Eu 2+ Doping Concentration‐Driven Site Selectivity Enables Tunable Luminescence in Sr 2 LuTaO 6 for Lighting and Optical Authentication
ABSTRACT Eu 2+ ‐activated phosphors are promising for various photonic applications; however, luminescence control and modification are always challenging. In this study, Eu 2+ doping concentration‐driven site‐selective luminescence is realized in monoclinic Sr 2 LuTaO 6 , with oxalic acid enhancing Eu 3+ →Eu 2+ conversion efficiency. Increasing Eu 2+ concentration drives its redistribution from SrO 8 sites to LuO 6 sites, giving rise to green emission at 534 nm under UV excitation and red emission at 612 nm under blue excitation. Eu 2+ at the SrO 8 site exhibits superior thermal stability, retaining 93% of its room‐temperature emission intensity at 150°C, compared with 70.2% for the LuO 6 site, due to its larger thermal activation barrier. These distinct luminescence properties enable the applications of Sr 2 LuTaO 6 :Eu 2+ phosphors in white‐light lighting and optical authentication. This work clearly shows the potential of site‐occupation engineering for the rational design of multifunctional phosphors.
Authors
- Zhiyu Yang (ORCID: https://orcid.org/0009-0003-3132-6556)
- Guangxiang Lu (ORCID: https://orcid.org/0009-0006-2959-6313)
- Tao Yang (ORCID: https://orcid.org/0000-0002-2276-4023)
- Zhiguo Xia (ORCID: https://orcid.org/0000-0002-9670-3223)
- Xianju Zhou (ORCID: https://orcid.org/0000-0002-8050-9688)
- Li Li (ORCID: https://orcid.org/0009-0001-3077-8273)
- Yongjie Wang (ORCID: https://orcid.org/0000-0002-5580-8555)
- Chonghuan Luo
- Jingyue Zhang
Institutions
- Chongqing University of Posts and Telecommunications (CN)
- Chongqing University (CN)
- State Key Laboratory of Luminescent Materials and Devices (CN)
- South China University of Technology (CN)
Publication Details
- Journal
- Laser & Photonics Review
- Published
- 2026-11-05
- DOI
- https://doi.org/10.1002/lpor.72196
- Primary Topic
- Luminescence Properties of Advanced Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00