198Bi的高自旋态结构研究

利用能量为85—105MeV的¹⁶O束流,通过¹⁸⁷Re(¹⁶O,5n)反应研究了¹⁹⁸Bi的高自旋态能级结构.用6台BGO(AC)HPGe探测器和一台用于探测低能γ跃迁的平面探测器进行了γ射线的激发函数、γ-γ—t符合及γ射线的角分布测量.基于这些测量,首次建立了包括26条γ跃迁的¹⁹⁸Bi的高自旋能级纲图,确定了一个半寿命为(8.0±3.6)ns,自旋和宇称为15+的同质异能态.基于较重的双奇铋核^200—206Bi能级结构的系统性,定性地对¹⁹⁸Bi的能级结构进行了解释.     

μs级充电时水介质同轴电容击穿实验研究

 研制了水介质同轴电容的实验装置，在此装置上进行了大量的实验。测得μs级充电时，水介质同轴电容分别在正脉冲和负脉冲充电时的击穿电压，负击穿电压的理论值与测量值相差较大，正击穿电压的理论值大于测量值的18%左右，对此实验结果进行了分析。此外，当去离子水的电阻率从13MΩ·cm降到5 MΩ·cm时，水介质同轴电容器的击穿电压基本不变。     

Orlicz capacities and Hausdorff measures on metric spaces

In the setting of doubling metric measure spaces with a 1-Poincaré inequality, we show that sets of Orlicz Φ-capacity zero have generalized Hausdorff h-measure zero provided thatwhere Θ⁻¹ is the inverse of the function Θ(t)=Φ(t)/t, and s is the “upper dimension” of the metric measure space. This condition is a generalization of a well known condition in Rⁿ. For spaces satisfying the weaker q-Poincaré inequality, we obtain a similar but slightly more restrictive condition. Several examples are also provided.     

Preparation and electrochemical properties of nano Al<Subscript>0.2</Subscript>V<Subscript>2</Subscript>O<Subscript>5.3−<Emphasis Type="BoldItalic">δ</Emphasis></Subscript> cathode materials for rechargeable lithium batteries

Nano-sized Al³⁺-doped V₂O₅ cathode materials, Al_0.2V₂O_5.3−δ , were prepared by an oxalic acid assisted sol–gel method at 350 °C (sample A) and 400 °C (sample B). X-ray diffraction confirmed that samples A and B were pure phase Al_0.2V₂O_5.3−δ with an orthorhombic structure close to that of V₂O₅. Scanning electron microscopy showed that sample A was in nanoscale with a mean particle size about 50 nm. Cyclic voltammetry showed the good electrochemical and structural reversibility of the Al_0.2V₂O_5.3−δ nanoparticles during the Li⁺ insertion/extraction process. The Al_0.2V₂O_5.3−δ nanoparticles exhibited excellent charge–discharge cycling performance and rate capability compared to that of bulky V₂O₅ electrodes. For instance, the materials delivered a reversible specific capacity about 180 mAh g⁻¹ (sample A) and 150 mAh g⁻¹ (sample B), in the potential window of 4.0–2.0 V at the current density of 150 mA g⁻¹. The Al_0.2V₂O_5.3−δ nanoparticles in particular showed almost no capacity fading for at least 50 cycles.     

基于二茂铁的两个查尔酮衍生物的合成及超快三阶非线性光学响应

二茂铁是合成新颖有机功能材料的基本单元之一。 本文设计并合成了两个基于二茂铁的同分异构查尔酮衍生物:1-二茂铁基-3-(噻吩-2-基)丙烯酮(a)和1-二茂铁基-3-(噻吩-3-基)丙烯酮(b)。 采用超快激光Z-扫描技术(脉宽180 fs,波长532 nm)测定了化合物a和b的三阶非线性光学性质。 结果表明,化合物a吸收系数β=-2.1×10^-12 m/W,折射率n₂=1.9×10^-19 m²/W,分子超极化率γ=5.37×10^-32 esu;化合物b:β=-1.2×10^-13 m/W,n₂=2.0×10^-19 m²/W,γ=4.48×10^-32 esu。 说明在飞秒激光激发下,电荷转移能够在化合物a和b分子内部快速进行,二者均具有优异的超快三阶非线性光学响应。 在B3LYP/6-311+G(d,p)理论水平下,计算了化合物a和b分子轨道能量、极化率和各基团在前线分子轨道中的占有率。 理论计算结果显示,二茂铁基团在化合物a和b前线分子轨道中占有率分别为97%和98%,对两化合物的非线性光学性能起主导作用。     

Enhancement of uranium(VI) biomineralization by Saccharomyces cerevisiae through addition of inorganic phosphorus

Journal of Radioanalytical and Nuclear Chemistry - Enhancement of U(VI) biomineralization by Saccharomyces cerevisiae through addition of inorganic phosphorus was studied in this work. The addition...     

Cu3V2O8 Nanoparticles as Intercalation‐Type Anode Material for Lithium‐Ion Batteries

Cu₃V₂O₈ nanoparticles with particle sizes of 40–50 nm have been prepared by the co‐precipitation method. The Cu₃V₂O₈ electrode delivers a discharge capacity of 462 mA h g^?1 for the first 10 cycles and then the specific capacity, surprisingly, increases to 773 mA h g^?1 after 50 cycles, possibly as a result of extra lithium interfacial storage through the reversible formation/decomposition of a solid electrolyte interface (SEI) film. In addition, the electrode shows good rate capability with discharge capacities of 218 mA h g^?1 under current densities of 1000 mA g^?1. Moreover, the lithium storage mechanism for Cu₃V₂O₈ nanoparticles is explained on the basis of ex situ X‐ray diffraction data and high‐resolution transmission electron microscopy analyses at different charge/discharge depths. It was evidenced that Cu₃V₂O₈ decomposes into copper metal and Li₃VO₄ on being initially discharged to 0.01 V, and the Li₃VO₄ is then likely to act as the host for lithium ions in subsequent cycles by means of the intercalation mechanism. Such an “in situ” compositing phenomenon during the electrochemical processes is novel and provides a very useful insight into the design of new anode materials for application in lithium‐ion batteries.     

基于Fe3O4@Ag壳核结构磁性纳米复合物的对杀螟硫磷的电化学传感

制备一种壳核结构的Fe3O4@Ag磁性纳米粒子,将该纳米粒子通过壳聚糖（CS）修饰在玻碳电极（GCE）表面,制备了对杀螟硫磷有灵敏电化学传感的Fe3O4@Ag/CS/GCE。应用透射电镜（TEM）和紫外可见光谱（UV-VIS）,对Fe3O4@Ag纳米粒子进行表征。运用电化学交流阻抗（EIS）、循环伏安法（CV）和时间电流法（I-T）来研究杀螟硫磷电化学特性。研究发现,在1.74×10-7～3.27×10–4 mol/L浓度范围内,该传感器可以实现对杀螟硫磷的快速检测,检测限为5.7×10-8 mol/L（S/N=3）     

碘喷孔位置的变化对激光性能的影响

 在主、副气流流量不变的情况下,仅改变氧碘化学激光器中碘喷孔的位置,数值模拟了其混合气体流场特性和小信号增益分布等的变化。计算结果表明,碘喷孔在喷管叶片上的位置沿气流方向往下游移动,混合状况变差,光腔中小信号增益降低,输出功率减小,饱和光强沿气流方向的衰减变得平缓。     

CW-COIL输出功率与输出孔径及光轴位置之间的依赖关系

 氧碘化学激光器由于复杂的动力学因素,激光介质的增益分布通常是不均匀的,这就使得激光输出功率并不完全随着激光输出孔径成线性增加,也由于这种增益分布的不均匀性,即使在激光输出孔径不变的情况下,激光输出功率也会随着光轴位置的改变而发生变化。为此,在激光器工作参数固定条件下,通过实验描述了激光输出功率与激光输出孔径及光轴位置之间存在着的一定的依赖关系。