Magnetic-nanoparticle diagnostics based on analysis of hyperfine structure of Mössbauer spectra in a weak magnetic field

2010 ◽  
Vol 55 (1) ◽  
pp. 6-12 ◽  
Author(s):  
M. A. Chuev ◽  
V. M. Cherepanov ◽  
M. A. Polikarpov
1983 ◽  
Vol 14 (1) ◽  
pp. 1-6 ◽  
Author(s):  
S. S. Yakimov ◽  
V. M. Cherepanov ◽  
M. A. Chuev ◽  
A. M. Afanas'ev ◽  
F. Parak

1971 ◽  
Vol 122 (3) ◽  
pp. 257-265 ◽  
Author(s):  
K. K. Rao ◽  
R. Cammack ◽  
D. O. Hall ◽  
C. E. Johnson

1. The Mössbauer spectra of Scenedesmus ferredoxin enriched in 57Fe were measured and found to be identical with those of two other plant-type ferredoxins (from spinach and Euglena) that had been previously measured. Better resolved Mössbauer spectra of spinach ferredoxin are also reported from protein enriched in 57Fe. All these iron–sulphur proteins are known to contain two iron atoms in a molecule that takes up one electron on reduction. 2. The Mössbauer spectra at 195°K have electric hyperfine structure only and show that on reduction the electron goes to one of the iron atoms, the other appearing to remain unchanged. 3. In the oxidized state, both iron atoms are in a similar chemical state, which appears from the chemical shift and quadrupole splitting to be high-spin Fe3+, but they are in slightly different environments. In the reduced state the iron atoms are different and the molecule appears to contain one high-spin Fe2+ and one high-spin Fe3+ atom. 4. At lower temperatures (77 and 4.2°K) the spectra of both iron atoms in the reduced proteins show magnetic hyperfine structure which suggests that the iron in the oxidized state also has unpaired electrons. This provides experimental evidence for earlier suggestions that in the oxidized state there is antiferromagnetic exchange coupling, which would result in a low value for the magnetic susceptibility. 5. In a small magnetic field the spectrum of the reduced ferredoxin shows a Zeeman splitting with hyperfine field (Hn) of 180kG at the nuclei. On application of a strong magnetic field H the spectrum splits into two spectra with effective fields Hn±H, thus confirming the presence of the two antiferromagnetically coupled iron atoms. 6. These results are in agreement with the model proposed by Gibson, Hall, Thornley & Whatley (1966); in the oxidized state there are two Fe3+ atoms (high spin) antiferromagnetically coupled and on reduction of the ferredoxin by one electron one of the ferric atoms becomes Fe2+ (high spin).


Author(s):  
Amel Kaibi ◽  
Abderrahim Guittoum ◽  
Nassim Souami ◽  
Mohamed Kechouane

Nanocrystalline Ni75Fe25 (Ni3Fe) powders were prepared by mechanical alloying process using a vario-planetary high-energy ball mill. The intermetallic Ni3Fe formation and different physical properties were investigated, as a function of milling time, t, (in the range 6 to 96 h range), using X-Ray Diffraction (XRD) and Mössbauer Spectroscopy techniques. X-ray diffraction were performed on the samples to understand the structural characteristics and get information about elements and phases present in the powder after different time of milling. The refinement of XRD spectra revealed the complete formation of fcc Ni (Fe) disordered solid solution after 24 h of milling time, the Fe and Ni elemental distributions are closely correlated. With increasing the milling time, the lattice parameter increases and the grains size decreases. The Mössbauer experiments were performed on the powders in order to follow the formation of Ni3Fe compound as a function of milling time. From the adjustment of Mössbauer spectra, we extracted the hyperfine parameters. The evolution of hyperfine magnetic field shows that the magnetic disordered Ni3Fe phase starts to form from 6 h of milling time and grow in intensity with milling time. For the milling time more than 24 h, only the Ni3Fe disordered phase is present with a mean hyperfine magnetic field of about 29.5 T. The interpretation of the Mossbauer spectra confirmed the results obtained by XRD.


1987 ◽  
Vol 20 (32) ◽  
pp. 5389-5399 ◽  
Author(s):  
M Winterer ◽  
E Morsen ◽  
B D Mosel ◽  
W Muller-Warmuth

Nanomaterials ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 24 ◽  
Author(s):  
Munirah Almessiere ◽  
Yassine Slimani ◽  
Hakan Güngüneş ◽  
Abdulhadi Baykal ◽  
S.V. Trukhanov ◽  
...  

Manganese (Mn)- and yttrium (Y)-substituted Sr-nanohexaferrites (MYSNHFs) of composition Sr1−xMnxFe12−xYxO19 (with 0.0 ≤ x ≤ 0.5) were prepared by citrate sol-gel autocombustion method. As-prepared MYSNHFs were characterized via diverse analytical techniques to determine the influence of Mn and Y cosubstitution on their microstructures and magnetic properties. 57Fe Mössbauer spectra of the MYSNHFs were used to evaluate the variation in the line width, isomer shift, quadrupole splitting, and hyperfine magnetic field values. It was shown that the dopant ions could preferentially occupy the 12k, 4f2, and 2b sites. Furthermore, the observed shift in the blocking temperatures of the studied MYSNHFs towards lower values with rising Mn2+ and Y3+ contents was attributed to the overall particles size reduction. Meanwhile, the AC susceptibility of the proposed MYSNHFs revealed that the magnetic interactions were weakened with the increase in dopant contents which was ascribed to the replacement of both Sr2+ and Fe3+ ions by the Mn2+ and Y3+ dopants.


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