Tunable Visible Light and Energy Transfer Mechanism in Tm3+ and Silver Nanoclusters within Co-Doped GeO2-PbO Glasses

This study introduces a novel method for producing Ag nanoclusters (NCs) within GeO2-PbO glasses doped with Tm3+ ions. Sample preparation involved the melt-quenching method, employing adequate heat treatment to facilitate Ag NC formation. Absorption spectroscopy confirmed trivalent rare-earth ion incorporation. Ag NC identification and the amorphous structure were observed using transmission electron microscopy. A tunable visible emission from blue to the yellow region was observed. The energy transfer mechanism from Ag NCs to Tm3+ ions was demonstrated by enhanced 800 nm emission under 380 and 400 nm excitations, mainly for samples with a higher concentration of Ag NCs; moreover, the long lifetime decrease of Ag NCs at 600 nm (excited at 380 and 400 nm) and the lifetime increase of Tm3+ ions at 800 nm (excitation of 405 nm) corroborated the energy transfer between those species. Therefore, we attribute this energy transfer mechanism to the decay processes from S-1 -> T-1 and T-1 -> S-0 levels of Ag NCs to the H-3(4) level of Tm3+ ions serving as the primary path of energy transfer in this system. GeO2-PbO glasses demonstrated potential as materials to host Ag NCs with applications for photonics as solar cell coatings, wideband light sources, and continuous-wave tunable lasers in the visible spectrum, among others.

Automated summary

This study introduces a novel method for producing Ag nanoclusters within GeO2-PbO glasses doped with Tm3+ ions. The research confirms the formation of Ag nanoclusters and their amorphous structure through transmission electron microscopy. The energy transfer mechanism between Ag nanoclusters and Tm3+ ions is demonstrated.