斜角入射沉积法制备渐变折射率薄膜的折射率分析

斜角入射沉积法是一种制备薄膜的新颖方法,它可以用来制备渐变折射率薄膜.本文首先探讨了膜料的沉积入射角为α,薄膜柱状生长倾斜角为β时的薄膜的填充系数;之后利用drude理论,分析研究了斜角入射沉积法制备渐变折射率薄膜的折射率与薄膜的入射角和生长方向的关系. 关键词： 斜角入射沉积 渐变折射率 填充系数     

LCC谐振变换器的优化设计与实现

LCC谐振变换器是电除尘高频高压电源的核心器件,十分适用于高压大功率场合,针对连续模式应用于电除尘高频高压电源的不足,采用LCC谐振变换器断续模式进行优化设计。分析了带RC负载的LCC谐振变换器断续模式(简称DCM)的工作原理及拓扑结构,采用状态空间法推导了其数学模型,研究并建立了新颖的LCC谐振变换器断续模式下的损耗模型。在此基础上提出了一种基于遗传粒子群算法的LCC谐振变换器优化设计方法,该方法直观并且准确,实现了软开关技术,提高了电源的工作效率。并在现场通过一台72KV/85KW的电除尘高频高压电源样机验证了本文的正确性。     

Oscillation of coercivity between positive and negative in MnxGe1-x：H ferromagnetic semiconductor films

Amorphous MnxGe1-x :H ferromagnetic semiconductor films prepared in mixed Ar with 20% H2 by magnetron cosputtering show global ferromagnetism with positive coercivity at low temperatures. With increasing temperature, the coercivity of MnxGe1-x :H films first changes from positive to negative, and then back to positive again, which was not found in the corresponding MnxGe1-x and other ferromagnetic semiconductors before. For Mn0.4Ge0.6 :H film, the inverted Hall loop is also observed at 30 K, which is consistent with the negative coercivity. The negative coercivity is explained by the antiferromagnetic exchange coupling between the H-rich ferromagnetic regions separated by the H-poor non-ferromagnetic spacers. Hydrogenation is a useful method to tune the magnetic properties of MnxGe1-x films for the application in spintronics.     

不同能量的氦原子与同位素分子H2(D2，T2)碰撞分波截面的理论计算

用Tang-Toennies势模型和密耦近似方法计算了不同能量下惰性气体原子He与H₂及其同位素D₂，T₂替代碰撞体系的振转激发碰撞截面. 通过分析He-H₂(D₂，T₂)各碰撞体系分波截面的差异，总结出在H₂分子的对称同位素替代情形下He-H₂(D₂，T₂)碰撞体系分波截面随量子数和体系     

单偏振控制器环形腔光纤激光器实验研究

理论分析了非线性偏振旋转环形腔作为类饱和可吸收体获得脉冲的物理机理。在光纤环形腔结构中,采用单个偏振控制器实现了非线性偏振旋转锁模,直接获得了脉冲宽度为131 fs的超短脉冲输出。实验中,采用性能稳定的976 nm半导体二极管激光器作为抽运源,使用高掺杂浓度的Er3 光纤为增益介质,通过调节偏振控制器,获得了光谱谱宽(3 dB带宽处)为23.5 nm的稳定锁模脉冲输出。脉冲中心波长为1535.9 nm,平均功率为5.91 mW,脉冲重复率为11.20 MHz。     

Synthesis and properties of Au-Fe3O4 and Ag-Fe3O4 heterodimeric nanoparticles

Monodisperse Au-Fe 3 O 4 heterodimeric nanoparticles (NPs) were prepared by injecting precursors into a hot reaction solution.The size of Au and Fe 3 O 4 particles can be controlled by changing the injection temperature.UV-Vis spectra show that the surface plasma resonance band of Au-Fe 3 O 4 heterodimeric NPs was evidently red-shifted compared with the resonance band of Au NPs of similar size.The as-prepared heterodimeric Au-Fe 3 O 4 NPs exhibited superparamagnetic properties at room temperature.The Ag-Fe 3 O 4 heterodimeric NPs were also prepared by this synthetic method simply using AgNO 3 as precursor instead of HAuCl 4.It is indicated that the reported method can be readily extended to the synthesis of other noble metal conjugated heterodimeric NPs.     

An analysis for features of geospatially rescaled range analysis method and spatial scaling behavior

We apply the rescaled range analysis (R/S) method to analyze the geospatial scaling behavior and its relevant features, including spatial heterogeneity, a spatially short-range correlation, spatial scale effects and spatial nonstationarity. Our goal is to provide a tentative finding about a theoretical framework construction of geospatial multifractality of attribution-variable-value distribution. To investigate the spatial scaling behavior, the conventional R/S method is extended to a two-dimensionally geographical space and a two-dimensional geospatially rescaled range analysis method is presented. Our analysis shows that this proposed method is reliable and effective in the analysis of spatial scaling behavior and its characteristics. Furthermore, on the basis of this approach, the theoretical framework of spatial multifractality associated with spatial distribution of attribution value is preliminarily developed. Our findings contribute by providing a potential method to investigate spatial scaling behavior and spatial multifractality.     

Density functional and spectroscopic studies of nitrogen inversion in substituted dizocilpines

While developing a synthesis towards tagged dizocilpine (MK‐801) analogues, we observed highly restricted inversion of a nitrogen centre in a number hydroxylamines obtained as key intermediates. These compounds are shown to possess some of the structural elements which are expected to significantly hinder the nitrogen inversion, potentially leading to hydroxylamines with a chiral nitrogen centre. Free energy barriers (ΔG^≠) of the nitrogen inversion were estimated to be ca. 22 kcal mol^?1 at temperatures near 420 K using variable temperature NMR measurements in DMSO‐d₆. Further density functional studies of a number model systems were undertaken in order to better rationalize the measured inversion barriers and follow the role of various structural factors in raising the barrier height of the nitrogen inversion process. Copyright © 2008 John Wiley & Sons, Ltd.