Abstract
Absorption transition from the ground 6H15/2 state to the superimposed (6H9/2, 6F11/2) states, inverse transition of which leads the Dy3+: 1.3 μm luminescence, in noncrystalline Ge-As-S alloys is dramatically modified upon a least compositional adjustment by Ga and CsBr. The change in oscillator strength of the Dy3+: 6H15/2 → 6F 11/2 transition in our modified glasses is more sensitive to the local coordination structure of rare-earths compared to other hypersensitive transitions that have been previously observed in solid-state dielectric hosts. Preferential highly symmetric coordination in nearest-neighbouring shell of dysprosium with bromine in [GaS3/2Br]- complexes, which are formed spontaneously during vitrification process of the host materials, is believed to be responsible for the behaviour.
Original language | English |
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Pages (from-to) | 29-34 |
Number of pages | 6 |
Journal | Chemical Physics Letters |
Volume | 403 |
Issue number | 1-3 |
DOIs | |
Publication status | Published - 14 Feb 2005 |