稀土掺杂碲铌锌系统玻璃的非线性光学性能

碲铌锌系统玻璃是一种性能优良的三阶非线性光学玻璃材料,综合品质优于其它非线性光学玻璃材料。在碲铌锌系统玻璃中引入稀土离子,利用其4f电子的跃迁提高谐波光子激发的可能性,从而提高玻璃的三阶光学非线性。研究表明,随着稀土离子的加入,532nm附近玻璃的光吸收明显增加,使由相同波长激光激发的光学非线性呈线性增长。掺入Ce3+、Ho3+、Y3+的玻璃三阶非线性极化率最高可达2.3×10-12esu。     

TeO2-Nb2O5系统玻璃的成玻性能研究

TeO2是一种线性和非线性光学性能优良、但无法单独形成玻璃的重金属氧化物玻璃系统,Nb2O5的引入有利于获得均匀而稳定的碲酸盐系统玻璃.研究发现,Nb2O5的引入会改变TeO2-Nb2O5系统玻璃中Te4 、Nb5 的配位数,进而对玻璃的结构和成玻能力、稳定性以及析晶性能均产生明显的影响.含有20-30wt%Nb2O5的碲酸盐系统玻璃表现出较好的综合品质.     

AgCl纳米晶掺杂铌碲酸盐系统非线性光学玻璃材料研究

铌碲酸盐非线性光学玻璃具有优良的三阶非线性光学效应,引入适量纳米晶体后,有望进一步提高玻璃的三阶非线性光学性能.本文采用在辅助电场诱导下的热处理方法在TeO2-Nb2O5-BaO-AgCl系统玻璃中析出AgCl纳米晶体,并研究了AgCl含量、热处理工艺及电场施加工艺对纳米晶析出和三阶非线性光学性能的影响.结果发现,在铌碲酸盐系统玻璃中引入0.1%～0.35%(质量分数)的AgCl,经热处理后可在玻璃中获得AgCl纳米晶体,而辅助电场提供的较小推动力可诱导更多的纳米晶体均匀析出,并且可以将其尺寸控制在20nm以下.采用辅助电场与热处理工艺相匹配的控制技术可以明显提高材料的三阶非线性光学性能.     

碲酸盐系统玻璃组成和结构对非线性光学性能的影响

碲酸盐系统重金属氧化物玻璃是一种优秀的非线性光学玻璃材料，具有较大的三阶非线性光学效应、超快光学响应、较宽红外透过范围、较好稳定性以及广泛应用前景。碲酸盐系统玻璃中的中间离子和网络外离子的加入会改变组成网络的配位多面体组成、键性和能带结构，进而影响玻璃的非线性光学性能。探讨了碲酸盐系统玻璃的网络结构，阐述了玻璃组成、结构以及纳米簇和非线性光学性能之间的相互关系。     

TeO2对氟铝酸盐玻璃性质和结构的影响

以10MgF2—20CaF2—10SrF2—10BaF2—15YF3—35AlF3氟铝酸盐玻璃为基玻璃引入不同含量的TeO2得到了新的氟碲铝酸盐玻璃．用差热分析方法研究了TeO2对氟铝酸盐玻璃性能的影响，通过拉曼光谱和红外吸收谱来研究玻璃的结构变化．差热分析表明TeO2的增加使玻璃开始析晶温度瓦升高，融化温度％降低，成玻璃能力增加．玻璃结构分析表明氟碲铝酸盐玻璃的结构中存在[FnAl-O—AlFn]、[TeO3]、[TeO2F]和[TeOF2]等多面体，这些多面体由F^-和O^2-离子连接．这种新的氟碲铝酸盐玻璃有着良好的成玻璃能力，在0．75～5．00μm范围内玻璃具有很高的透过率，是一种具有应用前景的新的红外光学玻璃材料．     

TeO2-Nb2O5-BaCl2-AlF3玻璃系统结构及光学性能研究

用传统熔融法制备了一种新型的氧卤碲酸盐玻璃:(80-x)TeO2-10Nb2O5-10BaCl2-xAlF3(x=10、20和30),用密度比重天平、玻璃热膨胀仪、棱镜耦合仪、显微拉曼光谱仪和红外-可见-紫外分光光度计研究了组分变化对物理性能、结构及光学性质的影响。研究结果表明,随着玻璃中AlF3含量增加,玻璃的密度和折射率减小;在Tg温度前,玻璃的平均线膨胀系数α减小;玻璃的热稳定性增强;玻璃结构中的双三角锥体[TeO4]和变形的双三角锥体[TeO3+1]以及三角棱锥体[TeO3]相对含量都相应减少;玻璃在紫外吸收边出现了蓝移现象,玻璃的直接和间接光学帯隙都增大。     

掺Er3+碲酸盐玻璃光谱性质和热稳定性的提高研究

用高温熔融法制备了摩尔组分百分比为70TeO2-20(ZnO、WO3,AlO1.5)-9NaO0.5-1ErO1.5的碲酸盐玻璃样品.测量了玻璃样品的吸收光谱和荧光光谱,用差热分析方法(DTA)测试了玻璃的热稳定性.结合Judd-Ofelt理论和McCumber理论分别计算得到了三种玻璃样品的强度参数Ω1(t=2,4,...     

掺铒TeO2-Nb2O5-ZnO系统玻璃的上转换发光性能

稀土离子掺杂碲酸盐系统玻璃是一类应用前景良好的上转换发光材料.研究了含铒TeO2-Nb2O5-ZnO系统玻璃在980nm抽运下的上转换光谱,结果发现存在3个上转换荧光谱带,分别对应于2H11/2→4I15/2、4S3/2→4I15/2和4F9/2→4I15/2,而且Er3 含量的增加可明显提高材料在530、550和660nm附近的发光性能.少量的ZnO引入既可以大幅提升材料的上转换发光强度,又能保持铌碲酸盐玻璃良好的化学稳定性.材料的发光机制主要是激发态吸收(ESA)和能量转移(ET),最大声子能量的降低是上转换发光增强的主要原因.     

TeO2-ZnCl2-BaO-NaF玻璃系统的结构及中红外透过特性的研究

制备了一种新型的氧卤碲酸盐玻璃：（80-x）TeO2—15ZnCl2-xBaO-5NaF（x=30、20、10、0mol％），对玻璃的机械强度、热稳定性、拉曼光谱、紫外吸收光谱、红外透过光谱等特性进行了研究．通过拉曼光谱分析研究了玻璃组分含量的变化对玻璃结构和红外透过性能的影响．结果表明，随着BaO含量的增加，玻璃在红外波段透过率显著增加，并且红外透过截止波长向长波方向移动，本文对这一实验结果进行了机理性的研究探讨．同时，通过在熔制过程中通入高纯O2，以及引入适量的卤化物有效地除去玻璃中的[OH]基团，使玻璃的红外透过性能得到进一步的提高．这种新型的氧卤碲酸盐玻璃在中红外区域有较高的透过（≥80％），中红外波段透过截止波长达6．5μm，是一种红外透过性能优良的光学玻璃材料．     

TeO2-AlF3(Al2O3)-LaF3-ZnF2玻璃的热稳定性和网络结构研究

制备了TeO2-AlF3 (Al2O3 )-LaF3-ZnF2体系氟氧化物玻璃.通过DSC和红外吸收光谱分析研究了Al2O3替代AlF3对氟氧化物碲酸盐玻璃热稳定性和网络结构的影响.结果表明:Al2O3替代AlF3使氟碲酸盐玻璃的玻璃转变温度和热稳定性明显提高,玻璃中形成的[AlO6]八面体使玻璃网络结构更加紧密.     

VLE data for CO2-CF2Cl2, N2-CO2, N2-CF2Cl2 and N2-CO2-CF2Cl

Knowledge about vapour-liquid (VLE) is required as a basis of reliable calculations for separation processes. Correlations available for the prediction of T, p, x, y data are less accurate for mixtures at high pressures and mixtures containing supercritical components. The results of VLE experiments are reported and compared with data calculated with equations of state.     

Preparation of ZrO2-CeO2 and HfO2-CeO2 nanopowders

We prepared weakly agglomerated powders of ZrO₂-CeO₂ and HfO₂-CeO₂ solid solutions 5–8 nm in particle size, consisting of monoclinic and tetragonal phases. After heat treatment at 1200°C, the crystallite size was 30 and 14 nm, respectively. We also examined the effect of precipitate freeze drying on the crystallization of hafnia-based solid solutions containing up to 20 mol % CeO₂.     

Thermal diffusion in binary mixtures H2-CCl2F2 and H2-CHClF2

Thermal diffusion coefficients were measured in two gaseous mixtures, in which one component was close to the critical temperature, in the pressure range (19.6–127.4)·10⁴ N/m² and at a freon concentration of 0.25–0.8.     

Comparison of the Electronic Structures of La2CuO4, Sr2CuO2Cl2, and Sr2CuO2F2

First-principles cluster calculations are reported of the local electronic structure of the three compounds: La₂CuO₄, Sr₂CuO₂Cl₂, and Sr₂CuO₂F₂. The copper ${\text{3d}}_{x^2 - y^2 } $ and the planar oxygen 2p _σ atomic orbitals exhibit a similar degree of covalency. The out-of-plane orbitals, however, are quite different with the ${\text{3}}d_{3z^2 - r^2 } $ atomic orbital lowered significantly in energy for chlorine and fluorine apical positions.     

Radial GRIN glasses in Li2O-Na2O-Al2O3-TiO2-SiO2 systems

A series of GRIN glass rods have been developed in Li2O-Na2O-Al2O3-TiO2-SiO2 systems. Negative radial refractive index profiles were generated by exchanging Na+ for Li+ ions in these glass rods. It has been observed that TiO2 plays a vital role in increase in the profile depth and maximum change in the refractive index because of its ambivalent nature. Change in the refractive index can be further increased by increasing the concentration of exchanging cation in the base glass.     

Thermoelectric power of single-phase samples of Tl2CaBa2Cu2O y and Ba2CaSr2Cu2O y

Single-phase 2122 samples of thallium and bismuth superconductors were made by the precursor matrix method. The thermopower of these samples was measured in the temperature range 250 K-T _c . The thermopower was positive and decreased linearly with increasing temperature aboveT _c (onset). The exponential enhancement of thermopower seen in the undoped and doped YBCO was not observed in these samples. The linear variation of thermopower can be explained on the basis of either a two-band model or a narrow band model.     

Si_2N_2O-Al_2O_3-La_2O_3和Si_2N_2O-Al_2O_3-CaO系统的亚固相关系

本文给出了 Si_2N_2O-Al_2O_3-La_2O_3和 Si_2N_2O-Al_2O_3-CaO 系统的亚固相图。实验结果表明:在 Si_2N_2O-Al_2O_3-CaO 系统中有一个未知结构的新化合物 CaO·Si_2N_2O,在3CaO·Si_2N_2O 和3CaO·Al_2O_3两化合物之间形成连续立方固溶体。而 Si_2N_2O-Al_2O_3-La_2O_3系统中则没有发现新化合物。在两个系统的富 Si_2N_2O区,过量的 Si_2N_2O 与 La_2O_3和 CaO 分别反应形成 Si_3N_4与 La_(10)[SiO_4]_(?)N_2(H-相)(和 CaSiO_3。所研究的这两个三元系统中,分别形成了如下几个四元相容性区。在 Si_2N_2O-Al_2O_3-La_2O_3系统内有:H-Si_3N_4-La_2O_3·Si_2N_2O-La_2O_3·Al_2O_3;H-Si_3N_4-La_2O_3·Al_2O_3-La_2O_3·11 Al_2O_3;H-Si_3N_4-La_2O_3·11 Al_2O_3-Al_2O_3;H-Si_3N_4-Al_2O_3-O′s.s;H-Si_3N_4-O′s.s-Si_2N_2O在 Si_2N_2O-Al_2O_3-CaO 系统内有:Si_3N_4-CaSiO_3-CaO·Si_2N_2O-3CaO·Al_2O_3;Si_3N_3-CaSiO_3-3CaO·Al_2O_3-2CaO·Al_2O_3·SiO_(?);Si_(?)N_(?)-CaSiO_3-2CaO·Al_2O_3·SiO_2-Al_2O_3;Si_3N_4-CaSiO_3-Al_2O_(?)-O′s.s;Si_3N_4-CaSiO_3-O′s.s-Si_(?)N_(?)O     

Elastic and Electronic Properties of Superconducting CaPd 2 As 2 and SrPd 2 As 2 vs. Non-superconducting BaPd 2 As 2

The first-principles calculations were performed to predict the elastic and electronic properties of the superconducting ThCr₂Si₂-type phases CaPd₂As₂ and SrPd₂As₂ in comparison with the non-superconducting CeMg₂Si₂-type phase BaPd₂As₂. Besides, the same properties were compared for CeMg₂Si₂- and ThCr₂Si₂-type polymorphs of BaPd₂As₂. We found that all these phases are mechanically stable and belong to soft materials with low hardness. The near-Fermi region is formed by the valence states of the blocks [Pd₂As₂] with decisive contributions of Pd 4d states. The values of N(E _F) increase in the sequence: CaPd₂As₂ < SrPd₂As₂ < BaPd₂As₂, i.e. in the reverse sequence relative to the transition temperatures T _C. Thus, the change in T _C cannot be explained by the electronic factor, i.e. by the simple correlation T _C～N(E _F). Most likely the decrease in T _C in the sequence CaPd₂As₂ → SrPd₂As₂ and the absence of a superconducting transition in BaPd₂As₂ are related to the structural factors and the peculiarities of the electron–phonon coupling mechanism.