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Excitation-Dependent Emission in Sb 3+ -Doped All-Inorganic Rare-Earth Double Perovskites for Anticounterfeiting Applications.

Wenzhi LiYuxi WangHong YinJunsheng ChenKe-Li HanFeng LiuRuiling Zhang
Published in: Inorganic chemistry (2024)
Achieving high-efficiency tunable emission in a single phosphor remains a significant challenge. Herein, we report a series of Sb 3+ -doped all-inorganic double perovskites, Sb 3+ :Cs 2 NaScCl 6 , with efficient excitation-dependent emission. In 0.5%Sb 3+ :Cs 2 NaScCl 6 , strong blue emission with a high photoluminescence quantum yield (PLQY) of 85% is obtained under 265 nm light irradiation, which turns into bright neutral white light with a PLQY of 56% when excited at 303 nm. Spectroscopic and computational investigations were performed to reveal the mechanism of this excitation-dependent emission. Sb 3+ doping induces two different excitation channels: the internal transition of Sb 3+ : 5s 2 → 5s5p and the electron transfer transition of Sb 3+ : 5s → Sc 3+ 3d. The former one generates excited Sb 3+ ions, which can undergo efficient energy transfer to populate the host self-trapped exciton (STE) state, yielding enhanced blue emission. The latter one leads to the formation of a new STE state with the hole localized on Sb 3+ and the electron delocalized on the nearest Sc 3+ , which accounts for the newly exhibited low-energy emission. The difference in the excitation pathways of the two emitting STE states results in the highly efficient excitation-dependent emission, making the doped systems promising anticounterfeiting materials.
Keyphrases
  • energy transfer
  • quantum dots
  • highly efficient
  • high efficiency
  • solid state
  • electron transfer
  • radiation therapy
  • solar cells
  • genome wide
  • molecular docking
  • water soluble