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A series of Dy/Eu co-doped Sc(MoO) (SMO) phosphors were synthesized a conventional solid-state reaction. Phase purity and morphology were characterized by X-ray diffraction with Rietveld refinement and scanning electron microscopy, confirming the formation of phase-pure orthorhombic crystals. The electronic structure was investigated through density functional theory calculations combined with diffuse reflectance spectroscopy. Under 266 and 352 nm excitation, the Dy doped SMO phosphors exhibited characteristic emission peaks at 488 nm (F → H), 578 nm (F → H), 667 nm (F → H), and 761 nm (F → H). In the Dy/Eu co-doped systems, detailed analysis of spectra and luminescence decay kinetics quantitatively confirmed efficient energy transfer from Dy to Eu. Finally, the optimized SMO:Dy, Eu phosphors achieved maximum relative ( ) and absolute ( ) sensitivities of 3.817% K and 0.018 K, respectively, demonstrating potential for ratiometric optical thermometry applications.
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http://dx.doi.org/10.1039/d5ra04860e | DOI Listing |
J Agric Food Chem
September 2025
Department of Applied Chemistry, College of Science, China Agriculture University, Beijing 100091, China.
l-glufosinate has garnered increasing attention as an ideal herbicide for weed control in agriculture. However, the underlying racemization process of l-glufosinate in the aqueous phase remains unclear. In this work, we elucidated the racemization mechanisms through heating reactions and theoretical calculations.
View Article and Find Full Text PDFEnviron Toxicol Chem
September 2025
Univ. Savoie Mont Blanc, CNRS. EDYTEM.
The environmental impact of Tire and Road Wear Particles (TRWP), arising from tire-road friction, has raised significant concerns. Like microplastics, TRWP contaminate air, water, and soil, with considerable annual emissions and runoff into freshwater ecosystems. Among TRWP compounds, 6PPD-Q, leached from tire particles, shows varying toxicity across species, notably affecting fish and invertebrates.
View Article and Find Full Text PDFInorg Chem
September 2025
College of Chemistry and Materials Science, The key Laboratory of Functional Molecular Solids, Ministry of Education, The Key Laboratory of Electrochemical Clean Energy of Anhui Higher Education Institutes, Anhui Provincial Engineering Laboratory for New-Energy Vehicle Battery Energy-Storage Materia
Conventional acid-catalyzed acetalization faces significant challenges in catalyst recovery and poses environmental concerns. Herein, we develop a CeO-supported Pd single-atom catalyst (Pd/CeO) that eliminates the reliance on liquid acids by creating a localized H-rich microenvironment through heterolytic H activation. X-ray absorption near-edge structure and extended X-ray absorption fine structure analyses confirm the atomic dispersion of Pd via Pd-O-Ce coordination, while density functional theory (DFT) calculations reveal strong metal-support interactions (SMSI) that facilitate electron transfer from CeO oxygen to Pd, downshifting the Pd d-band center and optimizing H activation.
View Article and Find Full Text PDFChaos
September 2025
Department of Physics, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
The absorption of laser energy by plasma is of paramount importance for various applications. Collisional and resonant processes are often invoked for this purpose. However, in some contexts (e.
View Article and Find Full Text PDFChem Sci
August 2025
College of Chemistry and Materials Science, Key Laboratory of Chemical Biology of Hebei Province, Hebei Research Center of the Basic Discipline of Synthetic Chemistry, Institute of Life Science and Green Development Hebei University Baoding Hebei 071002 P. R. China
The photocatalytic oxidative dipolar [3 + 2] cycloaddition reaction is a promising green approach for producing pyrrolo[2,1-]isoquinolines. However, developing sustainable cycloaddition methods with heterogeneous photocatalysts is still in its infancy, largely owing to their low reactivity and photostability. Herein, we propose a charge-oxygen synergy strategy through a dual-engineered covalent organic framework (COF) by integrating π-spacers with donor-acceptor motifs to promote intermolecular cycloaddition.
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