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  Co3O4-γ-Fe2O3 Nanocrystal Heterostructures with Enhanced Coercivity and Blocking Temperature

Nethravathi, C., Rajamathi, C. R., Caron, L., Kalache, A., Machado, J., Rajamathi, M., et al. (2020). Co3O4-γ-Fe2O3 Nanocrystal Heterostructures with Enhanced Coercivity and Blocking Temperature. The Journal of Physical Chemistry C, 124(2), 1623-1630. doi:10.1021/acs.jpcc.9b10858.

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 Urheber:
Nethravathi, C.1, Autor
Rajamathi, Catherine R.1, Autor
Caron, Luana1, Autor
Kalache, Adel2, Autor           
Machado, Jyothi1, Autor
Rajamathi, Michael1, Autor
Felser, Claudia3, Autor           
Affiliations:
1External Organizations, ou_persistent22              
2Inorganic Chemistry, Max Planck Institute for Chemical Physics of Solids, Max Planck Society, ou_1863425              
3Claudia Felser, Inorganic Chemistry, Max Planck Institute for Chemical Physics of Solids, Max Planck Society, ou_1863429              

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 Zusammenfassung: Reassembly of alpha-cobalt hydroxide nanosheets in the presence of citrate-capped gamma-Fe2O3 nanoparticles yields a-cobalt hydroxide-gamma-Fe(2)O(3 )hybrid in which the nanoparticles are trapped between the nanosheets. Thermal decomposition of the hybrid yields the Co3O4-gamma-Fe2O3 heterostructure. While the saturation magnetization (M-s) of gamma-Fe2O3 is preserved in the Co3O4-gamma-Fe(2)O(3 )heterostructure, the interface between the oxides in the heterostructure enhances the coercive field (H-C) to a large extent. The coercivity persists even above the Neel temperature of Co3O4 with the blocking temperature increased beyond room temperature. The unique morphology of the heterostructure wherein the Co3O4 and gamma-Fe2O3 particles are fused together to form a larger network leading to strong interparticle interactions, diffusion of Co atoms into the surface of gamma-Fe(2)O(3 )particles, and strain at the interfaces appear to be the reasons behind the improved magnetic behavior.

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Sprache(n): eng - English
 Datum: 2020-01-122020-01-12
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Art der Begutachtung: -
 Identifikatoren: ISI: 000508467700044
DOI: 10.1021/acs.jpcc.9b10858
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Titel: The Journal of Physical Chemistry C
  Kurztitel : J. Phys. Chem. C
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Washington, D.C. : American Chemical Society
Seiten: - Band / Heft: 124 (2) Artikelnummer: - Start- / Endseite: 1623 - 1630 Identifikator: ISSN: 1932-7447
CoNE: https://pure.mpg.de/cone/journals/resource/954926947766