Abstract
Coordination polymers (CPs) are promising for direct X-ray detection and imaging owing to higher designability and outstanding stability, however, it remains a challenge to achieve highly X-ray detection performance, particularly both high sensitivity and low detection limit at the same operating voltage. Herein, we construct a new conjugated CP {[Co(BPTTz)(DIPA)] ⋅ DMA}n (1, BPTTz=2,5-bis(pyridine-4-yl)thiazolo[5,4-d]thiazole, H2DIPA=2,5-diiodoterephthalic acid, DMA=N, N’-dimethylacetamide), with multi-channel charge transfer by regulating the linker mediated electronic-state, which reduces carrier losses resulting from recombination or quenching, enhances the efficiency of charge separation and transfer, thus further optimizes X-ray detection performance. The semiconductor prepared based on this strategy achieves record values including the highest mobility-lifetime product (μτ, 8.05×10−3 cm2 V−1) and the lowest detectable X-ray dose rate (128 nGyair S−1, 35 V) among CP-based direct radiation detectors, as well as a high sensitivity (172 μC Gyair−1 cm−2, 35 V) at the same operating voltage. This detector shows excellent long-time air stability under ambient conditions for over three months and operational stability. These findings demonstrate a rational structural design method to enhance the photoelectronic efficiency and stability of semiconductive CPs. © 2024 Wiley-VCH GmbH.
| Original language | English |
|---|---|
| Article number | e202419266 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 64 |
| Issue number | 7 |
| Online published | 3 Jan 2025 |
| DOIs | |
| Publication status | Published - 10 Feb 2025 |
Research Keywords
- coordination polymers
- direct X-ray detection
- electronic-state manipulation
- multi-channel charge transfer
- semiconductor
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