Abstract
Scintillator-based X-ray imaging technology is widely applied in medical diagnostics and nondestructive detection. Low-dimensional metal halide perovskites (MHPs) offer great potential in scintillation applications due to their flexible crystal structures. However, achieving strongly localized excitonic emission in low-dimensional MHPs remains challenging to further improve the photoemission performance. Herein, we report an entropy-engineering strategy to construct four-element Cs2MCl6(M = Te4+, Sn4+, Zr4+, and Hf4+) vacancy-ordered double-perovskite scintillators for enhanced X-ray detection, demonstrating an 8-fold enhancement in photoluminescence quantum yield, a 17-fold enhancement in photoluminescence intensity, and a low detection limit of 50.3 nGy s–1. Structural characterizations combined with theoretical calculations reveal that increased configurational entropy induces intense lattice distortion in [MCl6]2–octahedral clusters, increasing exciton transport barriers. Femtosecond transient absorption and temperature-dependent spectroscopic analyses indicate that this four-element Cs2MCl6shows strong electron–phonon and energy interactions between confined exciton states in isolated [MCl6]2–octahedral structures, thus promoting photoluminescence emission. A flexible scintillation screen containing high-entropy Cs2MCl6achieves a high resolution of over 20 lp mm–1for X-ray imaging. This work presents enhanced emission of MHPs by entropy engineering, providing potential implications for radiation detection and other optoelectronic applications.
| Original language | English |
|---|---|
| Pages (from-to) | 30396-30406 |
| Number of pages | 11 |
| Journal | ACS Nano |
| Volume | 19 |
| Issue number | 33 |
| DOIs | |
| State | Published - Aug 26 2025 |
Keywords
- entropy engineering
- exciton localization
- inorganic metal halide perovskites
- theoretical calculation
- X-ray imaging
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