双电荷交换反应与双重子共振态

提出了核双电荷交换反应的双重子共振态的反应机制,成功地解释了长期以来一直困惑着人们的共振区反应的角分布的实验结果.说明了共振区核双电荷交换反应是寻找双重子共振态的一个可能的途径.     

中子诱发12C反应的理论计算与分析

利用统一的Hauser–Feshbach理论和角动量相关的激子模型,以中子诱发¹²C反应为例,研究了轻核反应的反应机制和轻核反应的特点,并进行了理论计算,同时与实验数据进行了比较.     

量子微腔中原子大质心动量转移问题

讨论了双模量子环形微腔中二能级原子与腔场相互作用的动力学问题,分析了量子微腔的双模腔场和原子质心交换动量的过程。通过控制双模光场的光子数,得到了原子质心运动可同时吸收或发射多个光子的结论,从而可以实现较大的原子质心动量转移过程,使原子分束效应更为显著。     

650 kV/2 ns高压脉冲发生器研制

研制了一套峰值650 kV、脉宽2 ns的窄脉冲发生器,具有结构紧凑、体积小巧、便于移动和产生优质的纳秒高压脉冲等优点。该发生器基于三谐振脉冲变压器原理和脉冲形成压缩实现窄脉冲输出,采用紧凑双锥形绕组铁芯变压器、LC调谐回路和27 pF,30 脉冲形成线组成三谐振回路,油介质自击穿开关导通后在负载上获得高压脉冲。实验结果表明,该窄脉冲发生器可在80 电阻负载上输出脉冲峰值约650 kV,脉宽约2 ns,与理论分析的结果相吻合。     

Theoretical study on the mechanism for the excited-state double proton transfer process of an asymmetric Schiff base ligand

Excited-state double proton transfer (ESDPT) in the 1-[(2-hydroxy-3-methoxy-benzylidene)-hydrazonomethyl]-naphthalen-2-ol (HYDRAVH₂) ligand was studied by the density functional theory and time-dependent density functional theory method. The analysis of frontier molecular orbitals, infrared spectra, and non-covalent interactions have cross-validated that the asymmetric structure has an influence on the proton transfer, which makes the proton transfer ability of the two hydrogen protons different. The potential energy surfaces in both S₀ and S₁ states were scanned with varying O-H bond lengths. The results of potential energy surface analysis adequately proved that the HYDRAVH₂ can undergo the ESDPT process in the S₁ state and the double proton transfer process is a stepwise proton transfer mechanism. Our work can pave the way towards the design and synthesis of new molecules.     

Mg-doped layered oxide cathode for Na-ion batteries

Na-ion batteries (NIBs) are regarding as the optimum complement for Li-ion batteries along with the rapid development of stationary energy storage systems. In order to meet the commercial demands of cathodes for NIBs, O3-type Cu containing layered oxide Na_0.90Cu_0.22Fe_0.30Mn_0.48O₂ with good comprehensive performance and low-cost element components is very promising for the practical use. However, only part of the Cu³⁺/Cu²⁺ redox couple participated in the redox reaction, thus impairing the specific capacity of the cathode materials. Herein, Mg²⁺-doped O3-Na_0.90Mg_0.08Cu_0.22Fe_0.30Mn_0.40O₂ layered oxide without Mn³⁺ was synthesized successfully, which exhibited improved reversible specific capacity of 118 mAh/g in the voltage range of 2.4-4.0 V at 0.2 C, corresponding to the intercalation/deintercalation of 0.47 Na⁺ (0.1 more than that of Na_0.90Cu_0.22Fe_0.30Mn_0.48O₂). This work demonstrates an important strategy to obtain advanced layered oxide cathodes for NIBs.     

一种研究自旋翻转散射效应的新方法

金属中自旋翻转散射长度远长于电子平均自由程，近来关于自旋翻转散射效应的研究主要集中于扩散区域．文章作者提出了一种使用双势垒磁性隧道结来研究纳米尺度结构中弹道区域的自旋翻转散射效应的新方法．这种方法可以从磁电输运性质的测量，得出中间隔离层中的自旋翻转散射效应的温度和偏压关系，进一步可以得出诸如电子平均自由程和自旋翻转散射长度等自旋散射信息，以及中间层的态密度和量子阱信息．     

双随机相位编码光学加密系统的唯密文攻击

针对双随机相位编码光学加密系统的安全性分析表明，该系统属于线性对称分组密码系统，其线性性质为安全性留下极大隐患.在唯密文攻击下，仅根据密文估计出物面波函数的“支撑”(support)，然后利用迭代相位恢复算法获得物面波函数(其振幅是明文信息)，再根据物面波函数与频域密文的关系可推导出频谱平面的解密密钥.由于估计出来的物面波函数的“支撑”相对于真实的物面波函数的“支撑”有一定的平移，使得恢复的物面波函数与真实的物面波函数之间无论在振幅上还是相位上都存在平移，导致用推导出来的解密密钥去解密其他密文时所获得的明文与原始明文之间存在明显平移.然而，可依照这一先验信息，将估计出来的物面波函数的“支撑”在物面内遍历，从而找到逼近真实解密密钥的解.利用此解密密钥去解密其他密文时获得更好的解密效果. 关键词： 光学信息安全 双随机相位编码 唯密文攻击 函数支撑     

Exact coexistence surfaces containing double critical points for a three-component solution on the Bethe,honeycomb, and square lattices

A model is considered in which the bonds of a lattice are covered by rodlike molecules. Neighboring molecular ends interact with orientation-dependent interactions. The model exhibits closed -loop phase diagrams and double critical points. Exact coexistence surfaces are calculated for the model on the Bethe, honeycomb, and square lattices. The nature of the doubling of the critical exponent near a double critical point is calculated. The behavior of the critical line in the neighborhood of a double critical point is calculated exactly.     

Synthesis and Raman spectroscopic characterisation of hydrotalcites based on the formula Ca6Al2(CO3)(OH)16· 4H2O

We have successfully synthesised hydrotalcites (HTs) containing calcium, which are naturally occurring minerals. Insight into the unique structure of HTs has been obtained using a combination of X‐ray diffraction (XRD) as well as infrared and Raman spectroscopies. Calcium‐containing hydrotalcites (Ca‐HTs) of the formula Ca₄Al₂(CO₃)(OH)₁₂·4H₂O (2:1 Ca‐HT) to Ca₈Al₂(CO₃)(OH)₂₀· 4H₂O (4:1 Ca‐HT) have been successfully synthesised and characterised by XRD and Raman spectroscopy. XRD has shown that 3:1 calcium HTs have the largest interlayer distance. Raman spectroscopy complemented with selected infrared data has been used to characterise the synthesised Ca‐HTs. The Raman bands observed at around 1086 and 1077 cm⁻¹ were attributed to the ν₁ symmetric stretching modes of the (CO₃²⁻) units of calcite and carbonate intercalated into the HT interlayer. The corresponding ν₃ CO₃²⁻ antisymmetric stretching modes are found at around 1410 and 1475 cm⁻¹. Copyright © 2010 John Wiley & Sons, Ltd.