dc.contributor.author |
Bouet, L
|
|
dc.contributor.author |
Tailhades, P
|
|
dc.contributor.author |
Rousset, A
|
|
dc.contributor.author |
Kannan, K R
|
|
dc.contributor.author |
Verelst, M
|
|
dc.contributor.author |
Kulkarni, G U
|
|
dc.contributor.author |
Rao, C N R
|
|
dc.date.accessioned |
2012-10-31T11:23:53Z |
|
dc.date.available |
2012-10-31T11:23:53Z |
|
dc.date.issued |
1993-02 |
|
dc.identifier |
0022-4596 |
en_US |
dc.identifier.citation |
Journal of Solid State Chemistry 102(2), 414-422 (1993) |
en_US |
dc.identifier.uri |
https://libjncir.jncasr.ac.in/xmlui/10572/897 |
|
dc.description |
Restricted Access |
en_US |
dc.description.abstract |
Ferrites of the formula MoxFe3-xO4, prepared by a soft-chemistry route, show mixed valence states of both iron and molybdenum cations. Mössbauer studies show that Fe2+ and Fe3+ ions are present on both the A and B sites, giving Fe an average oxidation state between 2+ and 3+. Molybdenum is present in the 3+ and the 4+ states on the B sites. The presence of Mo in the 3+ state has been established by determining the Mo3+-O distance (2.2 Å), for the first time, by Mo K-EXAFS. The mixed valence of Fe on both the A and B sites and of Mo on the B sites is responsible for the fast electron transfer between the cations. All the Mössbauer parameters including the line width show a marked change at a composition (x ≈ 0.3) above which the concentration of Fe2+A increases rapidly. |
en_US |
dc.description.uri |
http://dx.doi.org/10.1006/jssc.1993.1053 |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Academic Press Inc |
en_US |
dc.rights |
© 1993 Academic Press Inc |
en_US |
dc.subject |
X-Ray |
en_US |
dc.subject |
Exchange |
en_US |
dc.title |
Fe-57 Mössbauer and Mo K-EXAFS Investigations of MoxFe3-xO4, an Interesting Mixed-Valent Oxide System |
en_US |
dc.type |
Article |
en_US |