scholarly journals Development of Sub-Second Synchrotron Powder Diffraction Measurement System Under Various Gas Atmospheres

2021 ◽  
Vol 63 (2) ◽  
pp. 121-128
Author(s):  
Shogo KAWAGUCHI
2020 ◽  
Vol 27 (3) ◽  
pp. 616-624 ◽  
Author(s):  
Shogo Kawaguchi ◽  
Michitaka Takemoto ◽  
Hideki Tanaka ◽  
Shotaro Hiraide ◽  
Kunihisa Sugimoto ◽  
...  

A gas- and vapour-pressure control system synchronized with the continuous data acquisition of millisecond high-resolution powder diffraction measurements was developed to study structural change processes in gas storage and reaction materials such as metal organic framework compounds, zeolite and layered double hydroxide. The apparatus, which can be set up on beamline BL02B2 at SPring-8, mainly comprises a pressure control system of gases and vapour, a gas cell for a capillary sample, and six one-dimensional solid-state (MYTHEN) detectors. The pressure control system can be remotely controlled via developed software connected to a diffraction measurement system and can be operated in the closed gas and vapour line system. By using the temperature-control system on the sample, high-resolution powder diffraction data can be obtained under gas and vapour pressures ranging from 1 Pa to 130 kPa in temperatures ranging from 30 to 1473 K. This system enables one to perform automatic and high-throughput in situ X-ray powder diffraction experiments even at extremely low pressures. Furthermore, this developed system is useful for studying crystal structures during the adsorption/desorption processes, as acquired by millisecond and continuous powder diffraction measurements. The acquisition of diffraction data can be synchronized with the control of the pressure with a high frame rate of up to 100 Hz. In situ and time-resolved powder diffraction measurements are demonstrated for nanoporous Cu coordination polymer in various gas and vapour atmospheres.


2017 ◽  
Vol 88 (8) ◽  
pp. 085111 ◽  
Author(s):  
S. Kawaguchi ◽  
M. Takemoto ◽  
K. Osaka ◽  
E. Nishibori ◽  
C. Moriyoshi ◽  
...  

2001 ◽  
Vol 156 (2) ◽  
pp. 428-436 ◽  
Author(s):  
G. Van Tendeloo ◽  
O. Garlea ◽  
C. Darie ◽  
C. Bougerol-Chaillout ◽  
P. Bordet

2014 ◽  
Vol 700 ◽  
pp. 113-116
Author(s):  
Yu Jie Chen ◽  
Feng Lan Han ◽  
Zhao Luo

Na2BaMgP2O8phosphors were synthesized by a standard solid state reaction and their luminescent properties were investigated. The phase structure was analyzed by X-ray powder diffraction measurement. Under the excitation of 365nm, Na2BaMgP2O8:Tb3+, Eu3+phosphors show two color bands of green and red color due to5D4−7F5transition of Tb3+ions and5D0−7F2transition of Eu3+ions, respectively. The emission intensity of Tb3+deceased with the increasing concentration of Eu3+, which verified that an effective energy transfer occurred from Tb3+to Eu3+in Na2BaMgP2O8host. The present study indicated that the phosphors have a high potential application in solid state lighting.


2019 ◽  
Vol 75 (1) ◽  
pp. 61-64 ◽  
Author(s):  
Prateek Bhojane ◽  
Armel Le Bail ◽  
Parasharam M. Shirage

The successful attempt to solve the crystal structure of Co(CO3)0.5(OH)·0.11H2O (denoted CCH), based on synchrotron powder diffraction data, leads to a drastic revision of the chemical formula to Co6(CO3)2(OH)8·H2O [hexacobalt(II) bis(carbonate) octahydroxide monohydrate] and to a hexagonal cell instead of the orthorhombic cell suggested previously [Porta et al. (1992). J. Chem. Soc. Faraday Trans. 88, 311–319]. This results in a new structure-type related to malachite involving infinite chains of [CoO6] octahedra sharing edges along a short c axis, delimiting tunnels having a three-branched star section. All reports discussing cobalt hydroxycarbonates (CCH) without any structural knowledge and especially its topotactic decomposition into Co3O4 have, as a result, to be reconsidered.


2008 ◽  
Vol 64 (6) ◽  
pp. 713-724 ◽  
Author(s):  
Florence Porcher ◽  
Elena Borissenko ◽  
Mohamed Souhassou ◽  
Masaki Takata ◽  
Kenichi Kato ◽  
...  

The crystal structure of a new phase consisting of the inclusion of the hyperpolarizable molecule p-N,N-dimethylnitroaniline (dimethyl-para-nitroaniline or dmpNA) in the large-pore zeolite mordenite (MOR) has been determined from high-resolution synchrotron powder diffraction at 300 and 90 K. The unit-cell parameters and space group at 300 K are similar to those of as-synthesized mordenite. The crystallographic study indicates that the MOR straight channels are almost fully loaded with molecules that are disordered over eight symmetry-related sites. As expected, the molecules are located in the large 12-membered ring channel, at the intersection with the secondary eight-membered channel with which they might form hydrogen bonds. The elongation axes (and then the dipole moments) of the molecules are slightly tilted (28.57°) from [001]. The configuration found suggests an interaction of dmpNA with framework O atoms through its methyl groups.


2020 ◽  
Vol 12 (6) ◽  
pp. 7710-7716
Author(s):  
Iurii Dovgaliuk ◽  
Vadim Dyadkin ◽  
Mathieu Vander Donckt ◽  
Yaroslav Filinchuk ◽  
Dmitry Chernyshov

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