Adsorption mechanism on metal organic frameworks of Cu-BTC, Fe-BTC and ZIF-8 for CO2 capture investigated by X-ray absorption fine structure

RSC Advances ◽  
2016 ◽  
Vol 6 (67) ◽  
pp. 62705-62716 ◽  
Author(s):  
Meng Du ◽  
Lina Li ◽  
Mingxing Li ◽  
Rui Si

XAFS analysis demonstrates the physical driving force, plus minor chemical transformation for the CO2 adsorption mechanism by MOFs.

2018 ◽  
Vol 140 (50) ◽  
pp. 17379-17383 ◽  
Author(s):  
Kirill A. Lomachenko ◽  
Jannick Jacobsen ◽  
Aram L. Bugaev ◽  
Cesare Atzori ◽  
Francesca Bonino ◽  
...  

2021 ◽  
Author(s):  
Gregory M. Su ◽  
Han Wang ◽  
Brandon R. Barnett ◽  
Jeffrey R. Long ◽  
David Prendergast ◽  
...  

In situ near edge X-ray absorption fine structure spectroscopy directly probes unoccupied states associated with backbonding interactions between the open metal site in a metal–organic framework and various small molecule guests.


2004 ◽  
Vol 831 ◽  
Author(s):  
V. Katchkanov ◽  
K.P. O'Donnell ◽  
J.F.W. Mosselmans ◽  
S. Hernandez ◽  
R.W. Martin ◽  
...  

ABSTRACTThe local structure around In atoms in InGaN epilayers grown by Molecular Beam Epitaxy (MBE) and by Metal-Organic Chemical Vapour Deposition (MOCVD) was studied by means of Extended X-ray Absorption Fine Structure (EXAFS). The averaged In fraction of MOCVD grown samples ranged from 10% to 40% as estimated by Electron Probe Microanalysis (EPMA). The In fraction of MBE grown samples spanned the range from 13% to 96%. The In–N bond length was found to vary slightly with composition, both for MBE and MOCVD grown samples. Moreover, for the same In content, the In-N bond lengths in MOCVD samples were longer than those in MBE grown samples. In contrast, the In-In radial separations in MOCVD and MBE samples were found to be indistinguishable for the same In molar fraction. The In-Ga bond length was observed to deviate from average cation-cation distance predicted by Vegard's law for MBE grown samples which indicates alloy compositional fluctuations.


2015 ◽  
Vol 17 (33) ◽  
pp. 21448-21457 ◽  
Author(s):  
Walter S. Drisdell ◽  
Roberta Poloni ◽  
Thomas M. McDonald ◽  
Tod A. Pascal ◽  
Liwen F. Wan ◽  
...  

In situ X-ray absorption spectroscopy, coupled with DFT calculations, uncovers the details of the novel mechanism for CO2 adsorption in diamine-appended metal–organic frameworks.


2000 ◽  
Vol 454-456 ◽  
pp. 723-728 ◽  
Author(s):  
H. Magnan ◽  
P. Le Fèvre ◽  
A. Midoir ◽  
D. Chandesris ◽  
H. Jaffrès ◽  
...  

Author(s):  
Kazumasa Murata ◽  
Junya Ohyama ◽  
Atsushi Satsuma

In the present study, the redispersion behavior of Ag particles on ZSM-5 in the presence of coke was observed using in situ X-ray absorption fine structure (XAFS) spectroscopy.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Hiroyuki Ikemoto ◽  
Takafumi Miyanaga

AbstractIn this review, we make a survey of the structure studies for the chalcogen elements and several chalcogenides in liquid, amorphous and nanosized state by using X-ray absorption fine structure (XAFS). The chalcogen elements have hierarchic structures; the chain structure constructed with the strong covalent bond as a primary structure, and the weaker interaction between chains as a secondary one. Existence of these two kinds of interactions induces exotic behaviors in the liquid, amorphous and nanosized state of the chalcogen and chalcogenides. XAFS is a powerful structure analysis technique for multi-element systems and the disordered materials, so it is suitable for the study of such as liquid, amorphous and nanosized mixtures. In section 2, the structures for the liquid state are discussed, which show the interesting semiconductor-metal transition depending on their temperatures and components. In section 3, the structure for the amorphous states are discussed. Especially, some of chalcogens and chalcogenides present the photostructural change, which is important industrial application. In section 4, the structures of nanosized state, nanoparticles and isolated chain confined into the narrow channel, are discussed. The studies of the nanoparticle and the isolated chain reveal the alternative role between the intrachain covalent bonds and the interchain interaction.


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