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CsCuI nanocrystals (NCs) are considered to be promising materials due to their high photoluminescence efficiency and X-ray hardness. However, the present strategy depends on tedious fabrication with excessive chemical waste. The evasive iodide ion dissociation, inadaptable ligand system, low stability, and relatively low light yield severely impede their applications. Herein, we develop an in situ fabrication strategy for a flexible and large-area Tl-doped CsCuI NC-polymer composite scintillation film with a high light yield (∼48800 photons/MeV) and improved stability. Tween 80 and phosphinic acid successfully inhibit the oxidation of iodide ions, and the films can be stored for at least six months. As a result, a high spatial resolution of 16.3 lp mm and a low detection limit of 305 nGy s were achieved. A radioluminescence intensity of >80% was maintained after a total irradiation dose of 604.8 Gy. These results indicate the promising application of these copper halide NCs in low-cost, flexible, and high-performance medical imaging.
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http://dx.doi.org/10.1021/acs.jpclett.2c00456 | DOI Listing |
Int J Biol Macromol
September 2025
Research Center of Advanced Catalytic Materials & Functional Molecular Synthesis, Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, School of Chemistry & Chemical Engineering, Shaoxing University, Shaoxing, 312000, China; Institute of Chemistry, Chinese Academy of Scien
Inspired by "the composition of catechol and amine groups in the adhesive proteins" of marine mussel and "brick-and-mortar" structure of nacre, we use polydopamine (PDA) as "mortar", graphene oxides (GO) nanosheets as "brick", and Pd ions as interfacial reinforcer, to fabricate nacre-like Pd enhanced PDA functionalized GO membranes (Pd@PDA/GO) with vacuum filtration-assisted assembly method. Meanwhile, in situ reduced Pd nanoclusters by PDA chains were well constrained within the resultant Pd@PDA/GO artificial nacre composites. Good interfacial adhesion with dense packing of the GO nanosheets was further confirmed with sub-nano level microstructure characterization by positron annihilation lifetime spectroscopy.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266580, PR China; Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), Qingdao 266580, PR China. Electronic address:
With the trend of heavy and inferior crude oil, the design of hydrodesulfurization (HDS) catalysts with excellent activity and high active metal utilization is an inevitable trend for the upgrading of refining technology. In this study, a highly dispersed Mo catalyst confined within nitrogen-doped porous carbon (xMo@NC) was prepared using an in situ encapsulation-pyrolysis approach and used in the HDS reaction of dibenzothiophene (DBT). The methods of XRD, HRTEM, HAADF-STEM, N physisorption, FT-IR, Raman, and XPS were used to carry out thorough microstructural characterization.
View Article and Find Full Text PDFACS Sens
September 2025
School of Physics and Electric Engineering, Linyi University, Linyi 276000, China.
In this study, employing a 2D electrodeposition in situ assembly method, a high-performance HS sensor based on a p-n type CuO-CuFeO heterostructure ordered nanowire arrays was successfully fabricated on silicon substrates. Compared to CuO, CuO-CuFeO nanowire arrays exhibits an ideal interfacial barrier structure and higher initial resistance, with a response to 10 ppm of HS at room temperature (20 ± 3 °C) increased by 225 times and a response time reduced by over 2400 s. The sensor demonstrates exceptional sensitivity (LOD = 10 ppb; response = 234.
View Article and Find Full Text PDFAnal Chem
September 2025
Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing 210023, P. R. China.
Electroactive bacteria (EAB) hold great promise for the development of electrochemical biosensors given their unique ability to transfer electrons extracellularly via specialized pathways, a process termed extracellular electron transfer (EET). Ongoing research aims to overcome current limitations and fully harness the potential of EABs for high-performance biosensing applications. Herein, we report the fabrication of an electrochemical microsensor based on biomineralized electroactive bacteria, specifically MR-1.
View Article and Find Full Text PDFAnal Chem
September 2025
Department of Chemistry, Wuhan University, Wuhan 430072, China.
Three-dimensional printing (3DP) technology enables the flexible fabrication of integrated monolithic microextraction chips for high-throughput sample pretreatment. Meanwhile, the extraction performance of 3DP-based channels is largely limited by printer resolution and the commercially available printing materials. In this work, a 3DP array monolithic microextraction chip (AMC) was fabricated by integrating 26-array helical monolithic microextraction channels for sample pretreatment and 52-array gas valves for fluid control.
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