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Na-alloy tailored 3D/0D metal halide heterostructures enabling efficient charge transfer for color-integrated white scintillators

Author

Listed:
  • Zhi Yang

    (Zhengzhou University)

  • Jiangtao Cui

    (Zhengzhou University)

  • Ying Sun

    (Zhengzhou University)

  • Jisong Yao

    (Zhengzhou University)

  • Shuang Yang

    (East China University of Science and Technology)

  • Jizhong Song

    (Zhengzhou University)

Abstract

Lead-free halide perovskites featuring broad emissions have attracted increasing interest as X-ray imaging scintillators. Currently, the radioluminescence spectrum is primarily tuned by dopants and crystal fields, thus exploring a heterostructure manner to extensively modulate emission intensity and linewidth presents an exciting opportunity. Herein, we synthesize 3D/0D Cs2NaLuCl6/Cs3LuCl6(Sb) heterostructures via a Na-alloying strategy to tailor the spectral feature of scintillators. We find that type I heterostructure can promote the emission of 0D Cs3LuCl6(Sb) through charge transfer mechanism, as corroborated by the combination of energy band alignment, ultrafast transient dynamics, microscopic photoluminescence and electrical conductivity. As a result, 3D/0D scintillator exhibits a 1.8-times higher radioluminescence intensity than 0D scintillator. Meanwhile, featuring a spectrum-flat white emission, 3D/0D scintillator provides a balanced RGB output enabling to extend the dynamic range in color-integrated X-ray imaging. These findings provide insights into constructing metal halide heterostructures with efficient charge transfer, and advance the design and application of lead-free perovskites and their derivatives.

Suggested Citation

  • Zhi Yang & Jiangtao Cui & Ying Sun & Jisong Yao & Shuang Yang & Jizhong Song, 2025. "Na-alloy tailored 3D/0D metal halide heterostructures enabling efficient charge transfer for color-integrated white scintillators," Nature Communications, Nature, vol. 16(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62195-x
    DOI: 10.1038/s41467-025-62195-x
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