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Divalent europium-activated chlorosilicate Ca6Sr4(Si2O7)3Cl2:Eu2+ phosphors were synthesized by a conventional solid-state reaction under reductive atmosphere. These phosphors can be efficiently excited by UV–visible light from 320 to 420 nm, which matches that of a near UV-emitting InGaN chip. Under the 360 nm excitation, Ca6Sr3.97(Si2O7)3Cl2:0.03Eu2+ phosphor shows a strong and broad emission centering at 515 nm, which is attributed to the 5d→4f transition of Eu2+ ion. The mechanism of concentration quenching was determined to be the dipole–dipole interaction and the critical energy-transfer distance of Eu2+ was calculated as 3.31 nm. The CIE chromaticity coordinates of Ca6Sr3.96(Si2O7)3Cl2:0.03Eu2+ phosphor are (0.127, 0.770) according to the emission spectrum. It can be expected that Ca6Sr4(Si2O7)3Cl2:Eu2+ phosphor is a promising candidate as the green component for near-ultraviolet InGaN-based white LED. 相似文献
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采用高温固相法合成Sr4-xCaxSi3O8Cl4:Eu^2+荧光材料,利用Van Uitert公式讨论Sr4-xCaxSi3O8Cl4:Eu^2+中yEu^2+的晶格环境和发光特性,确定晶体中有蓝色和黄绿色两种发光中心,并讨论了它们与光谱结构的对应关系。当0〈x〈0.5,Ca^2+固溶入Sr4Si3O8Cl4基质晶格,Eu^2+占据八配位Si^2+格位,晶体主要产生蓝色中心的蓝绿色发射;当0.5〈x〈2,较大的Ca^2+掺杂使晶胞参数变小,品格中的杂质束缚激子态的束缚增强,Eu^2+处于杂质束缚激子中心所形成的激发态能量进一步降低,发射位于长波段方向并具有较大的Stokes位移,Sr4-xCaxSi3O8Cl4:yEu^2+主要产生黄绿色中心的黄绿色发射光。 相似文献
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Here we reported photoluminescence properties of Eu2+ activated in novel and existing MgXAl10O17 (X = Sr, Ca) phosphor which has been prepared by combustion synthesis at 550 °C under UV and near UV excitation wavelength. The PL emission properties of MgSrAl10O17:Eu2+ were monitored at 254 nm and 354 nm respectively keeping emission wavelength at 469 nm. Whereas novel MgCaAl10O17:Eu2+ exhibit emission band at 452 nm keeping excitation at 378 nm. These blue emission corresponds to 4f65d1 → 4f7 transition of Eu2+ ions. Further phosphor was analyzed by XRD for the confirmation of desired phase and purity. 相似文献
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采用高温固相法制备了一种新型的白光LED用Ca3Si2O4N2∶Eu2+,Ce3+,K+荧光粉。利用X射线衍射仪对样品的物相结构进行了分析,结果表明:Ce3+和K+离子的掺杂没有改变Ca3Si2O4N2∶Eu2+荧光粉的主晶相。利用荧光光谱仪对样品的发光性能进行了测试,发现样品在355 nm激发下得到的发射光谱为峰值位于505 nm的单峰,是Eu2+离子5d-4f电子跃迁引起的。Ca3Si2O4N2∶Eu2+荧光粉通过Ce3+和K+离子的掺杂,发光明显增强。当Ce3+的摩尔分数为1%时,荧光粉的发光强度达到最大值,是单掺Eu2+离子荧光粉发光强度的168%。通过光谱重叠的方法计算Ce3+→Eu2+能量传递临界的距离为2.535 nm。 相似文献
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In this article, we have reported emission characteristics of Eu2+ activated Sr12Al10.6Si3.4O32Cl5.4 and Ca12Al10.6Si3.4O32Cl5.4 phosphors, prepared by combustion synthesis. The PL excitation was monitored at two different wavelengths 254 nm (mercury excitation) and 354 nm (mercury free excitation), which shows broad-blue emission bands at 432 nm, and 438 nm for 354 nm excitation wavelength. Under mercury excitation at 254 nm it shows emission wavelengths at 470 nm, 589 nm, 592 nm, and 617 nm for the prepared Sr12Al10.6Si3.4O32Cl5.4 and Ca12Al10.6Si3.4O32Cl5.4 phosphors. Further it was characterized by XRD, for the investigation of phase and purity of the phosphors. Thermal degradation of the phosphors was also studied at different temperatures. 相似文献
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Sr9Ca(PO4)6Cl2:Eu2+晶体中的两种发光中心 总被引:2,自引:0,他引:2
Sr9Ca(PO4)6Cl2:Eu2+是一种性能良好效率较高的发光材料.作者合成并生长了Sr9Ca(PO4)6Cl:Eu2+的单晶体.从晶体的结构测定和光谱学研究,确证了晶体中存在有两种发光中心,即Eu(Ⅰ)中心和Eu(Ⅱ)中心. 相似文献
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Ca$lt;sub$gt;2$lt;/sub$gt;Si(O$lt;sub$gt;4-$lt;i$gt;x$lt;/i$gt;$lt;/sub$gt;N$lt;sub$gt;$lt;i$gt;x$lt;/i$gt;$lt;/sub$gt;):Eu$lt;sup$gt;2+$lt;/sup$gt;绿色荧光粉的制备及其发光性能 下载免费PDF全文
利用在Ca-Si-O干凝胶前驱体中添加Si3N4的方法于非还原气氛下合成了含N固溶体Ca2Si(O4-xNx):Eu2+绿色荧光粉. 通过X射线衍射仪、扫描电子显微镜以及荧光分光光度计分别分析了产物的物相结构、颗粒形貌和发光性能. 结果显示,Si3N4与前驱体的混合物在非还原气氛(纯氮气)下于1100℃焙烧后获得含N固溶体Ca2Si(O4-xNx):Eu2+荧光粉,特别是其中Eu3+被还原为Eu2+,产物的晶体结构与βup -Ca2SiO4相一致. Ca2Si(O4-xNx):Eu2+能够被270–400 nm 范围内的紫外线有效激发,其发射光谱呈宽带发射. 随着N含量的增加,发射峰出现一定程度红移(501–504 nm),而且发光强度显著提高. 当Eu2+浓度为0.25 mol%时发光强度达最大值,浓度超过0.25 mol%时,发光强度显著降低,出现浓度猝灭 效应.
关键词:
白光LED
荧光粉
溶胶凝胶法
3N4')" href="#">Si3N4 相似文献
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The luminescence of SrAl12O19: Eu2+ consists of a 5d—4f broad-band emission and of 4f—4f lines, their relative intensities being strongly dependent on temperature. At 77°K mainly line emission is observed. 相似文献
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Abstract With increasing X on Ca1-xSrxF2 mixed crystals doped with Eu2+ (4f65d) ions, the absorption peak shifted linearly to that of SrF2:Eu, while the luminescence one moved parabolically with a minimum at around x=0.5. The linewidth broadened nearly twice as large as that of CaF2 in the vicinity of x=0.5 and subsequently renarrowed for x > 0.5. The temperature dependences of the luminescence intensity and life time revealed that the nonradiative activation energy has a minimum of 0.40 eV around x=0.5. From the calculated result of the lineshape, these non-linear behaviors against x were explained by adjusting the electron-phonon coupling strength. 相似文献
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Xinguo Zhang Jilin Zhang Zhiyue Dong Jianxin Shi Menglian Gong 《Journal of luminescence》2012,132(4):914-918
A piece-shaped phosphor Ca2BO3Cl: Eu2+ was synthesized by solid-state reaction method. This phosphor exhibited wide absorption in ultra-violet and visible range, and bright yellow emission band centering at 570 nm. The concentration quenching mechanism was verified to be a dipole–dipole interaction, and its critical transfer distance was about 17 Å by both calculated crystal structural method and experimental spectral method. This phosphor has a good thermal stability with a quenching temperature (T1/2) of 200 °C. Yellow and white LEDs were fabricated with this phosphor and near UV chips, and the yellow LED has a high color purity of 97.0% and promising current tolerant property, while the white LED shows a luminous efficiency of 11.68 lm/W. 相似文献
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Published in Zhurnal Prikladnoi Spektroskopii, Vol. 62, No. 4, pp. 30–37, July–August, 1995. 相似文献
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采用化学自燃烧法制备了不同Ag+掺杂浓度的Y2O3:Eu纳米晶体粉末样品([Y3+]:[Eu3+]:[Ag+]=99:1:X,X=0-3.5×10-2),以及通过退火处理得到了相应的体材料.根据X射线衍射谱确定所得纳米和体材料样品均为纯立方相.实验表明在纳米尺寸样品中随着Ag离子浓度的增加,荧光发射强度随之增加,当X=2×10-2时达到最大值,其发光强度比X=0时提高了近50%.当Ag离子浓度继续增加,样品发光强度保持不变.在相应的体材料样品中则没有观察到此现象.通过对各样品的发射光谱,激发光谱,X射线衍射图谱,透射电镜(TEM)照片和荧光衰减曲线的研究,分析了引起纳米样品荧光强度变化的原因是由于Ag离子与表面悬键氧结合,从而使这一无辐射通道阻断,使发光中心Eu3+的量子效率提高;Ag+的引入所带来的另一个效应是使激发更为有效.这两方面原因使发光效率得到了提高. 相似文献
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《Current Applied Physics》2009,9(3):618-621
Eu3+ doped SrAl2B2O7 phosphors were fabricated by the wet method. The structures of the phosphors were characterized by XRD. The doping content of Eu3+ ions in SrAl2B2O7:Eu3+ phosphors are 1%, 4%, 6%, 8%, 10% (molar fraction), respectively. Luminescence properties were analyzed by measuring the excitation and photoluminescence spectra. The luminescent properties of SrAl2B2O7:Eu3+ phosphors are discussed. It is shown that from 4% to 6% of doping content of Eu3+ ions under 392 nm excitation in SrAl2B2O7:Eu3+ phosphors is optimum. 相似文献
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BaMg2Si2O7:Eu3+和BaMg2Si2O7:Tb3+发光材料的合成及发光特性的研究 总被引:1,自引:1,他引:1
本文报道了首次合成的稀土离子激活的BaMg2Si2O7:Eu3+和BaMg2Si2O7:Tb3+光致发光材料,通过正交设计实验,确定了基质的最佳配比、烧结温度,探讨了影响材料发射强度的一些因素,测定了两种材料的发射光谱和激发光谱,对其发光性能也进行了分析和研究。 相似文献
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利用高温固相法制备了Eu3+掺杂的La2Mo2O9红色荧光粉,并对这种荧光粉的结构及发光性质进行了研究。XRD结果表明,实验合成了单一立方相的La2Mo2O9荧光粉体。该荧光粉的激发光谱由一宽带和一系列的锐峰组成;发射光谱由一系列锐峰组成,这些都与Eu3+的特征跃迁5DJ(J=0,1)和7FJ(J=1~4)相对应。结果表明该荧光粉可被395nm的紫外光和470nm的可见光有效激发,并发出峰值位于620nm左右的红光,亮度可达到传统红色荧光粉Y2O2S:Eu3+的1.5倍以上,这表明它可以作为蓝+黄模式白光LED的红色补光粉,也可以作为UV-LED激发三基色荧光粉体系中的红色荧光粉。研究了Eu3+的掺杂浓度以及不同助熔剂对样品发光性质的影响。Eu3+的摩尔分数为0.3时,发光强度达到最强。质量分数为3%的NH4Cl作为助熔剂时效果最好。 相似文献
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Eu2+掺杂浓度对BAM光谱特性的影响 总被引:1,自引:1,他引:1
采用燃烧法在低温成功合成了纳米Ba1-xMgAl10O17:xEu2 (0.05≤x≤0.4)蓝色荧光粉,着重研究了Eu2 掺人量对荧光粉光谱特性的影响.利用XRD和SEM对材料的物相和形貌进行了分析,采用荧光光谱仪测定了样品的发光特性.结果表明,合成的产物为纯相,且颗粒细小、分布均匀,平均粒径约30 nm.Eu2 的掺杂浓度对样品的发光性能有显著的影响,随Eu2 浓度增大,发光中心增多,Eu2 离子间相互作用增强,能量传递加快,发光强度逐渐增大.当Eu2 浓度为x=0.2时,能量传递速率与发射速率相等,Euz 的发光达到最大值;此后,随Eu2 的浓度进一步增加,Eu2 之间的能量传递速率将超过发射速率,Eu2 还未将光发射出去就发生能量的传递,使激发能通过晶格的迁移而消耗,呈现浓度猝灭特性. 相似文献
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采用CaCl2作助熔剂同时又作反应物,利用固相法在碳还原气氛下合成了Ca2MgSi2O7:Eu2+发光粉,确定其最佳的合成条件为按CaCO3、Mg(OH)2、SiO2、CaCl2的量的比1.5:1:2:2.4称取原料,烧结温度为900℃,烧结时间为3h。合成的样品可被360~480nm的光有效激发,得到发射峰值位于529nm的绿光。该发光粉Eu2+的最佳掺杂摩尔分数为0.02。与高温法相比,低温法制备的Ca2MgSi2O7:Eu2+发光粉激发光谱形状表现出一些差别,并且发射光强度显著增强,低温制备的Ca2MgSi2O7:0.02Eu2+的发射强度是高温制备样品的261%。 相似文献
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采用化学共沉淀法一次煅烧工艺合成了BaAl2Si2O8:Eu2+蓝色荧光粉.用X射线衍射仪和荧光分光光度计等对BaAl2Si2O8:Eu2+蓝色荧光粉的相结构、发光性能进行了测试.结果表明:化学共沉淀法一次煅烧工艺合成的BaAl2Si2O8:Eu2+蓝色荧光粉为单相;其激发光谱分布在240-410 nm的波长范围,峰值位于320 nm处,可以被InGaN管芯产生的350-410 nm辐射有效激发;在365 nm近紫外光的激发下,测得其发射光谱是位于465 nm附近的宽带峰.BaAl2Si2O8:Eu2+蓝色荧光粉的发光强度随Eu2+浓度的增大逐渐加强,当Eu2+掺杂的摩尔分数为3.5%时,发光强度达到最大值,而后随掺杂浓度的增加而减小,发生浓度猝灭;根据Dexter能量共振理论,该浓度猝灭是由于Eu2+的离子间交换相互作用引起的. 相似文献