scholarly journals Towards a Correlation between Structural, Magnetic, and Luminescence Properties of CeF3:Tb3+ Nanocrystals

Materials ◽  
2020 ◽  
Vol 13 (13) ◽  
pp. 2980
Author(s):  
Cristina Bartha ◽  
Corina Secu ◽  
Elena Matei ◽  
Catalin Negrila ◽  
Aurel Leca ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Magnetic Susceptibility ◽  
Uv Light ◽  
Nanocrystalline Phase ◽  
Magnetization Curves ◽  
X Ray Diffraction ◽  
Green Luminescence ◽  
X Ray ◽  
Light Excitation ◽  
Paramagnetic Properties

In this study, we report on the structural, magnetic, and optical properties of Tb3+-doped CeF3 nanocrystals prepared via a polyol-assisted route, followed by calcination. X-ray diffraction analysis and electron microscopy investigations have shown the formation of a dominant Ce0.75F3 nanocrystalline phase (of about 99%), with a relatively uniform distribution of nanocrystals about 15 nm in size. Magnetization curves showed typical paramagnetic properties related to the presence of Ce3+ and Tb3+ ions. The magnetic susceptibility showed a weak inflexion at about 150 K, assigned to the cerium ions’ crystal field splitting. Under UV light excitation of the Ce3+ ions, we observed Tb3+ green luminescence with a quantum yield of about 20%.

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.

Uniform Cerium-Based Coordination Polymer Microspheres: Preparation and Upconversion Emission

2016 ◽  
Vol 16 (4) ◽  
pp. 3705-3709 ◽  
Author(s):  
Zhi-Wen Nie ◽  
Cheng-Hui Zeng ◽  
Gang Xie ◽  
Sheng-Liang Zhong
Keyword(s):  
Electron Microscopy ◽  
Coordination Polymer ◽  
Large Scale ◽  
Upconversion Emission ◽  
X Ray Diffraction ◽  
X Ray ◽  
Band Emission ◽  
Transmission Electron ◽  
Light Excitation ◽  
Luminescent Spectra

Homogeneously doped Yb3+ and Er3+ cerium-based coordination polymer (CP) microspheres have been successfully synthesized on a large scale through a simple solvothermal route with 2, 5-pyridinedicarboxylic acid (2, 5-H2PDC) as the organic linker. CeO2:Yb3+, Er3+ porous microspheres were obtained by annealing the corresponding CP microspheres at 600 °C for 4 h under atmospheric pressure. These as-prepared products were characterized by Powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), energy-dispersion X-ray (EDX) spectroscopy, Thermogravimetric (TG) and derivative thermogravimetric (DTG) analysis. The room temperature upconversion luminescent spectra of the as-prepared microspheres were carried out by 980 nm NIR light excitation. Interestingly, Yb3+ and Er3+ codoped CP microspheres give a single-band emission centered at 673 nm, while the CeO2:Yb3+, Er3+ microspheres give emission in green and red region, with red being the dominant emission. The emission intensity of the CeO2:Yb3+, Er3+ microspheres were much stronger than that of the Yb3+ and Er3+ codoped CP microspheres.

scholarly journals Hydrothermal synthesis of ZnO quantum dot/KNb3O8 nanosheet photocatalysts for reducing carbon dioxide to methanol

2017 ◽  
Vol 8 ◽  
pp. 2264-2270 ◽  
Author(s):  
Xiao Shao ◽  
Weiyue Xin ◽  
Xiaohong Yin
Keyword(s):  
Electron Microscopy ◽  
Quantum Dots ◽  
Uv Light ◽  
Formation Rate ◽  
X Ray Diffraction ◽  
Methanol Production ◽  
X Ray ◽  
Transmission Electron ◽  
Methanol Formation ◽  
Zno Quantum Dots

ZnO quantum dots and KNb3O8 nanosheets were synthesized by a two-step hydrothermal method for the photocatalytic reduction of CO2 to methanol where isopropanol is simultaneously oxidized to acetone . The as-prepared photocatalysts were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and UV–vis absorption spectroscopy (UV–vis). The photocatalytic activity of the materials was evaluated by formation rate of methanol under UV light irradiation at ambient temperature and pressure. The methanol formation rate of pure KNb3O8 nanosheets was found to be 1257.21 μmol/g/h, and after deposition of 2 wt % ZnO quantum dots on the surface of KNb3O8 nanosheets, the methanol production rate was found to increase to 1539.77 μmol/g/h. Thus, the ZnO quantum dots obviously prompted separation of charge carriers, which was explained by a proposed mechanism for this photocatalytic reaction.

Solvothermal Synthesis of Novel 3D Peony-Like TiO2 Microstructures and its Enhanced Photocatalytic Activity

NANO ◽  
2018 ◽  
Vol 13 (05) ◽  
pp. 1850056 ◽  
Author(s):  
Yugan He ◽  
Qi Yan ◽  
Xiaoyu Chang ◽  
Meiying Zhu ◽  
Weiwei Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Reaction Time ◽  
Uv Light ◽  
X Ray Diffraction ◽  
Reaction Parameters ◽  
X Ray ◽  
Uv Light Irradiation ◽  
Transmission Electron ◽  
Irradiation Power ◽  
Degussa P25

A TiO2 photocatalyst with peony-like microstructures and a large percentage of exposed {001} facets was synthesized using a facile solvethermal method. The peony-like TiO2 was obtained using HF as a capping agent, TiCl4 as the precursor and ethanol as the solvothermal agent. The parameters which influence the mophology and formation mechanism of the products including the HF concentration, the reaction time and temperature and the solvothermal solvent, were investigated. The samples were characterized using field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction and N2 adsorption and desorption analysis. As the reaction time or reaction temperature increased, the morphology TiO2 changed from hexagonally assembled microspheres to peony-like microflowers which were composed of stacks of ultrathin nanosheets. The other reaction parameters also play a crucial role in the formation of the TiO2 microstuctures. Photocatalytic experiments showed that the synthesized TiO2 outperformed Degussa P25 in the photodegradation of methelene blue under a very weak UV light irradiation (power: 8[Formula: see text]W, light intensity: 0.4[Formula: see text]mW[Formula: see text]cm[Formula: see text]).

Darstellung und Charakterisierung des Silber(I,II,III)-oxidclathrates Ag7O8HCO3 / Synthesis and Characterization of the Silver(I,II,III) Oxide Clathrate Ag7O8HCO3

2000 ◽  
Vol 55 (9) ◽  
pp. 882-886 ◽  
Author(s):  
Martin Jansen ◽  
Sascha Vensky
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Scanning Electron Microscopy ◽  
Magnetic Susceptibility ◽  
Solid State Nmr ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

The silver(I,II,III) oxide clathrate Ag7O8HCO3 was synthesized by anodic oxidation of silver(I) in a suspension of Ag2CO3 in an aqueous AgF solution. The title compound was characterized by single crystal X-ray diffraction (cubic, Fm3̄m, a = 9.8085(3) Å, Z = 4), scanning electron microscopy, thermal analysis, IR spectroscopy, 1H-solid state-NMR and measurement of the magnetic susceptibility

scholarly journals Synthesis, Characterization, and Photocatalytic Performance of Mesoporous α-Mn2O3 Microspheres Prepared via a Precipitation Route

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Manoj Pudukudy ◽  
Zahira Yaakob
Keyword(s):  
Electron Microscopy ◽  
Uv Light ◽  
Thermal Transformation ◽  
Xrd Analysis ◽  
Structural Deformation ◽  
Blue Dye ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
X Ray ◽  
Transmission Electron

α-Mn2O3 microspheres with high phase purity, crystallinity, and surface area were synthesized by the thermal decomposition of precipitated MnCO3 microspheres without the use of any structure directing agents and tedious reaction conditions. The prepared Mn2O3 microspheres were characterized by Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) and photoluminescence (PL) studies. The complete thermal transformation of MnCO3 to Mn2O3 was clearly shown by the FTIR and XRD analysis. The electron microscopic images clearly confirmed the microsphere-like morphology of the products with some structural deformation for the calcined Mn2O3 sample. The mesoporous texture generated from the interaggregation of subnanoparticles in the microstructures is visibly evident from the TEM and BET studies. Moreover, the Mn2O3 microstructures showed a moderate photocatalytic activity for the degradation of methylene blue dye pollutant under UV light irradiation, using air as the potential oxidizing agent.

Hydrothermal Synthesis and Photocatalytic Properties of Flower-Like CdS Nanostructures

2011 ◽  
Vol 335-336 ◽  
pp. 460-463 ◽  
Author(s):  
Hong Mei Wang ◽  
Da Peng Zhou ◽  
Yuan Lian ◽  
Ming Pang ◽  
Dan Liu
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Uv Light ◽  
Sulfur Source ◽  
X Ray Diffraction ◽  
Facile Hydrothermal Method ◽  
X Ray ◽  
Transmission Electron ◽  
Cds Nanostructures

Hexagonal flower-like CdS nanostructures were successfully synthesized through a facile hydrothermal method with thiourea as sulfur source. By combining the results of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), the structural and morphological characterizations of the products were performed. The photocatalytic activity of CdS nanostructures had been tested by degradation of Rhodamine B (RB) under UV light compared to commercial CdS powders, which indicated that the as-syntherized CdS nanostructures exhibited enhanced photocatalytic activity for degradation of RB. The possible growth mechanism of CdS nanostructures was proposed in the end.

Synthesis of nanocomposite coating of electrodeposed amorphic layers of the Ni–P–W system

2020 ◽  
pp. 53-60
Author(s):  
A. V. Krasikov
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Differential Scanning Calorimetry ◽  
Phase Composition ◽  
Diffraction Analysis ◽  
Nanocomposite Coating ◽  
Nanocrystalline Phase ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray

The processes of the formation of the nanocomposite coating of Ni–11.5% P–5%W were studied during the heat treatment of amorphous electrodeposited layers. Using the method of differential scanning calorimetry, the temperature of the onset of crystallization of the nanocrystalline phase Ni3P was determined. X-ray diffraction analysis showed that heat treatment produces Ni3P phosphides and, presumably, Ni5P2, the size of which, according to electron microscopy, is 5–50 nm. The influence of the duration of heat treatment on the phase composition and microhardness of coatings is investigated.

Platinum Reduction Study on Pt/C Electro-catalysts for PEMFC

2013 ◽  
Vol 16 (3) ◽  
pp. 141-145
Author(s):  
M.L. Hernandez-Pichardo ◽  
R. Gonzalez-Huerta ◽  
P. del Angel ◽  
E. Palacios-Gonzalez ◽  
M. Tufiño-Velazquez ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Uv Light ◽  
Reducing Agents ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Synthesis Conditions ◽  
Platinum Species ◽  
Scanning Electron

Platinum reduction on Pt/C catalysts was studied on samples prepared by the impregnation method using different Pt precursors and reducing agents such as ethanol, sodium borohydride and ethanol-UV light (photo-assisted reduction), in order to compare the efficiency of the different reducing agents. The influence of the reduction level of the platinum species on the electrochemical behavior of these catalysts has been determined. The catalysts were characterized by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and linear and cyclic voltammetry. The results show that the reduction level depends mainly on the platinum precursor. Moreover, it was found that the higher electrochemical activity was found using catalysts reduced with ethanol, whereas by using NaBH4 as the reducing agent, the total reduction of the platinum precursor is very difficult in same synthesis conditions. The analysis of the XPS results shows that samples reduced with ethanol presented the lower PtOx/Pt reduction ratio.

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