In this work, germanate glasses of
composition 59GeO2-41PbO in mol% doped with Er3+ ions were synthesized using
the melt-quenching route. Au and Ag nanoparticles and Au@Ag bimetallic
nanoparticles were formed on the surface of the germanate glasses
by ion implantation followed by thermal treatments. X-ray diffraction
patterns confirmed the amorphous structure of the implanted glasses.
Molecular dynamics was used to simulate the GeO2–PbO
glass structure. Surface plasmon resonance bands centered at 486,
537, and 574 nm, obtained through ultraviolet–visible absorption
spectra, supported the formation of Ag, Au, and Au@Ag nanoparticles,
respectively. Transmission electron microscopy (TEM) revealed the
presence of spherical Au and Ag nanoparticles as well as the presence
of nonspherical Au@Ag bimetallic nanoalloys. Refractive index n and extinction coefficient k were measured
by ellipsometry. Judd–Ofelt theory was applied to evaluate
the phenomenological intensity parameters Ωλ
(λ = 2,4,6) , radiative parameters,
and stimulated emission cross-sections for glasses doped with Er3+ and implanted with Au @Ag bimetallic nanoalloys. Efficient
boosting of the near-infrared emission for the 4I13/2 → 4I15/2 transition was observed in
the glass doped with Er3+ ions due to the presence of Au@Ag
bimetallic nanoalloys. The possible cause of this improvement in luminescent
intensity was attributed to the strong local field effect due to the
efficient synergy between Au@Ag bimetallic nanoalloys and the Er3+ ions. The results obtained in this work indicate that the
vitreous system GeO2–PbO glass doped with Er3+ ions and with the incorporation of Au@Ag bimetallic nanoalloys
via ionic implantation exhibit excellent spectroscopic properties
compared to other vitreous host glasses doped with the Er3+, indicating its potential applications in optical amplifiers.