共查询到20条相似文献,搜索用时 31 毫秒
1.
Novel single-phased white light-emitting KCaY(PO(4))(2):Eu(2+),Mn(2+) phosphors for light-emitting diode (LED) applications were synthesized by conventional solid-state reaction. The emission hue could be controlled by tuning the Eu(2+)/Mn(2+) ratio via the energy transfer; the the emission hue of KCaY(PO(4))(2):Eu(2+),Mn(2+) varied from blue (0.1853, 0.2627) to white-light (0.3350, 0.3203) and eventually to purple (0.3919, 0.2867). The mechanism of energy transfer from a sensitizer Eu(2+) to an activator Mn(2+) in KCaY(PO(4))(2):Eu(2+),Mn(2+) phosphors was demonstrated to be an electric dipole-quadrupole interaction. Combining a NUV 405-nm chip and a white-emitting KCaY(PO(4))(2):1%Eu(2+),4%Mn(2+) phosphor produced a white-light NUV LED, demonstrating CIE chromaticity coordinates of (0.314, 0.329) and a color temperature of 6507 K. 相似文献
2.
Du F Zhu R Huang Y Tao Y Seo HJ 《Dalton transactions (Cambridge, England : 2003)》2011,40(43):11433-11440
A red-emitting phosphor, Eu(3+)-doped Ca(9)LiGd(2/3)(PO(4))(7), was synthesized by the conventional high-temperature solid-state reaction. X-ray powder diffraction (XRD) analyses confirmed the pure crystalline phase of Whitlockite-type structure. The excitation spectra of Eu(3+) doped Ca(9)LiGd(2/3)(PO(4))(7) were measured in the VUV and UV region indicating an efficient energy transfer process from the host and Gd(3+) to Eu(3+) ions. Upon excitation with VUV and UV radiation, the phosphor showed strong red emission around 611 nm corresponding to the forced electric dipole (5)D(0)→(7)F(2) transition of Eu(3+) ions. The VUV- and UV-excited luminescence spectra of Ca(9)LiGd(2/3)(PO(4))(7):Eu(3+) together with the dependence of the integrated emission intensities on the doping levels were investigated. The Eu(3+) ions were investigated by a tunable laser as an excitation source. The excitation spectra of (7)F(0)→(5)D(0) transitions suggest that there are two families of inequivalent sites for Eu(3+) in this host. The concentration quenching and crystallographic site-occupancy of Eu(3+) ions in Ca(9)LiGd(2/3)(PO(4))(7) host were discussed on the basis of the site selective excitation and emission spectra, the luminescence decay and its crystal structure. 相似文献
3.
A novel white-light-emitting phosphor Ca(9)Lu(PO(4))(7):Eu(2+),Mn(2+) has been prepared by solid-state reaction. The photoluminescence properties indicate that there is an efficient energy transfer from the Eu(2+) to Mn(2+) ions via a dipole-quadrupole reaction. The obtained phosphor exhibits a strong excitation band between 250 and 430 nm, matching well with the dominant emission band of a UV light-emitting-diode (LED) chip. Upon excitation of UV light, white light is realized by combining a broad blue-green emission band at 480 nm and a red emission band at 645 nm attributed to the Eu(2+) and Mn(2+) ions. The energy-transfer efficiency and critical distance were also calculated. Furthermore, the phosphors can generate lights from blue-green through white and eventually to red by properly tuning the relative ratio of the Eu(2+) to Mn(2+) ions through the principle of energy transfer. Preliminary studies showed that the phosphor might be promising as a single-phased white-light-emitting phosphor for a UV white-light LED. 相似文献
4.
A new family of chloroborate compounds, which was investigated from the viewpoint of rare earth ion activated phosphor materials, have been synthesized by a conventional high temperature solid-state reaction. The crystal structure and thermally stable luminescence of chloroborate phosphors Ba(2)Ln(BO(3))(2)Cl:Eu(2+) (Ln = Y, Gd, and Lu) have been reported in this paper. X-ray diffraction studies verify the successful isomorphic substitution for Ln(3+) sites in Ba(2)Ln(BO(3))(2)Cl by other smaller trivalent rare earth ions, such as Sm, Eu, Tb, Dy, Ho, Er, Tm, and Yb. The detailed structure information for Ba(2)Ln(BO(3))(2)Cl (Ln = Y, Gd, and Lu) by Rietveld analysis reveals that they all crystallize in a monoclinic P2(1)/m space group. These compounds display interesting and tunable photoluminescence (PL) properties after Eu(2+)-doping. Ba(2)Ln(BO(3))(2)Cl:Eu(2+) phosphors exhibit bluish-green/greenish-yellow light with peak wavelengths at 526, 548, and 511 nm under 365 UV light excitation for Ba(2)Y(BO(3))(2)Cl:Eu(2+), Ba(2)Gd(BO(3))(2)Cl:Eu(2+), and Ba(2)Lu(BO(3))(2)Cl:Eu(2+), respectively. Furthermore, they possess a high thermal quenching temperature. With the increase of temperature, the emission bands show blue shifts with broadening bandwidths and slightly decreasing emission intensities. It is expected that this series of chloroborate phosphors can be used in white-light UV-LEDs as a good wavelength-conversion phosphor. 相似文献
5.
Yu J Hao Z Zhang X Luo Y Zhang J 《Chemical communications (Cambridge, England)》2011,47(45):12376-12378
Eu(2+) singly and Eu(2+), Mn(2+) co-doped Sr(2)Mg(3)P(4)O(15) exhibit not only the well known blue emission band of Eu(2+) peaking at 448 nm but also a new band at 399 nm in violet. They are attributed to Eu(2+) on different Sr(2+) sites. The Eu(2+) for the violet band can transfer energy to the red emitting Mn(2+) more efficiently than Eu(2+) for the blue band. The new Eu(2+) band could enable Sr(2)Mg(3)P(4)O(15):Mn(2+), Eu(2+) to be a promising phosphor for enriching the red component of white LEDs. 相似文献
6.
Eu(2+)-activated Sr(8)MgY(PO(4))(7) and Sr(8)MgLa(PO(4))(7) yellow-emitting phosphors were successfully synthesized by solid-state reactions for applications in excellent color rendering index white light-emitting diodes (LEDs). The excitation and reflectance spectra of these phosphors show broad band excitation and absorption in the 250-450 nm near-ultraviolet region, which is ascribed to the 4f(7) → 4f(6)5d(1) transitions of Eu(2+). Therefore, these phosphors meet the application requirements for near-UV LED chips. Upon excitation at 400 nm, the Sr(8)MgY(PO(4))(7):Eu(2+) and Sr(8)MgLa(PO(4))(7):Eu(2+) phosphors exhibit strong yellow emissions centered at 518, 610, and 611 nm with better thermal stability than (Ba,Sr)(2)SiO(4) (570 nm) commodity phosphors. The composition-optimized concentrations of Eu(2+) in Sr(8)MgLa(PO(4))(7):Eu(2+) and Sr(8)MgY(PO(4))(7):Eu(2+) phosphors were determined to be 0.01 and 0.03 mol, respectively. A warm white-light near-UV LED was fabricated using a near-UV 400 nm chip pumped by a phosphor blend of blue-emitting BaMgAl(10)O(17):Eu(2+) and yellow-emitting Sr(8)MgY(PO(4))(7):0.01Eu(2+) or Sr(8)MgLa(PO(4))(7):0.03Eu(2+), driven by a 350 mA current. The Sr(8)MgY(PO(4))(7):0.01Eu(2+) and Sr(8)MgLa(PO(4))(7):0.03Eu(2+) containing LEDs produced a white light with Commission International de I'Eclairage (CIE) chromaticity coordinates of (0.348, 0.357) and (0.365, 0.328), warm correlated color temperatures of 4705 and 4100 K, and excellent color rendering indices of 95.375 and 91.75, respectively. 相似文献
7.
Zhou L Yi L Feng X 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,83(1):340-343
A series of Eu(2+) and Mn(2+) co-doped SrAl(2)B(2)O(7) phosphors were prepared by solid-state reaction method. X-ray powder diffraction (XRD) and photoluminescence excitation and emission were employed to characterize the phosphors. The results show that energy transfers between Eu(2+)and Mn(2+) ions. As the content of Ca(2+) ions in Ca(x)Sr(0.92-x)Al(2)B(2)O(7):Eu(2+)(0.06), Mn(2+)(0.02) phosphors increased, the CIE coordinates decreased and close to the white color standard mandated by the National Television Standard Committee (NTSC). Meanwhile, a white LED (light-emitting diode) was fabricated by combining the Ca(0.5)Sr(0.42)Al(2)B(2)O(7):Eu(2+)(0.06), Mn(2+)(0.02) phosphors with a 370 nm InGaN chip. The color coordinate of the fabricated white LED was also close to the white color standard, indicating that the Ca(0.5)Sr(0.42)Al(2)B(2)O(7):Eu(2+)(0.06), Mn(2+)(0.02) phosphor is a promising single-host phosphor that can be used in white LEDs. 相似文献
8.
Xue YN Xiao F Zhang QY 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,78(5):1445-1448
Ca(8)MgLa(PO(4))(7):Ce(3+),Mn(2+) phosphors have been prepared by a conventional solid state reaction under a weak reductive atmosphere. The crystal structure and photoluminescent properties were investigated. It was found that the red emission at 640nm originated from the (4)T(1)((4)G)→(6)A(1)((6)S) transition of Mn(2+) increases dramatically by a factor of 6.4 with the optimum Ce(3+) co-doping. The energy transfer from Ce(3+) to Mn(2+) was proposed to be resonance-type via an electric dipole-dipole mechanism and the energy transfer efficiency was also calculated by the relative emission intensity. With the broadband ultraviolet (UV) absorption of Ce(3+) and the suitable color coordinates, Ca(8)MgLa(PO(4))(7):Ce(3+),Mn(2+) phosphors might be a promising candidate as red phosphors in the field of UV-based white light-emitting diodes. 相似文献
9.
Ce(3+) and Eu(2+) singly doped and Ce(3+)/Eu(2+)-codoped Ca(7)Mg(SiO(4))(4) phosphors are synthesized by the conventional solid state reaction. The Ce(3+) activated sample exhibits intense blue emission under 350 nm excitation, the composition-optimized Ca(7)Mg(SiO(4))(4)?:?4%Ce(3+) shows better color purity than the commercial blue phosphor, BaMgAl(10)O(17)?:?Eu(2+) (BAM?:?Eu(2+)) and exhibits superior external quantum efficiency (65%). The Ca(7)Mg(SiO(4))(4)?:?Eu(2+) powder shows a broad emission band in the wavelength range of 400-600 nm with a maximum at about 500 nm. The strong excitation bands of the Ca(7)Mg(SiO(4))(4)?:?Eu(2+) in the wavelength range of 250-450 nm are favorable properties for applications as light-emitting-diode conversion phosphors. Furthermore, the energy transfer from the Ce(3+) to Eu(2+) ions is observed in the codoped samples, the resonance-type energy transfer is determined to be due to the dipole-dipole interaction mechanism and the critical distance is obtained through the spectral overlap approach and concentration quenching method. 相似文献
10.
Peng C Shang M Li G Hou Z Geng D Lin J 《Dalton transactions (Cambridge, England : 2003)》2012,41(16):4780-4788
One-dimensional La(9.33)(SiO(4))(6)O(2): Ln(3+) (Ln = Ce, Eu, Tb) microfibers were fabricated by a simple and cost-effective electrospinning method. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), photoluminescence (PL) and low voltage cathodoluminescence (CL) as well as kinetic decay were used to characterize the resulting samples. SEM and TEM results indicated that the diameter of the microfibers annealed at 1000 °C for 3 h was 200-245 nm. The microfibers were further composed of fine and closely linked nanoparticles. La(9.33)(SiO(4))(6)O(2): Ln(3+) (Ln = Ce, Eu, Tb) phosphors showed the characteristic emission of Ce(3+) (5d → 4f), Eu(3+) ((5)D(0)→(7)F(J)) and Tb(3+) ((5)D(3,4)→(7)F(J)) under ultraviolet excitation and low-voltage electron beams (3-5 kV) excitation. An energy transfer from Ce(3+) to Tb(3+) was observed in the La(9.33)(SiO(4))(6)O(2): Ce(3+), Tb(3+) phosphor under ultraviolet excitation and low-voltage electron beam excitation. Luminescence mechanisms were proposed to explain the observed phenomena. Blue, red and green emission can be realized in La(9.33)(SiO(4))(6)O(2): Ln(3+) (Ln = Ce, Eu, Tb) microfibers by changing the doping ions. So the La(9.33)(SiO(4))(6)O(2): Ln(3+) (Ln = Ce, Eu, Tb) phosphors have potential applications in full-color field emission displays. 相似文献
11.
A novel red-emitting Ba(2)Tb(BO(3))(2)Cl:Eu phosphor possessing a broad excitation band in the near-ultraviolet (n-UV) region was synthesized by the solid-state reaction. Versatile Ba(2)Tb(BO(3))(2)Cl compound has a rigid open framework, which can offer two types of sites for various valence's cations to occupy, and the coexistence of Eu(2+)/Eu(3+) and the red-emitting luminescence from Eu(3+) with the aid of efficient energy transfer of Eu(2+)-Eu(3+)(Tb(3+)) and Tb(3+)-Eu(3+) have been investigated. Ba(2)Tb(BO(3))(2)Cl emits green emission with the main peak around 543 nm, which originates from (5)D(4) → (7)F(5) transition of Tb(3+). Ba(2)Tb(BO(3))(2)Cl:Eu shows bright red emission from Eu(3+) with peaks around 594, 612, and 624 nm under n-UV excitation (350-420 nm). The existence of Eu(2+) can be testified by the broad-band excitation spectrum, UV-vis reflectance spectrum, X-ray photoelectron spectrum, and Eu L(3)-edge X-ray absorption spectrum. Decay time and time-resolved luminescence measurements indicated that the interesting luminescence behavior should be ascribed to efficient energy transfer of Eu(2+)-Eu(3+)(Tb(3+)) and Tb(3+)-Eu(3+) in Ba(2)Tb(BO(3))(2)Cl:Eu phosphors. 相似文献
12.
Three series of new ultraviolet-emitting Ca(9)Y(PO(4))(7):Ln(3+) (Ln = Ce, Gd, Pr) phosphors were synthesized, and their luminescence was investigated. Under vacuum ultraviolet excitation Ca(9)Y(PO(4))(7):Ce(3+) phosphors emit UVA light with one broad emission centered at 346 nm, on account of the 5d(1) → 4f(1) transition of Ce(3+) ions; the optimal doping concentration of these phosphors is 0.2 mol. Ca(9)Y(PO(4))(7):Gd(3+) phosphors show a strong 4f(7) → 4f(7) transition and a sharp UVB emission band at 312 nm; the optimal doping concentration of these phosphors is 0.7 mol. The PL spectra of Ca(9)Y(PO(4))(7):Pr(3+) show two broad UVC emission bands centered between 230 and 340 nm, owing to the 4f(1)5d(1) → 4f(2) transition of Pr(3+) ions; the optimal doping concentration of these phosphors is 0.2 mol. Under 172 nm excitation, we found that the luminescence intensity of the UVA-emitting Ca(9)Y(PO(4))(7):0.2Ce(3+) is 0.3675 times that of BaSi(2)O(5):0.05Pb(2+), that of the UVB-emitting Ca(9)Y(PO(4))(7):0.7Gd(3+) is 1.7 times that of YAl(3)(BO(3))(4):0.25Gd(3+), and that of the UVC-emitting Ca(9)Y(PO(4))(7):0.2Pr(3+) is 1.5 times that of LaPO(4):0.1Pr(3+). The thermal stability investigation indicated that the luminescence decay was only 9.2%, 18.2%, and 10.3% for Ca(9)Y(PO(4))(7):0.2Ce(3+), Ca(9)Y(PO(4))(7):0.7Gd(3+), and Ca(9)Y(PO(4))(7):0.2Pr(3+) at 250 °C relative to that at ambient temperature, respectively. The Ca(9)Y(PO(4))(7):Ln(3+) (Ln = Ce, Gd, Pr) phosphors exhibit high emission efficiency and excellent thermal stability. 相似文献
13.
Trivalent rare-earth (RE) ions (Eu(3+), Tb(3+) and Sm(3+)) activated multicolor emitting SrY(2)O(4) phosphors were synthesized by a sol-gel process. The structural and morphological studies were performed by the measurements of X-ray diffraction profiles and scanning electron microscope (SEM) images. The pure phase of SrY(2)O(4) appeared after annealing at 1300 °C and the doping of RE ions did not show any effect on the structural properties. From the SEM images, the closely packed particles were observed due to the roughness of each particle tip. The photoluminescence (PL) analysis of individual RE ions activated SrY(2)O(4) phosphors exhibits excellent emission properties in their respective regions. The Eu(3+) co-activated SrY(2)O(4):Tb(3+) phosphor creates different emissions by controlling the energy transfer from Tb(3+) to Eu(3+) ions. Based on the excitation wavelengths, multiple (green, orange and white) emissions were obtained by Sm(3+) ions co-activated with SrY(2)O(4):Tb(3+) phosphors. The decay measurements were carried out for analyzing the energy transfer efficiency and the possible ways of energy transfer from donor to acceptor. The cathodoluminescence properties of these phosphors show similar behavior as PL properties except the energy transfer process. The obtained results indicated that the energy transfer process was quite opposite to the PL properties. The calculated CIE chromaticity coordinates of RE ions activated SrY(2)O(4) phosphors confirmed the red, green, orange and white emissions. 相似文献
14.
A series of Bi3+-doped YAG:Ce3+, Mn2+ ceramics was synthesized successfully by gel-casting method and structurally characterized by XRD and SEM. The doping effect and related mechanism of Bi3+ upon the luminescent property were studied. It can be assigned to the energy transfer of multipolar interaction from Bi3+ to Ce3+, leading to the improvement of emission intensity about 58% for 0.0001 Bi3+ and 0.05 Mn2+ doping. In addition, the emission is significantly red-shifted with the peak at 590 nm for the Y2.9939 Ce0.006 Bi0.0001 Al4.96 Mn0.02 Si0.02 O12 ceramic specimen with in-line transmittance 81.6% at 1100 nm. The LED module assembled from Y2.9939 Ce0.006 Bi0.0001 Al4.96 Mn0.02 Si0.02 O12 ceramic owns correlated color temperature(CCT) of 3960 K and luminous efficiency(LE) of 92 lm/W, implying that doping Bi3+ shows a good sensitization effect in the YAG:Ce3+, Mn2+ ceramic system and further serving as an attracting phosphor candidates for warm WLEDs applications. 相似文献
15.
Huang S Zhang X Wang L Bai L Xu J Li C Yang P 《Dalton transactions (Cambridge, England : 2003)》2012,41(18):5634-5642
Yttrium tungstate precursors with novel 3D hierarchical architectures assembled from nanosheet building blocks were successfully synthesized by a hydrothermal method with the assistance of sodium dodecyl benzenesulfonate (SDBS). After calcination, the precursors were easily converted to Y(2)(WO(4))(3) without an obvious change in morphology. The as-prepared precursors and Y(2)(WO(4))(3) were characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM), and photoluminescence (PL) spectra, respectively. The results reveal that the morphology and dimensions of the as-prepared precursors can be effectively tuned by altering the amounts of organic SDBS and the reaction time, and the possible formation mechanism was also proposed. Upon ultraviolet (UV) excitation, the emission of Y(2)(WO(4))(3):x mol% Eu(3+) microcrystals can be tuned from white to red, and the doping concentration of Eu(3+) has been optimized. Furthermore, the up-conversion (UC) luminescence properties as well as the emission mechanisms of Y(2)(WO(4))(3):Yb(3+)/Ln(3+) (Ln = Er, Tm, Ho) microcrystals were systematically investigated, which show green (Er(3+), (4)S(3/2), (2)H(11/2)→(4)I(15/2)), blue (Tm(3+), (1)G(4)→(3)H(6)) and yellow (Ho(3+), (5)S(2)→(5)I(8)) luminescence under 980 nm NIR excitation. Moreover, the doping concentration of the Yb(3+) has been optimized under a fixed concentration of Er(3+) for the UC emission of Y(2)(WO(4))(3):Yb(3+)/Er(3+). 相似文献
16.
The VUV-vis spectroscopic properties of Tb(3+) activated fluoro-apatite phosphors Ca(6)Ln(2-x)Tb(x)Na(2)(PO(4))(6)F(2) (Ln = Gd, La) were studied. The results show that phosphors Ca(6)Gd(2-x)Tb(x)Na(2)(PO(4))(6)F(2) with Gd(3+) ions as sensitizers have intense absorption in the VUV range. The emission color of both phosphors can be tuned from blue to green by changing the doping concentration of Tb(3+) under 172 nm excitation. The visible quantum cutting (QC) via cross relaxation between Tb(3+) ions was observed in cases with and without Gd(3+). Though QC can be realized in phosphors Ca(6)La(2-x)Tb(x)Na(2)(PO(4))(6)F(2), we found that Gd(3+)-containg phosphors have a higher QC efficiency, confirming that the Gd(3+) ion indeed plays an important role during the quantum cutting process. In addition, the energy transfer process from Gd(3+) to Tb(3+) as well as (5)D(3)-(5)D(4) cross relaxation was investigated and discussed in terms of luminescence spectra and decay curves. 相似文献
17.
Eu^2+和Mn^2+在Sr3MgSi2O8中的光致发光研究 总被引:7,自引:1,他引:7
研究了Eu^2+和Mn^2+共激活的Sr3MgSi2O8的荧光性质。Eu^2+和Mn^2+在460nm和690nm的发射峰分别由Eu^2+的5d→4f跃迁和Mn^2+的^4T1(^4G)→^6A1g(^6S)跃迁产生。未观察到单掺杂Mn^2+的Sr3MgSi2O8的荧光发射,而掺入Eu^2+后则出现了Mn^2+的690nm光致发光峰,表明Eu^2+对Mn^2+有敏化作用。Eu^2+的荧光寿命也受M 相似文献
18.
Preparation of Sr2CeO4:Eu3+,Dy3+ white luminescence phosphor particles and thin films by using an emulsion liquid membrane system 总被引:3,自引:0,他引:3
Sr(2)CeO(4) and Sr(2)CeO(4):Eu(3+),Dy(3+) phosphor particles and thin films were prepared by using an emulsion liquid membrane (ELM, water-in-oil-in-water (W/O/W) emulsion) system, containing VA-10 (2-methyl-2-ethylheptanoic acid) as extractant (cation carrier). A two-step extraction enabled efficient extraction for Sr(3+) and rare earth ions, and the resulting precursor metal oxalate particles produced in the internal water phase of the ELM system were about 60 nm in diameter. Calcination of the oxalate particles in air gave submicrometer-sized Sr(2)CeO(4) and Sr(2)CeO(4):Eu(3+),Dy(3+) particles, which showed blue and white luminescence, respectively, by UV excitation. Blue and white luminescence phosphor thin films were also prepared by soaking alumina substrates into the W/O emulsion containing precursor oxalate particles, followed by calcination in air. 相似文献
19.
掺杂铕和铽的卤硼酸盐荧光体的制备及光谱特征 总被引:1,自引:0,他引:1
采用高温固相法在空气中合成了一系列掺杂稀土离子的卤硼酸盐荧光体, 研究了其发光性质和基质组成对稀土离子共掺杂的荧光体发光性质的影响. 研究结果表明, 在Eu3+和Tb3+共掺杂的体系中存在电子转移, 因此出现了Eu3+, Eu2+和 Tb3+共存于同一基质共同发射的现象. Ce3+对Eu2+和Tb3+具有敏化作用, 可增强其发射强度. 基质的组成对稀土离子的发射峰位和发射强度有明显影响. 相似文献
20.
Eu3+在碱土金属卤磷酸盐中的格位对称性及电荷迁移态 总被引:2,自引:0,他引:2
在254nm紫外光激发下研究了Eu~(3+)在Sr_3Ca_2(PO_4)_3Cl基质中的发光光谱.以Eu~(3+)为结构探针测定了Eu~(3+)所处晶格的点对称性.研究了M_5(PO_4)_3X(M=Ca,Sr,Ba;X=F,Cl,Br)基质组成改变对Eu~(3+)电荷迁移态的影响,以及温度对Ca_5(PO_4)_3Cl:Eu~(3+)发光强度的影响. 相似文献