射频辉光放电CH4等离子体中电子的能量分布

通过求解Lorentz简化的玻尔兹曼方程,得到射频放电CH₄等离子体中电子的能量分布函数.求解过程中使用一个简化的射频电场模型代替泊松方程求解放电电场.共计包含6类环境气体及27种电子碰撞反应.通过EEDF对等离子体中的电子反应率系数、电子平均能量、电子的传输率系数等进行求解分析.结果表明,在等离子体鞘层区域电子能量具有Maxwell分布形式,在正柱区域具有Druyvesteyn分布形式.最高电子能量和最大反应率系数出现在鞘层区域.电子的迁移率系数和扩散率系数随射频周期的演化时空分布不均匀.     

射频辉光放电CH4等离子体一维流体动力学模拟

完整建立一个关于射频辉光放电CH₄等离子体的流体动力学模型.模型包括基于迁移-扩散近似的粒子平衡方程、电子能量平衡方程,共包含了20种粒子(环境气体粒子,激发态粒子,离子和电子)和49类化学反应(电子-中性环境粒子、离子-中性环境粒子、激发态粒子-激发态粒子(中性环境粒子)).结果表明,在强电场区域有较高的电子反应率系数;等离子体中除源气体CH₄外,H₂,C₂H₆,C₃H₈,C₂H₄和C₂H₂也有较高的密度含量;激发态粒子中,CH₃含量最高,密度约为10¹⁹m^-3;在较低放电压力时(如18 Pa),CH₅⁺在离子成分中密度含量最高,当放电压力较高时(如67Pa),C₂H₅⁺在离子成分中占主导地位;除C₂H₅⁺外,其它各离子和激发态粒子在极板上的粒子流量随功率的增大逐渐升高.     

改性硫氧镁胶凝材料的配制及性能研究

为确定工业级轻烧氧化镁粉与七水硫酸镁溶液配制改性硫氧镁胶凝材料的最优参数,分别研究了不同氧化镁/七水硫酸镁摩尔比,硫酸镁溶液浓度及水稳剂水玻璃对硫氧镁胶凝材料工作和力学性能的影响.结果表明:随着氧化镁/硫酸镁摩尔比的提高,硫氧镁水泥的初凝时间逐渐缩短,流动性逐渐降低,抗压和抗折强度逐渐提高;随着七水硫酸镁浓度的提高,硫氧镁水泥的抗压抗折强度也呈现增长趋势,MgO:MgSO4·7H2O:H2O摩尔比为14:1:12时,硫氧镁胶凝材浆体的28d抗压和抗折强度分别达到38.3MPa和7.0MPa.耐水性研究表明,加入氧化镁质量2%的水玻璃可以很好地改善硫氧镁水泥的耐水性.     

天目铁木愈伤组织和芽苗诱导技术

以天目铁木嫩茎尖为外植体,应用均匀设计法筛选其基部愈伤组织诱导和愈伤组织再分化芽苗的最适合培养基.结果表明,最适合的嫩茎尖基部愈伤组织诱导培养基为1/2DR+TDZ 2.30 mg·L^-1+2,4-D 0.55 mg·L^-1,诱导率为93.5%;愈伤组织芽苗再分化培养基为1/2DR+TDZ 3.30 mg·L^-1+KT 0.70 mg·L^-1,分化率达99.8%以上. 成功建立了天目铁木嫩茎尖离体诱导愈伤组织和芽苗再分化体系,且再生芽苗与野生植株染色体数目相同.     

Isochronal synchronization in networks and chaos-based TDMA communication

Pairs of delay-coupled chaotic systems were shown to be able to achieve isochronal synchronization under bidirectional coupling and self-feedback. Such identical-in-time behavior was demonstrated to be stable under a set of conditions and to support simultaneous bidirectional communication between pairs of chaotic oscillators coupled with time-delay. More recently, it was shown that isochronal synchronization can emerge in networks with several hundreds of oscillators, which allows its exploitation for communication in distributed systems. In this paper, we introduce a conceptual framework for the application of isochronal synchronization to TDMA communication in networks of delay-coupled chaotic oscillators. On the basis of the stable and identical-in-time behavior of delay-coupled chaotic systems, the chaotic dynamics of distributed oscillators is used to support and sustain coordinate communication among nodes over the network. On the basis of the unique features of chaotic systems in isochronal synchronization, the chaotic signals are used to timestamp clock readings at the physical layer such that logical clock synchronization among the nodes (a prerequisite for TDMA) can be exploited using the same basic structure. The result is a standalone network communication scheme that can be advantageously applied in the context of ad-hoc networks or alike, especially short-ranged ones that yield low values of time-delay. As explored to its depths in practical implementations, this conceptual framework is argued to have potential to provide gain in simplicity, security and efficiency in communication schemes for autonomous/standalone network applications.     

Molecular tethering or aggregation: is the existence of charge-transfer bands indicative of the formation of blue-box/tetrathiafulvalene inclusion complexes?

The interaction between tetrathiafulvalene and tetracation cyclobis(paraquat-p-phenylene) fragments-the key elements of many rotaxane systems-was investigated theoretically by using ab-initio second-order perturbation methods. In addition to the inclusion complex observed in the solid state, a thermodynamically stable "exterior" complex was identified. Calculation of the UV/Vis spectra for the inclusion and the exterior complexes indicated that the charge-transfer band that is often used to predict the formation of the inclusion complexes in solution is, in reality, due to the exterior mode of complexation. These results suggest that UV/Vis spectroscopy is not a reliable method for assigning the complexation modes in TTF:BB(4+) rotaxanes and related systems.     

Chemical network algorithms for the risk assessment and management of chemical threats

A network of chemical threats: Current regulatory protocols are insufficient to monitor and block many short-route syntheses of chemical weapons, including those that start from household products. Network searches combined with game-theory algorithms provide an effective means of identifying and eliminating chemical threats. (Picture: an algorithm-detected pathway that yields sarin (bright red node) in three steps from unregulated substances.).     

Great expectations: can artificial molecular machines deliver on their promise?

The development and fabrication of mechanical devices powered by artificial molecular machines is one of the contemporary goals of nanoscience. Before this goal can be realized, however, we must learn how to control the coupling/uncoupling to the environment of individual switchable molecules, and also how to integrate these bistable molecules into organized, hierarchical assemblies that can perform significant work on their immediate environment at nano-, micro- and macroscopic levels. In this tutorial review, we seek to draw an all-important distinction between artificial molecular switches which are now ten a penny-or a dime a dozen-in the chemical literature and artificial molecular machines which are few and far between despite the ubiquitous presence of their naturally occurring counterparts in living systems. At the single molecule level, a prevailing perspective as to how machine-like characteristics may be achieved focuses on harnessing, rather than competing with, the ineluctable effects of thermal noise. At the macroscopic level, one of the major challenges inherent to the construction of machine-like assemblies lies in our ability to control the spatial ordering of switchable molecules-e.g., into linear chains and then into muscle-like bundles-and to influence the cross-talk between their switching kinetics. In this regard, situations where all the bistable molecules switch synchronously appear desirable for maximizing mechanical power generated. On the other hand, when the bistable molecules switch "out of phase," the assemblies could develop intricate spatial or spatiotemporal patterns. Assembling and controlling synergistically artificial molecular machines housed in highly interactive and robust architectural domains heralds a game-changer for chemical synthesis and a defining moment for nanofabrication.     

一维新型阶梯函数光子晶体透射特性

研究了阶梯型折射率n22、n11(阶梯分布高度)的大小、对应的分布厚度、不同入射角以及缺陷模对阶梯函数型光子晶体透射特性的影响.由费马原理给出光在函数光子晶体中的运动方程,再由电磁传播理论给出函数光子晶体的传输矩阵,进一步推导出函数光子晶体的透射率以及电场分布的表达式.研究表明,1)随n22,n11大小或者厚度改变,其禁带变宽;2)随光的入射角增加,其禁带变窄;3)当加入缺陷层时,随着缺陷层介质折射率增加,缺陷模强度减小且位置发生红移;4)在函数光子晶体中,缺陷层前电场分布保持不变,而在缺陷层处以及之后的电场强度都明显增强,这不同于常规光子晶体的电场分布仅在缺陷层处局域增强.