In Situ X‐Ray Absorption Near Edge Structure Study of the Potential Dependence of the Formation of the Passive Film on Iron in Borate Buffer

1997 ◽  
Vol 144 (7) ◽  
pp. 2398-2404 ◽  
Author(s):  
L. J. Oblonsky ◽  
A. J. Davenport ◽  
M. P. Ryan ◽  
H. S. Isaacs ◽  
R. C. Newman
Keyword(s):  
Passive Film ◽  
Structure Study ◽  
Borate Buffer ◽  
Edge Structure ◽  
X Ray ◽  
Potential Dependence ◽  
X Ray Absorption

Fluorescence Extended X-Ray Absorption Fine Structure Study on Local Structures of Rare-Earth-Doped InGaGdN

2016 ◽  
Vol 1133 ◽  
pp. 429-433
Author(s):  
Siti Nooraya Mohd Tawil ◽  
Shuichi Emura ◽  
Daivasigamani Krishnamurthy ◽  
Hajime Asahi
Keyword(s):  
Fine Structure ◽  
Rare Earth ◽  
Nearest Neighbor ◽  
Structure Study ◽  
Edge Structure ◽  
X Ray ◽  
Local Structures ◽  
Absorption Fine ◽  
X Ray Absorption

Local structures around gadolinium atoms in rare-earth (RE)-doped InGaGdN thin films were studied by means of fluorescence extended X-ray absorption fine structure (EXAFS) measured at the Gd LIII-edges. The samples were doped with Gd in-situ during growth by plasma-assisted molecular beam epitaxy (PAMBE). Gd LIII-edge EXAFS signal from the GaGdN, GdN and Gd foil were also measured as reference. The X-ray absorption near edge structure (XANES) spectra around Gd LIII absorption edge of InGaGdN samples observed at room temperature indicated the enhancement of intensities with the increase of Gd composition. Further EXAFS analysis inferred that the Gd atoms in InGaN were surrounded by similar atomic shells as in the case of GaGdN with the evidence indicating majority of Gd atoms substituted into Ga sites of InGaGdN. A slight elongation of bond length for the 2nd nearest-neighbor (Gd–Ga) of sample with higher Gd concentration was also observed.

ChemInform Abstract: In situ Time-Resolved X-Ray Absorption Near Edge Structure Study of the Nickel Oxide Electrode

ChemInform ◽  
1989 ◽  
Vol 20 (48) ◽  
Author(s):  
J. MCBREEN ◽  
W. E. O'GRADY ◽  
G. TOURILLON ◽  
E. DARTYGE ◽  
A. FONTAINE ◽  
...  
Keyword(s):  
Nickel Oxide ◽  
Structure Study ◽  
Oxide Electrode ◽  
Time Resolved ◽  
Edge Structure ◽  
X Ray ◽  
Nickel Oxide Electrode ◽  
X Ray Absorption

In situ micro X-ray absorption near edge structure study of microbiologically reduced selenite (SeO32−)

2004 ◽  
Vol 59 (10-11) ◽  
pp. 1681-1686 ◽  
Author(s):  
Phil M. Oger ◽  
I. Daniel ◽  
B. Cournoyer ◽  
A. Simionovici
Keyword(s):  
Structure Study ◽  
Edge Structure ◽  
X Ray ◽  
X Ray Absorption

In Situ X-ray Absorption Near-Edge Structure Study of Advanced NiFe(OH)x Electrocatalyst on Carbon Paper for Water Oxidation

2015 ◽  
Vol 119 (34) ◽  
pp. 19573-19583 ◽  
Author(s):  
Dongniu Wang ◽  
Jigang Zhou ◽  
Yongfeng Hu ◽  
Jinli Yang ◽  
Na Han ◽  
...  
Keyword(s):  
Water Oxidation ◽  
Structure Study ◽  
Carbon Paper ◽  
Edge Structure ◽  
X Ray ◽  
X Ray Absorption

In situ time-resolved x-ray absorption near edge structure study of the nickel oxide electrode

1989 ◽  
Vol 93 (17) ◽  
pp. 6308-6311 ◽  
Author(s):  
J. McBreen ◽  
W. E. O'Grady ◽  
G. Tourillon ◽  
E. Dartyge ◽  
A. Fontaine ◽  
...  
Keyword(s):  
Nickel Oxide ◽  
Structure Study ◽  
Oxide Electrode ◽  
Time Resolved ◽  
Edge Structure ◽  
X Ray ◽  
Nickel Oxide Electrode ◽  
X Ray Absorption

scholarly journals High-energy resolution X-ray absorption and emission spectroscopy reveals insight into unique selectivity of La-based nanoparticles for CO2

2015 ◽  
Vol 112 (52) ◽  
pp. 15803-15808 ◽  
Author(s):  
Ofer Hirsch ◽  
Kristina O. Kvashnina ◽  
Li Luo ◽  
Martin J. Süess ◽  
Pieter Glatzel ◽  
...  
Keyword(s):  
Energy Resolution ◽  
Emission Spectroscopy ◽  
High Energy ◽  
Unit Cell ◽  
High Energy Resolution ◽  
Electron Configuration ◽  
Edge Structure ◽  
X Ray ◽  
X Ray Absorption

The lanthanum-based materials, due to their layered structure and f-electron configuration, are relevant for electrochemical application. Particularly, La2O2CO3 shows a prominent chemoresistive response to CO2. However, surprisingly less is known about its atomic and electronic structure and electrochemically significant sites and therefore, its structure–functions relationships have yet to be established. Here we determine the position of the different constituents within the unit cell of monoclinic La2O2CO3 and use this information to interpret in situ high-energy resolution fluorescence-detected (HERFD) X-ray absorption near-edge structure (XANES) and valence-to-core X-ray emission spectroscopy (vtc XES). Compared with La(OH)3 or previously known hexagonal La2O2CO3 structures, La in the monoclinic unit cell has a much lower number of neighboring oxygen atoms, which is manifested in the whiteline broadening in XANES spectra. Such a superior sensitivity to subtle changes is given by HERFD method, which is essential for in situ studying of the interaction with CO2. Here, we study La2O2CO3-based sensors in real operando conditions at 250 °C in the presence of oxygen and water vapors. We identify that the distribution of unoccupied La d-states and occupied O p- and La d-states changes during CO2 chemoresistive sensing of La2O2CO3. The correlation between these spectroscopic findings with electrical resistance measurements leads to a more comprehensive understanding of the selective adsorption at La site and may enable the design of new materials for CO2 electrochemical applications.

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