scholarly journals EuTiO3magnetic structure studied by neutron powder diffraction and resonant x-ray scattering

2012 ◽  
Vol 86 (9) ◽  
Author(s):  
Valerio Scagnoli ◽  
Mattia Allieta ◽  
Helen Walker ◽  
Marco Scavini ◽  
Takuro Katsufuji ◽  
...  
1995 ◽  
Vol 28 (5) ◽  
pp. 630-632
Author(s):  
M. Lorenzen ◽  
C. Ferrero ◽  
O. Diat ◽  
C. Riekel ◽  
U. Mayerhofer

A set of macros based on CERN's program package PAW has been developed for interactive preprocessing of two-dimensional detector data at ESRF prior to more detailed data analysis. Various types of image operations (averaging, cuts, background correction etc.) are available. The main use of the package is at present in small- and wide-angle X-ray scattering (SAXS and WAXS). The flexibility of the package allows, however, easy adaptation to other areas such as fibre or powder diffraction.


2019 ◽  
Vol 624 ◽  
pp. A136
Author(s):  
S. P. Thompson ◽  
A. Herlihy ◽  
C. A. Murray ◽  
A. R. Baker ◽  
S. J. Day ◽  
...  

Context. Laboratory analogues can provide physical constraints to the interpretation of astronomical observations of cosmic dust but clearly do not experience the same formation conditions. To distinguish between properties intrinsic to the material and properties imprinted by their means of formation requires extensive characterisation. Aims. Sol–gel methods can produce amorphous silicates with potentially high reproducibility, but often require long drying times (24+ h) at elevated temperatures in air, controlled atmosphere, or vacuum. We investigate the possibility that microwave drying can be used to form amorphous silicate on a timescale of ∼10 min and characterise their structural and spectroscopic properties relative to silicates produced by other drying methods. Methods. Microwave-dried amorphous MgSiO3, Fe0.1Mg0.9SiO3 and Mg2SiO4 are characterised using X-ray powder diffraction, total X-ray scattering, small angle X-ray scattering and mid-IR FTIR spectroscopy, and compared to samples produced from the same gels but dried in-air and under vacuum. The development of crystalline structure in the microwave-dried silicates via thermal annealing up to 999°C is also investigated using in situ X-ray powder diffraction. Results. At the inter-atomic level the silicate structures are largely independent of drying method, however larger-scale structured domains, ranging from a ∼few × 10 Å to ∼100’s Å in size, are observed. These are ordered as mass fractals with discernible variation caused by the drying processes. The mid-IR 10 μm band profile is also found to be influenced by the drying process, likely due to the way removal of water and bonded OH influences the distribution of tetrahedral species. However, microwave drying also allows Fe to be easily incorporated into the silicate structure. In situ annealing shows that for amorphous MgSiO3 crystalline forsterite, enstatite and cristobalite are high temperature phases, while for Mg2SiO4 forsterite crystallises at lower temperatures followed by cristobalite at high temperature. For Fe0.1Mg0.9SiO3 the crystallisation temperature is significantly increased and only forsterite is observed. Crystalline SiO2 may be diagnostic of Mg-rich, Fe-poor grain mineralogies. The results are discussed in relation to the different thermal conditions required for dust to crystallise within protoplanetary disk lifetimes. Conclusions. Sol–gel microwave drying provides a fast and easy method of producing amorphous Mg- and Fe,Mg-silicates of both pyroxene and olivine compositions. Their structure and spectroscopic characteristics although similar to silicates produced using other drying methods, exhibit subtle variations which are particularly manifest spectroscopically in the mid-IR, and structurally over medium- and long-range length scales.


1982 ◽  
Vol 25 (4) ◽  
pp. 2472-2476 ◽  
Author(s):  
C. -E. Chen ◽  
Y. Schlesinger ◽  
A. J. Heeger

1965 ◽  
Vol 43 (10) ◽  
pp. 2812-2826 ◽  
Author(s):  
Osvald Knop ◽  
François Brisse ◽  
Lotte Castelliz

The crystal structure of erbium titanate, Er2Ti2O7, has been shown by X-ray and neutron powder diffraction to be of the cubic pyrochlore type, with ao = 10.0762 ± 6 Å. Least-squares isotropic refinement based on resolved single reflections gave x(O2) = 0.4200 ± 10 and R = 2.25%. Ionic and neutral X-ray scattering factors gave practically identical results. The six equal Ti—O2 distances in the distorted coordination octahedron of the Ti atom are 1.955 ± 5 Å. The two short (apparent) Er—O distances are 2.1815 ± 5 Å (Er—O1) and 2.471 ± 8 Å (Er—O2). The infrared spectrum of the titanate in the region 1 600 to 250 cm−1 shows features similar to those encountered in the spectra of other simple oxygen compounds of titanium.


2013 ◽  
Vol 46 (2) ◽  
pp. 573-576 ◽  
Author(s):  
Attila Bóta

A novel type of X-ray collimation system attached to commercial powder diffractometers makes the structural characterization of nanomaterials possible in a wide size range from <0.1 to 100 nm by combination of the small- and wide-angle X-ray scattering techniques. There is no dead interval in the detection between the small- and wide-angle regimes. This device can be attached to any existing `θ/θ' powder diffractometer, providing a multi-functional small- and wide-angle X-ray scattering/diffraction (SWAXS) apparatus. After proper alignment and adjustment, the device can be removed and re-attached at any time to switch between normal and SWAXS functions.


2021 ◽  
Vol 28 (3) ◽  
pp. 804-811
Author(s):  
Daisuke Ishikawa ◽  
Alfred Q. R. Baron

Several different ways of measuring the energy resolution for meV-resolved inelastic X-ray scattering (IXS) are compared: using scattering from poly(methyl methacrylate), PMMA, using scattering from borosilicate glass (Tempax), and using powder diffraction from aluminium. All of these methods provide a reasonable first approximation to the energy resolution, but, also, in all cases, inelastic contributions appear over some range of energy transfers. Over a range of ±15 meV energy transfer there is good agreement between the measurements of PMMA and Tempax at low temperature, and room-temperature powder diffraction from aluminium, so we consider this to be a good indication of the true resolution of our ∼1.3 meV spectrometer. The resolution over a wider energy range is self-consistently determined using the temperature, momentum and sample dependence of the measured response. The inelastic contributions from the PMMA and Tempax, and their dependence on momentum transfer and temperature, are then quantitatively investigated. The resulting data allow us to determine the resolution of our multi-analyzer array efficiently using a single scan. The importance of this procedure is demonstrated by showing that the results of the analysis of a spectrum from a glass are changed by using the properly deconvolved resolution function. The impact of radiation damage on the scattering from PMMA and Tempax is also discussed.


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