Facile Combustion Synthesis of (Y,Pr)2O3 Red Phosphor: Study of Luminescence Dependence on Dopant Concentration and Enhancement by the Effect of Co-dopant

2020 ◽  
Vol 75 (4) ◽  
pp. 357-371
Author(s):  
K. Vini ◽  
K. M. Nissamudeen
Keyword(s):  
Luminescence Intensity ◽  
Dopant Concentration ◽  
Combustion Method ◽  
X Ray Diffraction ◽  
Praseodymium Oxide ◽  
Co Doping ◽  
Luminescence Efficiency ◽  
Transmission Electron ◽  
Munk Function ◽  
20 Nm

AbstractThere occurs a great interest in explaining the dependence of dopant concentration on the luminescence efficiency of rare earth oxides. Unambiguously, this study explains that luminescence intensity increases with increase in dopant concentration only up to optimised value. The syntheses of doped and co-doped yttrium oxide (Y2O3) nanophosphors in this study were carried out by making use of combustion method. This method produces the nanophosphors that have sizes ranging between 5 and 20 nm as confirmed by transmission electron microscopy. X-ray diffraction pattern confirms that the incorporation of praseodymium oxide (Pr3+) and gadolinium oxide (Gd3+) does not cause any change in the cubic structure of Y2O3. The phase purity has been confirmed by Fourier transform infrared spectrum. Diffuse reflectance spectra reveal that the bandgap increases with increase in annealing temperature. Bandgap has been calculated by making use of the Kubelka–Munk function. Strongest emission was observed at 605 nm with 2 wt% of Pr3+ as optimised concentration. Replacement of Y3+ by Gd3+ partially enhances the 605-nm emission linearly. The [Y:Pr:Gd] exhibits luminescence intensity of 2.705 times more than that of Y:Pr nanophosphors. This is for the first time our team has made a detailed study regarding the effects of co-doping in the case of Y2O3:Pr powders. We have successfully presented the changes that happen to the particle after co-doping especially in the particle size and luminescence properties.

scholarly journals Enhanced Photocatalytic Activity of Vanadium-Doped SnO2 Nanoparticles in Rhodamine B Degradation

2019 ◽  
Vol 2019 ◽  
pp. 1-11 ◽  
Author(s):  
H. Letifi ◽  
Y. Litaiem ◽  
D. Dridi ◽  
S. Ammar ◽  
R. Chtourou
Keyword(s):  
Photocatalytic Activity ◽  
Rhodamine B ◽  
Crystal Size ◽  
Sno2 Nanoparticles ◽  
X Ray Diffraction ◽  
Optical Studies ◽  
Vanadium Concentration ◽  
X Ray ◽  
Transmission Electron ◽  
20 Nm

In this paper, we have reported a novel photocatalytic study of vanadium-doped SnO2 nanoparticles (SnO2: V NPs) in rhodamine B degradation. These NPs have been prepared with vanadium concentrations varying from 0% to 4% via the coprecipitation method. Structural, morphological, and optical properties of the prepared nanoparticles have been investigated by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, transmission electron microscope (TEM), and UV-Vis and photoluminescence (PL) spectroscopy. Structural properties showed that both undoped and SnO2: V NPs exhibited the tetragonal structure, and the average crystal size has been decreased from 20 nm to 10 nm with the increasing doping level of vanadium. Optical studies showed that the absorption edge of SnO2: V NPs showed a redshift with the increasing vanadium concentration. This redshift leads to the decrease in the optical band gap from 3.25 eV to 2.55 eV. A quenching in luminescence intensity has been observed in SnO2: V NPs, as compared to the undoped sample. Rhodamine B dye (RhB) has been used to study the photocatalytic degradation of all synthesized NPs. As compared to undoped SnO2 NPs, the photocatalytic activity of SnO2: V NPs has been improved. RhB dye was considerably degraded by 95% within 150 min over on the SnO2: V NPs.

scholarly journals Synthesis, Structure, and Luminescent Properties of Europium-Doped Hydroxyapatite Nanocrystalline Powders

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Carmen Steluta Ciobanu ◽  
Simona Liliana Iconaru ◽  
Florian Massuyeau ◽  
Liliana Violeta Constantin ◽  
Adrian Costescu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Textural Properties ◽  
Average Crystallite Size ◽  
Luminescent Properties ◽  
Nanocrystalline Powders ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vibrational Studies ◽  
20 Nm

The luminescent europium-doped hydroxyapatite (Eu:HAp, Ca10−xEux(PO4)6(OH)2) with0≤x≤0.2nanocrystalline powders was synthesized by coprecipitation. The structural, morphological, and textural properties were well characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The vibrational studies were performed by Fourier transform infrared, Raman, and photoluminescence spectroscopies. The X-ray diffraction analysis revealed that hydroxyapatite is the unique crystalline constituent of all the samples, indicating that Eu has been successfully inserted into the HAp lattice. Eu doping inhibits HAp crystallization, leading to a decrease of the average crystallite size from around 20 nm in the undoped sample to around 7 nm in the sample with the highest Eu concentration. Furthermore, the samples show the characteristic5D0→7F0transition observed at 578 nm related to Eu3+ions distributed on Ca2+sites of the apatitic structure.

Ferromagnetism, Raman Spectra and Photoluminescence of Sn0.91Co0.05Ce0.04O2 and Sn0.91Fe0.05Ce0.04O2 Nanorods

2012 ◽  
Vol 488-489 ◽  
pp. 226-229
Author(s):  
Jasneet Kaur ◽  
R.K. Kotnala ◽  
Vinay Gupta ◽  
Kuldeep Chand Verma
Keyword(s):  
Raman Spectroscopy ◽  
Magnetic Measurements ◽  
Room Temperature Ferromagnetism ◽  
Sol Gel ◽  
Stoichiometric Ratio ◽  
Chemical Route ◽  
Structural Modifications ◽  
Co Doping ◽  
Transmission Electron ◽  
20 Nm

In the present work, we have fabricated Sn0.91Co0.05Ce0.04O2 (SCC54) and Sn0.91Fe0.05Ce0.04O2 (SFC54) nanorods by a chemical route similar to sol-gel method. X-ray diffraction (XRD), transmission electron microscopy (TEM), Raman spectroscopy, photoluminescence (PL) and magnetic measurements are used to characterize these nanorods. XRD pattern shows the polycrystalline nature of rods and TEM confirms that the diameter of rods lie in the range of 15-20 nm and length 100-200 nm. It is observed that on Ce3+ co-doping, nanoparticles assembled themselves into rod like structures. The SCC54 and SFC54 specimens exhibit room temperature ferromagnetism. Their saturated magnetic moment and phase transition temperature is sensitive to their size and stoichiometric ratio. Raman spectroscopy shows an intensity loss of classical cassiterite SnO2 vibration lines, which is indication of significant structural modifications like crystallinity and nano metric size effects on the vibrational properties. From PL spectra, an intense blue luminescence centred at a wavelength of 532 nm is observed in the prepared SnO2 nanostructures, attributed to oxygen-related defects, introduced during the growth process.

Characterization and their Fluorescence of Fe3+-Doped La2Zr2O7 Nanocrystals by a Salt-Assistant Combustion Method

2011 ◽  
Vol 306-307 ◽  
pp. 1257-1261 ◽  
Author(s):  
Yun Shan Bai ◽  
Lu De Lu ◽  
Jian Chun Bao
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Solid Solutions ◽  
Low Cost ◽  
Combustion Process ◽  
Combustion Method ◽  
Crystal Form ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
Transmission Electron

Nanocrystalline Fe3+-doped La2Zr2O7 series solid solutions were prepared by a convenient salt-assisted combustion process using glycine as fuel. The samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM). The results showed the La ion can be partially replaced by Fe ion. The partial substituted products were still single-phase solid solutions and the crystal form remained unchanged. TEM images reveal that the products are composed of well-dispersed square-shaped nanocrystals. The method provides a convenient and low-cost route for the synthesis of nanostructures of oxide materials. The fluorescence of La1.8Fe0.2Zr2O7 nanocrystals was evaluated by the UV-visible absorption spectra and the fluorescence spectra. The results indicate that (LaxFe1-x)2Zr2O7 nanocrystals prepared by this method are a kind of potential fluorescent-emitted material.

Nanoporous Ni and Ni-Cu Fabricated by Dealloying

2009 ◽  
Vol 1228 ◽  
Author(s):  
Masataka Hakamada ◽  
Yasumasa Chino ◽  
Mamoru Mabuchi
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Noble Metals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
The Difference ◽  
20 Nm ◽  
Good Workability ◽  
Scanning Electron

AbstractMetallic nanoporous architecture can be spontaneously attained by dealloying of a binary alloy. The nanoporous architecture can be often fabricated in noble metals such as Au and Pt. In this study, nanoporous Ni, Ni-Cu are fabricated by dealloying rolled Ni-Mn and Cu-Ni-Mn alloys, respectively. Unlike conventional Raney nickel composed of brittle Ni-Al or Cu-Al intermetallic compounds, the initial alloys had good workability probably because of their fcc crystal structures. After the electrolysis of the alloys in (NH4)2SO4 aqueous solution, nanoporous architectures of Ni and Ni-Cu with pore and ligament sizes of 10–20 nm were confirmed by scanning electron microscopy and transmission electron microscopy. X-ray diffraction analyses suggested that Ni and Cu atoms form a homogeneous solid solution in the Ni-Cu nanoporous architecture. The ligament sizes of nanoporous Ni and Ni-Cu were smaller than that of nanoporous Cu, reflecting the difference between diffusivities of Ni and Cu at solid/electrolyte interface. Ni can reduce the pore and ligament sizes of resulting nanoporous architecture when added to initial Cu-Mn alloys.

Mechanical Stress, Grain-boundary Relaxation, and Oxidation of Sputtered CuNi(Mn) Films

1999 ◽  
Vol 14 (4) ◽  
pp. 1286-1294 ◽  
Author(s):  
W. Brückner ◽  
W. Pitschke ◽  
S. Baunack ◽  
J. Thomas
Keyword(s):  
Grain Boundary ◽  
Microstructural Characterization ◽  
Excess Vacancy ◽  
X Ray Diffraction ◽  
Force Microscopy ◽  
Atomic Force ◽  
Transmission Electron ◽  
Boundary Relaxation ◽  
20 Nm ◽  
Atomic Rearrangement

This paper focuses on understanding stress development in CuNi42Mn1 thin films during annealing in Ar. In addition to stress-temperature measurements, resistance-temperature investigations and chemical and microstructural characterization by Auger electron spectroscopy, scanning and transmission electron microscopy, x-ray diffraction, and atomic force microscopy were also carried out. The films are polycrystalline with a grain size of 20 nm up to 450 °C. To explain the stress evolution above 120 °C, atomic rearrangement (excess-vacancy annihilation, grain-boundary relaxation, and shrinkage of grain-boundary voids) and oxidation were considered. Grain-boundary relaxation was found to be the dominating process up to 250–300 °C. A sharp transition from compressive to tensile stress between 300 and 380 °C is explained by the formation of a NiO surface layer due to reaction with the remaining oxygen in the Ar atmosphere. This oxidation is masking the inherent structural relaxation above 300 °C.

TiO2 Nanoparticles Synthesized with Ti(SO4)2 as Precursor via the Hydrothermal Method and their Optical Absorption Properties

2017 ◽  
Vol 727 ◽  
pp. 280-283
Author(s):  
Xiao Ming Fu
Keyword(s):  
Hydrothermal Method ◽  
Ph Value ◽  
Blue Shift ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Absorption Properties ◽  
Tem Analysis ◽  
Visible Absorption ◽  
Transmission Electron ◽  
20 Nm

Anatase TiO2 particles of about 20 nm in the diameter were successfully synthesized with Ti (SO4)2 as titanium source and stronger ammonia water as precipitant at 240°C for 48 h with pH=5 using the hydrothermal method. The samples were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM) and ultraviolet-visible absorption spectroscopy (UV-VIS). XRD analysis showed that the phase of the samples was anatase TiO2. TEM analysis confirmed that TiO2 particles of about 50 nm in the diameter were obtained when the pH value was 0.12. With the increasement of the pH value, the size of as-prepared TiO2 particles became remarkably fine. However, with the further increase of the pH value, the size of TiO2 particles was not obvious. TiO2 particles of about 20 nm in the diameter were obtained when the pH value was 5. And UV-VIS results showed that the size of anatase TiO2 nanoparticles, which became small, was propitious to the blue shift of their absorption peak.

Frequency dependence and fuel effect on optical properties of nano TiO2-based structures

2016 ◽  
Vol 30 (18) ◽  
pp. 1650247 ◽  
Author(s):  
Mahdi Ghasemifard ◽  
Misagh Ghamari ◽  
Meysam Iziy
Keyword(s):  
Particle Size ◽  
Optical Properties ◽  
Average Particle Size ◽  
Combustion Method ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Nano Tio2 ◽  
Transmission Electron ◽  
Auto Combustion ◽  
Xrd Patterns

TiO2-(Ti[Formula: see text]Si[Formula: see text]O2 nanopowders (TS-NPs) with average particle size around 90 nm were successfully synthesized by controlled auto-combustion method by using citric acid/nitric acid (AC:NA) and urea/metal cation (U:MC). The structure of powders was studied based on their X-ray diffraction (XRD) patterns. The XRD of TS-NPs shows that rutile and anatase are the main phases of TS-NPs for AC:NA and U:MC, respectively. Particle size and histogram of nanopowders were characterized by transmission electron microscopy (TEM) and dynamic light scattering (DLS). Optical properties of TS-NPs were calculated by Fourier transform infrared spectroscopy (FTIR) and Kramers–Kroning (KK) relation. Plasma frequencies of TS-NPs obtained from energy loss functions depend on fuels as a result of changes in crystal structure, particle size distribution, and morphology.

Nanocrystallization of gas atomized Cu47Ti33Zr11Ni8Si1 metallic glass

2006 ◽  
Vol 21 (3) ◽  
pp. 597-607 ◽  
Author(s):  
S. Venkataraman ◽  
S. Scudino ◽  
J. Eckert ◽  
T. Gemming ◽  
C. Mickel ◽  
...  
Keyword(s):  
Metallic Glass ◽  
Primary Crystallization ◽  
Nanocrystalline Phase ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
High Resolution Tem ◽  
20 Nm ◽  
Annealing Experiments

Cu47Ti33Zr11Ni8Si1 metallic glass powder was prepared by gas atomization. Decomposition in the amorphous alloy and primary crystallization has been studied by differential scanning calorimetry (DSC), x-ray diffraction (XRD), and transmission electron microscopy (TEM). The glassy powder exhibits a broad DSC exotherm prior to bulk crystallization. Controlled annealing experiments reveal that this exotherm corresponds to a combination of structural relaxation and nanocrystallization. A uniform featureless amorphous contrast is observed in the TEM prior to the detection of nanocrystals of 4–6 nm in size. High-resolution TEM studies indicate that this nanocrystalline phase has a close crystallographic relationship with the γ–CuTi phase having a tetragonal structure. The product of the main crystallization event is also nanocrystalline, hexagonal Cu51Zr14, having dimensions of 20 nm. However, there is no evidence for possible amorphous phase separation prior to the nanocrystallization events.

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