Luminescence-site symmetry correlations in Dy3+ doped alkali-alkaline earth orthoborates of the type XZBO3 with X = Li, Na, K and Z = Mg, Ca, Ba

2022 ◽  
Vol 241 ◽  
pp. 118429
Author(s):  
Andreas Herrmann ◽  
Elizabeth Tsekrekas ◽  
Doris Möncke ◽  
Alexis G. Clare
Keyword(s):  
Author(s):  
Ghaleb Alhakmi ◽  
Abderrazzak Assani ◽  
Mohamed Saadi ◽  
Lahcen El Ammari

Two new orthophosphates, BaMn2Fe(PO4)3[barium dimanganese(II) iron(III) tris(orthophosphate)] and SrMn2Fe(PO4)3[strontium dimanganese(II) iron(III) tris(orthophosphate)], were synthesized by solid-state reactions. They are isotypic and crystallize in the orthorhombic system with space group typePbcn. Their crystal structures comprise infinite zigzag chains of edge-sharing FeO6octahedra (point group symmetry .2.) and Mn2O10double octahedra running parallel to [001], linked by two types of PO4tetrahedra. The so-formed three-dimensional framework delineates channels running along [001], in which the alkaline earth cations (site symmetry .2.) are located within a neighbourhood of eight O atoms.


2016 ◽  
Vol 72 (11) ◽  
pp. 1532-1535 ◽  
Author(s):  
Matthias Weil ◽  
Mahdi Shirkhanlou

The asymmetric unit of the title basic strontium oxotellurate(IV), Sr5Te4O12(OH)2{systematic name pentastrontium tetrakis[oxotellurate(IV)] dihydroxide}, comprises three SrIIcations (one with site symmetry 2) and two TeIVatoms, as well as seven O atoms. The coordination numbers of the alkaline earth cations to nearby O atoms range from seven (2 ×) to eight, and the TeIVatoms are surrounded by three oxygen partners in the form of trigonal pyramids. The SrOxpolyhedra share corners and edges to build up a three-dimensional framework structure encapsulating channels propagating along [010]. The TeIVatoms flank the framework O atoms and are situated at the outer array of the channels with the 5s2lone electron pairs protruding into the empty space of the channels (diameter ≃ 4 Å). Although the H atom of the OH group could not be located, bond-valence-sum calculations and typical O...O distances (range 2.81–3.06 Å) clearly indicate hydrogen bonding of medium to weak strengths.


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.


1976 ◽  
Vol 37 (C7) ◽  
pp. C7-158-C7-158
Author(s):  
A. RASCÓN ◽  
J. L. ALVAREZ RIVAS

2019 ◽  
Author(s):  
Nga Phung ◽  
Hans Köbler ◽  
Diego Di Girolamo ◽  
Thi Tuyen Ngo ◽  
Gabrielle Sousa e Silva ◽  
...  

2020 ◽  
pp. 25-34
Author(s):  
V. P. Ermakova ◽  
◽  
S. Yu. Melchakov ◽  
V. G. Smirnova ◽  
L. A. Ovchinnikova ◽  
...  

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