Drastic Change of the Ferromagnetic Properties of the Ternary Germanide GdTiGe through Hydrogen Insertion
Author(s) -
Etienne Gaudin,
Samir F. Matar,
Rainer Pöttgen,
Matthias Eul,
Bernard Chevalier
Publication year - 2011
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/ic201579r
Subject(s) - chemistry , antiferromagnetism , ferromagnetism , germanide , paramagnetism , hydride , magnetism , delocalized electron , ternary operation , hydrogen , condensed matter physics , crystallography , curie temperature , physics , germanium , organic chemistry , silicon , computer science , programming language
Hydrogen absorption of the CeFeSi- and CeScSi-type forms of GdTiGe was performed. Before hydrogenation they show an antiferromagnetic transition at around 412 K and a ferromagnetic transition at 376 K, respectively. Hydrogenation of both forms leads to formation of the same hydride GdTiGeH which crystallizes with a filled CeScSi-type structure where all the [Gd(4)] tetrahedra are filled by hydrogen. This hydride is paramagnetic in the temperature range 4-300 K. The slightly negative value of the paramagnetic Curie temperature θ(p) confirms that all ferromagnetic interactions were destroyed in the case of the CeScSi-type form. From first-principles calculations with the PAW GGA methodology, the localization of hydrogen within the [Gd(4)] tetrahedra was confirmed through energetic stabilization. It was also seen that the energy changes significantly with volume, indicating the itinerant (delocalized) role of the electrons in the magnetism.
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