Colour-tunable and warm white light emitting thermally stable Dy3+/Sm3+ co-activated tungstate-tellurite glasses for photonic applications

Transparent single Dy3+, Sm3+, and Dy3+/Sm3+ co-activated tungstate-tellurite (TWKZBi) glass matrices were synthesized via melt-quenching process. The optical features of the prepared glass matrices were examined with the aid of the absorption spectra. Under various excitation wavelengths (366, 388 and 454 nm), Dy3+ doped TWKZBi (TWKZBiDy) glasses revealed a prevailing emission peak similar to 575 nm related to the yellow band (F-4(9/2) -> H-6(13/2)) transition, while Sm3+ doped TWKZBi (TWKZBiSm) glass matrices reveal strong intense emission peak at similar to 600 nm associated with the orange-red band ((4)G(5/2) -> H-6(7/2)) transition. The emission intensity progressively surges with an increment in Sm3+ ion content (up to 1.5 mol%), confirming the ET mechanism between Dy3+ and Sm3+ ions. Application of Dexter's ET formulation with the Reisfeld's approximation revealed that the ET mechanism involves a non-radiative dipole-dipole (d-d) interaction between Dy3+ and Sm3+ ions. The average lifetime (tau(avg)) values for the F-4(9/2) state of Dy3+ ions in the TWKZBiDySm glass sample was measured and found that these values decreased with increasing Sm3+ ion content. In addition, the ET efficiencies (eta(Dy -> Sm)) of the TWKZBiDySm glass matrices were evaluated using the lifetime curves. The color coordinates (x, y) and the correlated color temperature (CCT) values of the co-activated glass samples were estimated. Based on the chromaticity coordinates and CCT values, it was found that the desired color of the TWKZBiDySm glass samples can be modulated from warm white light to orange-red light via precisely adjusting the concentration of Sm3+ ions and at selected excitation wavelengths. Furthermore, the emission intensity observed at 373 K was 83.83 % compared to the emission intensity at ambient temperature, indicating the excellent thermal stability of the TWKZBiDySm glasses prepared. The above results confirm that the prepared Dy3+/Sm3+ co-activated TWKZBi glass matrix can be a promising candidate for white light and other photonic devices.