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1.
Abstract

The fluorescence spectra of Y2O3:Eu3+ nanoparticles have been measured under the pressure of up to 78 kbar at room temperature. In this pressure range, a red-shift of 0.02(1) nm/kbar?1 is noticed for the 0–2 line (5D07F2 transition). This shift is explained by the change of negative charge of the surrounding ligands. Compatibility between measured and calculated values for the 0–2 line position was obtained. The luminescence decay curves of the 5D07F2 transition were studied up to 78 kbar and were found to behave exponentially for all pressures studied. The fluorescence lifetime τ for the 0–2 line (5D07F2 transition) slowly decreased with pressure. The pressure effect on τ for the 0–2 line (5D07F2 transition) was explained by a model which considers the pressure effect on the line position, inter-ionic distance, ion volume and polarizability, molecular volume and polarizability, molecular refractive index and the refractive index medium n med of the surrounding hydrostatic medium. The fluorescence lifetime calculated by the present model is in close correspondence with the experimental values.  相似文献   

2.
采用溶胶凝胶法制备了Sr3Al2O6: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Sr3Al2O6,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Sr3Al2O6:Eu2+和Sr3Al2O6:Eu2+,Dy3+的激发光谱均为激发峰位于473 nm的宽带谱.Sr3Al2O6:Dy3+的发射峰位于530.1 nm,对应于Dy3+代替Sr2+位置后基质中形成的施主-受主对Dy·Sr-V″Sr的重新组合.Sr3-0.02-yAl2O6:0.02Eu2+,yDy3+(0相似文献   

3.
采用高温固相法合成发光样品Y2O3:Eu3+0.01和Y2O3:Eu3+0.01,Dy3+0.01.X射线衍射分析(XRD)表明样品保持Y2O3晶格结构,掺入的Eu3+和Dy3+对Y2关键词: 长余辉 2O3')" href="#">Y2O3 稀土掺杂 陷阱  相似文献   

4.
以甘氨酸为燃料,采用溶液燃烧法制备了Y2O3:Eu3 (3%)纳米粉末,并研究了制备过程中前驱溶液的pH值对Y2O3:Eu3 发光性质的影响.从XRD和SEM分析得到,随着溶液pH值的增大,样品颗粒逐渐变大,并且多孔粉末变得越来越致密.通过对样品发光性质的测量得到,随着pH值的增大,样品发光逐渐增强,但寿命逐渐变短.激发谱显示,基质吸收和电荷迁移带的相对强度比随着pH值的增大逐渐减小.  相似文献   

5.
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7.
Pyrochlore‐structured yttrium titanate phosphors activated by trivalent europium ions (Y2Ti2O7(YT):Eu3+), with spherical morphology, were synthesized at different pH values by a solvothermal process. From the structural and morphological measurements, the annealing temperature had no effect on the spherical morphology of the YT:Eu3+ sample. The photoluminescence excitation and emission spectra were taken by activating the Eu3+ ions in the YT host lattice as functions of Eu3+ ion concentration and annealing temperature. The optimal doping concentration was found to be 4 mol%, exhibiting an excellent orange–red emission due to the highest intensity of the 5D07F1 transition. When the YT:Eu3+ phosphor was mixed with YAG:Ce3+ phosphor, a brilliant white light emission was achieved. (© 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

8.
The Eu3+ ion occupies two different crystallographic sites in (Y1−xEux)2O3 and (Gd1−xEux)2O3, with site symmetry S6 and C2. Energy transfer over more than 7 Å occurs from Eu3+ (S6) ions to Eu3+ (C2) ions. This is shown to be a direct one-phonon assisted process, in combination with a one-site resonant two-phonon assisted process at higher temperatures. For x = 1 there is energy migration over the Eu3+ (C2) sublattice to quenching impurities. The presence of cooperative absorption points to superexchange interaction between the Eu3+ ions.  相似文献   

9.
 在低温条件下分别用爆轰法和燃烧法制备出了SrAl2O4:Eu2+,Dy3+ 纳米发光粉。从合成条件、热处理温度等方面详细对比了爆轰法和燃烧法对所制备的SrAl2O4:Eu2+,Dy3+纳米发光粉的晶体生长行为、粒子形貌和光学性质等的影响。研究表明,随着热处理温度的升高,爆轰法制备的纳米发光粉的平均粒径逐渐增大,而燃烧法制备的纳米发光粉的平均粒径先减小后增大,在600 ℃时平均粒径存在一个极小值。在同样热处理温度下,爆轰法制备的纳米发光粉的平均粒径增长明显高于燃烧法合成的纳米发光粉的平均粒径。最后讨论了长余辉的发光机理,并给出了如何改进合成方法的建议。  相似文献   

10.
《Radiation measurements》2008,43(7):1191-1197
CaSO4:Dy is a well-known phosphor for radiation dosimetry using thermoluminescence. CaSO4:Eu, phosphors also find applications in radio-photoluminescence dosimetry and PLLCD. Various syntheses of these phosphors are described and optimum procedures are suggested. Effects of various preparation methods on luminescence characteristics are discussed in terms of elimination of unwanted impurities, grain size, etc.  相似文献   

11.
151Eu Mössbauer spectroscopy was applied to distinguish among different Eu microenvironments and phases in spherical Y2O3:Eu3?+? and core-shell Y2O3@Eu3?+? phosphor nanoparticles prepared by using homogeneous precipitation method. 151Eu isomer shift revealed that Eu atoms exist only in oxidation state Eu3?+? in all spherical and core-shell phosphors. Significant differences have been found between the Mössbauer parameters (isomer shift, principal component of EFG and linewidth) characteristic of spherical Y2O3:Eu3?+? and core-shell Y2O3@Eu3?+? phosphor nanoparticles. The Mössbauer parameters of spherical Y2O3:Eu3?+? were associated with Eu substituting Y in the Y2O3, while Mössbauer parameters of core-shell Y2O3@Eu3?+? phosphor were attributed to Eu being in the Eu2O3 shell, proving the structural model and the successful preparation of these phosphors.  相似文献   

12.
A novel hydrothermal approach for the preparation of europium(III)-doped yttrium oxide (Y2O3:Eu3+) nanocrystals was reported. The as-synthesized Y2O3:Eu3+ nanocrystals with diameter of about 5 nm are highly uniform and dispersed in water. The Y2O3:Eu3+ nanocrystals were characterized by high-resolution transmission electron microscopy and fluorescence spectroscopy. Due to their well dispersity in water, low toxicity, and good photoluminescence, the Y2O3:Eu3+ nanocrystals can potentially be used in high-definition displays and fluorescence probe in bioimaging.  相似文献   

13.
作者用燃烧法制备了8nm-50nm的系列纳米晶Y2O3:Eu3+,利用XRD谱确定了纳米晶的晶体结构及晶粒大小。利用两套由不同波长的激光所激发的拉曼光谱,指认了纳米晶Y2O3:Eu3+的拉曼振动模,研究其拉曼光谱。与传统的拉曼光谱学相比较,光谱呈现出明显的反常,其一,是斯托克斯与相对应的反斯托克斯谱峰波数不相等;其二,随晶粒的减小,拉曼谱有明显的变化,包括谱峰的微移、半高宽的增加,以及谱峰强度比的强烈变化;其三,随着激发波长的变化,光谱也呈现出峰位移动的明显变化。这些反常的散射光谱的变化源于纳米结构的本征缺陷。  相似文献   

14.
Sun LN  Meng QY  Feng XH  Zuo L  Yu CH  Ma L 《光谱学与光谱分析》2011,31(12):3218-3222
用沉淀法合成了Y10W2O21:Eu纳米发光材料,利用X射线衍射谱(XRD)和场发射扫描电镜(FE-SEM),对样品的结构和形貌进行了表征.测量了各样品的激发光谱、发射光谱,绘制了Eu3+发光的浓度猝灭图,计算了各样品的部分J-O参数和EC+5 D0能级量子效率,对Eu3+掺杂的Y10W2O21纳米发光材料的光致发光性...  相似文献   

15.
共掺杂效应对Y2O3:Eu3+和Gd2O3:Eu3+发光影响的理论研究   总被引:2,自引:0,他引:2       下载免费PDF全文
张睿  顾牡  刘小林  刘冰洁 《发光学报》2007,28(3):383-388
通过在Y2O3:Eu3 和Gd2O3:Eu3 发光材料中掺入Li ,Mg2 ,Al3 等离子能有效地提高材料的发光强度,根据分子动力学和密度泛函计算的结果,认为这些离子多倾向于形成C2格位附近的间隙缺陷对,导致部分Y(Gd)-O的键长增加,提高了材料的量子效率的同时使得激发峰位出现红移,是引起材料发光增强的一个原因.  相似文献   

16.
Large-scale spindle-like YVO4 particles with an euatorial diameter of 100–150 nm and a length of 300–350 nm were synthesized by utilizing the Y(OH)CO3 colloid spheres as the precursor and NH4VO3 as the vanadium source through a simple solution-based hydrothermal process, for the first time. In the first stage of the reaction, hierarchical flower-like YVO4 spheres were formed. Then, petals of spindle-like YVO4 particles were obtained via a following self-abscission process from these flower spheres. The possible formation mechanism has been discussed in detail. Moreover, the photoluminescent properties of spindle-like YVO4:Ln3+ (Ln=Eu, Dy) nanoparticles were investigated. They might have potential application in advanced flat panel display, minioptoelectronic devices, and biological labeling.  相似文献   

17.
SrAl2O4:Eu2+,Dy3+的上转换发光特性   总被引:1,自引:0,他引:1  
铕镝共掺的铝酸锶是一种新型的绿色长余辉荧光材料 ,经可见 -紫外光激发后 ,能发出超长时间的余辉。本文首次用 980nm的红外激发光源激发SrAl2 O4 :Eu2 ,Dy3 磷光体后 ,在室温下观测到了SrAl2 O4 :Eu2 ,Dy3 的绿色上转换荧光。并测得了其上转换荧光光谱图。与其正常的荧光光谱图相比 ,两者的峰形及波峰的位置有很大的差异 ,这预示着两者有不同的发光机理 ,并就其发光机理进行了初步的探讨。所用的样品经高温固相法合成后 ,用XRD表征。两种荧光光谱用荧光光谱仪测定。  相似文献   

18.
Ag+掺杂的立方相Y2O3:Eu纳米晶体粉末发光强度研究   总被引:2,自引:1,他引:2       下载免费PDF全文
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   

19.
为进一步提高Y2O2S:Eu^3+的发光性能,采用改善主要原材料Y2O3结晶性的方法,使Y2O2S:Eu^3+红色荧光粉在20kV和25kV下发光强度分别增强5%和10%,且不影响色度、粒度、粉体分散性等主要考核指标。提高了粉体的耐电压特性(发射强度与激发电压间的关系特性)。讨论和分析了发射强度增强、电压特性改善的原因:主要原材料Y2O3的结晶性的改善,使得合成的Y2O2S:Eu^3+具有更好的晶体质量,Eu^3+离子品场环境得到进一步改善,从而减弱了无辐射过程及因晶格畸变所造成的能量损失,发光效率得到增强,电压特性得刮改善。文验表明,获取高质量多晶Y2O3的最佳分解温度为1400℃左右。  相似文献   

20.
In this study we have synthesized Y2O3 (yttria) nanopowders with 1 % Nd3+ concentration by using a thermal decomposition method and investigated the effect of annealing temperature on the particle sizes and the effect of particle sizes on the spectroscopic properties of these systems. The particle sizes were effectively controlled by synthesis and annealing temperatures; the sizes were found to vary in the 15–290 nm range. The particle sizes and cubic phase of the yttria were determined by using XRD patterns and confirmed by SEM and TEM measurements. We note that the particle sizes increase by increasing the synthesis and annealing temperatures. Temperature dependence of the width and position of a selected spectral line were successfully fitted with the theoretical expressions. We studied thoroughly the behavior of the samples under pulsed excitation and give plausible explanations of the measured effects.  相似文献   

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