Influence of fluoride on f-f transitions of Eu in LiEuM2O8 (M=Mo, W)

The influence of fluoride on the luminescence of LiEuM₂O₈ (M=Mo, W) was studied. LiEuMo₂O₈ and LiEuW₂O₈ formed the whole range of solid solutions, which emitted intense red luminescence under the excitations by 395, 465 and 535 nm wavelengths. When doped with fluoride, the materials also formed solid solutions and the luminescent intensity was remarkably enhanced. The phosphor with optimized compositions in this system would be a promising red component for solid-state lighting devices based on GaN light-emitting diodes.     

冠心病微量元素谱的计算机模式识别

用计算机多元分析研究冠心病微量元素谱，识别冠心病患者与健康者；非线性映射法判别率男性８６．６％，女性９６．２％；ＳＩＭＣＡ差别法正确回判率男性８５．０％，女性８８．３％。     

聚醋酸乙烯酯/聚丙烯酸甲酯互穿网络聚合物的研究——1.聚合条件对体系相容性的影响

用分步法合成了聚醋酸乙烯酯/聚丙烯酸甲酯互穿网络聚合物(PVAc/PMA-IPN),PVAc和PMA的交联剂分别是丁二酸二烯丙酯(DAS),和二乙烯基苯(DVB)。当DAS用量较小时,VAc聚合时的接枝反应较明显,PVAc网络的交联密度高于化学当量的计算值。动态力学的实验结果表明,丙烯酸甲酯的聚合温度和聚合过程中的溶胶-凝胶转变对PVAc/PMA-IPN体系的相容性有很大影响。     

Size-dependent visible photoluminescence from ZnO nanoparticles prepared via SiO2 network

This study reports a simple method for the synthesis of different size of wurtzite ZnO nanoparticles in assistance of tetraethyl orthosilicate (TEOS). With the increase of the amount of TEOS added, the average size of ZnO nanoparticles was found decreased from ∼14.6 to ∼1.9 nm by characterization of X-ray diffraction (XRD) and high-resolution electron microscopy (HRTEM). The growth of ZnO nanoparticles is proposed to be controlled by the density of the SiO₂ chain mesh which is determined by TEOS amount in precursor. Ultraviolet–visible (UV–VIS) absorption and photoluminescence (PL) spectra show both shift to higher energy in cut-off edge and in visible emission bands respectively. The electron transition process in the mechanism of the visible emission shift was described and related to quantum size effect in ZnO nanoparticles.     

磁致伸缩-压电联合激励凹筒型发射换能器

设计制作了一种新型磁致伸缩-压电联合激励凹筒型发射换能器,采用稀土超磁致伸缩材料Terfenol-D与PZT压电陶瓷作为联合激励元件,模拟计算与实测结果均表明,与采用单一振子激励的凹筒型发射换能器相比,此种新型换能器在保持尺寸小、频率低等优点的同时,显著拓宽了工作频带并提高了辐射声功率.换能器外型尺寸为φ88 mm×316 mm,水中谐振频率1.30 kHz,-3 dB带通Q值1.43,谐振频率下发射电压响应级135.1 dB.     

Lithium aluminosilicate glass-ceramic containing Na2O for low-temperature anodic bonding in microelectronic mechanical systems

In this study, one kind of lithium aluminosilicate-β-quartz glass-ceramic containing Na₂O has been chosen, which can be used for low-temperature bonding with a higher bonding rate for the manufacture of microelectronic mechanical systems. The microstructure of the glass-ceramic is analyzed by transmission electron microscopy, high resolution transmission electron microscopy, selected-area diffraction, energy dispersive spectrometry and X-ray diffraction. The influence of the heat treatment process of the glass on the properties and the microstructure of the glass-ceramics is discussed. The microstructure of the glass-ceramic has the continuous glassy region with higher alkali metal ion content, which benefits the low-temperature anodic bonding.     

The BEM for solving the nonhomogeneous Helmholtz equation with variable coefficients

Considering the fundamental solution of the Laplace equation as the weight function, we give the iterative format for solving the nonhomogeneous Helmholtz equation with variable coefficients. Furthermore, the iteration method of BEM for solving the equation mentioned above is obtained. The numerical example is given in this paper. Finally, the iteration method of BEM mentioned above is compared with the coupled method of BEM that was presented before then by authors.     

Exploring Reversible Quenching of Fluorescence from a Pyrazolo[3,4‐b]quinoline Derivative by Protonation

Pyrazolo[3,4‐b]quinoline derivatives are reported to be highly efficient organic fluorescent materials suitable for applications in light‐emitting devices. Although their fluorescence remains stable in organic solvents or in aqueous solution even in the presence of H₂O, halide salts (LiCl), alkali (NaOH) and weak acid (acetic acid), it suffers an efficient quenching process in the presence of protic acid (HCl) in aqueous or ethanolic solution. This quenching process is accompanied by a change in the UV spectrum, but it is reversible and can be fully recovered. Both steady‐state and transient fluorescence spectra of 1‐phenyl‐3,4‐dimethyl‐1H‐pyrazolo‐[3,4‐b]quinoline (PAQ5) during quenching are measured and analyzed. It is found that a combined dynamic and static quenching mechanism is responsible for the quenching processes. The ground‐state proton‐transfer complex [PAQ5 ??? H⁺] is responsible for static quenching. It changes linearly with proton concentration [H⁺] with a bimolecular association constant K_S=1.95 M ^?1 controlled by the equilibrium dissociation of HCl in ethanol. A dynamic quenching constant K_D=22.4 M ^?1 is obtained by fitting to the Stern–Volmer equation, with a bimolecular dynamic quenching rate constant k_d=1.03×10⁹ s^?1 M ^?1 under ambient conditions. A change in electron distribution is simulated and explains the experiment results.