scholarly journals Study on Luminescence of KCl:Eu2+ Crystals after X-ray Irradiation at Room Temperature

Crystals ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 331 ◽  
Author(s):  
Yohichi Kohzuki ◽  
Tomiyasu Ohgaku

Bleaching with the F-light at the excitation bandpass of 20 nm results in the phenomenon that F-centre peak and thermoluminescence (TL) glow peaks due to Fz- and F-centres identically decrease with the F-bleach time, whereas TL glow peak due to Fz-centre only remains almost constant irrespective of its time in the case of that at the excitation bandpass of 5 nm. Analysing the data on bleaching effects, absorption spectrum of X-ray irradiated KCl:Eu2+ crystal has a peak due to Fz-centre approximately within 20 nm of the wavelength 560 nm at F-centre peak. Electrons released from Fz-centres at 370 K and from F-centres at 450 K combine with Eu3+ ions, leading to the excited Eu2+ ions from which the luminescence at 420 nm is emitted.

2014 ◽  
Vol 979 ◽  
pp. 184-187
Author(s):  
Weerachon Phoohinkong ◽  
Thitinat Sukonket ◽  
Udomsak Kitthawee

Zinc sulfide (ZnS) nanostructures are important materials for many technologies such as sensors, infrared windows, transistors, LED displays, and solar cells. However, many methods of synthesizing ZnS nanostructures are complex and require expensive equipment. In this study, a liquid-solid chemical reaction without surfactant was used to synthesize ZnS at room temperature. In addition, commercial grade zinc oxide (ZnO) particles were used as a precursor. The effect of the addition of acids and inorganic salts were investigated. The products were characterized by field emission scanning electron microscopy (FESEM) coupled with energy-dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). The results show that the nanoparticles of ZnS were obtained in hydrochloric acid and acetic acid addition. The diameters were in the range of 10 to 20 nm and 50 to 100 nm, respectively. In the case of a sodium chloride salt addition, a ZnS structure was obtained with a particle size of approximately 5 nm and a flake-like morphology.


2021 ◽  
Author(s):  
Yuri Mikhlin ◽  
Roman Borisov ◽  
Sergey Vorobyev ◽  
Yevgeny Tomashevich ◽  
Alexander Romanchenko ◽  
...  

Two-dimensional phenomena are attracting enormous interest at present and the search for novel 2D materials is very challenging. We propose here the layered material valleriite composed of altering atomic sheets of Cu-Fe sulfide and Mg-based hydroxide synthesized via a simple hydrothermal pathway as particles of 50-200 nm in the lateral size and 10-20 nm thick. The solid products and aqueous colloids prepared with various precursor ratios were examined using XRD, TEM, EDS, X-ray photoelectron spectroscopy (XPS), reflection electron energy loss spectroscopy (REELS), Raman, Mössbauer, UV-vis-NIR spectroscopies, magnetic, dynamic light scattering, zeta potential measurements. The material properties are largely determined by the narrow-gap (less than 0.5 eV) sulfide layers containing Cu+ and Fe3+ cations, monosulfide and minor polysulfide anions but are strongly affected by the hydroxide counterparts. Particularly, Fe distribution between sulfide (55-90%) and magnesium hydroxide layers is controlled through insertion of Al into the hydroxide part and by Cr and Co dopants entering both layers. Room-temperature Mössbauer signals of paramagnetic Fe3+ transformed to several Zeeman sextets with hyperfine magnetic fields up to 500 kOe in the sulfide layers at 4 K. Paramagnetic or more complicated characters were observed for valleriites with higher and lower Fe concentrations in hydroxide sheets, respectively. Valleriite colloids showed negative zeta potentials, suggesting negative electric charging of the hydroxide sheets, and optical absorption maxima between 500 nm and 700 nm, also depended on the Fe distribution. The last features observed also in the REELS spectra may be due to localized surface plasmon or, more likely, quasi-static dielectric resonance. The tunable composition, electronic, magnetic, optic and surface properties highlight valleriites as a rich platform for novel 2D composites promising for numerous applications.


1982 ◽  
Vol 46 (341) ◽  
pp. 453-457 ◽  
Author(s):  
R. J. Hill ◽  
J. H. Canterford ◽  
F. J. Moyle

AbstractEuhedral crystals of the low-temperature mineral lansfordite, MgCO3 · 5H2O, have been prepared from saturated magnesium bicarbonate solutions at temperatures below 10°C. The crystals are monoclinic P21/a with a = 12.4758(7), b = 7.6258(4), c = 7.3463(6)Å, β = 101.762(6)°, V = 684.24Å3, Dcalc. = 1.693 g cm−3, Dobs. = 1.70(1) g m−3. At room temperature, the crystals slowly effloresce to produce pseudomorphs of nesquehonite, MgCO3 · 3H2O. Dehydration is complete at 300°C, with decarbonation taking place in the interval to 560°C. A new X-ray powder diffraction pattern is presented, and details of the infra-red absorption spectrum are discussed.


2009 ◽  
Vol 1201 ◽  
Author(s):  
Nola Li ◽  
Shen-Jie Wang ◽  
William E. Fenwick ◽  
Andrew Melton ◽  
Chung-Lung Huang ◽  
...  

AbstractGaN and InGaN layers were grown on annealed 20 and 50nm Al2O3/ZnO substrates by metalorganic chemical vapor deposition (MOCVD). GaN was only observed by high resolution x-ray diffraction (HRXRD) on 20 nm Al2O3/ZnO substrates. Room temperature photoluminescence (RT-PL) showed the red shift of the GaN near band-edge emission, which might be from oxygen incorporation forming a shallow donor-related level in GaN. HRXRD measurements revealed that (0002) InGaN layers were also successfully grown on 20nm Al2O3/ZnO substrates. In addition, thick InGaN layers (∼200-300nm) were successfully grown on Al2O3/ZnO and bare ZnO substrates. These results are significant as previous studies showed decomposition of the layer at InGaN thicknesses of 100nm or less.


2005 ◽  
Vol 475-479 ◽  
pp. 3729-3732
Author(s):  
Cong Mian Zhen ◽  
Xiao Xia Zhai ◽  
Chengfu Pan ◽  
Xiangfu Nie

FePt/C mutilayer films were successfully prepared by using RF and DC magnetron sputtering system. FePt nanoparticles embedded in a C matrix were formed by consequently annealing. X-ray diffraction (XRD) results show the degree of atomic ordering of the L10 structure increases with higher temperature annealing. Room temperature magnetic measurements reveal that in-plane coercivity HC, and squareness Mr/MS depend on the thickness of carbon layer. Relatively High HC (3245.1Oe) and squareness (0.67) were obtained when the thickness of C layer is 2.0 nm. The carbon layer not only isolates the FePt grain, but also suppresses the growth of fct FePt grains. When the thickness of carbon layer is 2.0 nm, the FePt grain size decreases down to ~20 nm measured by Scan Probe Microscope (SPM). Interactions between particles can be tuned to near zero when we select the proper thickness of C layer.


2018 ◽  
Vol 31 (1) ◽  
pp. 37 ◽  
Author(s):  
Iman Hameed Khudayer ◽  
Bushra Hashem Hussein Ali ◽  
Mohammed Hamid Mustafa ◽  
Ayser Jumah Ibrahim

  The Silver1Indium1Selenide (AgInSe2) (AIS) thin1films of (3001±20) nm thickness  have been1prepared2from the compound alloys2using thermal evaporation2 technique onto the glass2substrate at room temperature, with a deposition rate2(3±0.1) nm2sec-1. The2structural, optical and electrical3properties have been studied3at different annealing3temperatures (Ta=450, 550 and 650) K. The amount3or (concentration) of the elements3(Ag, In, Se) in the  prepared alloy3was verified using  an energy dispersive3x-ray spectrometer (EDS)3technology. X-ray diffraction3analysis shows that AIS alloy  prepared as (powder) and the thin films3are polycrystalline  of tetragonal3structure with preferential orientation3(112). The crystalline3size increases  as a function3of annealing temperature. The atomic force3microscope (AFM) technique  was used to examine3the  topography  and  estimate3the surface roughness, also the  average grain3size of the films. The results show3that the grain size increases3with annealing3temperature.   The optical4band gap of the films lies4in the range 1.6-1.9 eV. The films4appear to be4n-type indicating that the electrons4as a dominant charge4carrier. The electrical conductivity4increases  with a corresponding4increase in annealing4temperature.  


2016 ◽  
Vol 16 (4) ◽  
pp. 4012-4015 ◽  
Author(s):  
Li Peng ◽  
Liu Yun ◽  
Shi Xiaolei ◽  
Guo Yaxin ◽  
Zhu Gangqiang

Large-scale, rod-like nanostructures of LaPO4:Eu3+ phosphors were synthesized using a simple hydrothermal method. The phase composition, structure and morphology of the final products were characterized by XRD, FE-SEM and TEM. Highly crystalline material was obtained as confirmed by X-ray powder diffraction measurements. The FE-SEM and TEM observations indicate that the obtained LaPO4:Eu3+ nanorods have a diameter of about 10–20 nm, and a length of about 100–600 nm. Meanwhile, the excitation and emission spectra of the products at room temperature were measured using a fluorescence spectrometer. The effects of pH and Eu3+-doping on the morphology and luminescence properties of the as-prepared powders were investigated. The photoluminescence (PL) spectra show that the emission intensity of the LaPO4:Eu3+ phosphors improved with increases in concentrations of Eu3+ from 3 mol% to 14 mol%, and then decreased for higher concentrations.


Author(s):  
T. Malis ◽  
M. C. Chaturvedi

Ottawa, Ontario, Canada. KlA 0G1 Winnipeg, Manitoba, Canada. R3T 2N2 Energy dispersive X-ray analysis (EDS) has been used in conjunction with STEM microscopy to characterize interfacial segregation. Segregation via solute-vacancy pair migration to grain boundaries has been proposed to influence the hydrogen embrittlement, or stress corrosion cracking, of Al-Zn-Mg alloys. In addition, it has been seen that substantial variations exist in the distribution of boundary precipitates in such alloys. Thus, there is a need for more rigorous characterization of boundary segregation than the normal approach of obtaining elemental profiles across boundaries. Accordingly, specimens of A1 8-wt% Mg were water-quenched from 350°C, aged at room temperature, and EDS profiles were obtained along suitable boundaries from thin foils of both conditions. The traces were in the form of 10-15 point analyses (nominal beam diameter of 20 nm) spaced at 100 nm intervals along the boundary.


2014 ◽  
Vol 606 ◽  
pp. 105-109
Author(s):  
Zulhelmi Alif Abdul Halim ◽  
Muhamad Azizi Mat Yajid ◽  
Zulkifli Mohd Rosli ◽  
Riyaz Ahmad M. Ali

In this work, the effects of room temperature deposition on the structural properties of Al-Cu bilayers thin films were investigated. The bilayers were sputter deposited by RF magnetron sputtering on Si {100} wafers without substrate heating. The thickness of each layer is approximately 500 nm thick. Characterization were performed with grazing incidence X-ray diffraction (XRD) cross-sectional field emission scanning electron microscope (FE-SEM) with chemical analysis by energy dispersive X-ray (EDX) and atomic force microscope (AFM). It was found polycrystalline Al and Cu thin films have been grown with {111} preferred growth orientation with very fine crystallites size (less than 20 nm). The bilayers were in non-strained condition, but each layer shows different morphologies between the columnar and non columnar structure. AFM analysis revealed that the bilayers top surface appears to have higher surface roughness (Ra= 20 nm) due to low adatoms surface mobility during room temperature deposition.


Author(s):  
C. Wolpers ◽  
R. Blaschke

Scanning microscopy was used to study the surface of human gallstones and the surface of fractures. The specimens were obtained by operation, washed with water, dried at room temperature and shadowcasted with carbon and aluminum. Most of the specimens belong to patients from a series of X-ray follow-up study, examined during the last twenty years. So it was possible to evaluate approximately the age of these gallstones and to get information on the intensity of growing and solving.Cholesterol, a group of bile pigment substances and different salts of calcium, are the main components of human gallstones. By X-ray diffraction technique, infra-red spectroscopy and by chemical analysis it was demonstrated that all three components can be found in any gallstone. In the presence of water cholesterol crystallizes in pane-like plates of the triclinic crystal system.


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