EXAFS Study of Annealing Effects on Mg65Cu25Gd10 Metallic Glass

2007 ◽  
Vol 546-549 ◽  
pp. 477-480
Author(s):  
Guo Qiang Li ◽  
Li Jing Zheng ◽  
Z.F. Zhang ◽  
Huan Xi Li ◽  
M.F. Hashmi ◽  
...  
Keyword(s):  
Structural Changes ◽  
Local Environment ◽  
Test Machine ◽  
Compression Tests ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Heat Treated ◽  
Annealing Effects ◽  
Exafs Study ◽  
X Ray Absorption

The effect of heat treatment on mechanical prosperities of Mg65Cu25Gd10 glass has been studied in this paper. The thermal stability and the structure of as-spun and heat treated Mg65Cu25Gd10 alloys were examined by differential scanning calorimetry (DSC) and X-ray diffractometry (XRD). The compression tests were performed using a computer controlled tensile test machine. Extended X-ray absorption fine structure (EXAFS) was applied to study the structural changes of Mg65Cu25Gd10 glass during annealing. Results showed that the decline of mechanical properties for Mg65Cu25Gd10 glass after annealing was closely related to the changes in local environment of Cu atoms and appearance of crystalline phases, and not the Gd local structure.

Extended x-ray absorption fine structure study of incorporation of Bi and Pb atoms into the crystal structure of Ba4.5Nd9Ti18O54

1997 ◽  
Vol 12 (3) ◽  
pp. 799-804 ◽  
Author(s):  
M. Valant ◽  
I. Arčon ◽  
D. Suvorov ◽  
A. Kodre ◽  
T. Negas ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Fine Structure ◽  
Local Environment ◽  
Structure Study ◽  
X Ray ◽  
Absorption Fine ◽  
Exafs Study ◽  
X Ray Absorption

In the extended x-ray absorption fine structure (EXAFS) study of the local environment of Bi3+ and Pb2+ ions incorporated in Ba4.5Nd9Ti18O54, actual sites of Bi- and Pb-incorporation are determined. Evidence is given that dopant ions are not distributed randomly on all theoretically possible sites; Bi3+ selectively enters one out of three possible channels, corresponding to the sites x = 0.9484, y = 0.2500, z = 0.2939, and/or x = 0.0455, y = 0.2500, z = 0.6928 previously occupied by Nd3+, while Pb2+ selectively enters site x = 0.4940, y = 0.2500, and z = 0.4993 previously shared by Ba2+ and Nd3+.

Combined TDPAC and EXAFS Study of InPt/FER Catalysts

2000 ◽  
Vol 55 (1-2) ◽  
pp. 327-330 ◽  
Author(s):  
J. M. Ramallo-López ◽  
F. G. Requejo ◽  
A. G. Bibiloni ◽  
M. Rentería ◽  
L. Gutierrez ◽  
...  
Keyword(s):  
Perturbed Angular Correlation ◽  
Local Environment ◽  
X Ray ◽  
Time Differential ◽  
Before And After ◽  
Nuclear Quadrupole Moment ◽  
Exafs Study ◽  
Nuclear Quadrupole ◽  
X Ray Absorption ◽  
Asymmetry Parameters

Time Differential Perturbed Angular Correlation (TDPAC) experiments using 111In as probe were performed in order to determine the nature of In-sites in In-ferrierite (In/FER), before and after the incorporation of Pt through the hyperfine interaction between the nuclear quadrupole moment of the probe's nucleus and the extranuclear electric field gradient (EFG). Extended X-ray Absorption Fine Structure (EXAFS) measurements were performed to measure the absorbance above the Pt's LIII absorption edge in the transmission mode in order to determine the local environment of Pt atoms in Pt/FER and In Pt/FER catalysts. TDPAC spectra of 111In in In/FER and InPt/FER taken at 500°C in air indicated that there are no changes in the indium surroundings after the incorporation of Pt. Three sites were found for indium in both samples. Two of them correspond to the two sites of indium in ln2O3 and the third one is attributed to In in exchange sites of the zeolites. Their population, quadrupole frequencies and asymmetry parameters didn't change with the incorporation of Pt. EXAFS experiments showed similar near neighborhood Pt-0 distances and Pt coordination number in Pt/FER and In Pt/FER samples. There is no evidence of the presence of any In-Pt bimetallic entity in In Pt/FER catalyst.

Local atomic structure in tetragonal pure ZrO2nanopowders

2010 ◽  
Vol 43 (2) ◽  
pp. 227-236 ◽  
Author(s):  
Leandro M. Acuña ◽  
Diego G. Lamas ◽  
Rodolfo O. Fuentes ◽  
Ismael O. Fábregas ◽  
Márcia C. A. Fantini ◽  
...  
Keyword(s):  
Tetragonal Phase ◽  
Local Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Atomic Structures ◽  
Crystallite Sizes ◽  
Exafs Study ◽  
The Difference ◽  
X Ray Absorption ◽  
Good Agreement

The local atomic structures around the Zr atom of pure (undoped) ZrO2nanopowders with different average crystallite sizes, ranging from 7 to 40 nm, have been investigated. The nanopowders were synthesized by different wet-chemical routes, but all exhibit the high-temperature tetragonal phase stabilized at room temperature, as established by synchrotron radiation X-ray diffraction. The extended X-ray absorption fine structure (EXAFS) technique was applied to analyze the local structure around the Zr atoms. Several authors have studied this system using the EXAFS technique without obtaining a good agreement between crystallographic and EXAFS data. In this work, it is shown that the local structure of ZrO2nanopowders can be described by a model consisting of two oxygen subshells (4 + 4 atoms) with different Zr—O distances, in agreement with those independently determined by X-ray diffraction. However, the EXAFS study shows that the second oxygen subshell exhibits a Debye–Waller (DW) parameter much higher than that of the first oxygen subshell, a result that cannot be explained by the crystallographic model accepted for the tetragonal phase of zirconia-based materials. However, as proposed by other authors, the difference in the DW parameters between the two oxygen subshells around the Zr atoms can be explained by the existence of oxygen displacements perpendicular to thezdirection; these mainly affect the second oxygen subshell because of the directional character of the EXAFS DW parameter, in contradiction to the crystallographic value. It is also established that this model is similar to another model having three oxygen subshells, with a 4 + 2 + 2 distribution of atoms, with only one DW parameter for all oxygen subshells. Both models are in good agreement with the crystal structure determined by X-ray diffraction experiments.

scholarly journals Structural Evolution in Wet Mechanically Alloyed Co-Fe-(Ta,W)-B Alloys

Metals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 800
Author(s):  
Vladimír Girman ◽  
Maksym Lisnichuk ◽  
Daria Yudina ◽  
Miloš Matvija ◽  
Pavol Sovák ◽  
...  
Keyword(s):  
Structural Changes ◽  
Magnetic Measurements ◽  
Structural Evolution ◽  
High Energy ◽  
Control Agent ◽  
X Ray Diffraction ◽  
Mechanically Alloyed ◽  
X Ray ◽  
Transmission Electron ◽  
X Ray Absorption

In the present study, the effect of wet mechanical alloying (MA) on the glass-forming ability (GFA) of Co43Fe20X5.5B31.5 (X = Ta, W) alloys was studied. The structural evolution during MA was investigated using high-energy X-ray diffraction, X-ray absorption spectroscopy, high-resolution transmission electron microscopy and magnetic measurements. Pair distribution function and extended X-ray absorption fine structure spectroscopy were used to characterize local atomic structure at various stages of MA. Besides structural changes, the magnetic properties of both compositions were investigated employing a vibrating sample magnetometer and thermomagnetic measurements. It was shown that using hexane as a process control agent during wet MA resulted in the formation of fully amorphous Co-Fe-Ta-B powder material at a shorter milling time (100 h) as compared to dry MA. It has also been shown that substituting Ta with W effectively suppresses GFA. After 100 h of MA of Co-Fe-W-B mixture, a nanocomposite material consisting of amorphous and nanocrystalline bcc-W phase was synthesized.

Size dependent behavior of Fe3O4crystals during electrochemical (de)lithiation: an in situ X-ray diffraction, ex situ X-ray absorption spectroscopy, transmission electron microscopy and theoretical investigation

2017 ◽  
Vol 19 (31) ◽  
pp. 20867-20880 ◽  
Author(s):  
David C. Bock ◽  
Christopher J. Pelliccione ◽  
Wei Zhang ◽  
Janis Timoshenko ◽  
K. W. Knehr ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Structural Changes ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
X Ray ◽  
Size Dependent ◽  
Transmission Electron ◽  
Dependent Behavior ◽  
X Ray Absorption

Crystal and atomic structural changes of Fe3O4upon electrochemical (de)lithiation were determined.

Ascertaining the nanocluster formation within an ion-irradiated Pt/Ni/C multi-trilayer with X-ray absorption spectroscopy

2012 ◽  
Vol 20 (1) ◽  
pp. 137-144
Author(s):  
Nitya Ramanan ◽  
Sumalay Roy ◽  
Debdutta Lahiri ◽  
Surinder M. Sharma ◽  
B. N. Dev
Keyword(s):  
Absorption Spectroscopy ◽  
Structural Changes ◽  
Nearest Neighbor ◽  
Ion Irradiation ◽  
Physical Adsorption ◽  
X Ray ◽  
Bimetallic Nanoclusters ◽  
Wave Technique ◽  
Wide Scale ◽  
X Ray Absorption

In this work nanoclusters formed in a Pt/Ni/C multi-trilayer by the ion-irradiated method of synthesis are characterized. In particular, an attempt to understand the role of interfaces in the synthesis is made. With this objective, ion-irradiation-induced structural changes in a Pt/Ni/C multi-trilayer using X-ray absorption spectroscopy (at the NiK-edge) in conjunction with the X-ray standing-wave technique are investigated. The XANES analysis identifies chemical binding at pristine Ni/C and Ni/Pt interfaces, in contrast with physical adsorption at the Pt/C interface. The chemical nature of the interfaces determines their relative stability with respect to irradiation and controls the extent of metallic diffusion. The most interesting structural change, upon irradiation, is the disruption of the Pt/C interface and subsequent migration of Pt atoms towards pre-diffused Ni atoms within the C layer, leading to the formation of Ni-centered Ni–Pt bimetallic nanoclusters (with Ni:Pt = 60:40). These clusters are highly disordered beyond their nearest neighbor and find wide-scale applications as, for example, magnetic devicesetc. The implications of these findings on the design goals are discussed.

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