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At least 91 records · Page 5

Understanding and controlling chromaticity shift in LED devices

Chromaticity shift in light-emitting diode (LED) devices arises from multiple mechanisms, and at least five different chromaticity shift modes (CSMs) have been identified to date. This paper focuses on the impacts of irreversible phosphor degradation as a cause of chromaticity shifts in LED devices. The nitride phosphors used to produce warm white LEDs are especially vulnerable to degradation due to thermal and chemical effects such as reactions with oxygen and water. As a result, LED devices utilizing these phosphors were found to undergo either a green shift or, less commonly, a red shift depending on the phosphor mix in the LED devices. These types of chromaticity shifts are classified as CSM-2 (green shift) and CSM-5 (red shift). This paper provides an overview of the kinetic processes responsible for green and red chromaticity shifts along with examples from accelerated stress testing of 6” downlights. Both CSMs appear to proceed through analogous mechanisms that are initiated at the surface of the phosphor. A green shift is produced by the surface oxidation of the nitride phosphor that changes the emission profile to lower wavelengths. As the surface oxidation reaction proceeds, reactant limitations slow the rate and bulk oxidation processes become more prevalent. We found that a red chromaticity shift arises from quenching of the green phosphor, also possibly due to surface reactions of oxygen, which shift the emission chromaticity in the red direction. In conclusion, we discuss the implications of these findings on projecting chromaticity.

Davis, Lynn↗

Synthesis and photoluminescence properties of LiSrPO{sub 4}:Eu{sup 2+} phosphor for solid state lighting

A novel method to prepare orthophosphate LiSrPO{sub 4}: Eu{sup 2+} phosphor for white light-emitting diodes (w-LEDs) is given in this paper. Phosphor was successfully synthesized by Pechini (citrate gel) method which is efficient than conventional high temperature solid state reaction. X-ray powder diffraction (XRD) analysis confirmed the single phase formation of LiSrPO{sub 4}:Eu{sup 2+} with monoclinic crystal structure. Luminescence results showed that the phosphor could be efficiently excited by near UV and exhibited bright blue emission at λ{sub em} = 420 nm corresponding to 5d– 4f transition of Eu{sup 2+}. The phosphor exhibits blue emission bands under 350 nm excitation. This mercury-free excitation is useful for solid state lighting and light-emitting diode (LED). Hence it could be useful for solid state lighting and light-emitting diode (LED) application.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Crystal structure, thermally stability and photoluminescence properties of novel Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} phosphors

A series of novel luminescent phosphors Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} with apatite structure were synthesized via a high temperature solid-state reaction. The phase structure, photoluminescence (PL) properties, the PL thermal stability, as well as the fluorescence decay curves of the samples were investigated to characterize the resulting samples, and the selected Sr{sub 9.97}(PO{sub 4}){sub 6}O:0.03Eu{sup 2+} phosphor exhibits strong thermal quenching resistance, retaining the luminance of 88.73% at 150 °C. The quenching concentration of Eu{sup 2+} in Sr{sub 10}(PO{sub 4}){sub 6}O was about 0.03 attributing to the dipole–quadrupole interaction. The Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} phosphor exhibited a broad-band blue emission at 439 nm upon excitation at 346 nm. The results indicate that Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} phosphors have potential applications as near UV-convertible phosphors for white-light UV LEDs. - Graphical abstract: Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} phosphors have potential applications as near UV-convertible phosphors for white-light UV LEDs. - Highlights: • Sr{sub 9.97}(PO{sub 4}){sub 6}O:0.03Eu{sup 2+} phosphor exhibits strong thermal quenching resistance. • Two different Eu{sup 2+} emission centers exists in Sr{sub 10}(PO{sub 4}){sub 6}O. • The activation energy was also estimated for the Eu{sup 2+} luminescence center.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Photoluminescent and thermal properties of (Sr{sub 0.995−x−y−z}Ca{sub x}Ba{sub y}Mg{sub z}){sub 2}SiO{sub 4}:0.01Eu{sup 2+} phosphors for warm white light-emitting diodes

Highlights: • The photoluminescent property of Sr{sub 2}SiO{sub 4}:Eu{sup 2+} is improved by doping Ca{sup 2+} and Ba{sup 2+}. • The emission spectra red-shift obviously by doping Ca{sup 2+} into Sr{sub 2}SiO{sub 4}:Eu{sup 2+}. • The thermal stability is enhanced by doping Ba{sup 2+} into (Sr,Ca){sub 2}SiO{sub 4}:Eu{sup 2+}. • The improved phosphors can combine blue-LED chips to generate warm white light. - Abstract: A series of phosphors (Sr{sub 0.995−x−y−z}Ca{sub x}Ba{sub y}Mg{sub z}){sub 2}SiO{sub 4}:0.01Eu{sup 2+} (0 ≤ x ≤ 0.45, 0 ≤ y ≤ 0.015, 0 ≤ z ≤ 0.35) were synthesized by solid state reaction. Their phase compositions and photoluminescent properties were investigated in detail. The X-ray diffraction analysis indicates the impurity phase of SrSiO{sub 3} is formed only when z ≥ 0.25. A photoluminescence investigation shows, with x increasing the emission spectra of the phosphors (0 ≤ x ≤ 0.45, 0 ≤ y ≤ 0.015, z = 0) obviously red-shift, the corresponding color tones shift from yellow to orange–yellow and their CCTs reduce from 2875 to 2237 K. All the results are beneficial for the phosphors to combining blue light-emitting diode chips to generate warm white light. Besides, the thermal stability of the phosphor (x = 0.36, y = z = 0) is enhanced by doping Ba{sup 2+}, due to the greater activation energy for the compounds containing barium.

36 MATERIALS SCIENCE↗

Phosphor Ceramic Composite for Tunable Warm White Light

Composite phosphor ceramics for warm white LED lighting were fabricated with K 2 SiF 6 :Mn 4+ (KSF) as both a narrowband red phosphor and a translucent matrix in which yellow-emitting Y 3 Al 5 O 12 :Ce 3+ (YAG) particles were dispersed. The emission spectra of these composites under blue LED excitation were studied as a function of YAG loading and thickness. Warm white light with a color temperature of 2716 K, a high CRI of 92.6, and an R9 of 77.6 was achieved. A modest improvement in the thermal conductivity of the KSF ceramic of up to 9% was observed with the addition of YAG particles. In addition, a simple model was developed for predicting the emission spectra based on several parameters of the composite ceramics and validated with the experimental results. The emission spectrum can be tuned by varying the dopant concentrations, thickness, YAG loading, and YAG particle size. This work demonstrates the utility of KSF/YAG composite phosphor ceramics as a means of producing warm white light, which are potentially suitable for higher-drive applications due to their increased thermal conductivity and reduced droop compared with silicone-dispersed phosphor powders.

36 MATERIALS SCIENCE↗

Preparation and investigation of Dy3+-doped Ca9LiGd2/3(PO4)7 single-phase full-color phosphor

Highlights: • A novel single-phased Ca{sub 9}LiGd{sub 2/3}(PO{sub 4}){sub 7}:xDy{sup 3+} phosphor was firstly synthesized. • Its structure, luminescent properties are well studied and characterized. • It was promising as a single-component white-light-emitting phosphor for w-LEDs. - Abstract: Novel single-phased white-light-emitting Ca{sub 9}LiGd{sub 2/3}(PO{sub 4}){sub 7}:xDy{sup 3+} (x = 0.02, 0.05, 0.10, 0.15, 0.20, 0.25, and 0.30) β-Ca{sub 3}(PO{sub 4}){sub 2}-type phosphate phosphors were synthesized. The phase structure, luminescence, and thermal stability of the phosphors were characterized by X-ray powder diffraction analysis, photoluminescence excitation and emission spectra, thermal quenching, and decay curves. XRD analysis confirmed the phase formation of Ca{sub 9}LiGd{sub 2/3}(PO{sub 4}){sub 7}:Dy{sup 3+} materials. Under the excitation of 352 nm, the emission of the Ca{sub 9}LiGd{sub 2/3}(PO{sub 4}){sub 7}:0.20Dy{sup 3+} sample centered at blue (488 nm) and yellow (580 nm), which corresponded to {sup 4}F{sub 9/2}–{sup 6}H{sub 15/2} transition and {sup 4}F{sub 9/2}–{sup 6}H{sub 13/2} transition. The optimum dopant concentration of Dy{sup 3+} ions was around 20 mol%, and the critical transfer distance of Dy{sup 3+} was calculated as 18 Å. The thermal-quenching temperature was above 500 K for Ca{sub 9}LiGd{sub 2/3}(PO{sub 4}){sub 7}:0.20Dy{sup 3+}. The developed phosphor has a great potential as a single-component white-light-emitting phosphor for UV-light-emitting diodes.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Electrical current leakage and open-core threading dislocations in AlGaN-based deep ultraviolet light-emitting diodes

Electrical current transport through leakage paths in AlGaN-based deep ultraviolet (DUV) light-emitting diodes (LEDs) and their effect on LED performance are investigated. Open-core threading dislocations, or nanopipes, are found to conduct current through nominally insulating Al{sub 0.7}Ga{sub 0.3}N layers and limit the performance of DUV-LEDs. A defect-sensitive phosphoric acid etch reveals these open-core threading dislocations in the form of large, micron-scale hexagonal etch pits visible with optical microscopy, while closed-core screw-, edge-, and mixed-type threading dislocations are represented by smaller and more numerous nanometer-scale pits visible by atomic-force microscopy. The electrical and optical performances of DUV-LEDs fabricated on similar Si-doped Al{sub 0.7}Ga{sub 0.3}N templates are found to have a strong correlation to the density of these nanopipes, despite their small fraction (<0.1% in this study) of the total density of threading dislocations.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Crystal structure and luminescence properties of a novel red-emitting phosphor BaAlBO{sub 3}F{sub 2}:Eu{sup 3+}

A series of novel red-emitting phosphors BaAlBO{sub 3}F{sub 2}:xEu{sup 3+} (0.001≤x≤0.08) were first synthesized via a high temperature solid-state reaction. X-ray diffraction and photoluminescence spectroscopy were used to characterize the crystal structure and photoluminescence properties of the phosphor, respectively. The phosphor can be effectively excited with a 395 nm light, and shows a dominant {sup 5}D{sub 0}−{sup 7}F{sub 2} emission with chromatic coordination of 0.628 and 0.372. The optimal doping concentration is about 0.04. Rietveld refinement results and the luminescence behavior of Eu{sup 3+} indicate that the Eu{sup 3+} ion occupies a C{sub 3} symmetry site, and the host BaAlBO{sub 3}F{sub 2} has a hexagonal structure with P-6 space group. In addition, the phosphor could be a potential candidate as red-emitting phosphor for application in white light-emitting diode. - Graphical abstract: The luminescence behavior and Rietveld refinement of BaAlBO{sub 3}F{sub 2}:Eu{sup 3+} indicate that the red-emitting phosphor has potential application in white LED and the host has a hexagonal structure with P-6 space group. - Highlights: • A novel red-emitting phosphor BaAlBO{sub 3}F{sub 2}:Eu{sup 3+} is first synthesized. • The crystal structure of BaAlBO{sub 3}F{sub 2} is confirmed. • The phosphor shows potential application in white LED.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Structure and photoluminescence properties of Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} phosphors for solid-state lighting application

Novel phosphors of Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+} and Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} were synthesized by a solid-state process and characterized with X-ray diffraction, photoluminescence (PL), PL excitation (PLE), and fluorescence decay time. The relationship between the observed Ce{sup 3+} emission properties and the crystal structure of Na{sub 2}Y{sub 2}B{sub 2}O{sub 7} is built and the result shows that Ce{sup 3+} ions occupy two non-equivalent Y{sup 3+} sites in the host. The codoping of Tb{sup 3+} in Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+} can tune the emitting colour from blue to green and increase the luminescence quantum efficiency to 75.2% by the energy transfer of Ce{sup 3+}→Tb{sup 3+}. The energy transfer processes of Ce{sup 3+}–Ce{sup 3+} and Ce{sup 3+}–Tb{sup 3+} are analysed and determined to be electric dipole–dipole and dipole–quadrupole, respectively. The broad PLE spectra of Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+} and Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} are well matched with the emission from near UV LED chips, which indicates that they are promising blue and green phosphors for phosphor-converted white LEDs. - Graphical abstract: Colour-tunable phosphors Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} with optimal quantum yield of 75.2% are synthesized and the phosphors can be served as n-UV pumped materials for LEDs. - Highlights: • Green phosphor Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} with quantum efficiency of 75.2% for n-UV application is synthesized. • The site occupation of Ce{sup 3+} in Na{sub 2}Y{sub 2}B{sub 2}O{sub 7} is investigated with the crystal structure and photoluminescence spectra. • The energy transfer of Ce{sup 3+}–Ce{sup 3+} and Ce{sup 3+}–Tb{sup 3+}, which is responsible to the tunable emitting colour of the phosphor, is demonstrated and the mechanism is studied.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

White LEDs with limit luminous efficacy

In most promising widespread gallium nitride based LEDs emission is generated in the blue spectral region with a maximum at about 450 nm which is converted to visible light with the desired spectrum by means of phosphor. The thermal energy in the conversion is determined by the difference in the energies of excitation and emission quanta and the phosphor quantum yield. Heat losses manifest themselves as decrease in the luminous efficacy. LED heating significantly reduces its efficiency and life. In addition, while heating, the emission generation output and the efficiency of the emission conversion decrease. Therefore, the reduction of the energy losses caused by heating is crucial for LED development. In this paper, heat losses in phosphor-converted LEDs (hereinafter chips) during spectrum conversion are estimated. The limit values of the luminous efficacy for white LEDs are evaluated.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Near infrared emission of TbAG:Ce{sup 3+},Yb{sup 3+} phosphor for solar cell applications

Luminescent materials doped with rare earth ions are used for many devices such as optical amplifiers in telecommunication, phosphors for white light emitting diodes (LEDs), displays, and so on. Recently, they also have attracted a great interest for photovoltaic applications to improve solar cell efficiency by modifying solar spectrum. Crystal silicon (c-Si) solar cells most effectively convert photons of energy close to the semiconductor band gap. The mis-match between the incident solar spectrum and the spectral response of solar cells is one of the main reasons to limit the cell efficiency. The efficiency limit of the c-Si has been estimated to be 29% by Shockley and Queisser. However, this limit is estimated to be improved up to 38.4% by modifying the solar spectrum by a quantum cutting (down converting) phosphor which converts one photon of high energy into two photons of lower energy. The phenomenon such as the quantum cutting or the down conversion of rare earth ions have been investigated since Dexter reported the possibility of a luminescent quantum yield greater than unity in 1957. In the past, the quantum cutting from a vacuum ultraviolet photon to visible photons for Pr{sup 3+}, Gd{sup 3+},Gd{sup 3+}–Eu{sup 3+}, and Er{sup 3+}–Tb{sup 3+} had been studied. Recently, a new quantum cutting phenomenon from visible photon shorter than 500 nm to two infrared photons for Tb{sup 3+}–Yb{sup 3+}, Pr{sup 3+}–Yb{sup 3+}, and Tm{sup 3+}–Yb{sup 3+} has been reported. The Yb{sup 3+} ion is suitable as an acceptor and emitter because luminescent quantum efficiency of Yb{sup 3+} is close to 100% and the energy of the only excited level of Yb{sup 3+} (1.2 eV) is roughly in accordance with the band gap of Si (1.1 eV). In addition, the Ce{sup 3+}-doped Tb{sub 3}Al{sub 5}O{sub 12} (TbAG), used as a phosphor for white LED, has broad absorption bands in the range of 300–500 nm due to strong ligand field and high luminescent quantum efficiency. Therefore, the Ce{sup 3+} ions in the TbAG can be suitable as an excellent sensitizing donor for down conversion materials of Si solar cells. In this paper, Ce{sup 3+} –Yb{sup 3+}-codoped TbAG ceramics were prepared and the energy transfer (ET) including down conversion mechanism in Ce{sup 3+} – Yb{sup 3+} codoped TbAG ceramics have been evaluated by the photoluminescence (PL), the photoluminescence excitation (PLE), the lifetime and the quantum yield (QY), which was measured directly using an integrating sphere.

36 MATERIALS SCIENCE↗

2D photonic crystal layer assisted thiosilicate ceramic plate with red-emitting film for high quality w -LEDs

In this work, we have succeeded in obtaining high quality warm w-light-emitting-diodes (LEDs) by adopting hybrid two-dimensional (2D) structure of SiNx photonic crystal layer (PCL) assisted cyan-emitting ceramic-plate thiosilicate SrLa2Si2S8:Ce3+ with red-emitting film SrLiAl3N4:Eu2+ phosphor on a 430 nm blue LED chip at 350 mA. 2D SiNx PCL was capped with thiosilicate is because it can enhance the luminous efficacy and maintain the low correlated color temperature (CCT) and high color-rendering index (CRI). High luminous efficacy (82.3 lm/W), high special CRI (R9=75) as well as the low CCT (5431 K) of the optimal w-LED was obtained due to the assistances of 2D SiNx PCL and narrow-band red-emitting phosphor with the doping percentage at 10 wt%. The synthesis processes, structural analysis, optical properties and LED device performances were detailed investigated to find out the relationship between the optimum composition and good optical properties. Based on intriguing luminescence properties by the 2D SiNx PCL and red-emitting film phosphor introducing, we proclaim this method could also have high potential application in other phosphor-converted w-LEDs.

36 MATERIALS SCIENCE↗

High-Power Warm-White Hybrid LED Package for Illumination

In this project, an integrated warm-white hybrid light engine was developed. The hybrid approach involves combining phosphor-converted off-white InGaN LEDs and direct-emitting red AlInGaP LEDs in a single light engine to achieve high efficacy together with high color rendering index. We developed and integrated technology improvements in InGaN and AlInGaP die technology, phosphor technology, package architecture and encapsulation, to realize a hybrid warm-white LED package with an efficacy of 140 lm/W at a correlated color temperature of 3000K and a color rendering index of 90, measured under representative operating conditions. This efficacy is 26% higher than the best warm-white LEDs of similar specification that are commercially available at the end of the project. Since the InGaN- and AlInGaP-based LEDs used in the hybrid engine show different behavior as a function of current and temperature, a control system needs to be in place to ensure a stable color point over all operating conditions. In this project, we developed an electronic control circuit that is fully integrated into the light engine in such a way that the module can simply be driven by a conventional single-channel driver. The integrated control circuit uses a switch-mode boost converter topology to control the LED drive currents based on the temperature and the input current of the light engine. A color control performance of 5 SDCM was demonstrated, and improvement to 3 SDCM is considered well within reach. The combination of high efficacy and ease of integration with existing single-channel drivers is expected to facilitate the adoption of the hybrid technology and accelerate the energy savings associated with solid-state lighting. In the product commercialization plan, downlights and indirect-lit troffers have been selected as the first target applications for this product concept. Fully functional integrated prototypes have been developed for both applications, and the business case evaluation is ongoing as of the end of the project.

32 ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATI↗

A far‐red‐emitting (Gd,Y) 3 (Ga,Al) 5 O 12 :Mn 2+ ceramic phosphor with enhanced thermal stability for plant cultivation

Abstract As for plants, far‐red (FR) light with wavelength from 700 nm to 740 nm is critical for processes of photosynthesis and photomorphogenesis. Light‐controlled development depends on light to control cell differentiation, structural and functional changes, and finally converge into the formation of tissues and organs. Phosphor converted FR emission under LED excitation is a cost‐effective and high‐efficient way to provide artificial FR light source. With the aim to develop an efficient FR phosphor that can promote the plant growth, a series of gadolinium yttrium gallium garnet (GYGAG) transparent ceramic phosphors co‐doped with Mn 2+ and Si 4+ have been fabricated via chemical co‐precipitation method, followed sintered in O 2 and hot isostatic pressing in this work. Under UV excitation, the phosphor exhibited two bright and broadband red emission spectra due to Mn 2+ : 4 T 1 → 6 A 1 spin‐forbidden transition, and one of which located in the right FR region. And then, Ce 3+ ions were co‐doped as the activator to enhance the absorption at blue light region and the emission of Mn 2+ . It turns out that the emission band of GYGAG transparent ceramic phosphors matches well with the absorption band of phytochrome P FR , which means they are promising to be applied in plant cultivation light‐emitting diodes (LEDs) for modulating plant growth. Besides, the thermal stability of this material was investigated systematically, and an energy transferring model involves defects was also proposed to explain the phenomenon of abnormal temperature quenching.

Qiu, Xuting↗

On the Mn 4+ R-line emission intensity and its tunability in solids

The spectroscopic properties of Mn 4+ ions in solids are analyzed to establish key parameters that are responsible for the energy and the intensity of the 2 E g → 4 A 2g zero-phonon emission transition (R-line). These two factors of the emission spectrum are critical in determining the phosphor luminosity or brightness. The emission energy is chiefly determined by the “Mn 4+ -ligand” bonding covalence. In fluorides, the Mn-F bonding covalence is weak, and the R-line occur at higher energy. In oxides, the stronger Mn-O bonding covalence reduces the energy of the 2 E g state. In oxides, the R-line shifts to higher energy with increasing local distortion of the MnO 6 octahedral moiety. Those host crystals that locate the Mn 4+ ion at a noncentrosymmetric site (absence of inversion symmetry) relax the parity section rule, which enhances the R-line intensity. Increased R-line intensity in the emission spectrum produces color changes that increases phosphor luminosity. The influence of second coordination sphere (next-nearest neighbors) on the R-line intensity is considered. This article establishes guidelines for the development of host crystals that meet the requirements of high luminosity phosphors for general illumination applications.

36 MATERIALS SCIENCE↗

The potential of ill-nitride laser diodes for solid-state lighting [Advantages of III-Nitride Laser Diodes in Solid-State Lighting]

III-nitride laser diodes (LDs) are an interesting light source for solid-state lighting (SSL). Modelling of LDs is performed to reveal the potential advantages over traditionally used light-emitting diodes (LEDs). The first, and most notable, advantage is LDs have higher efficiency at higher currents when compared to LEDs. This is because Auger recombination that causes efficiency droop can no longer grow after laser threshold. Second, the same phosphor-converted methods used with LEDs can also be used with LDs to produce white light with similar color rendering and color temperature. Third, producing white light from direct emitters is equally challenging for both LEDs and LDs, with neither source having a direct advantage. Lastly, the LD emission is directional and can be more readily captured and focused, leading to the possibility of novel and more compact luminaires. These advantages make LDs a compelling source for future SSL.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Color-tunable photoluminescence phosphors of Ce{sup 3+} and Tb{sup 3+} co-doped Sr{sub 2}La{sub 8}(SiO{sub 4}){sub 6}O{sub 2} for UV w-LEDs

A series of new luminescent emission-tunable phosphors Sr{sub 2}La{sub 8}(SiO{sub 4}){sub 6}O{sub 2}:Ce{sup 3+}, Tb{sup 3+} with apatite structure have been synthesized by a high temperature solid-state reaction. The phase structure, photoluminescence emission and excitation spectra, lifetime, as well as the effect of Tb{sup 3+} concentration are investigated to characterize the resulting samples. The critical distance was calculated to be 8.26 Å by using the concentration quenching method. The intense green emission was observed in the Sr{sub 2}La{sub 8}(SiO{sub 4}){sub 6}O{sub 2}:Ce{sup 3+}, Tb{sup 3+} phosphors on the basis of the efficient energy transfer from Ce{sup 3+} to Tb{sup 3+} with an efficiency of 68.55%. And a possible mechanism of the energy-transfer from Ce{sup 3+} to Tb{sup 3+} ion is also proposed. The results indicate that Sr{sub 2}La{sub 8}(SiO{sub 4}){sub 6}O{sub 2}:Ce{sup 3+}, Tb{sup 3+} phosphors have potential applications to be used as near UV-convertible phosphors for white light-emitting diodes because of the broad excitation in the near-ultraviolet range and the efficient green emission light. - Graphical abstract: Crystal structure and luminescence properties of Sr{sub 2}La{sub 8}(SiO{sub 4}){sub 6}O{sub 2}:Ce{sup 3+},Tb{sup 3+} phosphors have been discussed. - Highlights: • Ce{sup 3+} and Tb{sup 3+} ions entered both La sites in SLSO. • The energy transfer efficiency can reach at 68.55%. • The emitting color of SLSO phosphors shifted from the blue to green region.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗