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Efficient energy upconversion of cw radiation at 1.064 μm into blue, red, and near infrared emission in Tm3+-doped Yb3+-sensitized 60TeO2-10GeO2-10K2O-10Li2O-10Nb2O5 glasses is reported. Intense blue upconversion luminescence at 485 nm corresponding to the Tm3+ 1G4→3H6 transition with a measured absolute power of 0.1 μW for 800 mW excitation power at room temperature is observed. The experimental results also revealed a sevenfold enhancement in the upconversion efficiency when the sample was heated from room temperature to 235 °C yielding 0.7 μW of blue absolute fluorescence power for 800 mW pump power. High brightness emission around 800 nm (3F4→3H6) in addition to a less intense 655 nm (1G4→3H4 and 3F2,3→3H6) fluorescence is also recorded. The energy upconversion excitation mechanism for thulium emitting levels is assigned to multiphonon-assisted anti-Stokes excitation of the ytterbium-sensitizer followed by multiphonon-assisted sequential energy-transfer processes.

Stable and intense second-order nonlinearity in soda lime glass is investigated tailoring the induced electric current. This procedure allows the determination of the relative contributions of the dipole orientation as well as the ionic contributions to the poling process. The experiments are developed in the light of multiple-carrier models controlling the output power supply applied current to tailor the frozen-in induced electric field — Edc. This method permits the induction of the stable nonlinearity for applied electric fields above ∼5kV∕cm and temperatures ∼250°C. It is also possible to reach higher temperatures than the ones used in normal poling procedures avoiding the electric current breakdown. The controlled Edc formation enables it to participate in essential chemical reactions that determine the intensity and stability of the nonlinearity. The induced d33 of ∼0.41pm∕V measured 20 days after poling reduced only ∼50% during the next seven months.