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High-performance X-ray detectors are essential for 3D X-ray imaging in computed tomography (CT), but conventional systems require high radiation doses to achieve fine resolution. All-In-One (AIO) Cu(I) halide complexes, capable of forming both ionic and coordinate bonds within a single structure, offer efficient scintillation at lower doses, yet their performance remains limited by nonradiative energy losses during indirect X-ray-to-light conversion. Here, we develop rigid-cation-assisted AIO Cu(I) halide complexes by introducing π-π interactions to suppress the nonradiative pathways, achieving near-unity photoluminescence quantum yield (PLQY). In particular, the rigid (benzyl-DABCO)CuI (Bz-CuI) complex stabilizes triplet emissive states, thereby facilitating high-efficiency radiative recombination and excellent radioluminescence (RL) properties. When incorporated into flexible scintillator film, Bz-CuI demonstrates remarkable X-ray imaging performance, enabling a high spatial resolution exceeding 20 lp mm and a low radiation dose of 71.2 nGy s. Importantly, 3D X-ray image reconstruction of small electronic components reveals fine structural details, highlighting the potential of Bz-CuI as a next-generation X-ray scintillator for low-dose CT imaging.
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http://dx.doi.org/10.1002/anie.202512471 | DOI Listing |
Nat Commun
September 2025
Key Lab of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Department of Chemistry, Tsinghua University, Beijing, China.
Perovskite quantum dot light-emitting diodes have rapidly achieved high external quantum efficiencies of over 25%; however, hindered by limited operating stability originating from surface defects or ion migration in quantum dots. Here, we design a lattice-matched anchoring molecule, tris(4-methoxyphenyl)phosphine oxide (TMeOPPO-p), to anchor the multi-site defects and stabilise the lattice. The target quantum dots exhibit high exciton recombination features with near-unity photoluminescence quantum yields (97%), and the as-fabricated quantum dot light-emitting diodes present a maximum external quantum efficiency of up to 27% at 693 nm, a low efficiency roll-off (over 20% at a current density of 100 mA cm for the typical device) and an operating half-life of over 23,000 h.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Key Laboratory of Textile Fiber and Products, Wuhan Textile University, Ministry of Education, Wuhan, 430200, China.
0D hybrid manganese halides represent an emerging class of luminescent materials, yet their practical application has been hindered by the intrinsic trade-off between optical performance and mechanical flexibility. Here, a green synthesis of 0D (ECMP)MnBr crystal is reported, exhibiting unprecedented triple-mode emission (photoluminescence, X-ray scintillation, and mechanoluminescence) through rationally designed highly symmetric [MnBr] tetrahedra, achieving near-unity photoluminescence quantum yield (98.97%), record-low X-ray detection limit (15.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Chemical Physics and NanoLund, Lund University, Box 124, Lund, 22100, Sweden.
High-performance X-ray detectors are essential for 3D X-ray imaging in computed tomography (CT), but conventional systems require high radiation doses to achieve fine resolution. All-In-One (AIO) Cu(I) halide complexes, capable of forming both ionic and coordinate bonds within a single structure, offer efficient scintillation at lower doses, yet their performance remains limited by nonradiative energy losses during indirect X-ray-to-light conversion. Here, we develop rigid-cation-assisted AIO Cu(I) halide complexes by introducing π-π interactions to suppress the nonradiative pathways, achieving near-unity photoluminescence quantum yield (PLQY).
View Article and Find Full Text PDFNano Lett
August 2025
Key Laboratory of Materials Physics of Ministry of Education, School of Physics, Zhengzhou University, Daxue Road 75, Zhengzhou 450052, China.
Chiral perovskite nanocrystals (PeNCs) scintillators hold great potential for reducing optical crosstalk in X-ray imaging, due to their circularly polarized radioluminescence (CPRL) properties. However, due to the weak binding of chiral ligands and inefficient chirality transfer, achieving chiral PeNCs with high radioluminescence dissymmetry factors () remains a challenge. Here, we introduce polydimethylsiloxane (PDMS) as a CPRL-enhancing modifier that anchors chiral ligands to PeNCs surfaces through σ-π interactions.
View Article and Find Full Text PDFInorg Chem
September 2025
Main Group Organometallics Optoelectronic Materials and Catalysis Lab, Department of Chemistry, National Institute of Technology, Calicut 673601, India.
Unlocking the full potential of solid-state organic luminophores remains a central challenge in materials chemistry, particularly in overcoming the limitations of traditional donor-acceptor (D-A) architectures. In this study, we introduce a pioneering frontier in main-group-organic hybrid design by presenting the foremost triarylborane-integrated carbazole-cyanostilbene () conjugate ( featuring a duryl-linked dimesitylborane (TAB) unit strategically fused into the D-A framework to construct an Acceptor-Donor-π-Acceptor (A-D-π-A) system. This molecular blueprint capitalizes on the rigidifying character of -BMes to minimize the nonradiative decay channels and unlock record level solid-state performance.
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