Structural observation of nano-structured and amorphous hydrogen storage materials by neutron diffraction

被引:27
作者
Fukunaga, T [1 ]
Itoh, K
Orimo, S
Aoki, K
机构
[1] Kyoto Univ, Inst Res Reactor, Kumatori, Osaka 5900494, Japan
[2] Tohoku Univ, Inst Mat Res, Aoba Ku, Sendai, Miyagi 9808577, Japan
[3] Kitami Inst Technol, Dept Mat Sci, Kitami, Hokkaido 0908507, Japan
来源
MATERIALS SCIENCE AND ENGINEERING B-SOLID STATE MATERIALS FOR ADVANCED TECHNOLOGY | 2004年 / 108卷 / 1-2期
关键词
neutron diffraction; structure; hydrogen; RMC modeling;
D O I
10.1016/j.mseb.2003.10.059
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Neutron diffraction is a powerful tool to elucidate the structure of hydrogen storage materials. H/D isotopic substitution was employed to observe the location of deuterium atoms because the coherent scattering length of deuterium is large enough to observe in comparison with that of the other atoms forming hydride materials. This work focused on two kinds of hydrogen storage materials to investigate the location of deuterium atoms. One is the deuterated nano-graphite prepared by mechanical milling under deuterium gas atmosphere and the other is a hydrogen-induced amorphized material. The structure of graphite was changed by a creation of dangling bonds and deuterium was absorbed by the solid-gas reaction when the trilling proceeds. The RDF(r) observed by neutron diffraction indicates two kinds of locations of deuterium atoms, that is, some deuterium atoms bond with the carbon atoms and others exist between layers of the graphite. The structure around a deuterium atom in the crystalline intermetallic compound TbFe2D3.8 and amorphous TbFe2Dx (x = 3.0, 2.0) informs us not only the location of the deuterium atoms but also rearrangement of metal atoms with transformation from a crystalline to an amorphous phase. In crystalline TbFe2 = D-3.8 deuterium atoms occupy the tetrahedral unit consisting of 2Tb+2Fe. On the other hand, a tetrahedral unit consisting mainly of Tb atoms becomes a stable site of D atoms in the amorphous TbFe2Dx. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:105 / 113
页数:9
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