254 resultados para LAPO4-CE
Resumo:
Ce3+ and/or Tb3+ doped LaPO4 nanofibers and microbelts have been prepared by a combination method of sol-gel process and electrospinning. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), photoluminescence (PL), low voltage cathodoluminescence (CL) and time-resolved emission spectra as well as kinetic decays were used to characterize the resulting samples. SEM and TEM results indicate the as-formed precursor fibers and belts are smooth. and the as-prepared nanofibers and microbelts consist of nanoparticles. The doped rare-earth ions show their characteristic emission under ultraviolet excitation, i.e. Ce3+ 5d-4f and Tb3+ D-5(4)-F-7(j) (J = 6-3) transitions, respectively. The energy transfer process from Ce3+ to Tb3+ in LaPO4:Ce3+, Tb3+ nanofibers was further studied by the time-resolved emission spectra.
Resumo:
利用溶胶-凝胶法合成了一系列稀土离子掺杂的发光薄膜,包括三元氧磷灰石稀土硅酸盐Ca2RS(SiO4)6O2(R=YGd)体系,YVO4体系,LaPO4体系以及钒磷酸盐形成的固熔体体系1并研究了稀土离子Eu3+,Tb3+,Dy3+,Sm3+,Er3+和类汞离子Pb2+在这些薄膜中的发光性质和能量传递性质。同时利用软石印法结合毛细管微模板技术实现了发光薄膜的图案化。SEM以及AFM结果表明,利用溶胶一凝胶法制备的发光薄膜表面致密均匀,无开裂。通过增加镀膜溶液的粘度、镀膜的次数可以有效的控制薄膜的厚度,使其达到理想的范围。由此可见溶胶一凝胶法是一种比较理想的制备发光薄膜的方法。在三元氧磷灰石稀土硅酸盐Ca2R8(SiO4)6O2(R=YGd)体系中,稀土离子Eu3+,Tb3+在Ca2Y8(SiO4)6O2基质中占据低刘·称性格位6h(Cs)和4f(C3),并以其特征的红光发射(5Do-7F2)和绿光发射(5D4-7F5)为主。Eu3+,Tb3+发光的最佳浓度分别为Y3+的10mol%和6mol%,Ca2Y8(51O4)6O2:Eu3+薄膜样品的发光强度和寿命随着烧结温度的升高而增加,Ca2Y8(SiO4)6O2:Tb3+薄膜样品的发光强度和寿命在800℃时最大,随后又随烧结温度的升高有所下降,Pb2+可以敏化Ca2Gd8(SiO4 )6O2中Gd3+的基质晶格,通过Pb2+→Gd3十→(Gd3+)n→A3+形式传递和转移能量。在YVO4体系中,利用Pechini溶胶一凝胶法以无机盐为主要原料,柠檬酸为络合剂,利用聚乙二醇调节镀膜溶液的粘度,制备了YvO4:A(A=Eu3+ Dy3+,Sm3+,Er3+)纳米发光薄膜。结合软石印法,通过简单工艺实现了发光薄膜图案化烧结过程中图案化薄膜有一定程度的收缩,存在一定的缺陷。得到的条纹在紫外灯下发出明亮的红光。掺杂的稀土离子在YVO4薄膜中显示它们特征发射,同时VO43-和稀土离子之间存在能量传递。Dy3+,Sm3+,Er3十发光的最佳浓度皆为Y3+的2mol%,这三者的发光淬灭是由交叉驰豫引起的。在LaPO4发光薄膜中,Etl3+以591nm的5Do-7Fl跃迁发射为主,呈现红橙光;Tb3+以543nm的5D4-7F5发射为主,属于绿光发射。Ce3+则由其特有的5d-4f双峰发射组成。Tb3+和Eu3+掺杂的样品发光强度和荧光寿命随烧结温度的升局而增加。Tb3+和Eu3+的寿命曲线符合指数衰减,但Tb3十在LaPO4:Ce,Tb薄膜中,所得的寿命曲线不符合单指数衰减。Ce3+和Tb3+之间存在吸收能量传递。通过计算得到能量传递效率可以达到95%以上。XRD结果表明,从x=0到x=1 YVxP1-xO4:Eu3+薄膜形成了一系列具有错石结构的固熔体。在YVxP1-xO4:Eu3+(0≤x≤1)系列薄膜中,随着x值的增加,Eu3+的发光强度和红橙比逐渐增大。除x=0,其它的Eu3+的红橙比都大于1,说明在发射光谱中,以Eu3+禁戒5Do一7F2电偶极跃迁为主,Etls十在基质中处于低对称性格位。当x=0时,即Y0.98Eu0.l2PO4薄膜中,Eu3+,仍处于D2d低对称性格位,但5D0一7FI橙光发射却比SD0一7F2红光发射强。x对Y0.98Eu0.02VxP1-xO4(0≤x≤l)薄膜寿命曲线有很大的影响,当0≤x≤0.5时,Eu3+5 D0-7F2发射呈单指数衰减;当x≥0.6时,Eu3+5D0-7F2发射的衰减曲线比较复杂,不能用单指数拟合。YVxP1-xO4:A3+(0≤x≤1,A=Er,Sm)薄膜中,由于存在VO43-A3+,以及VO43-(VO43-)n-A3+(n≥1)形式的能量传递,同时由于浓度淬灭,VO43-的蓝光发射在0.1≤x≤1范围内,随x的增加而减弱,当x=1时,VO43-的蓝光发射被完全淬灭,而A3+发光强度随x的增加而增加。在RVO4:A3+(R=Y,La,Gd,A=Eu,Sm,Er)纳米发光薄膜中,R对稀土离子发光性质的影响主要是由于基质晶体结构的不同。A3+在YVO4和GdVO4中属于D2d对称性,在YVO4和GdVO4薄膜中A3+的光谱性质基本相同,而LaVO4属于单斜晶系,具有独居石结构。A3+在LaVO4中属于C1对称性。C1对称性比D2d对称性低,A3+的发光光谱中谱线的位置以及谱线的劈裂数目都略有不同。由于Gd3+和发光离子之间的能量传递,A3+在GdVO4基质中的发光最强。
Resumo:
Uniform lanthanide orthophosphate LnPO(4) (Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho) nanoparticles have been systematically synthesized via a facile, fast, efficient ultrasonic irradiation of inorganic salt aqueous solution under ambient conditions without any surfactant or template. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), photoluminescence (PL) spectra as well as kinetic decays were employed to characterize the samples. The SEM and the TEM images show that the hexagonal structured lanthanide orthophosphate LnPO(4) (Ln = La, Ce, Pr, Nd. Sm, Eu, Gd) products have nanorod bundles morphology, while the tetragonal LnPO(4) (Ln = Tb, Dy, Ho) samples prepared under the same experimental conditions are composed of nanoparticles. HRTEM micrographs and SAED results prove that these nanostructures are polycrystalline in nature.
Resumo:
Thin film phosphors with compositions of RP1-xVxO4: A (R = Y, Gd, La; A = Sm3+, Et3+; x = 0, 0.5, 1) have been prepared by a Pechini sol-gel process. X-Ray diffraction, atomic force microscopy (AFM), photoluminescence excitation and emission spectra were utilized to characterize the thin film phosphors. The results of XRD showed that a solid solution formed in YVxP1-xO4: A film series from x = 0 to x = 1 with zircon structure, which also held for GdVO4: A film. However, LaVO4: A film crystallized with a different structure, monazite. AFM study revealed that the phosphor films consisted of homogeneous particles ranging from 90 to 400 nm depending on the compositions. Upon short ultraviolet excitation, the films exhibit the characteristic Sm(3+ 4)G(5/2)-H-6(J) (J=5/2, 7/2, 9/2) emission in the red region and Er3+ H-2(11/2), S-4(3/2)-I-4(15/2) emission in the green region, respectively With the increase of x values in YVxP1-xO4: SM3+ (Er3+) films, the emission intensity Of SM3+ (Er3+) increases due to the increase of energy transfer probability from VO43- to Sm3+ (Er3+). Due to the structural effects, the Sm3+ (Er3+) shows similar spectral properties in YVO4 and GdVO4 films, which are much different from those in LaVO4 film.
Resumo:
The room temperature creep behaviors of Ce-based bulk metallic glasses were examined by the use of nanoindentation. The creep rate and creep rate sensitivity of Ce-based BMGs were derived from indentation creep curves. The low creep rate sensitivity of Ce-based BMGs indicates that the room temperature creep is dominated by localized shear flow. The experimental creep curves can be described by a generalized Kelvin model. Furthermore, the creep retardation spectrum is calculated for the Ce-based metallic glasses. The results showed that creep retardation spectrum consists of two relatively separated peaks with the well defined characteristic relaxation times.
Resumo:
The strain rate dependence of plastic deformation of Ce60Al15CU10Ni15 bulk metallic glass was studied by nanoindentation. Even though the ratio of room temperature to the glass transition temperature was very high (0.72) for this alloy, the plastic deformation was dominated by shear banding under nanoindentation. The alloy exhibited a critical loading rate dependent serrated flow feature. That is, with increasing loading rate, the alloy exhibited a transition from less prominent serrated flow to pronounced serrated flow during continuous loading but from serrated to smoother flow during stepped loading.
Resumo:
An improved two-dimensional space-time conservation element and solution element ( CE/ SE) method with second-order accuracy is proposed, examined and extended to simulate the detonation propagations using detailed chemical reaction models. The numerical results of planar and cellular detonation are compared with corresponding results by the Chapman-Jouguet theory and experiments, and prove that the method is a new reliable way for numerical simulations of detonation propagation.
Resumo:
The deformation behavior and the effect of the loading rate on the plastic deformation features in (numbers indicate at.%) Ce60Al15Cu10Ni15, Ce65Al10Cu10Ni10Nb5, Ce68Al10Cu20Nb2, and Ce70Al10Cu20 bulk metallic glasses (BMGs) were investigated through nanoindentation. The load-displacement (P-h) curves of Ce65Al10Cu10Ni10Nb5, Ce68Al10Cu2, and Ce70Al10Cu20 BMGs exhibited a continuous plastic deformation at all studied loading rate. Whereas, the P-h curves of Ce60Al15Cu10Ni15 BMG showed a quite unique feature, i.e. homogeneous plastic deformation at low loading rates, and a distinct serrated flow at high strain rates. Moreover, a creep deformation during the load holding segment was observed for the four Ce-based BMGs at room temperature. The mechanism for the appearance of the "anomalous" plastic deformation behavior in the Ce-based BMGs was discussed. (c) 2006 Elsevier B.V. All rights reserved.
Resumo:
The viscoelastic deformation of Ce-based bulk metallic glasses (BMGs) with low glass transition temperature is investigated at room temperature. Contact stiffness and elastic modulus of Ce-based BMGs cannot be derived using the conventional Oliver-Pharr method [W. C. Oliver and G. M. Pharr, J. Mater. Res. 7, 1564 (1992)]. The present work shows that the time dependent displacement of unloading segments can be described well by a generalized Kelvin model. Thus, a modified Oliver-Pharr method is proposed to evaluate the contact stiffness and elastic modulus, which does, in fact, reproduce the values obtained via uniaxial compression tests. (c) 2007 American Institute of Physics.
Resumo:
利用纳米压入技术研究了Ce基大块非晶合金的变形行为,以及加载速率对塑性变形行为的影响规律.结果表明,Ce基大块非晶合金在纳米压入过程中表现出的变形行为与其他体系大块非晶有显著差别.Ce60Al15Cu10Ni15合金在低加载速率下为连续的塑性变形,在高加载速率下表现出显著的锯齿流变特征;而Ce65Al10Cu10Ni10Nb5合金,在所研究的加载速率范围内均为连续的塑性变形.但是,这两种合金都出现了室温蠕变现象.另外,探讨了Ce基大块非晶合金的反常塑性变形行为的产生机理.
Resumo:
通过提出一种新的守恒元和解元划分方式对二维时-空守恒元解元算法(CE/SE)进行了改进,推导了改进CE/SE算法的一、二阶精度计算格式,并给出了更高阶精度计算格式的构造方法。利用得到的改进CE/SE格式对激波反射问题、后台阶扰流问题及隔墙坑道传播问题进行了数值模拟。数值结果表明,对CE/SE算法的改进是成功的。改进CE/SE算法有诸多优点,值得在数值模拟中推广使用。
Resumo:
将CE/SE方法推广到二维固体流体弹塑性问题的数值计算,同时结合杂交粒子水平集方法追踪物质界面和合适的边界条件,提出一套完整的二维Euler型流体弹塑性计算方案.通过长钨杆侵彻装甲钢实验的数值模拟,对方法的精度和有效性进行验证.
Resumo:
<正>时-空守恒元解元方法(space-timeconservationelementandsolutionelementmethod,CE/SE)是近年来兴起的一种全新的守恒方程型方程计算方法。它最早由NASALewis研究中心的Chang于1995年提出来的。这种方法从根本上区别于传统的方法:它将时间和空间统一起来同等对待;利用守恒
Resumo:
时-空守恒元解元方法是近年来兴起的一种全新的高分辨率守恒方程型方程计算方法。它具有物理概念清晰,计算精度高和格式构造简单等优点,是一种具有广阔发展前景的计算流体力学方法。本文介绍了CE/SE方法的基本理论、格式构造、发展历史、应用情况和最新进展,并指出了应解决的问题和发展方向。