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 originale | Inglese |
|---|---|
| Rivista | Materials Research Bulletin |
| DOI | |
| Stato di pubblicazione | Pubblicato - 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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