隔离式低压大电流输出DC/DC变换器拓扑分析

从拓扑、应用方面论述了低压大电流变换器技术近期的发展。对隔离式DC/DC变换器原边和副边拓扑进行了分析和比较,得出了隔离式低压大电流输出DC/DC变换器的优选拓扑结构。阐述了带倍流整流的桥式拓扑、推挽正激拓扑以及改进型推挽正激拓扑的优点和工作特点。同时,介绍了能提高变换器效率的同步整流技术。     

基于亲水表面处理的GaAs/GaN晶片直接键合

对晶片进行亲水表面处理,在氮气保护下500℃热处理10min,成功实现GaAs与GaN晶片的直接键合,键合质量较好.扫描电子显微镜观测结果表明,键合界面没有空洞.光致发光谱观测结果表明,键合工艺对晶体内部结构的影响很小.可见光透射谱测试结果表明,键合界面具有良好的透光特性.GaAs与GaN晶片直接键合的成功,为实现GaAs和GaN材料的集成提供了实验依据.     

甲基红掺杂液晶E7的光限幅特性研究

研究了甲基红染料掺杂的液晶混合物E7对波长为 5 32nm的纳秒脉冲激光的光限幅特性 ,观察了激光通过液晶盒后的远场光强分布及其随入射光能量的变化。实验发现 ,对于厚度为 4 6 μm ,重量体积比为 6mg/ 0 5ml的甲基红染料掺杂的液晶混合物E7薄膜 ,其最初三次测试的箝位输出值分别为 0 70 μJ,1.0 0 μJ和 1 5 2 μJ ,输入限幅阈值在 2 3～ 2 8μJ之间。这种薄膜的极低箝位输出特性对用于人眼和传感器保护的光限幅应用很有意义     

脉冲泄流时土壤条件对冲击接地阻抗的影响

 为了探寻电流脉冲泄流时，设备的接地是否有效可靠，用FDTD法分析了脉冲泄流时均一土壤、分层土壤及局部改善土壤的电导率对冲击接地阻抗（TGR）的影响。结果表明：大地电导率对冲击接地阻抗的影响很大；对均一土壤，TGR随大地电导率的增大而减小，大地电导率越大，TGR对接地体的埋深越不敏感。对分层土壤，接地体要埋在大地电导率大的土壤层中，且不要靠近交界面；局部改善大地导电性能对降低TGR效果明显，TGR对改善区域的体积非常敏感，而当电导率大于一定值时，大地电导率的再增加，对TGR的影响不明显。     

高空核电磁脉冲模拟波形的双指数函数拟合法

 许多标准和公开出版物中都用双指数函数描述高空核电磁脉冲典型波形。通过数值方法，研究了双指数函数一项重要的性质。根据该性质，详细讨论了高空核电磁脉冲模拟波形数值拟合中，双指数函数特征参数与脉冲峰值、前沿、后沿以及半宽等物理参数的关系，从而提出一种简单有效的脉冲参数计算方法。通过IEC标准中规定的高空核电磁脉冲参数的估计与一个实测高空核电磁脉冲模拟波形的数值拟合，验证了该方法的有效性和可靠性。该方法能够适应多种峰值、前沿和半宽的高宽核电磁脉冲模拟波形的数值拟合。     

能量选择中子成像技术及其应用

能量选择中子成像技术是利用特定范围波长(能量)的中子进行成像。在热/冷中子范围内(<25meV),能量选择中子成像技术主要基于布拉格边效应和衍射机制,相比常规中子成像技术不但可以显著提高图像对比度,而且能分析应变、应力、织构。在超热中子范围内(>1eV),能量选择中子成像技术主要基于中子共振吸收,中子截面随能量变化是同位素特有的,存在明显的共振吸收峰,因此可以进行同位素的“指纹”识别。能量选择中子成像技术在工程、材料、化学、物理、生物、考古等众多科研领域中有着非常广阔的应用前景。     

连续波雷达中对较大加速度的一种估计方法

在连续波雷达信号事后处理过程中,当目标的加速度比较大、信噪比又比较低时,各种算法很难处理出正确的结果。而目标的径向加速度是一个非常关键的参数。对它的成功的估计是后续处理中得到目标速度与距离的一个重要前提。本文针对这种情况,对连续波雷达回波频谱幅度产生原因进行分析,提出了二次曲线拟合频谱幅度来估计加速度的方法。仿真证明该方法的有效性。     

Enhancing cell membrane phase separation for inhibiting cancer metastasis with a stimuli-responsive DNA nanodevice

Phase separation in cell membranes promotes the assembly of transmembrane receptors to initiate signal transduction in response to environmental cues. Many cellular behaviors are manipulated by promoting membrane phase separation through binding to multivalent extracellular ligands. However, available extracellular molecule tools that enable manipulating the clustering of transmembrane receptors in a controllable manner are rare. In the present study, we report a DNA nanodevice that enhances membrane phase separation through the clustering of dynamic lipid rafts. This DNA nanodevice is anchored in the lipid raft region of the cell membrane and initiated by ATP. In a tumor microenvironment, this device could be activated to form a long DNA duplex on the cell membrane, which not only enhances membrane phase separation, but also blocks the interaction between the transmembrane surface adhesion receptor and extracellular matrix, leading to reduced migration. We demonstrate that the ATP-activated DNA nanodevice could inhibit cancer cell migration both in vitro and in vivo. The concept of using DNA to regulate membrane phase separation provides new possibilities for manipulating versatile cell functions through rational design of functional DNA structures.

A DNA nanodevice is developed to enhance the cell membrane phase separation in a tumor microenvironment to weaken the formation of focal adhesion. As a result, the migration of cancer cells is inhibited both in vitro and in vivo.     

双模压缩真空态在Tavis-Cummings模型中量子态保真度

考虑了原子的偶极相互作用,通过计算Tavis-Cummings模型下压缩真空态的保真度,阐明了在双模压缩真空态与环境(原子)通过双光子发生相互作用过程中量子信息的保真程度随时间的演化关。通过计算机模拟出两原子处于各种初态下时原子、光场和系统的保真度随时间的演化图象,分析出三者在压缩指数r、偶极相互作用常数ga和相位(?)等改变时的变化情况,结果表明r和k值的改变对于提高保真度具有重要意义。当两原子处于基态时减小r和当两原子处于一Bell基时增大都可以显著的提高体系的保真度。     

Visible Light-Driven Alkyne-Grafted Ethylene-Bridged Azobenzene Chromophores for Photothermal Utilization

Molecular photoswitches are considered to be important candidates in the field of solar energy storage due to their sensitive and reversible bidirectional optical response. Nevertheless, it is still a daunting challenge to design a molecular photoswitch to improve the low solar spectrum utilization and quantum yields while achieving charging and discharging of heat without solvent assistance. Herein, a series of visible-light-driven ethylene-bridged azobenzene (b-Azo) chromophores with different alkyne substituents which can undergo isomerization reactions promoted in both directions by visible light are reported. Their visible light responsiveness improves their solar spectrum utilization while also having high quantum yields. In addition, as the compounds are liquids, there is no need to dissolve the compounds in order to exploit this switching. The photoisomerization of b-Azo can be adjusted by alkyne-related substituents, and hexyne-substituted b-Azo is able to store and release photothermal energy with a high density of 106.1 J·g⁻¹, and can achieve a temperature increase of 1.8 °C at a low temperature of −1 °C.