Abstract
X-ray detection and imaging are crucial in many fields, yet most conventional scintillators suffer from brittleness, limited light yield, and incompatibility with flexible or confined-space applications. Here, we report the first synthesis of transparent single crystals of (C8H20N)2Cu2I4((TEA)2Cu2I4), the iodide analogue of (TEA)2Cu2Br4. Although (TEA)2Cu2Br4has shown remarkable scintillation performance, its iodide counterpart, expected to deliver stronger X-ray absorption and higher efficiency, had remained inaccessible. Single-crystal diffraction reveals that TEA+cations fully encapsulate [CuI2]−units, forming spatially isolated 0D motifs that promote efficient self-trapped exciton recombination. The crystals emit deep-blue light at 450 nm with a photoluminescence quantum yield of 96% and a microsecond STE lifetime. Under X-ray excitation, (TEA)2Cu2I4achieves a record light yield of 115,000 Photons/MeV, a detection limit of 167 nGyair/s, and an imaging resolution of 11.9 lp/mm. These findings establish (TEA)2Cu2I4as the first structurally well-defined iodide analogue in this family, and they highlight structural design as a viable strategy for developing high-performance lead-free Cu(I)-halide scintillators.
| Original language | English |
|---|---|
| Pages (from-to) | 12997-13006 |
| Number of pages | 10 |
| Journal | Journal of Physical Chemistry Letters |
| Volume | 16 |
| DOIs | |
| State | Published - 4 Nov 2025 |
| Externally published | Yes |
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