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1.
Ce3+/Eu2+ co‐doped Na3Ca6(PO4)5 phosphors were prepared using a combustion‐assisted synthesis method. X‐Ray powder diffraction (XRD) analysis confirmed the formation of a Na3Ca6(PO4)5 crystal phase. Na3Ca6(PO4)5:Eu2+ phosphors have an efficient bluish‐green emission band that peaks at 489 nm, whereas Ce3+‐doped Na3Ca6(PO4)5 showed a bright emission band at 391 nm. Analysis of the experimental results suggests that enhancement of the Eu2+ emission intensity in co‐doped Na3Ca6(PO4)5:Eu2+,Ce3+ phosphors is due to a resonance‐type energy transfer from Ce3+ to Eu2+ ions, which is predominantly governed by an exchange interaction mechanism. These results indicate that Ce3+/Eu2+ co‐doped Na3Ca6(PO4)5 is potentially useful as a highly efficient, bluish‐green emitting, UV‐convertible phosphor for white‐light‐emitting diodes. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

2.
Novel red‐emitting phosphors, Eu3+‐activated M7Sn(PO4)6 (M = Sr, Ba), were synthesized at 1200°C by conventional solid‐state reaction method. The luminescent properties of M7Sn(PO4)6:Eu3+ (M = Sr, Ba) phosphors were investigated, and the critical concentration of the activator (Eu3+) concentration were found to be 0.175 mol and 0.21 mol per formula unit for Sr7‐xSn(PO4)6:xEu3+ and Ba7‐xSn(PO4)6:xEu3+, respectively. These phosphors presented red luminescence under the excitation of 395 or 465 nm, perfectly matching with the emissions wavelength of near‐ultraviolet (UV) light‐emitting diodes (LEDs) and InGaN blue LED.  相似文献   

3.
Triple whitlockite‐type structure‐based red phosphors Ca8MgBi1?x(PO4)7:xEu3+ (x = 0.10, 0.20, 0.30, 0.40, 0.50, 0.60, 0.70, 0.80 and 1.00) were synthesized by a conventional solid‐state reaction route and characterized by their X‐ray crystal structures. The X‐ray diffraction (XRD) patterns, Fourier transform infrared spectra, morphologies, photoluminescence spectra, UV/Vis reflectance spectra, decay times and the International Commission on Illumination (CIE) chromaticity coordinates of Ca8MgBi1?x(PO4)7:xEu3+ were analyzed. Eu‐doped Ca8MgBi(PO4)7 phosphors exhibited strong red luminescence with peaks at 616 nm due to the 5D07 F2 electric dipole transition of Eu3+ ions after excitation at 396 nm. The UV/Vis spectra indicated that the band gap of Ca8MgBi0.30(PO4)7:0.70Eu3+ is larger than that of Ca8MgBi(PO4)7. The phosphor developed in this study has great potential as a red‐light‐emitting phosphor for UV light‐emitting diodes. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

4.
A series of Eu3+‐, Ce3+‐, Dy3+‐ and Tb3+‐doped (Y,Gd)BO3 phosphors was synthesized by a solid‐state diffusion method. X‐Ray diffraction confirmed their hexagonal structure and the scanning electron microscopy results showed crystalline particles. The excitation spectra revealed that (Y,Gd)BO3 phosphors doped with Eu3+, Ce3+ , Dy3+ and Tb3+ are effectively excited with near UV‐light of 395 nm/blue light, 364, 351 and 314 nm, respectively. Photoluminescence spectra of Eu3+‐, Ce3+‐ and Tb3+/Dy3+‐doped phosphor showed intense emission of reddish orange, blue and white light, respectively. The phosphor Y0.60Gd0.38BO3:Ce0.02 showed CIE 1931 color coordinates of (0.158, 0.031) and better color purity compared with commercially available blue BAM:Eu2+ phosphor. The phosphor (Y,Gd)BO3 doped with Eu3+, Dy3+ and Tb3+ showed CIE 1931 color coordinates of (0.667, 0.332), (0.251, 0.299) and (0.333, 0.391) respectively. Significant photoluminescence characteristics of the prepared phosphors indicate that they might serve as potential candidates for blue chip and near‐UV white light‐emitting diode applications. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

5.
A solid‐state reaction route‐based LiTi2 ? xEux(PO4)3 was phosphor synthesized for the first time to evaluate its luminescence performance by excitation, emission and lifetime (τ) measurements. The LiTi2 ? xEux(PO4)3 phosphor was excited at λexci. = 397 nm to give an intense orange–red (597 nm) emission attributed to the 5D07F1 magnetic dipole (ΔJ = ±1) transition and red (616 nm) emission (5D07F2), which is an electric dipole (ΔJ = ±2) transition of the Eu3+ ion. Beside this, excitation and emission spectra of host LiTi2(PO4)3 powder were also reported. The effect of Eu3+ concentration on luminescence characteristics was explained from emission and lifetime profiles. Concentration quenching in the LiTi2 ? xEux(PO4)3 phosphor was studied from the Dexter's model. Dipole–quadrupole interaction is found to be responsible for energy transfer among Eu3+ ions in the host lattice. The LiTi2 ? xEux(PO4)3 phosphor displayed a reddish‐orange colour realized from a CIE chromaticity diagram. We therefore suggest that this new phosphor could be used as an optical material of technological importance in the field of display devices. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

6.
In order to improve the luminescent performance of silicate blue phosphors, Sr(1.5‐x)‐(1.5y)Mg0.5SiO4:xEu2+,yCe3+ phosphors were synthesized using one‐step calcination of a precursor prepared by chemical co‐precipitation. The crystal structure and luminescent properties of the phosphors were analyzed using X‐ray diffraction and fluorescence spectrophotometry, respectively. Because the activated ions (Eu2+) can occupy two different types of sites (Sr1 and Sr2), the emission spectrum of Eu2+ excited at 350 nm contains two single bands (EM1 and EM2) in the wavelength range 400–550 nm, centered at 463 nm, and the emission intensity first increases and then decreases with increasing concentrations of Eu2+ ions. Co‐doping of Ce3+ ions can greatly enhance the emission intensity of Eu2+ by transferring its excitation energy to Eu2+. Because of concentration quenching, a higher substitution concentration of Ce3+ can lead to a decrease in the intensity. Meanwhile, the quantum efficiency of the phosphor is improved after doping with Ce3+, and a blue shift phenomenon is observed in the CIE chromaticity diagram. The results indicate that Sr(1.5‐x)‐(1.5y)Mg0.5SiO4:xEu2+,yCe3+ can be used as a potential new blue phosphor for white light‐emitting diodes.  相似文献   

7.
A new halophosphor K3Ca2(SO4)3 F activated by Eu or Ce and K3Ca2(SO4)3 F:Ce,Eu co‐doped halosulfate phosphor has been synthesized by the co‐precipitation method and characterized for its photoluminescence (PL). The PL emission spectra of the K3Ca2(SO4)3 F :Ce phosphor show emission at 334 nm when excited at 278 nm due to 5d → 4f transition of Ce3+ ions. In the K3Ca2(SO4)3 F:Eu lattice, Eu2+ (440 nm) as well as Eu3+ (596 nm and 615 nm) emissions have been observed showing 5D07 F1 and 5D07 F2 transition of the Eu3+ ion, which is in the blue and red region of the visible spectrum respectively. The trivalent europium ion is very useful for studying the nature of metal coordination in various systems owing to its non‐degenerate emitting 5D0 state. K3Ca2(SO4)3 F:Ce,Eu is suitable for Ce3+ → Eu2+ → Eu3+ energy transfer in which Ce3+and Eu2+ play the role of sensitizers and Eu2+ and Eu3+ act as the activators. The observations presented in this paper are relevant for lamp phosphors. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

8.
K. N. Shinde  K. Park 《Luminescence》2013,28(5):793-796
A series of efficient Li3Al2(PO4)3:Eu2+ novel phosphors were synthesized by the facile combustion method. The effects of dopant on the luminescence behavior of Li3Al2(PO4)3 phosphor were also investigated. The phosphors were characterized by X‐ray diffraction, field emission scanning electron microscope and photoluminescence techniques. The result shows that all samples can be excited efficiently by near‐ultraviolet excitation under 310 nm. The emission was observed for Li3Al2(PO4)3:Eu2+ phosphor at 425 nm, which corresponded to the d → f transition. The concentration quenching of Eu2+ was observed in Li3Al2(PO4)3:Eu2+ when the Eu concentration was at 0.5 mol%. The prepared powders exhibited intense blue emission at the 425 nm owing to the Eu2+ ion by Hg‐free excitation at 310 nm (i.e., solid‐state lighting excitation). Consequently, the availability of such a phosphor will significantly help in the development of blue‐emitting solid‐state lighting applications. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

9.
Eu3+‐activated MAl(SO4)2Br phosphors (where M = Mg or Sr) are successfully prepared using a wet chemical reaction technique. The samples are characterized by X‐ray diffraction (XRD) and photoluminescence (PL) spectroscopies. The XRD pattern revealed that both the samples are microcrystalline in nature. PL of Eu3+‐doped SrAl(SO4)2Br and MgAl(SO4)2Br phosphors exhibited characteristic red emission coming from the 5D07F2 (616 nm) electron transition, when excited by 396 nm wavelength of light. The maximum intensity of luminescence was observed at a concentration of 1 mol% Eu3+. The intensity of the electric dipole transition at 616 nm is greater than that of the magnetic dipole transition at 594 nm. The results showed that MAl(SO4)2Br:Eu3+, (M = Mg, Sr) phosphors have potential application in near‐UV light‐emitting diodes as efficient red‐emitting phosphor. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

10.
The individual emission and energy transfer between Ce3+ and Eu2+ or Dy3+ in BaCa(SO4)2 mixed alkaline earth sulfate phosphor prepared using a co‐precipitation method is described. The phosphor was characterized by X‐ray diffraction (XRD) and photoluminescence (PL) studies and doped by Ce;Eu and Dy rare earths. All phosphors showed excellent blue–orange emission on excitation with UV light. PL measurements reveal that the emission intensity of Eu2+ or Dy3+ dopants is greater than when they are co‐doped with Ce3+. An efficient Ce3+ → Eu2+ [2T2g(4f65d) → 8S7/2(4f7)] and Ce3+ → Dy3+ (4 F9/26H15/2 and 4 F9/26H13/2) energy transfer takes place in the BaCa(SO4)2 host. A strong blue emission peak was observed at 462 nm for Eu2+ ions and an orange emission peak at 574 nm for Dy3+ ions. Hence, this phosphor may be used as a lamp phosphor. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

11.
In this article, we report the synthesis of Na2Sr1‐x(PO4)F:Eux phosphor via a combustion method. The influence of different annealing temperatures on the photoluminescence properties was investigated. The phosphor was excited at both 254 and 393 nm. Na2Sr1‐x(PO4)F:Eux3+ phosphors emit strong orange and red color at 593 and 612 nm, respectively, under both excitation wavelengths. Na2Sr1‐x(PO4)F:Eux3+ phosphors annealed at 1050°C showed stronger emission intensity compared with 600, 900 and 1200°C. Moreover, Na2Sr1‐x(PO4)F:Eux3+ phosphor was found to be more intense when compared with commercial Y2O3:Eu3+ phosphor. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

12.
Ca3SiO4Cl2 co‐doped with Ce3+,Eu2+ was prepared by high temperature reaction. The structure, luminescent properties and the energy transfer process of Ca3SiO4Cl2: Ce3+,Eu2+ were investigated. Eu2+ ions can give enhanced green emission through Ce3+ → Eu2+ energy transfer in these phosphors. The green phosphor Ca2.9775SiO4Cl2:0.0045Ce3+,0.018Eu2+ showed intense green emission with broader excitation in the near‐ultraviolet light range. A green light‐emitting diode (LED) based on this phosphor was made, and bright green light from this green LED could be observed by the naked eye under 20 mA current excitation. Hence it is considered to be a good candidate for the green component of a three‐band white LED. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

13.
We report the photoluminescence characterization of Dy3+‐activated NaM4(VO4)3 (M = Ca, Ba, Sr) phosphors prepared by a solid‐state method. The synthesis was confirmed by X‐ray diffraction (XRD) characterization and photoluminescence (PL) emission results showed sharp blue and yellow bands for NaM4(VO4)3 (M = Ca, Ba, Sr):Dy3+ phosphors at the excitation wavelength of 323 nm, which is near‐UV excitation. Thus, these phosphors could be applicable for near‐UV excited solid‐state lighting devices. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

14.
A series of phosphors KAl1‐xPO4Cl:Eux3+ (0.1 ≤ x ≤ 1.0) was synthesized using a facile combustion method using urea as a fuel and their structural, morphological and photoluminescence properties were investigated. It was found that the particle size was in the range of 1–2 µm with an irregular shape. The f–f transitions of Eu3+ in the host lattice were assigned and discussed. The excitation and emission spectra indicated that this phosphor can be efficiently excited by ultraviolet (395 nm), and exhibit reddish orange emission corresponding to the 5D07FJ (J = 0, 1, 2) transitions of Eu3+. The impact of the Eu3+ concentration on the relative emission intensity was investigated, and the best doping concentration is 0.5. The present study suggests that the KAl0.5PO4Cl: Eu0.53+ phosphor is a strong candidate as a red component for phosphor‐ converted white light‐emitting diodes (LEDs). Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

15.
A novel phosphor LiBaPO4 doped with rare earths Eu and Dy prepared by high temperature solid‐state reaction method is reported. The phosphors were characterized by X‐ray powder diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence (PL). The emission and excitation spectra of these materials were measured at room temperature with a spectrofluorophotometer. The excitation spectra of LiBaPO4:Eu3+ phosphor can be efficiently excited by 394 nm, which is matched well with the emission wavelength of near‐UV light‐emitting diode (LED) chip. PL properties of Eu3+‐doped LiBaPO4 exhibited the characteristic red emission coming from 5D07 F1 (593 nm) and 5D07 F2 (617 nm) electronic transitions with color co‐ordinations of (0.680, 0.315). The results demonstrated that LiBaPO4:Eu3+ is a potential red‐emitting phosphor for near‐UV LEDs. Emission spectra of LiBaPO4:Dy3+ phosphors showed efficient blue (481 nm) and yellow (574 nm) bands, which originated from 4 F9/26H15/2 and 4 F9/26H13/2 transitions of the Dy3+ ion, respectively. The 574 nm line is more intense than the 481 nm lines, which indicates that the site Dy3+ is located with low symmetry. This article summarizes fundamentals and possible applications of optically useful inorganic phosphates with visible photoluminescence of Eu3+ and Dy3+ ions. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

16.
A series of Ba2P2O7:xEu2+,yCe3+,zTb3+ phosphors was synthesized via a co‐precipitation method, then their crystal structure, quantum efficiency and luminescent properties were analyzed by XRD and FL, respectively. The results showed that these phosphors not only presented the excitation characteristics of Ba2P2O7:xEu2+,zTb3+, but also exhibited that of the Ba2P2O7:yCe3+,zTb3+ phosphor. Meanwhile, the tri‐doped phosphor showed a stronger absorption around 320 nm in contrast with the Eu2+/Ce3+:Tb3+ co‐doped phosphor. Not only can energy transfer from Ce3+→Eu2+ be observed; the energy transfer mechanism from Eu2+ to Tb3+ is discussed in the tri‐doped system. Ce3+ affects the luminescence properties of Ba2P2O7:xEu2+,yCe3+,zTb3+ phosphors just as the sensitizer whereas Eu2+ is considered both as the sensitizer and the activator. The chromaticity coordinates of tri‐doped phosphors excited at 320 nm stayed steadily in the bluish‐white light region,and the emitted color and color temperature (CCT) of these phosphors could be tuned by adjusting the relative contents of Eu2+, Ce3+ and Tb3+. Hence, the single phase Ba2P2O7:xEu2+,yCe3+,zTb3+ phosphors may be considered as potential candidates for white light‐emitting diodes.  相似文献   

17.
The synthesis, X‐ray diffraction, photoluminescence, TGA/DTA and FTIR techniques in Dy3+ activated Na2Sr(PO4)F phosphor are reported in this paper. The prepared phosphor gave blue, yellow and red emission in the visible region of the spectrum at 348 nm excitation. CIE color co‐ordinates of Na2Sr(PO4)F:Dy3+ are suitable as white light‐emitting phosphors. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

18.
In the present study, Na3(SO4)X (X = F or Cl) halosulphate phosphors have been synthesized by the solid‐state diffusion method. The phase formation of the compounds Na3(SO4)F and Na3(SO4)Cl were confirmed by X‐ray powder diffraction (XRD) measurement. Photoluminescence (PL) excitation spectrum measurement of Na3(SO4)F:Ce3+ and Na3(SO4)Cl:Ce3+ shows this phosphor can be efficiently excited by near‐ultraviolet (UV) light and presents a dominant luminescence band centred at 341 nm for Ce3+, which is responsible for energy transfer to Dy3+and Mn2+ ions. The efficient Ce3+ → Dy3+ energy transfer in Na3(SO4)F and Na3(SO4)Cl under UV wavelength was observed due to 4 F9/2 to 6H15/2 and 6H13/2 level, while Ce3+ → Mn2+ was observed due to 4 T1 state to 6A1. The purpose of the present study is to develop and understanding the photoluminescence properties of Ce3+‐, Dy3+‐ and Mn2+‐doped fluoride and chloride Na3(SO4)X (X = F or Cl) luminescent material, which can be the efficient phosphors in many applications, such as scintillation applications, TL dosimetry and the lamp industry, etc. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

19.
A series of Ca2Mg0.25Al1.5Si1.25O7:Ce3+/Eu2+/Tb3+ phosphors was been prepared via a conventional high temperature solid‐state reaction and their luminescence properties were studied. The emission spectra of Ca2Mg0.25Al1.5Si1.25O7:Ce3+,Eu2+ and Ca2Mg0.25Al1.5Si1.25O7:Ce3+,Tb3+ phosphors show not only a band due to Ce3+ ions (409 nm) but also as a band due to Eu2+ (520 nm) and Tb3+ (542 nm) ions. More importantly, the effective energy transfer from Ce3+ to Eu2+ and Tb3+ ions was confirmed and investigated by emission/excitation spectra and luminescent decay behaviors. Furthermore, the energy level scheme and energy transfer mechanism were investigated and were demonstrated to be of resonant type via dipole–dipole (Ce3+ to Eu2+) and dipole–quadrupole (Ce3+ to Tb3+) reactions, respectively. Under excitation at 350 nm, the emitting color could be changed from blue to green by adjusting the relative doping concentration of Ce3+ and Eu2+ ions as well as Ce3+ and Tb3+ ions. The above results indicate that Ca2Mg0.25Al1.5Si1.25O7:Ce3+,Eu2+/Tb3+ are promising single‐phase blue‐to‐green phosphors for application in phosphor conversion white‐light‐emitting diodes. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

20.
A series of Sr2ZnWO6 phosphors co‐doped with Eu3+, Bi3+ and Li+ were prepared using the Pechini method. The samples were tested using X‐ray diffraction and luminescence spectroscopy. The results show that the samples can be effectively excited by near‐ultraviolet (UV) and UV light. The introduction of Bi3+ and Li+ significantly enhances the fluorescence emission of Sr2ZnWO6:Eu3+ and changes the light emitted by the phosphors from bluish‐green to white. When excited at 371 nm, Sr2–x–zZn1–yWO6:xEu3+,yBi3+,zLi+ (x = 0.05, y = 0.05, z = 0.05, 0.1 and 0.15) samples emit high‐performance white light. Intense red–orange emission is also observed when excited by UV light. The obtained phosphor is a potential white‐emitting phosphor that could meet the needs of excitation sources with near‐UV chips. In addition, this phosphor might have promising application as a red–orange emitting phosphor for white light‐emitting diodes based on UV light‐emitting diodes. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

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