Co-doped Dy3+ and Pr3+ Ga5Ge20Sb10S65 fibers for mid-infrared broad emission.

Rare earth ion doped materials are means to obtain cost-effective infrared light sources, with enough brilliance for applications such as gas sensing. Within a sulfide matrix, the simultaneous luminescence of both Pr3+ and Dy3+ in the Ga5Ge20Sb10S65 glass is reported. The use of these two rare earths is giving rise to a broad continuous luminescence in the 2.2-5.5 µm wavelength range, which could be used as a mid-infrared light source for gas-sensing applications. The demonstration of CO2 and CH4 detection using a fiber drawn from these materials is reported.

Control of the radiative properties via photon-plasmon interaction in Er3+ -Tm3+ -codoped tellurite glasses in the near infrared region.

The novelty of this paper is that it reports on the tuning of the spectral properties of Er3+ -Tm3+ ions in tellurite glasses in the near-infrared region through the incorporation of silver or gold nanoparticles. These noble metal nanoparticles can improve the emission intensity and expand the bandwidth of the luminescence spectrum centered at 1535 nm, covering practically all the optical telecommunication bands (S, C + L and U), and extended up to 2010 nm wavelength under excitation by a 976 nm laser diode. Both effects are obtained by the combined emission of Er3+ and Tm3+ ions due to efficient energy transfer processes promoted by the presence of silver or gold nanoparticles for the (Er3+)4I(11/2)→(Tm3+)3H5, (Er3+)4I(13/2)→(Tm3+)3H4 and (Er3+)4I(13/2)→(Tm3+)3F4 transitions. The interactions between the electronic transitions of Er3+ and Tm3+ ions that provide a tunable emission are associated with the dynamic coupling mechanism described by the variations generated by the Hamiltonian H DC in either the oscillator strength or the local crystal field, i.e. the line shape changes in the near-infrared emission band. The Hamiltonian is expressed as eigenmodes associated with the density of the conduction electron generated by the different nanoparticles through its collective free oscillations at each resonance frequency of the nanoparticle and their geometric dependence. A complete description of photon-plasmon interactions of noble metal nanoparticles with the Er3+ and Tm3+ ions is provided.

Localized surface plasmon resonance interaction with Er3+-doped tellurite glass.

We show the annealing effect on silver and Erbium-doped tellurite glasses in the formation of nanoparticles (NPs) of silver, produced by the reduction of silver (Ag+ → Ag0), aiming to an fluorescence enhancement. The absorption spectra show typical Localized Surface Plasmon Resonance (LSPR) band of Ag0 NP in addition to the distinctive absorption peaks of Er3+ ions. Both observations demonstrate that the photoluminescence enhancement is due to the coupling of dipoles formed by NPs with the Er3+ 4I(13/2) → 4I(15/2) transition. This plasmon energy transfer to the Er3+ ions was observed in the fluorescence spectrum with a blue-shift of the peaks.