Achieving tunable luminescence in Eu2+ and Eu3+ codoped MAl2B2O7:Eu (M = Ca2+, Sr2+, and Ba2+) phosphor by structure defect designing and site symmetry controlling

2021 ◽  
Vol 122 ◽  
pp. 111673
Author(s):  
Wanping Chen
Author(s):  
A. G. Jackson ◽  
M. Rowe

Diffraction intensities from intermetallic compounds are, in the kinematic approximation, proportional to the scattering amplitude from the element doing the scattering. More detailed calculations have shown that site symmetry and occupation by various atom species also affects the intensity in a diffracted beam. [1] Hence, by measuring the intensities of beams, or their ratios, the occupancy can be estimated. Measurement of the intensity values also allows structure calculations to be made to determine the spatial distribution of the potentials doing the scattering. Thermal effects are also present as a background contribution. Inelastic effects such as loss or absorption/excitation complicate the intensity behavior, and dynamical theory is required to estimate the intensity value.The dynamic range of currents in diffracted beams can be 104or 105:1. Hence, detection of such information requires a means for collecting the intensity over a signal-to-noise range beyond that obtainable with a single film plate, which has a S/N of about 103:1. Although such a collection system is not available currently, a simple system consisting of instrumentation on an existing STEM can be used as a proof of concept which has a S/N of about 255:1, limited by the 8 bit pixel attributes used in the electronics. Use of 24 bit pixel attributes would easily allowthe desired noise range to be attained in the processing instrumentation. The S/N of the scintillator used by the photoelectron sensor is about 106 to 1, well beyond the S/N goal. The trade-off that must be made is the time for acquiring the signal, since the pattern can be obtained in seconds using film plates, compared to 10 to 20 minutes for a pattern to be acquired using the digital scan. Parallel acquisition would, of course, speed up this process immensely.


Author(s):  
Robert A. Evarestov ◽  
Vyacheslav P. Smirnov
Keyword(s):  

1985 ◽  
Vol 50 (12) ◽  
pp. 2715-2721
Author(s):  
Bohumil Hájek ◽  
Alexander Muck ◽  
Eva Šantavá

The mutual replacement of SO32- and SO42- anions was studied in Na2SO3.7 H2O crystals where sulphite is slowly oxidized to sulphate by air oxygen. In a series of Na2(SO3, SO4).7 H2O samples, the C1 or Cs site symmetry appears for the SO32- anion and the site symmetry of the SO42- anion is lowered gradually from Td through D2d or C3v to C1. The replacement was also studied for anhydrous sodium sulphite obtained by dehydration or by evaporation from aqueous solution. Despite the different structures of Na2SO3 and Na2SO4 crystals (C3i1 and D2h24, respectively), the favourable dimensions of the sterically different anions allow the SO42- ions, with their own symmetry Td, to be located in the C3 sites of the SO32- ions in Na2SO3.


1982 ◽  
Vol 47 (4) ◽  
pp. 1176-1183 ◽  
Author(s):  
Alexander Muck ◽  
Olga Smrčková ◽  
Bohumil Hájek

Infrared spectra of mixed crystals Sc(PO4, VO4) and Y(PO4, VO4) have been studied from the point of view of group analysis. These systems form substitution mixed crystals in tetragonal space group D194h. The anions having proper symmetry Td or D2d in site symmetry D2d exhibit in spectra lowering of the site symmetry to effective C2 as a result of lattice vibrations of the type T(B2).


2013 ◽  
Vol 22 ◽  
pp. 284-291 ◽  
Author(s):  
CH. SRINIVASU ◽  
M. A. SAMI ◽  
A. EDUKONDALU ◽  
SYED RAHMAN

Electron paramagnetic resonance (EPR) and optical absorption spectra of copper ions in xLiF-(50-x)Li2O-20SrO-30Bi2O3 glass system have been studied. MDSC studies showed that the glass transition temperature decreases with LiF content. Optical absorption spectra of the pure glasses reveled that the cut off wave length increased and optical band gap energy decreased with increase in LiF content. EPR spectra of all the glass samples exhibit resonance signals characteristic of Cu2+ ions. The Cu2+ ions are in well-defined axial sites but subjected to small distortion leading to the broadening of the spectra. The spin-Hamiltonian parameter values indicate that the ground state of Cu2+ is d x2 y2 and the site symmetry around Cu2+ ions is tetragonally distorted octahedral. The optical absorption spectra exhibited a broad band corresponding to the d-d transition bands of Cu2+ ion. By correlating EPR and optical absorption data, the bond parameters are evaluated from various techniques.


1991 ◽  
Vol 30 (Part 1, No. 6) ◽  
pp. 1169-1175 ◽  
Author(s):  
Jun-Yuan Chen ◽  
Jenn-Gee Lo ◽  
Luke Su Lu

2015 ◽  
Vol 71 (11) ◽  
pp. 1384-1387
Author(s):  
Marwen Chouri ◽  
Habib Boughzala

The title compound bis(1,4-diazoniabicyclo[2.2.2]octane) di-μ-chlorido-bis[tetrachloridobismuthate(III)] dihydrate, (C6H14N2)2[Bi2Cl10]·2H2O, was obtained by slow evaporation at room temperature of a hydrochloric aqueous solution (pH = 1) containing bismuth(III) nitrate and 1,4-diazabicyclo[2.2.2]octane (DABCO) in a 1:2 molar ratio. The structure displays a two-dimensional arrangement parallel to (100) of isolated [Bi2Cl10]4−bioctahedra (site symmetry -1) separated by layers of organic 1,4-diazoniabicyclo[2.2.2]octane dications [(DABCOH2)2+] and water molecules. O—H...Cl, N—H...O and N—H...Cl hydrogen bonds lead to additional cohesion of the structure.


2006 ◽  
Vol 62 (5) ◽  
pp. m1112-m1113
Author(s):  
Djulia Onggo ◽  
Fatimah Martak ◽  
Ismunandar ◽  
Bohari M. Yamin ◽  
Seik Weng Ng

The crystal structure of the title compound, [Fe(C6H4NO2)(C6H4.5NO2)(C6H5NO2)](BF4)0.5, is regarded as consisting of disordered mononuclear [FeII(C6H4.5NO2)3]0.5+ cations and tetrafluoroborate anions. The N,O-chelated Fe lies on a special position of site symmetry 3 and the acid H atom on a special position of site symmetry \overline{1}. The B atom is located on a special position of site symmetry \overline{3}. The disordered mononuclear units are linked through the acid H atom into a layer motif.


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