SEM), and Transmission electron microscopy (TEM). The SEM and TEM confirm the microencapsulation of LA with SiO2. Thermogravimetric analysis (TGA) revealed better thermal stability of microencapsulated LA/SiO2 compared to pure LA. PCM with 50% LA i.e. LAPC-6 exhibited the highest encapsulation efficiency (96.50%) and encapsulation ratio (96.15%) through Differential scanning calorimetry (DSC) as well as good thermal reliability even after 30th cycle of heating and cooling process.

Ferroelectric Tunability Studies in Doped BaTiO3 and Ba1−xSrxTiO3

2000 ◽  
Vol 658 ◽  
Author(s):  
Dong Li ◽  
M. A. Subramanian
Keyword(s):  
Curie Temperature ◽  
Phase Change ◽  
Tetragonal Phase ◽  
Cryogenic Temperature ◽  
Room Temperature ◽  
Co Doping ◽  
Structure Changes

ABSTRACTAcceptor and Donor codoped BaTiO3 and Ba1−xSrxTiO3 are prepared. For Ba1−xLaxTi1−xFexO3,BaTiO3 remains as tetragonal phase up to about 5mol% LaFeO3. For x ≥0.06, the structure changes to cubic at room temperature. The phase change shifts the Curie temperature to lower value and increases the tunability at room temperature. Doping of other acceptor (Al, Cr) and donor (Sm, Gd, Dy) ions has the same effect although with varying levels of tuning. BaTiO3: 4%LaFeO3 has the highest tunability among the studied systems, which is even higher than Ba0.6Sr0.4TiO3. Co-doping of (La, Fe) and (La, Al) in Ba1−xSrxTiO3 also lowers the Curie temperature and increases the tunability of high Ba content samples at cryogenic temperature.

scholarly journals A Highly Sensitive Room Temperature CO2 Gas Sensor Based on SnO2-rGO Hybrid Composite

Materials ◽  
2021 ◽  
Vol 14 (3) ◽  
pp. 522
Author(s):  
Zhi Yan Lee ◽  
Huzein Fahmi bin Hawari ◽  
Gunawan Witjaksono bin Djaswadi ◽  
Kamarulzaman Kamarudin
Keyword(s):  
Electron Microscopy ◽  
Carbon Dioxide ◽  
Gas Sensor ◽  
Photoelectron Spectroscopy ◽  
Hybrid Composite ◽  
Room Temperature ◽  
Co2 Gas ◽  
X Ray ◽  
Wide Range ◽  
Co2 Gas Sensor

A tin oxide (SnO2) and reduced graphene oxide (rGO) hybrid composite gas sensor for high-performance carbon dioxide (CO2) gas detection at room temperature was studied. Since it can be used independently from a heater, it emerges as a promising candidate for reducing the complexity of device circuitry, packaging size, and fabrication cost; furthermore, it favors integration into portable devices with a low energy density battery. In this study, SnO2-rGO was prepared via an in-situ chemical reduction route. Dedicated material characterization techniques including field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), energy dispersive X-ray (EDX) spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS) were conducted. The gas sensor based on the synthesized hybrid composite was successfully tested over a wide range of carbon dioxide concentrations where it exhibited excellent response magnitudes, good linearity, and low detection limit. The synergistic effect can explain the obtained hybrid gas sensor’s prominent sensing properties between SnO2 and rGO that provide excellent charge transport capability and an abundance of sensing sites.

ROOM TEMPERATURE PHOTOLUMINESCENCE OF POLYCRYSTALLINE SIC PREPARED FROM CARBON-SATURATED SI MELT

2002 ◽  
Vol 16 (06n07) ◽  
pp. 1047-1051
Author(s):  
JIANPING MA ◽  
ZHIMING CHEN ◽  
GANG LU ◽  
MINGBIN YU ◽  
LIANMAO HANG ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Uv Light ◽  
X Ray Diffraction ◽  
X Ray ◽  
Room Temperature Photoluminescence ◽  
Composition And Structure ◽  
Light Excitation ◽  
Scanning Electron

Intense photoluminescence (PL) has been observed at room temperature from the polycrystalline SiC samples prepared from carbon-saturated Si melt at a temperature ranging from 1500 to 1650°C. Composition and structure of the samples have been confirmed by means of X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. PL measurements with 325 nm UV light excitation revealed that the room temperature PL spectrum of the samples consists of 3 luminescent bands, the peak energies of which are 2.38 eV, 2.77 eV and 3.06 eV, respectively. The 2.38 eV band is much stronger than the others. It is suggested that some extrinsic PL mechanisms associated with defect or interface states would be responsible to the intensive PL observed at room temperature.

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