X-ray absorption fine structure study on the formation of Cu–Br bonds in (Br + Cu) ion implanted silica glass

2003 ◽  
Vol 18 (4) ◽  
pp. 885-894 ◽  
Author(s):  
Kohei Fukumi ◽  
Akiyoshi Chayahara ◽  
Atsushi Kinomura ◽  
Hiroyuki Kageyama ◽  
Kohei Kadono ◽  
...  

The valence and coordination structure of implanted Cu and Br ions were investigated by x-ray absorption fine structure spectroscopy in (2.4 MeV 6 × 1016 Br2+ ions cm−2+ 2 MeV 6 × 1016 Cu+ ions cm−2)-implanted silica glass. It was found that the implanted Cu and Br atoms were coordinated by oxygen atoms and silicon atoms, respectively, in as-implanted glass. After heating at 600 °C, at least two-thirds of the Cu atoms were coordinated by Br atoms without the formation of crystals. The γCuBr crystal was formed after heating to 1100 °C. It was deduced that the coordination structure of Cu and Br atoms depends on defects as well as thermochemical stability and mass transport processes.

1998 ◽  
Vol 13 (9) ◽  
pp. 2649-2654
Author(s):  
Kohei Fukumi ◽  
Hiroyuki Kageyama ◽  
Kohei Kadono ◽  
Akiyoshi Chayahara ◽  
Nagao Kamijo ◽  
...  

Coordination state of gold atoms implanted in silica glass to an energy of 1.5 MeV and a dose of 1 × 1017 ions/cm2 has been studied by x-ray absorption fine structure spectroscopy. It was found that most of the gold atoms form gold clusters in which the nearest neighboring Au–Au interatomic distance is shorter by 0.05 °A than that in bulk gold. The contraction of Au–Au interatomic distance of gold clusters in silica glass is less than that reported in the previous studies on gold clusters within the other substrates. Gold atoms are coordinated by about four gold atoms in average. In addition, it was found that Au–O bonds are formed at the gold clusters/silica glass interface. It was deduced that the formation of Au–O bond at the gold clusters/silica glass interface depresses the contraction of Au–Au interatomic distance.


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.


1984 ◽  
Vol 30 (2) ◽  
pp. 672-677 ◽  
Author(s):  
P. A. Montano ◽  
W. Schulze ◽  
B. Tesche ◽  
G. K. Shenoy ◽  
T. I. Morrison

1995 ◽  
Author(s):  
I. Pop ◽  
O. Pop ◽  
Ioan Burda ◽  
C. Oprea ◽  
I. Nazarenco ◽  
...  

2001 ◽  
Vol 63 (22) ◽  
Author(s):  
Shiqiang Wei ◽  
Hiroyuki Oyanagi ◽  
Zhongrui Li ◽  
Xinyi Zhang ◽  
Wenhan Liu ◽  
...  

1997 ◽  
Vol 11 (16n17) ◽  
pp. 745-748 ◽  
Author(s):  
Rebekah Min-Fang Hsu ◽  
Kai-Jan Lin ◽  
Cheng Tien ◽  
Lin-Yan Jang

X-ray absorption fine structure XAFS spectroscopy has been used to determine the valence system for the Fe atom in ilmenite, FeTiO3 . This is the first XAFS data in FeTiO3 to our knowledge. The α- Fe2O3 data served as the standard in determining the ionization of the Fe atom in FeTiO3 . Observation of intensity and k-space are consistent. There was no evidence of mixed valence on comparing the FeTiO3 near edge X-ray absorption spectrum with α- Fe2O3 data. The absorption spectra suggest that iron is in the trivalent state in ilmenite.


1986 ◽  
Vol 47 (C8) ◽  
pp. C8-473-C8-478 ◽  
Author(s):  
U. DÖBLER ◽  
L. WENZEL ◽  
D. ARVANITIS ◽  
K. BABERSCHKE

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