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1.
Yellow-green-emitting Sr Si2O2N2:Eu2+phosphors were synthesized with Sr2Si O4:Eu2+as precursor.The effects of flux and the concentration of Eu2+on the crystal structure and luminescent properties of the phosphors were investigated.Results suggested that the optimal content of flux Na2CO3 was 1 wt%and the optimal doping concentration of Eu2+was 0.05 mol.The emission spectra showed the most intense peaks located at 535 nm which corresponded to the 4f65d→4f7 transition of Eu2+.The excitation spectra showed that these phosphors could be effectively excited by near-ultraviolet and blue light,whichwas consistent with the widely applied output wavelengths of near-ultraviolet and blue-white light-emitting diode(LED)chips.When the influence of flux on the luminescent properties of Sr Si2O2N2:Eu2+phosphor was analyzed,the X-ray diffraction(XRD)patterns indicated that the flux could help the crystallization of the phosphors.No other phases except the triclinic structure of Sr Si2O2N2 were formed.The thermal stability and the emission intensity of synthesized Sr Si2O2N2:Eu2+phosphor were examined and compared with commercial YAG yellow phosphors.All results indicate that the yellow-green-emitting phosphor is a suitable candidate for the fabrication of white LEDs.  相似文献   

2.
LiSrBO3 :Eu3+ phosphor is synthesized by a high solid-state reaction method, and its luminescent characteristics are investigated. The emission and excitation spectra of LiSrBO3:Eu3+ phosphors exhibit that the phosphors can be effectively excited by near ultraviolet (401 nm) and blue (471 nm) light, and emit 615nm red light. The effect of Eua+ concentration on the emission spectrum of LiSrBO3:Eu3+ phosphor is studied; the results show that the emission intensity increases with increasing Eu3+ concentration, and then decreases because of concentration quenching. It reaches the maximum at 3mol%, and the concentration self-quenching mechanism is the dipoledipole interaction according to the Dexter theory. Under the conditions of charge compensation Li+, Na+ or K+ incorporated in LiSrBO3, the luminescent intensities of LiSrBO3 :Eua+ phosphor are enhanced.  相似文献   

3.
周天亮  宋振  宋西平  边柳  刘泉林 《中国物理 B》2010,19(12):127808-127808
Sr2ScAlO5:Eu2+,a red oxide phosphor with a perovskite-type structure,has been synthesized through a solid-state reaction and its luminescence properties have been investigated.An absorption band centering at 450 nm is observed from the diffuse reflection spectra and the excitation spectra,indicating that the phosphor can match perfectly with the blue light of InGaN light-emitting diodes.A broad red emission band at 620 nm is found from the emission spectra,originating from the 4f 6 5d-4f 7 transition of the Eu 2+ ions.The best doping content of Eu in this material is about 5%.Sr2ScAlO5:Eu2+is a highly promising red phosphor for use in white light-emitting diodes.  相似文献   

4.
Yb 3+ /Dy 3+ co-doped Al2O3 nanopowders have been prepared by the non-aqueous sol-gel method and their up- conversion photoluminescence spectra are measured under excitation by a 980-nm semiconductor laser. The results show that there are comparatively abundant spectra of up-conversion emissions centered at 378, 408, 527 and 543, and 663 nm, corresponding to4G9/2 → 6H13/2,4G9/2→6H11/2 ,4I15/2 →6H13/2 , and 4F9/2 → 6H11/2 transitions of Dy 3+ , respectively. Two-photon and three-photon processes are involved in ultraviolet, violet, green, and red up-conversion emissions. The energy transition between Yb3+ and Dy3+ is discussed.  相似文献   

5.
A series of SrIn2 O4 :Eu3+ phosphors are synthesized by a high temperature solid-state method, and their luminescent properties are investigated. They can be excited by 395-nm radiation, and produce red emission (619 nm); however, they have a low absorption of near-ultraviolet light with the wavelength of 400nm-405 nm. When co-doped with A+ (A=Li, Na, K), the emission intensity of SrIn2O4 :Eu3+ is significantly enhanced, but its emission and excitation spectral profile is unchanged. With co-doping Sm3+ , not only is the emission intensity of SrIn2 O4 :Eu3+ enhanced, but also the absorption is broadened and strengthened in the range of 400 nm-405nm. The effect of Sm3+ -doped content on the emission intensity of SrIn2O4 :Eu3+ , Sm3+ is investigated, and the optimal Sm3+ content is 0.02 mol.  相似文献   

6.
Fluoride nanoparticles of Ln3+(Ln3+=Pr3+,Nd3+,Sm3+,Gd3+,Tb3+Dy3+,Ho3+,Er3+,Tm3+,Yb3+)/Eu3+:LaOF and Eu3+ :LaOF with rhombohedral crystal structure were prepared by a hydrothermal-sintering method. The red fluorescence emission of Eu3+ ions was found to be enhanced with most of the co-dopant Ln3+ ions. Compared with strong fluorescence emission at 610 nm of Eu3+ :LaOF nanoparticles, the enhancement factors was up to ten times in Ln3+(Ln3+ =Gd3+,Dy3+,Tm3+)/Eu3+ :LaOF co-doped nanoparticles. The results show that the asymmetry of the local environment of Eu3+ ion was reduced by co-doping Ln3+ ion into the nanoparticles, and that energy transfer might occur between Eu3+ and codopant Ln3+ ions, which is suggested as the source of the observed fluorescence enhancement.  相似文献   

7.
Optical absorption,excitation,and fluorescence were investigated in Eu ion-doped CdWO4 single crystal grown by a modified Bridgman method.The results indicate that Eu2+ and Eu3+ ions coexist in CdWO4 crystal and an energy transfer occurs between these Eu2+ and Eu3+ ions.When the crystal is excited by 266-nm light,the energy corresponding to the 4f65d to 8S7/2 transition of Eu2+ ions results in the excitation of the Eu3+ ions to the 5DJ level.The effect on fluorescence of annealing in oxygen at various temperatures was investigated.The excitation intensity of Eu2+ ions at 266 nm decreases as annealing temperature increases from 300 K to 1073 K,but it remains at a certain equilibrium level when the annealing temperature is further increased.  相似文献   

8.
王国利  周效信 《中国物理 B》2009,18(9):3833-3838
There can be found some notable discrepancies with regard to the resonance structures when R-matrix calculations from the Opacity Project and other sources are compared with recent absolute experimental measurements of Bizau et al [Astron.Astrophts.439 387(2005)] for B-like ions N2+,O3+ and F4+.We performed close-coupling calculations based on the R-matrix formalism for the photoionizations of ions mentioned above both for the ground states and first excited states in the near threshold regions.The present results are compared with experimental ones given by Bizau et al and earlier theoretical ones.Excellent agreement is obtained between our theoretical results and the experimental photoionization cross sections.The present calculations show a significant improvement over the previous theoretical results.  相似文献   

9.
A luminescence kinetic model for the green-emission long-afterglow phosphor (Sr0.5 Ca1.5)MgSi2O7:Eu^2 ,Dy^3 is proposed based on the studies of the thermoluminescence and isothermal decay curves at different temperatures.The isothermal decay curves at different temperatures meet the hyperbolic law and show to be dependent on temperature. Combined with the decay curves and the thermoluminescence curves, it can be concluded that the long afterglow of this material originates from the traps with energy distribution rather than a single level trap.Upon illumination with ultra-violet or visible light, the trap filling can proceed via excitation of 4f electrons to the 5d level of Eu^2 ions. After excitation, 5d electrons can be transferred to the trap related to Dy3 ions, and Eu^3 is left behind. Upon subsequent heating, the electron is released from this trap and recombines with Eu^3 to produce Eu^2 emission.  相似文献   

10.
The structure and photoluminescence (PL) properties of Sr3 SiO5: Sm3+ and Li+-doped Sr3SiOs: Sm3+ red-emitting phosphors were investigated. Samples were prepared by the high-temperature solid-state method. PL spectra show that the concentration quenching occurs when the Sm3+ concentration is beyond 1.3 mol% in Sr3SiOs: Sm3+ phosphor without doping Li+ ions. The concentration-quenching mechanism can be explained by the electric dipole-dipole interaction of Sm3+ ions. The incorporation of Li+ ions into Sr3SiOs: Sm3+ phosphors, as a charge compensator, improves the PL properties. The lithium ions also suppress the concentration quenching in Sm3+ with concentration increased from 1.3 tool% to 1.7 tool%.  相似文献   

11.
崔彩娥  王森  黄平 《物理学报》2009,58(5):3565-3571
采用溶胶凝胶法制备了Sr3Al26:Eu2+,Dy3+红色长余辉发光材料,利用X射线衍射仪对材料的物相进行了分析,结果表明,1200℃下制备的样品的物相为Sr3Al26,少量的Eu和Dy掺杂没有影响样品的相组成.采用荧光分光光度计、照度计测定了样品的发光特性.结果表明Sr3Al2关键词: 红色长余辉 3Al26')" href="#">Sr3Al26 溶胶凝胶法  相似文献   

12.
Sr2MgSi2O7:Eu2+, Dy3+ phosphors were prepared by the (aminopropyl)-triethoxysilane (APTES) co-precipitation method. Effects of synthesis temperature on the crystal characteristics, luminescent properties and afterglow performance of Sr2MgSi2O7:Eu2+, Dy3+ phosphors have been discussed in detail and compared with the corresponding commercial product. The experimental results indicated that the sample could be synthesized at a relatively lower temperature and had better performance on the above-mentioned properties using the co-precipitation method.  相似文献   

13.
The spectroscopic properties in UV-excitable range for the phosphors of Sr3La2(BO3)4:RE3+ (RE3+=Eu3+, Ce3+, Tb3+) were investigated. The phosphors were synthesized by conventional solid-state reactions. The photoluminescence (PL) spectra and commission international de I'Eclairage (CIE) coordinates of Sr3La2(BO3)4:RE3+ were investigated. The f-d transitions of Eu3+, Ce3+ and Tb3+ in the host lattices are assumed and corroborated. The PL and PL excitation (PLE) spectra indicate that the main emission wavelength of Sr3La2(BO3)4:Eu3+ is 611 nm, and Sr3La2(BO3)4:Ce3+ shows dominating emission peak at 425 nm, while Sr3La2(BO3)4:Tb3+ displays green emission at 487, 542, 582 and 620 nm. These phosphors were prepared by simple solid-state reaction at 1000 °C. There are lower reactive temperature and more convenient than commercial phosphors. The Sr3La2(BO3)4:Tb3+ applied to cold cathode fluorescent lamp was found to emit green light and have a major peak wavelength at around 542 nm. These phosphors may provide a new kind of luminescent materials under ultraviolet excitation.  相似文献   

14.
Eu3+掺杂的Sr2CeO4发光材料的光致发光研究   总被引:1,自引:0,他引:1       下载免费PDF全文
符史流  尹涛  丁球科  赵韦人 《物理学报》2006,55(9):4940-4945
利用高温固相反应法制备了Eu3+掺杂的Sr2CeO4样品,并对其吸附水前后的光谱特性进行了研究.结果发现,对于刚制备的Sr2-xEuxCeO4+x/2样品, 在Ce4+—O2-的电荷迁移激发中,只有强激发带(~35700cm-1)与Eu3+离子间存在能量传递,而弱激发带 (~29400cm-1)只是引起Ce4+—O2-的电荷迁移发射;在Sr2-xEuxCeO4+x/2样品吸附水后,Eu3+的线状吸收跃迁强度显著增加, Ce4+—O2-两个激发带均向Eu3+离子传递能量. Ce4+—O2-强激发带通过交换作用向Eu3+离子传递能量,而弱激发带与Eu3+离子间的能量传递机理是非辐射多极子近场力的相互作用. 关键词: 2-xEuxCeO4+x/2')" href="#">Sr2-xEuxCeO4+x/2 发光性质 能量传递 吸附水  相似文献   

15.
采用高温固相法制备了LiBaBO3:Eu2+绿色发光材料.测量了Eu2+浓度为1mol%时样品的激发与发射光谱,其发射光谱为双峰宽谱,主峰分别为482和507nm,与理论计算值符合很好;监测482nm发射峰时,对应激发光谱的峰值为287和365nm,监测507nm发射峰时,对应的激发峰为365和405nm.研究了Eu2+浓度对材料发射光谱的影响,结果显示,随Eu2+浓度的增大,蓝、绿发射峰均发生了  相似文献   

16.
Eu2+-doped Sr3Al2O6 (Sr3−xEuxAl2O6) was synthesized by a solid-state reaction under either H2 and N2 atmosphere or CO atmosphere. When H2 was used as the reducing agent, the phosphor exhibited green emission under near UV excitation, while CO was used as the reducing agent, the phosphor mainly showed red emission under blue light excitation. Both emissions belong to the d-f transition of Eu2+ ion. The relationship between the emission wavelengths and the occupation of Eu2+ at different crystallographic sites was studied. The preferential substitution of Eu2+ into different Sr2+ cites at different reaction periods and the substitution rates under different atmospheres were discussed. Finally, green-emitting and red-emitting LEDs were fabricated by coating the phosphor onto near UV- or blue-emitting InGaN chips.  相似文献   

17.
In this work, we report the high temperature solid-state synthesis of red phosphors Sr2MgSi2O7: Eu3+ with various Eu3+ concentrations. Their luminescent properties at room temperature are investigated. The X-ray diffraction patterns indicate that the red phosphors powder conforms to the tetragonal Sr2MgSi2O7. Impurity structure appears when more than 20% Eu3+ is doped. The samples show a strong emission line at 615 nm and the intensity increases with the increase of Eu3+ concentration until concentration quenching occurs. Charge compensation assists in the reduction of the impurity structure and vacancies; hence the luminescent intensity is enhanced. The decay measurement indicates that the lifetime of Eu3+ emission is about 2-3 ms. Some of the Eu3+ can be reduced to Eu2+; this is also discussed.  相似文献   

18.
This paper reports the photoluminescence and afterglow behavior of Eu2+ and Eu3+ in Sr3Al2O6 matrix co-doped with Dy3+. The samples containing Eu2+ and Eu3+ were prepared via solid-state reaction. X-ray diffraction (XRD), photo luminescent spectroscope (PLS) and thermal luminescent spectroscope (TLS) were employed to characterize the phosphors. The comparison between the emission spectra revealed that Sr3Al2O6 phosphors doped with Eu2+, Dy3+ and Eu3+, Dy3+ showed different photoluminescence. The phosphor doped with Eu3+, Dy3+ showed an intrinsic f-f transition generated from Eu3+, with two significant emissions at 591 and 610 nm. However, the phosphor doped with Eu2+, Dy3+ revealed a broad d-f emission centering around 512 nm. After the UV source was turned off, Eu2+, Dy3+ activated Sr3Al2O6 phosphor showed excellent afterglow while Eu3+, Dy3+ activated phosphor almost showed no afterglow. Thermal simulated luminescence study indicated that the persistent afterglow of Sr3Al2O6: Eu2+, Dy3+ phosphor was generated by suitable electron traps formed by the co-doped rare-earth ions (Dy3+) within the host.  相似文献   

19.
The Eu2+and Dy3+ activated Sr3Al2O6 (S3A2O-ED) nanophosphors were synthesized by a new microwave method. The S3A2O-ED sample calcined in microwave oven at around 650 °C for 20 min possesses a cubic Sr3Al2O6 single phase. The sample showed small size (80–100 nm) and spherical shape. The excitation and emission spectra indicated that excitation broad band chiefly sited in visible range and the nanophosphors emitted strong light at 611 nm under around 473 nm excitation. Comparing with conventional method, the microwave synthesis of S3A2O-ED greatly decreased the calcining temperature and time. However, the brightness of S3A2O-ED nanophosphors was reduced. The change of luminescent intensity in S3A2O-ED nanophosphors could be attributed to the effect of surface energy.  相似文献   

20.
采用高温固相法制备了Ca2SiO4:Dy3+发光材料.在365nm紫外光激发下,测得Ca2SiO4:Dy3+材料的发射光谱为一多峰宽谱,主峰分别位于486nm,575nm和665nm处;监测575nm发射峰,测得材料的激发光谱为一多峰宽谱,主峰分别位于331nm,361nm,371nm,397nm,435nm,461nm和478nm处.研究了Dy3+掺杂浓度对Ca2SiO4:Dy3+材料发射光谱及发光强度的影响,结果显示,随Dy3+浓度的增大,黄、蓝发射峰强度比(Y/B)逐渐增大,利用Judd-Ofelt理论解释了其原因;随Dy3+浓度的增大,Ca2SiO4:Dy3+材料发光强度先增大,在Dy3+浓度为4 mol%时到达峰值,而后减小,根据Dexter理论其浓度猝灭机理为电偶极-电偶极相互作用.研究了电荷补偿剂Li+,Na+和K+对Ca2SiO4:Dy3+材料发射光谱的影响,结果显示,不同电荷补偿剂下,随电荷补偿剂掺杂浓度的增大,Ca2SiO4:Dy3+材料发射光谱强度的演化趋势相同,即Ca2SiO4:Dy3+材料发射峰强度先增大后减小,但不同电荷补偿剂下,材料发射峰强度最大处对应的补偿剂浓度不同,对应Li+,Na+和K+时,浓度分别为4mol%,4mol%和3mol%. 关键词: 白光LED 2SiO4:Dy3+')" href="#">Ca2SiO4:Dy3+ 发光特性 电荷补偿  相似文献   

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