拓扑分子格的弱分离公理

本文是文［１］的继续，我们以Ｑ－远域为工具，首先引入和研究了拓扑分子格的ＳＴｉ分离公理（ｉ＝－１，０，１，２，３，４）。其次我们引入了Ｓ－不定序同态和Ｓ－同胚序同态等概念，给出了它们的若干特征性质。最后我们得到了各种ＳＴｉ分离公理是Ｓ－同胚序同态下保持不变的性质。     

加快我国信用卡市场发展的思考

自1986年中国银行发行了我国的第一张信用卡——长城卡以来，我国的信用卡市场经历了一个起步、探索的阶段，“电子货币”正逐渐改变着人们的生活方式。但由于缺乏规范、统一的管理，经营粗放；产品定位不当，管理手段落后；个人信用体系不健全；特约商户发展缓慢等原因，阻碍着我国信用卡业的进一步发展。鉴于此，就如何加快信用卡业的发展提出了一些对策和建议。     

浅论提高高校电子阅览室利用率的措施

分析了高校电子阅览室利用率低的原因，从加大宣传力度，加强电子信息资源的建设和管理，创建网络导航数据库，加强对读者的信息教育等方面提出了提高电子阅览室利用率的措施。     

Molecular dynamics study on the structure I helium hydrate

A 368- water molecule structure I gas hydrate, encased by the number of helium (He) molecules ranging from two to twenty-two, are calculated by molecular dynamical simulations. The potential TIP4P (transferable intermolecular potentical with four sites) is used for water interactions and Lennard-Jones for He-He and He-water interactions. He molecules do not affect the water lattice and can stabilize the hydrate when their concentration is small. A trough signature of He encased is found at 80～90 meV in the phonon density of states. He molecules prefer to be more off-center in 51262 cages. Heavier isotope He are energetically favorable to be filled in cages.     

基于Protel的通信电子线路仿真分析

简要介绍了Protel的主要组成及其仿真特性，分析了它在通信电子线路实验教学中的应用前景一实用、安全、高效、所见即所得．通过对MC1496双差分对平衡调制电路的仿真分析，直观、清晰、实用、简明而严谨的对理论进行了验证，做到了理论联系实际．     

不对称D—A反应区域选择性及其理论解析

本文以教学研究为基础,系统研究不对称D—A反应区域选译性规律,并运用前线分子轨道理论,采用图解量子化学方法予以理论解析。     

有机化学中烷基的电子效应

主要从分析烷基对有机分子和离子的影响讨论烷基的电子效应，指出仅用烷基的“供电”或“吸电”来表述烷基的电子效应是不够全面的。     

基于MAX155和KMZ52的电子指南针的实现

介绍了电子指南针的工作原理，采用高速A／D转换器MAX155，完成了对KMZ52二维磁阻传感器输出信号的同时采样，提高了系统的精度．同时，采用跳转技术对偏差及温度漂移进行了补偿，减少了温度等因素对本系统造成的影响．     

从电子设计竞赛看单片机实验教学的改革与创新

结合电子设计竞赛的内容及特点,从当前社会发展对高素质、创新人才的需求出发,为提高学生运用理论知识去解决实际问题的能力,对单片机原理及应用课程实验内容和方法的改革进行了探讨.     

Ab initio study of the effects of Ag/Mn doping on the electronic structure of LiFePO_4

Based on density functional theory (DFT) of the first-principle for the cathode materials of lithium ion battery, the electronic structures of Li(Fe1-xMex)PO4 (Me = Ag/Mn, x = 0―0.40) are calculated by plane wave pseudo-potential method using Cambridge serial total energy package (CASTEP) program. The calculated results show that the Fermi level of mixed atoms Fe1-xAgx moves into its conduction bands (CBs) due to the Ag doping. The Li(Fe1-xAgx)PO4 system displays the periodic direct semiconductor characteristic with the increase of Ag-doped concentration. However, for Fe1-xMnx mixed atoms, the Fermi level is pined at the bottom of conduction bands (CBs), which is ascribed to the interaction be-tween Mn(3d) electrons and Fe(4s) electrons. The intensity of the partial density of states (PDOS) near the bottom of CBs becomes stronger with the increase of Mn-doped concentration. The Fermi energy of the Li(Fe1-xMnx)PO4 reaches maximum at x = 0.25, which is consistent with the experimental value of x = 0.20. The whole conduction property of Mn-doped LiFePO4 is superior to that of Ag-doped LiFePO4 cathode material, but the structural stability is reverse.