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Quantum cutting properties of Tb3+/Yb3+ co-doped ZrO2-SiO2 nano-crystalized glasses synthesized via a sol-gel route
Tb3+/Yb3+ co-doped ZrO2-SiO2 nano-crystallized glasses were prepared by a sol-gel process. The crystal structure and optical properties including down-conversion photoluminescence (or, quantum cutting) of the Tb3+-Yb3+ system with respect to gel heat treatment temperature were investigated by X-ray...
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Published in: | Journal of alloys and compounds 2019-04, Vol.781, p.315-320 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Tb3+/Yb3+ co-doped ZrO2-SiO2 nano-crystallized glasses were prepared by a sol-gel process. The crystal structure and optical properties including down-conversion photoluminescence (or, quantum cutting) of the Tb3+-Yb3+ system with respect to gel heat treatment temperature were investigated by X-ray diffraction (XRD), Raman, photoluminescence (PL), and PL decay curves analysis. The energy transfer efficiency from Tb3+ to Yb3+ ions, which converts one photon to two photons with lower energy, increased with heat-treatment temperature. Furthermore, the oxidation state of Tb4+ ions was suspected to influence the emission intensity of Tb3+ and energy conversion efficiency. Thus, a post-treatment reduction was applied to the sample heated at 1100 °C by annealing it at 1100 °C for 1 h under 5%H2/95%N2 reductive atmosphere. Consequently, the thermodynamically generated Tb4+ ions were reduced to a trivalent state, leading to higher energy transfer efficiency.
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•Sol-gel method was applied to fabricate transparent Tb3+/Yb3+ co-doped ZrO2-SiO2 nanocomposites.•Thermal evolution of the precipitation of ZrO2 nanocrystals in SiO2 glass was investigated.•Tb3+-Yb3+ quantum cutting properties in ZrO2 nanocrystals was studied.•The high quantum cutting efficiency of 183% was obtained.•The impact of Tb valence state on the quantum cutting behavior was elucidated. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2018.11.380 |