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Influence of Host Lattice Ions on the Dynamics of Transient Multiband Upconversion in Yb–Er Codoped NaLnF4 and LiLnF4 Microcrystals (Ln: Y, Lu, Gd)

Inorganic host matrices provide a tunable luminescence environment for lanthanide ions, allowing for the modulation of upconversion luminescence (UCL) properties. AREF4 (A = alkali metal, RE = rare earth) have a low phonon energy and a high optical damage threshold, making them widely used as the ho...

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Bibliographic Details
Published in:ACS omega 2024-09, Vol.9 (38), p.39893-39903
Main Authors: Li, Mingchen, Yuan, Maohui, Cui, Wenda, Huang, Hanchang, Guo, Chuan, Han, Kai
Format: Article
Language:English
Online Access:Get full text
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Summary:Inorganic host matrices provide a tunable luminescence environment for lanthanide ions, allowing for the modulation of upconversion luminescence (UCL) properties. AREF4 (A = alkali metal, RE = rare earth) have a low phonon energy and a high optical damage threshold, making them widely used as the host matrix for UCL materials. However, the impact mechanism of alkali metal ions and lanthanide lattice ions on transient UCL dynamics in AREF4 remains unclear. This study utilized a high-power nanosecond-pulsed laser at 976 nm to excite Yb–Er codoped NaLnF4 and LiLnF4 (Ln: Y, Lu, and Gd) microcrystals (MCs). All samples exhibit multiband emission, and the transient UC dynamics are discussed in detail. Compared with LiLnF4, NaLnF4 has higher UC efficiency and red to green (R/G) ratio. Lanthanide ions (Y, Lu, and Gd) affect the energy transfer (ET) distance in Yb–Er codoped systems, thereby altering UC efficiency and the R/G ratio. The energy level coupling between Gd3+ and Er3+ prolongs the duration of the UC emission. Specifically, the red emission lifetime of NaGdF4 is five times longer than that of NaYF4. Our research contributes to exploring excellent alternative host matrices for NaYF4 in the fields of rapid-response optoelectronic devices, micro–nano lasers, and stimulated emission depletion (STED) microscopy.
ISSN:2470-1343
2470-1343
DOI:10.1021/acsomega.4c05453