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Probing the site occupancies of Co-, Ni-, and Mn-substituted biogenic magnetite using XAS and XMCD

Authors :
Carolyn I. Pearce
Neil D. Telling
Elke Arenholz
Jonathan R. Lloyd
Richard A. D. Pattrick
John M. Charnock
Gerrit van der Laan
Victoria S. Coker
Source :
American Mineralogist. 93:1119-1132
Publication Year :
2008
Publisher :
Mineralogical Society of America, 2008.

Abstract

Ferrimagnetic nanoparticles have many uses in industry including in magnetic recording media and transformers, however these particles are often expensive to synthesize. In this study, the Fe3+-reducing bacteria Geobacter sulfurreducens and Shewanella oneidensis were used to synthesize spinel ferrite nanoparticles of the general chemical formula M x Fe3– x O4, where M is either Co, Ni, Mn, Zn, or a combination of Mn and Zn. This was done at ambient temperatures through the dissimilatory reduction of Fe3+-oxyhydroxides containing the appropriate substitutional cations. A combination of L -edge and K -edge X-ray absorption spectroscopy (XAS) and L -edge X-ray magnetic circular dichroism (XMCD) was used to determine the site occupancies, valence, and local structure of the Fe and substitutional cations within the spinels. The Ni and Co ferrites produced using each bacterium were very similar and therefore this study concludes that, despite the difference in reduction mechanism of the bacteria used, the end-product is remarkably unaltered. Nickel ferrites contained only Ni2+, with at least 80% in Oh coordination. Cobalt ferrites contained only Co2+ but with a significant proportion (up to 45%) in Td coordination, showing a slight preference for Td sites. The Mn-ferrites contained Mn2+ only on the Oh sites but a mixture of Mn2+ and Mn3+ on Td sites when the amount of Mn exceeded 3% (compared to the amount of Fe) or some Zn was also present. This study successfully produced a range of nanoparticulate ferrites that could be produced industrially using relatively environmentally benign methodologies.

Details

ISSN :
0003004X
Volume :
93
Database :
OpenAIRE
Journal :
American Mineralogist
Accession number :
edsair.doi...........cfd10010697f479685db20ef2e9cfde2
Full Text :
https://doi.org/10.2138/am.2008.2681