Miaohui Tong

Highly efficient Sr3Y2(Si3O9)2:Ce3+,Tb3+/Mn2+/Eu2+ phosphors for white LEDs: structure refinement, color tuning and energy transfer

A series of highly efficient and emission-tunable Sr3Y2(Si3O9)2(SYSO):Ce3+,Tb3+/Mn2+/Eu2+ phosphors have been prepared via a solid-state reaction. The structure refinement indicates that the as-prepared phosphors crystallized in a monoclinic phase with a space group of C2/c (no. 15), and there are three kinds of cation sites in the host lattice for the doped ions to occupy. The Ce3+ emission at different lattice sites in the SYSO host has been firstly identified and discussed. When introducing other doping ions into these cation sites, there exist efficient energy transfers from Ce3+ ions to these doping ions (Tb3+, Mn2+, and Eu2+) under UV excitation. The corresponding energy transfer mechanisms from Ce3+ to Tb3+/Mn2+/Eu2+ in SYSO:Ce3+,Tb3+/Mn2+/Eu2+ systems have been studied systematically. These energy transfers not only can enhance the luminescent efficiencies and broaden the width of emission spectra of SYSO:Ce3+,Tb3+/Mn2+/Eu2+ phosphors but also can modulate their emission colors from blue to green, orange or cyan, respectively. For example, the maximum quantum yields (QYs) of as-prepared SYSO:0.15Ce3+,xTb3+/yMn2+ phosphors can reach 90.4% and 74% at x = 0.70, y = 0.01, respectively. Based on these experiment results, the as-prepared SYSO:Ce3+,Tb3+/Mn2+/Eu2+ phosphors can act as potential color-tunable and emission band-widened phosphors for possible applications in ultraviolet light based white LEDs.

Molten salt synthesis and photoluminescence properties of novel red emitting phosphors Ba5(VO4)3Cl:Eu3+,K+

Abstract A series of Ba5(VO4)3Cl:Eu3+,K+ phosphors have been synthesized by the molten salt synthesis method. The crystalline structure, morphology, photoluminescence properties and lifetimes were characterized using X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM) and photoluminescence spectroscopy, respectively. XRD indicates that the Ba5(VO4)3Cl:Eu3+,K+ phosphors are synthesized successfully via molten salt method. SEM image demonstrates that the obtained phosphors have hexagonal polyhedron morphology. The photoluminescence spectra reveal that the as-prepared phosphors exhibit a bright red emission under the excitation of blue or near ultraviolet light. The concentration quenching was also investigated, and the dipole–dipole interaction is responsible for the concentration quenching of fluorescence emission of Eu3+ ions in Ba5(VO4)3Cl phosphor. The present work suggests that the Ba5(VO4)3Cl:Eu3+,K+ phosphors would be a potential candidate for light emitting devices.

Synthesis and characterization of micro/nano-structured BaHPO4/Ba3(PO4)2/Ba5(PO4)3OH phases and their luminescence

Microspheres covered with microcuboids/nanorods and nanoparticles of BaHPO4/Ba3(PO4)2/Ba5(PO4)3OH phases have been successfully synthesized by a facile hydrothermal (HT) method using the citric acid as a surfactant at different pH values. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and fluorescence spectrometry were used to characterize the samples. It was found that the pH value was a crucial factor for the phase formation and shape determination of the final products, which were discussed in detail. Attractively, the as-prepared BaHPO4/Ba3(PO4)2/Ba5(PO4)3OH samples emitted an intense blue light in a broad band from 380 to 625 nm, for which the mechanism was complex ions luminescence originating from the transition of 3T1 → 1A1 in PO43−. Meanwhile, an obvious red shift for the emission band was observed between nano- and bulk-Ba3(PO4)2 synthesized by HT and conventional solid-state (CSS) reactions, respectively, which was due to the effect of the product being nanosized. The same effect was also revealed by the fact that the decay time of the latter was about 2.5 times that of the former. Moreover, the decay mode of Ba5(PO4)3OH was different from those of BaHPO4 and Ba3(PO4)2, which was ascribed to the effect of the substitution of three OH− for one PO43− on their electronic structures.

Investigation of the luminescence properties and thermal stability of dysprosium, terbium, and europium ions singly- and co-doped strontium yttrium borate phosphors

ABSTRACT A series of trivalent rare-earth element ions (europium, terbium, dysprosium) singly- and co-doped strontium yttrium borate phosphors was synthesized via the sol–gel method. The phase formation, luminescence properties, decay times, and energy transfer behaviors from terbium ions to europium ions, the thermal stability, and the Commission Internationale de L’Eclairage coordinates were investigated. Under the excitation of ultraviolet light, the singly doped phosphors exhibited green emission of terbium ions, white emission of dysprosium ions, and red emission of europium ions, respectively. For the terbium and europium ions co-doped strontium yttrium borate samples, a white emission can be realized by blending the doping concentration of terbium and europium ions. The critical distance between terbium and europium ions has been calculated to be about 14.52 Å and the energy transfer from terbium to europium occurred through the dipole–quadrupole interaction. At 150°C, the emission intensity of terbium and europium in the 12 mol% terbium and 14 mol% europium co-doped strontium yttrium borate sample was maintained at about 74% and 87% of their corresponding initial values, respectively, and the dysprosium ions singly doped strontium yttrium borate sample showed about 70% of its initial emission intensity at room temperature. The above results suggested that europium, terbium, dysprosium ions singly- and co-doped strontium yttrium borate phosphors have potential applications as ultraviolet-convertible phosphors.