A Dual-Mode Magnetic–Luminescent Hybrid: Fe3O4 + Y2O3:Yb3+,Tm3+ Decorated with a Eu3+ β-Diketonate Complex

  • André Lucas Costa
  • , Clara Johanna Pacheco
  • , Julieth Caro Patiño
  • , Angelo Márcio de Souza Gomes
  • , FLAVIA ARTIZZU
  • , Sergio Antonio Marques Lima
  • , Airton Germano Bispo-Jr
  • , Ana Maria Pires

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

We report the fabrication of multifunctional core@shell nanostructures integrating photonic and magnetic properties via a stepwise synthetic approach. The Fe3O4 + Y2O3:Yb,Tm@SiO2 hybrid was prepared through co-precipitation, homogeneous precipitation with urea, and silica coating, followed by functionalization with isocyanate groups. Subsequent coupling with 4-(aminomethyl)benzoic acid (pamba) enabled Eu3+ coordination through carboxylate moieties. Finally, the β-diketonate ligand 1-(4-chlorophenyl)-4,4,4-trifluoro-1,3-butanedione (4-Cl-btfa) was coordinated to Eu3+, promoting efficient ligand-to-metal energy transfer. The resulting nanostructure exhibited a saturation magnetization of 0.58 emu g−1 with negligible coercivity, consistent with related systems. Under 980 nm excitation (1500 mW), bright blue upconversion emission from Yb3+/Tm3+ in the Y2O3 matrix was observed. In contrast, ultraviolet excitation (335 nm) produced intense red emission with an absolute quantum yield of 12.7 %, arising from Eu3+ β-diketonate complexes on the surface. These findings demonstrate tunable emission behavior depending on excitation wavelength and highlight the potential of rational core@shell assembly for multifunctional nanoplatforms.

Lingua originaleInglese
RivistaMaterials Research Bulletin
DOI
Stato di pubblicazionePubblicato - 2025

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Keywords

  • 3-butanedione (4-Cl-btfa) was coordinated to Eu3+
  • 4
  • 4-trifluoro-1
  • Tm@SiO2 hybrid was prepared through co-precipitation
  • We report the fabrication of multifunctional core@shell nanostructures integrating photonic and magnetic properties via a stepwise synthetic approach. The Fe3O4 + Y2O3:Yb
  • and silica coating
  • arising from Eu3+ β-diketonate complexes at the surface. These findings demonstrate tunable emission behavior depending on excitation wavelength and highlight the potential of rational core@shell assembly for multifunctional nanoplatforms.
  • bright blue upconversion emission from Yb3+/Tm3+ in the Y2O3 matrix was observed. In contrast
  • consistent with related systems. Under 980 nm excitation (1500 mW)
  • followed by functionalization with isocyanate groups. Subsequent coupling with 4-(aminomethyl)benzoic acid (pamba) enabled Eu3+ coordination through carboxylate moieties. Finally
  • homogeneous precipitation with urea
  • promoting efficient ligand-to-metal energy transfer. The resulting nanostructure exhibited a saturation magnetization of 0.58 emu g−1 with negligible coercivity
  • the β-diketonate ligand 1-(4-chlorophenyl)-4
  • ultraviolet excitation (335 nm) produced intense red emission with an absolute quantum yield of 12.7%

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