Synthesis of Lanthanide-Ion-Doped NaYF4 RGB Up-Conversion Nanoparticles for Anti-Counterfeiting Application

2018 ◽  
Vol 18 (12) ◽  
pp. 8207-8215 ◽  
Author(s):  
Guo Gong ◽  
Shaowen Xie ◽  
Ya Song ◽  
Haihu Tan ◽  
Jianxiong Xu ◽  
...  
Keyword(s):  
Hexagonal Phase ◽  
Lanthanide Ions ◽  
X Ray Diffraction ◽  
Uniform Size ◽  
Lanthanide Ion ◽  
Molar Ratios ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Luminescent Polymer ◽  
Luminescent Ink

Well-defined and mono-dispersed lanthanide-ion-doped NaYF4 up-conversion nanoparticles (UCNPs) were synthesized via thermal decomposition using lanthanide oleate as the precursor. By rational selecting the dopant pairs of the doped lanthanide ions (Y3+, Yb3+, Er3+ and Tm3+) with accurate molar ratios, three-primary-color (RGB) UCNPs which exhibited green (UCNPs-G), blue (UCNPs-B) and red (UCNPs-R) fluorescence, respectively, were prepared. The X-ray diffraction (XRD) patterns showed that the three UCNPs were purely hexagonal-phase NaYF4 crystals. Transmission electron microscopy (TEM) images revealed that the synthesized UCNPs exhibited well-defined nanosphere morphology with uniform size distribution. The average diameters were 23.95±3.35 nm for UCNPs-G, 20.63±2.59 nm for UCNPs-B, and 19.24±2.37 nm for UCNPs-R, respectively. After surface modification employing polyacrylic acid (PAA) as modifier, the obtained UCNPs were converted to be hydrophilic, which can be used as fillers to construct luminescent polymer films and luminescent ink in anti-counterfeiting application.

scholarly journals Solvothermal Synthesis ofGd2O3 : Eu3+Luminescent Nanowires

2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Guixia Liu ◽  
Song Zhang ◽  
Xiangting Dong ◽  
Jinxian Wang
Keyword(s):  
Large Scale ◽  
Hexagonal Phase ◽  
Infrared Spectrometry ◽  
Cubic Phase ◽  
X Ray Diffraction ◽  
Display Devices ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Facile Solvothermal Method ◽  
Better Than

UniformGd2O3 : Eu3+luminescent nanowires were prepared on a large scale by a facile solvothermal method using polyethylene glycol (PEG-2000) as template and ethanol as solvent; the properties and the structure were characterized. X-ray diffraction (XRD) patterns and Fourier transform infrared spectrometry (FTIR) showed that the precursors are hexagonal phaseGd(OH)3crystals, and the samples calcined at 800C°are cubic phaseGd2O3. Transmission Electron Microscopy (TEM) images indicated that the samples are nanowires with a diameter of 30 nm and a length of a few microns. Photoluminescence (PL) spectra showed that the ratio ofD50→F72toD50→F71transition peak of the calcined samples is stronger than that of the precursors, which confirmed that the color purity of theGd2O3 : Eu3+is better than that of the precursors. The as-obtainedGd2O3 : Eu3+luminescent nanowires show a strong red emission corresponding toD50→F72transition (610 nm) ofEu3+under ultraviolet excitation (250 nm), which have potential application in red-emitting phosphors and field emission display devices.

scholarly journals Effect of anions on the structural, morphological and dielectric properties of hydrothermally synthesized hydroxyapatite nanoparticles

2019 ◽  
Vol 2 (1) ◽  
Author(s):  
Lakshmanaperumal Sundarabharathi ◽  
Deepalekshmi Ponnamma ◽  
Hemalatha Parangusan ◽  
Mahendran Chinnaswamy ◽  
Mariam Al Ali Al-Maadeed
Keyword(s):  
Electron Microscopy ◽  
Dielectric Properties ◽  
Hexagonal Phase ◽  
Biological Properties ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Polarized Surface ◽  
Egg Shell ◽  
Xrd Patterns ◽  
Source Materials

Abstract Synthetic nano hydroxyapatites (HA) have been considered as potential biomaterials for bone tissue engineering applications because of its excellent biological properties. The present work deals with the synthesis of HA nanoparticles from different anion source materials via autoclave assisted hydrothermal method. All the prepared HA nanoparticles were characterized by X-ray diffraction (XRD), Fourier transformation infrared spectra, field emission scanning electron microscopy, energy dispersive spectra and high resolution transmission electron microscopy. The XRD patterns reveal the pure and hexagonal phase structure with smaller crystallite size for HA obtained from various calcium salt precursors. HA particles prepared from nitrate precursors show spherical morphology with 32 nm grain size whereas those derived from the acetate, chloride and egg shell precursors respectively show needle-like, irregular and oval morphology. The effect of different anions on the dielectric properties and alternating conductivity of HA is investigated, as a polarized surface can trigger biological reactions. For the particles obtained from nitrate, acetate, chloride and egg shell precursors respectively give dielectric constant (εʹ) values of 9.96, 13.22, 9.92 and 10.86 at 5 MHz. The εʹ and dielectric loss (εʹʹ) values for the HA nanoparticles decrease with increase in the applied frequency as well. The alternating current conductivity values confirm that the as-synthesized HA samples exhibit insulating behavior. In short this article provides the various applicability of HA particles in optoelectronics and drug delivery. Graphic abstract

Microstructure Characterization of Metal Mixed Oxides

MRS Advances ◽  
2017 ◽  
Vol 2 (64) ◽  
pp. 4025-4030 ◽  
Author(s):  
T. Kryshtab ◽  
H. A. Calderon ◽  
A. Kryvko
Keyword(s):  
Mixed Oxides ◽  
Profile Analysis ◽  
Atomic Resolution ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Reconstruction Procedure ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Co Precipitation

ABSTRACTThe microstructure of Ni-Mg-Al mixed oxides obtained by thermal decomposition of hydrotalcite-like compounds synthesized by a co-precipitation method has been studied by using X-ray diffraction (XRD) and atomic resolution transmission electron microscopy (TEM). XRD patterns revealed the formation of NixMg1-xO (x=0÷1), α-Al2O3 and traces of MgAl2O4 and NiAl2O4 phases. The peaks profile analysis indicated a small grain size, microdeformations and partial overlapping of peaks due to phases with different, but similar interplanar spacings. The microdeformations point out the presence of dislocations and the peaks shift associated with the presence of excess vacancies. The use of atomic resolution TEM made it possible to identify the phases, directly observe dislocations and demonstrate the vacancies excess. Atomic resolution TEM is achieved by applying an Exit Wave Reconstruction procedure with 40 low dose images taken at different defocus. The current results suggest that vacancies of metals are predominant in MgO (NiO) crystals and that vacancies of Oxygen are predominant in Al2O3 crystals.

Solvothermal Synthesis of Bi2Se3 Hexagonal Nanosheet Crystals

2011 ◽  
Vol 236-238 ◽  
pp. 1712-1716 ◽  
Author(s):  
Hai Tao Liu ◽  
Jun Dai ◽  
Jia Jia Zhang ◽  
Wei Dong Xiang
Keyword(s):  
Electron Microscope ◽  
Solvothermal Synthesis ◽  
Solvothermal Method ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Uniform Size ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Scanning Electron

Bismuth selenide (Bi2Se3) hexagonal nanosheet crystals with uniform size were successfully prepared via a solvothermal method at 160°C for 22 h using bismuth trichloride(BiCl3) and selenium powder(Se) as raw materials, sodium bisulfite(NaHSO3) as a reducing agent, diethylene glycol(DEG) as solvent, and ammonia as pH regulator. Various techniques such as X-ray diffraction (XRD), field-emission scanning electron microscope (FESEM), high-resolution transmission electron microscope (HRTEM), and selected area electron diffraction (SAED) were used to characterize the obtained products. Results show that the as-synthesized samples are pure Bi2Se3 hexagonal nanosheet crystals. A possible growth mechanism for Bi2Se3 hexagonal nanosheet crystals is also discussed based on the experiment.

The effect of silver concentration and calcination temperature on structural and optical properties of ZnO:Ag nanoparticles

2015 ◽  
Vol 29 (01) ◽  
pp. 1450254 ◽  
Author(s):  
M. Shayani Rad ◽  
A. Kompany ◽  
A. Khorsand Zak ◽  
M. E. Abrishami
Keyword(s):  
Calcination Temperature ◽  
Sol Gel ◽  
Visible Emission ◽  
X Ray Diffraction ◽  
Ag Nps ◽  
Zno Nps ◽  
Calcination Temperatures ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Average Size

Pure and silver added zinc oxide nanoparticles ( ZnO -NPs and ZnO : Ag -NPs) were synthesized through a modified sol–gel method. The prepared samples were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM) and photoluminescence (PL) spectroscopy. In the XRD patterns, silver diffracted peaks were also observed for the samples synthesized at different calcination temperatures of 500°C, 700°C, 900°C except 1100°C, in addition to ZnO . TEM images indicated that the average size of ZnO : Ag -NPs increases with the amount of Ag concentration. The PL spectra of the samples revealed that the increase of Ag concentration results in the increase of the visible emission intensity, whereas by increasing the calcination temperature the intensity of visible emission of the samples decreases.

scholarly journals Cypermethrin elimination using Fe-TiO2 nanoparticles supported on coconut palm spathe in a solar flat plate photoreactor

2020 ◽  
Vol 29 ◽  
pp. 2633366X2090616
Author(s):  
Ricardo Andrés Solano Pizarro ◽  
Adriana Patricia Herrera Barros
Keyword(s):  
Electron Microscopy ◽  
Flat Plate ◽  
Diffuse Reflectance Spectroscopy ◽  
Cocos Nucifera ◽  
Operating Costs ◽  
Bet Surface Area ◽  
Gas Chromatography Mass Spectrometry ◽  
X Ray Diffraction ◽  
Molar Ratios ◽  
Transmission Electron

In this research, the photocatalytic degradation of cypermethrin using iron-titanium dioxide (Fe-TiO2) nanoparticles supported in a biomaterial was evaluated. The nanoparticles of TiO2 were synthesized by the green chemistry method assisted by ultrasound and doped by chemical impregnation using Fe+3:Ti molar ratios of 0, 0.05, 0.075 and 0.1 to make efficient use of direct sunlight ( λ > 310 nm). All nanoparticles were immobilized on the surface of coconut spathe ( Cocos nucifera). The degradation was carried out at room temperature and natural pH in a flat plate solar reactor, on which the composite material was subjected. The concentration of cypermethrin was determined after 12,000 J m−2 of accumulated radiation from gas chromatography–mass spectrometry and the resulting material was characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, ultraviolet–visible diffuse reflectance spectroscopy, and Brunauer-Emmett-Teller (BET) surface area. The best results were achieved with the use of Evonik TiO2 P-25, Fe:Ti = 0 and Fe:Ti = 0.05 in suspension, with percentages of degradation of cypermethrin of 99.84%, 99.62%, and 100%, respectively. However, the materials supported on the biomaterial of coconut allowed to reach degradation percentages higher than 80%, with the advantage that it minimizes operating costs, as they are not necessarily filtering or centrifuging processes to separate the catalyst.

scholarly journals Synthesis and optical properties of self-assembled flower-like CdS architectures by mixed solvothermal process

2010 ◽  
Vol 8 (5) ◽  
pp. 1027-1033 ◽  
Author(s):  
Junhao Zhang ◽  
Yuhui Wu ◽  
Jia Zhu ◽  
Shaoxing Huang ◽  
Dongjing Zhang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Optical Properties ◽  
X Ray Diffraction ◽  
Wurtzite Phase ◽  
Strong Emission ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Self Assembled ◽  
Xrd Patterns ◽  
Hexagonal Wurtzite Phase

AbstractSelf-assembled CdS architectures with flower-like structures have been synthesized by a mixed solvothermal method using ethylene glycol and oleic acid as the mixed solvent at 160°C for 12 h. The results of X-ray diffraction (XRD) patterns, field-emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) images indicate that the product exists as the hexagonal wurtzite phase and conatins of larger numbers of flower-like CdS architectures with diameters of 1.8–3 μm. The selected-area electron diffraction (SAED) pattern and the high resolution transmission electron microscope (HRTEM) image reveal that the grain has better crystallinity. The optical properties of flower-like CdS architectures were also investigated by ultraviolet-visable (UV-vis) and photoluminescence spectroscopy at room temperature. A strong peak at 490 nm is shown in the UV-vis absorption, while an emission at 486 nm and another strong emission at 712 nm are shown in the PL spectrum.

Synthesis and Characterization of Nanometer Copper Ferrite by Auto-Combustion

2011 ◽  
Vol 347-353 ◽  
pp. 3472-3476
Author(s):  
Guang Xiu Cao ◽  
Tian Liu ◽  
Qing Hong Zhang ◽  
Hong Zhi Wang
Keyword(s):  
Raw Materials ◽  
Combustion Process ◽  
Copper Nitrate ◽  
Copper Ferrite ◽  
X Ray Diffraction ◽  
Uniform Size ◽  
Simple Method ◽  
Transmission Electron ◽  
Auto Combustion ◽  
Average Size

A simple method for preparing nanoscale copper ferrite particles with narrow distribution and uniform size was developed by auto-combusting the precursor using copper nitrate, iron nitrate, and malic acid as raw materials. The constituents and the thermal decomposition process of the precursor were studied by Fourier transform infrared (FT-IR), thermogravimetry-differental thermal analysis (TG-DTA) and X-ray diffraction (XRD). The results showed that the carboxyl and nitrate ion take part in the reaction during the auto-combustion process. The precursor decomposed completely at about 199 °C, to yield single phase product. Transmission electron microscopy (TEM) indicated that the average size of the as-burnt sample was about 90 nm.

Photocatalytic Analysis and Characterization of Zn2SnO4 Nanoparticles Synthesized via Hydrothermal Method with Na2CO3 Mineralizer

2010 ◽  
Vol 97-101 ◽  
pp. 19-22 ◽  
Author(s):  
Yu Shiang Wu ◽  
Wen Ku Chang ◽  
Min Jou
Keyword(s):  
Photocatalytic Activity ◽  
Hydrothermal Process ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
Transmission Electron ◽  
Excellent Photocatalytic Activity ◽  
Face Centered ◽  
Xrd Patterns

Zinc stannate Zn2SnO4 (ZTO) nanoparticles were synthesized via a hydrothermal process utilizing sodium carbonate (Na2CO3) as a weak basic mineralizer. The samples were hydrothermally treated at 150, 200, and 250oC for 48 h. The X-ray diffraction (XRD) patterns show that the highly-crystalline ZTO nanostructure could be formed in a well-dispersed manner for the 250°C sample at a particle size of less than 50 nm. As determined from transmission electron microscopy (TEM) results, ZTO nanoparticles are face-centered cubic single crystals agglomerated together. The Raman spectra results showed that the ZTO nanocrystals have a spinel structure. Furthermore, photocatalytic activity was tested with methylene blue (MB) by UV irradiation. The ZTO synthesized by the 2 M Na2CO3 mineralizer at 250oC demonstrated excellent photocatalytic activity. The ZTO treated three different ways had three distinct UV-Visible absorption curves, which directly influences their corresponding photocatalytic activity.

Single-molecule precursor-based approaches to cobalt sulphide nanostructures

2010 ◽  
Vol 368 (1927) ◽  
pp. 4249-4260 ◽  
Author(s):  
Karthik Ramasamy ◽  
Weerakanya Maneerprakorn ◽  
Mohammad A. Malik ◽  
Paul O'Brien
Keyword(s):  
Electron Microscopy ◽  
Single Molecule ◽  
Size Range ◽  
Hexagonal Phase ◽  
Cobalt Complexes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Cobalt Sulphide ◽  
Microscopy Images

Cobalt complexes of 1,1,5,5-tetramethyl-2,4-dithiobiuret, [Co{N(SCNMe 2 ) 2 } 3 ] ( 1 ), and 1,1,5,5-tetraisopropyl-2-thiobiuret, [Co{N(SOCN i Pr 2 ) 2 } 2 ] ( 2 ), have been synthesized and characterized. Both complexes were used as single-molecule precursors for the preparation of cobalt sulphide nanoparticles by thermolysis in hexadecylamine, octadecylamine or oleylamine. The powder X-ray diffraction pattern of as-prepared nanoparticles showed the hexagonal phase of Co 1− x S from complex 1 and mixtures of cubic and hexagonal Co 4 S 3 from complex 2 . Transmission electron microscopy images of material prepared from complex 1 showed spherical and trigonally shaped particles in the size range of 10–15 nm; whereas spheres, rods, trigonal prisms and pentagonally and hexagonally faceted crystallites were observed from complex 2 . This observation is the first of the Co 4 S 3 phase in a nanodispersed form.

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