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Functional materials with stable and adjustable luminescence have recently become a research hotspot for their broad application prospects. Tunable luminescence can be realized by the doping of hetero-valent europium ions. High-temperature hydrogen atmosphere reduction is required in the traditional preparation of Eu-doped phosphors. Herein, an anoxic molten-salt medium environment was established to form oxygen vacancy defects in the reaction system and induce the self-reduction of Eu ions to obtain Eu ions. X-ray photoelectron spectroscopy (XPS) results confirm the existence of Eu and Eu ions in the samples, and the fluorescence spectrum shows that hetero-valent Eu ions can synergistically emit light effectively. Under 266 nm ultraviolet light excitation, the white light emission was successfully realized for a BaInTaO:Eu phosphor by different emission combinations of Eu and Eu ions. In addition, the BaInTaO:Eu phosphor exhibits adjustable luminescence from greenish-yellow to red exciting at 390-490 nm, which has superior stability in a high-temperature and high-humidity environment. Therefore, it is very promising that BaInTaO:Eu will be used as multi-color functional materials in many fields such as communication encryption and colorful decoration.
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http://dx.doi.org/10.1021/acs.inorgchem.1c03312 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
State Key Laboratory of Chemical Resource Engineering, Beijing 100029, China.
Circularly polarized luminescence (CPL) has emerged as a critical technology for anticounterfeiting and optical display applications due to its unique chiroptical properties. We report a multicolor CPL-emitting elastomeric film (P37/PSK@SiO-PDMS) that synergistically combines chiral helical polyacetylene (P37) and a surface-engineered perovskite (PSK@SiO) through hydrogen-bond-directed assembly. Confinement within the PDMS matrix drives P37 to self-assemble into a chiral supramolecular structure through hydrogen bonding, inducing a chiroptical inversion.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Nanochemistry Department, Max Planck Institute for Solid State Research, Heisenbergstraße 1, 70569 Stuttgart, Germany.
Covalent organic frameworks (COFs) have been emerging as versatile reticular materials due to their tunable structures and functionalities, enabled by precise molecular engineering at the atomic level. While the integration of multiple components into COFs has substantially expanded their structural complexity, the strategic engineering of diverse functionalities within a single framework the random distribution of linkers with varying lengths remains largely unexplored. Here, we report a series of highly crystalline mixed-length multivariate COFs synthesized using azobenzene and bipyridine as linkers, where tuning the ratio of linkers and incorporating palladium effectively modulates the balance between near-infrared (NIR) light absorption and catalytic sites for NIR-generation of hydrogen peroxide (HO).
View Article and Find Full Text PDFThe formation of heterostructure interfaces from quantum dots (or nanocrystals) and lower-dimensional (2D or quasi-2D) materials enables interfacial and optoelectronic property tuning. However, this strategy has not been sufficiently characterized, for example, the application of cesium halide nanocrystals to quasi-2D perovskite structures is underexplored, and the mechanisms of the resulting structural modifications and specific nanocrystal roles are not fully understood. Herein, the effects of postsynthetically surface-modifying quasi-2D perovskite films with CsX ( = Cl, Br, I) nanocrystals are examined to bridge this gap.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Material Science & Engineering, City University of Hong Kong, Kowloon, 999077, Hong Kong P.R. China.
Organic solar cells (OSCs) with p-i-n architecture usually exhibit decent efficiency due to the easily tunable energy levels of organic interfacial layers (ILs). However, their operational lifetime is limited by the morphological instability of organic ILs especially the electron-transporting layer (ETL) that shows strong self-aggregation tendency. Besides, organic ETLs are confronted with significant challenges including large batch-to-batch variations and high costs.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Department of Advanced Materials Engineering for Information & Electronics, Kyung Hee University, Gyeonggi-do 17104, Republic of Korea. Electronic address:
We present a supramolecular templating strategy for inducing chirality in hybrid perovskites via confined crystallization within chiral super spaces-nanoconfined, helically ordered cavities formed by the self-assembly of achiral bent-core molecules with chiral additives. Upon removal of the additives, the resulting porous films retain permanent chirality. Quasi-2D hybrid organic-inorganic perovskites crystallized within these templates exhibit distinct chiroptical activity, including mirror-image circular dichroism and circularly polarized light emitting (CPLE), with CPLE dissymmetry factors reaching up to 1.
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