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A new disordered langbeinite-type compound, K <sub/>2</sub> Tb <sub/>1.5</sub> Ta <sub/>0.5</sub> P <sub/>3</sub> O <sub/>12</sub> , and Eu <sup>3+</sup> -doped multicolour light-emitting properties
摘要： For the first time, a new langbeinite-type phosphate, namely potassium terbium tantalum tris(phosphate), K2Tb1.5Ta0.5(PO4)3, has been prepared successfully using a high-temperature flux method and has been structurally characterized by single-crystal X-ray diffraction. The results show that its structure can be described as a three-dimensional open framework of [Tb1.5Ta0.5(PO4)3] interconnected by K+ ions. The TbIII and TaV cations in the structure are disordered and occupy the same crystallographic sites. The IR spectrum, the UV–Vis spectrum, the morphology and the Eu3+-activated photoluminescence spectroscopic properties were studied. A series of Eu3+-doped phosphors, i.e. K2Tb1.5–xTa0.5(PO4)3:xEu3+ (x = 0.01, 0.03, 0.05, 0.07, 0.10), were prepared via a solid-state reaction and the photoluminescence properties were studied. The results show that under near-UV excitation, the luminescence colour can be tuned from green through yellow to red by simply adjusting the Eu3+ concentration from 0 to 0.1, because of the efficient Tb3+→Eu3+ energy-transfer mechanism.
关键词： photoluminescence,Langbeinite-type phosphate,crystal structure,energy-transfer mechanism,multicolour light
更新于2025-11-14 15:23:50
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Efficient blue-white color luminescence with near-ultraviolet excitation in Dy3+/Tm3+:Na3Gd(PO4)2 nanophosphor for white LEDs
摘要： The Dy3t/Tm3t ions co-activated Na3Gd(PO4)2 phosphors were synthesized by the citrate-gel based combustion technique. The structural properties of as-synthesized phosphors were studied through X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). The influence of Tm3t concentration on the fluorescence properties of Na3Gd(PO4)2:Dy3t phosphors were systematically investigated under near-UV light irradiation of 359 and 352 nm. The energy transfer efficiency (ηET) of as-prepared phosphors increases gradually from 17 to 42%, and the critical distance (Rc) between Dy3t and Tm3t ions is calculated to be 4.76 ?. For better understanding the energy transfer mechanism (ET:Dy3t →Tm3t), the decay curves were utilized on the basis of Dexter’s energy transfer formula and Reisfeld’s approximation. More importantly, the obtained CIE color coordinates of Na3Gd(PO4)2:Dy3t/Tm3t phosphors located at blue-white region under near-UV light irradiation. The results demonstrate the promising application of Na3Gd(PO4)2:Dy3t/Tm3t phosphor for near-UV white LEDs.
关键词： Citrate-gel combustion technique,Decay times-Energy transfer mechanism,Photoluminescence,White-light,Dy3t/Tm3t
更新于2025-09-16 10:30:52
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Facile Synthesis and Controllable Emission of Tm <sup>3+</sup> /Er <sup>3+</sup> -Doped and -Co-doped α-NaYbF <sub/>4</sub> Upconversion Nanocrystals
摘要： Tm3+, Er3+-doped and -co-doped α-NaYbF4 nanoparticles were synthesized via a facile hydrothermal route with oleic acid as the capping agent. Experimental results showed that the doped NaYbF4 nanoparticles possessed a cubic phase with the average size of ～13 nm. Upon excitation by a 980 nm laser, the as-synthesized nanoparticles exhibited blue and red upconversion emissions corresponding to the monodoped Tm3+, Er3+ in the cubic-phase NaYbF4, respectively, and intense green and red emissions in the Tm3+/Er3+-co-doped NaYbF4 nanoparticles. Furthermore, the possible energy transfer mechanism among Yb3+/Tm3+/Er3+ in α-NaYbF4 nanoparticles was also proposed. The cell toxicity test revealed that the as-synthesized upconversion nanoparticles possessed remarkably low cytotoxicity. All of the advantageous features including facile synthesis, controllable emission, and low cytotoxicity make the upconversion nanoparticles promising for multicolor bioimaging and anti-counterfeiting applications.
关键词： anti-counterfeiting applications,multicolor bioimaging,upconversion nanocrystals,hydrothermal synthesis,energy transfer mechanism,α-NaYbF4,low cytotoxicity,Tm3+/Er3+-doped
更新于2025-09-04 15:30:14