Article (Scientific journals)
Determination of the antimony valence state in Eu10Mn6Sb13
Brown, D. E.; Johnson, C. E.; Grandjean, Fernande et al.
2004In Inorganic Chemistry, 43 (4), p. 1229-1234
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Abstract :
[en] The antimony-121 Mossbauer spectra of Eu10Mn6Sb13 have been measured between 2 and 295 K. Although the Zintl formalism indicates that the nine crystallographically distinct antimony sites in Eu10Mn6Sb13 should have formal valence states of -2, -1, 0, and +1, the Mossbauer spectral isomer shifts reveal that the valence states of the 4.0 different sites are all quite similar and correspond to an average electronic configuration for antimony of 5s(1.7)5p(4.0). This configuration corresponds to an excess of negative charge on the antimony of 0.7 or an average valence of -0.7, a valence which is rather consistent with the average antimony valence of -0.61 obtained from the Zintl formalism for the nine antimony sites in Eu10Mn6Sb13. The spectra obtained between 90 and 295 K are more consistent with the absence rather than the presence of any transferred magnetic hyperfine field at the antimony. In contrast, the spectra obtained at 2 and 5 K reveal the presence of an average transferred magnetic hyperfine field of ca. 8 T, a field that arises from the ferromagnetic ordering of the near-neighbor manganese(II) ions.
Disciplines :
Chemistry
Author, co-author :
Brown, D. E.
Johnson, C. E.
Grandjean, Fernande ;  Université de Liège - ULiège > Département de physique > Département de physique
Hermann, Raphaël ;  Université de Liège - ULiège > Département de physique > Département de physique
Kauzlarich, S. M.
Holm, A. P.
Long, G. J.
Language :
English
Title :
Determination of the antimony valence state in Eu10Mn6Sb13
Publication date :
2004
Journal title :
Inorganic Chemistry
ISSN :
0020-1669
eISSN :
1520-510X
Publisher :
American Chemical Society, Washington, United States - District of Columbia
Volume :
43
Issue :
4
Pages :
1229-1234
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 19 October 2011

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