Weidenthaler, C.

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  • Weidenthaler, C. (1)
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Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles

Antić, Bratislav; Kremenović, Aleksandar S.; Jović, Nataša G.; Pavlović, Miodrag B.; Jovalekić, Čedomir; Nikolić, Aleksandar S.; Goya, Gerardo F.; Weidenthaler, C.

(2012)

TY  - JOUR
AU  - Antić, Bratislav
AU  - Kremenović, Aleksandar S.
AU  - Jović, Nataša G.
AU  - Pavlović, Miodrag B.
AU  - Jovalekić, Čedomir
AU  - Nikolić, Aleksandar S.
AU  - Goya, Gerardo F.
AU  - Weidenthaler, C.
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6946
AB  - We present a study of the structural and magnetic properties of (Mn,Fe)(3-delta)O-4 nanoparticles synthesized by soft mechanochemistry using Mn(OH)(2) x 2 H2O and Fe(OH)(3) powders as starting compounds. The resulting nanoparticles with a composition of the (Mn,Fe)(3-delta)O-4 type are found to have a core/shell structure with different Mn/Fe ratios in the core and at the surface. XPS analysis points to valences of +2, +3, and +4 for Mn and +3 for Fe at the particle surface. Combined results of XRPD, Mossbauer spectroscopy, and EDX analysis suggest that there is a deviation from stoichiometry in the nanoparticle core compared to the shell, accompanied by creation of cation polyvalence and vacancies. The value of saturation magnetization, M-S, of 73.5 emu/g at room temperature, is among the highest reported so far among nanocrystalline ferrite systems of similar composition. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.3700228]
T2  - Journal of Applied Physics
T1  - Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles
VL  - 111
IS  - 7
DO  - 10.1063/1.3700228
ER  - 
@article{
author = "Antić, Bratislav and Kremenović, Aleksandar S. and Jović, Nataša G. and Pavlović, Miodrag B. and Jovalekić, Čedomir and Nikolić, Aleksandar S. and Goya, Gerardo F. and Weidenthaler, C.",
year = "2012",
abstract = "We present a study of the structural and magnetic properties of (Mn,Fe)(3-delta)O-4 nanoparticles synthesized by soft mechanochemistry using Mn(OH)(2) x 2 H2O and Fe(OH)(3) powders as starting compounds. The resulting nanoparticles with a composition of the (Mn,Fe)(3-delta)O-4 type are found to have a core/shell structure with different Mn/Fe ratios in the core and at the surface. XPS analysis points to valences of +2, +3, and +4 for Mn and +3 for Fe at the particle surface. Combined results of XRPD, Mossbauer spectroscopy, and EDX analysis suggest that there is a deviation from stoichiometry in the nanoparticle core compared to the shell, accompanied by creation of cation polyvalence and vacancies. The value of saturation magnetization, M-S, of 73.5 emu/g at room temperature, is among the highest reported so far among nanocrystalline ferrite systems of similar composition. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.3700228]",
journal = "Journal of Applied Physics",
title = "Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles",
volume = "111",
number = "7",
doi = "10.1063/1.3700228"
}
Antić, B., Kremenović, A. S., Jović, N. G., Pavlović, M. B., Jovalekić, Č., Nikolić, A. S., Goya, G. F.,& Weidenthaler, C.. (2012). Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles. in Journal of Applied Physics, 111(7).
https://doi.org/10.1063/1.3700228
Antić B, Kremenović AS, Jović NG, Pavlović MB, Jovalekić Č, Nikolić AS, Goya GF, Weidenthaler C. Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles. in Journal of Applied Physics. 2012;111(7).
doi:10.1063/1.3700228 .
Antić, Bratislav, Kremenović, Aleksandar S., Jović, Nataša G., Pavlović, Miodrag B., Jovalekić, Čedomir, Nikolić, Aleksandar S., Goya, Gerardo F., Weidenthaler, C., "Magnetization enhancement and cation valences in nonstoichiometric (Mn,Fe)(3-delta)O-4 nanoparticles" in Journal of Applied Physics, 111, no. 7 (2012),
https://doi.org/10.1063/1.3700228 . .
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