The polar ionosphere at Zhongshan station on May 11, 1999, the day the solar wind almost disappeared

The solar wind almost disappeared on May 11, 1999: the solar wind plasma density and dynamic pressure were less than 1cm⁻³ and 0.1 nPa respectively, while the interplanetary magnetic field was northward. The polar ionospheric data observed by the multi-instruments at Zhongshan Station in Antarctica on such special event day was compared with those of the control day (May 14). It was shown that geomagnetic activity was very quiet on May 11 at Zhongshan. The magnetic pulsation, which usually occurred at about magnetic noon, did not appear. The ionosphere was steady and stratified, and the F₂ layer spread very little. The critical frequency of day-side F₂ layer, f₀F₂, was larger than that of control day, and the peak of f₀F₂ appeared 2 hours earlier. The ionospheric drift velocity was less than usual. There were intensive auroral E_s appearing at magnetic noon. All this indicates that the polar ionosphere was extremely quiet and geomagnetic field was much more dipolar on May 11. There were some signatures of auroral substorm before midnight, such as the negative deviation of the geomagnetic H component, accompanied with auroral E_s and weak Pc3 pulsation.

     

Analysis of Aperture Field of Circular Groove Guide Horn Antenna by Using FD-TD Method

This paper presents an instance of using FD-TD method to analyze the aperture field of circular groove guide horn antenna. This process is one part of a hybrid method to solve the radiation field of aperture antenna. To verify the calculated aperture field the radiation pattern is computed from it and compared with the measured one. Good agreement is reached.     

CsNiCl3晶体的光谱精细结构、零场分裂参量及Jahn-Teller效应

应用不可约张量理论构造了三角对称晶场中3d²/3d⁸态离子的45阶可完全对角化的微扰哈密顿矩阵，研究了CsNiCl₃晶体的光谱精细结构、晶体结构、零场分裂参量、Jahn-Telller效应以及自旋单重态对Ni²⁺离子基态能级的影响，理论与实验相符合.在此基础上，进一步研究了以前工作中被忽略的自旋-自旋耦合作用和Trees修正对CsNiCl₃晶体的光谱精细结构和零场分裂参量的影响，发现有四种机理会影响零场分裂参量：1)自旋-轨道耦合机理，2)自旋-自旋耦合机理；3)自旋-轨道与自旋-自旋联合耦合机理；4)自旋-轨道与Trees修正联合耦合机理，其中自旋-轨道耦合机理是最主要的，其他三种机理也是不可忽略的. 关键词： 基态能级 精细结构 零场分裂 自旋-自旋耦合     

含外规范场和动力学费米子自能的狄拉克算符及费米子凝聚

将非阿贝尔规范理论中狄拉克算符行列式的计算从传统的只能含有硬费米子质量项的情况推广到可以含有动量相关的费米子自能的情况，并且行列式与费米子凝聚的计算都被推广到使之能够含有任意的外规范场. 关键词： 费米子自能 外规范场 狄拉克算符的行列式 费米子凝聚     

磁各向异性色散介质散射的Pad啨时域有限差分方法分析

根据矩阵Pad啨逼近理论,把磁化色散介质的相对磁导率张量表示成以jω为自变量的矩阵函数形式,用/t代替jω后过渡到时域,再引入离散时域移位算子代替时间微分算子.进而导出磁化色散介质中的磁感应强度B和磁场强度H在离散时域的色散关系,并将其具体应用于旋磁介质,得到了这种磁化色散介质的Pad啨时域有限差分方法的递推表达式.作为验证,用这种方法计算了磁化铁氧体球的后向雷达散射截面,所得结果与文献结果一致.理论推导及算例表明,该方法是正确和有效的.     

场发射平板显示高低压电平转换电路

提出适用于场发射高压驱动的高低压电平转换电路设计及性能分析。通过模拟,此电路可以在100V的驱动工作电压以及10mA的驱动电流条件下安全工作,最高工作频率可达20MH_z。在50pF输出负载下上升时间和下降时间分别为14,25ns。同时分析了高压CMOS器件与0.8μm标准CMOS工艺兼容过程中的厚栅氧化对于低压器件及高压N管的阈值特性影响。     

掺入Ni元素的LiCoO2晶体光谱结构及电子顺磁共振g因子

在弱场图像下,利用Racah不可约张量算符方法得到了三角对称3d4/3d6电子组态的210阶可完全对角化的微扰哈密顿矩阵、最近邻点电荷模型晶体结构常量公式和电子顺磁共振g因子公式.研究了LiCoO2晶体和掺入Ni的LiCoO2:Ni晶体中Co3+的基态能级、晶体结构和电子顺磁共振g因子.考虑了LiCoO2晶体和LiCoO2:Ni晶体中自旋单重态和三重态对Co3+基态能级的影响,讨论了LiCoO2晶体和在LiCoO2晶体中掺杂Ni后Co3+局域结构常量大小的变化是引起Co3+的基态能级变化的主要原因,理论和实验都证实了这一点.还计算了掺杂前后的电子顺磁共振g因子,计算结果与实验值符合得较好.     

左手介质椭圆光波导基模传播特性

在椭圆柱坐标系中，采用分离变量方法，得出了左手介质椭圆光波导本征方程的近似解，通过数值计算，分析了椭圆波导偏心率、左手介质的电容率、磁导率对椭圆光波导基模传播特性的影响，并将左介质光波导与右手介质光波导基模特性进行对比，得出左手介质光波导的基模特性与右手介质光波导基模特性差别不大的结论.     

极化子导电到能带导电的转变

采用交流法测量大功率商用钛酸钡(BT)陶瓷加热器的电阻和加热功率随温度的变化关系.结果显示,BT陶瓷的电导特性在80℃附近出现了明显的转变,从低温时的极化子跳跃导电转变为高温时的能带导电,此时,电阻出现极小值,而加热功率出现极大值.     

New ligands for the Fe(III)‐mediated reverse atom transfer radical polymerization of methyl methacrylate

A series of (di)picolinic acids and their derivates are investigated as novel complexing tridentate or bidentate ligands in the iron‐mediated reverse atom transfer radical polymerization of methyl methacrylate in N,N‐dimethylformamide at 100 °C with 2,2′‐azobisisobutyrontrile as an initiator. The polymerization rates and polydispersity indices (1.32–1.8) of the resulting polymers are dependent on the structures of the ligands employed. Different iron complexes may be involved in iron‐mediated reverse atom transfer radical polymerization, depending on the type of acid used. ¹H NMR spectroscopy has been used to study the structure of the resulting polymers. Chain‐extension reactions have been performed to further confirm the living nature of this catalytic system. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2912–2921, 2006