从CET-4新题型看大学英语词汇教学

本文结合最新的四级题型,分析了大学英语新四级考试中词汇的测试特点,对大学英语词汇教学提出了一些有效的教学方法.     

几类完全4-部图的邻强边染色

得到了几类完全4-部图的邻强边色数.     

S桶空间的几个性质(Ⅱ)

讨论了S桶空间在归纳限和稠密子空间方面的一些基本性质．     

N阶幻体及其初等性质

幻方和幻立方是组合数学中古老问题,它们体现了数字间关系的优美性与和谐性.本文基于幻方和幻立方的理论引入了幻体,给出了其存在性定理的证明,并进一步讨论了幻体的初等性质.     

co—H空间上自同伦等价群的若干结果

研究有关co H 空间上的自同伦等价.当co H 空间X是1 连通的有限CW 复形时,εSP(SX)是有限生成的群.另外本文还得到εco H(X)是有限群的一个充分条件.     

展览建筑中受众选择性注意的应用研究

分析了展览建筑设计中受众选择性注意的社会因素,提出了展览建筑设计中针对受众选择性注意的设计原则。     

交换子在Morrey-Herz空间上的有界性

T^mb表示由函数b∈BMO（R^n）和强奇异积分算子T生成的m阶交换子。T^mb在L^q（R^n）上的有界性结果已经存在。利用不等式技巧进一步研究了T^mb在Herz和Morrey-Herz空间上的有界性质，所得结果更具有一般性。     

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.     

论莱辛《第五个孩子》的空间意义

从现代空间小说特征来看,长篇小说《第五个孩子》在形式上可谓一部空间小说;从福柯关于空间及权力关系的理论看,空间成了暴力的象征,这种暴力可能是压迫的,也可能是叛逆的。由此,实在的空间上升为具有象征意义的空间。     

Theoretical study on the lithium bond interaction of furan homologues C_4H_4Y (Y=O, S) with LiCH_3 via DFT and MP2

The optimizations geometries and interaction energy corrected by BSSE of the complexes between C4H4Y (Y=O, S) and CH3Li have been calculated at the B3LYP/6-311 G** and MP2/6-311 G** levels. Three complexes were obtained. Abnormally, the calculations showed that all the C10—Li14 bond lengths increased obviously but the blue-shift of C10—Li14 stretching frequency occurred after formed complexes. The calculated binding energy with basis set super-position error (BSSE) and zero-point vibrational energy corrections of complexes I―III is ?45.757, ?35.700 and ?39.107 kJ·mol?1, respectively. The analyses on the combining interaction with the atom-in-molecules theory (AIM) also showed that a relatively strong lithium bond interaction presented in furan homologues C4H4Y---LiCH3 systems. Natural bond orbital theory (NBO) analysis has been performed, and the results revealed that the com- plex I is formed with n-σ type lithium bond interaction between C4H4O and LiCH3, complex II is formed with π-s type lithium bond interaction between C4H4O and LiCH3, and complex III is formed with π-s and n-s type lithium bond interactions between C4H4S and LiCH3, respectively.