一维辐射系统吸收系数的反问题

辐射反问题是当前的研究热点之一。本文采用离散坐标法求解正问题,用共轭梯度法求解一维系统吸收系数的反问题。用正问题的计算结果加上误差作为反问题的求解条件。数值计算的结果表明,共轭梯度法可以比较好的反演辐射系统的吸收系数。在考虑散射时,反演效果比不考虑散射的反演效果好。     

Isomorphism of two realizations of quantum affine algebraU_q (\widehat{\mathfrak{g}\mathfrak{l}{\text{(}}n{\text{)}}})

We establish an explicit isomorphism between two realizations of the quantum affine algebra given previously by Drinfeld and Reshetikhin-Semenov-Tian-Shansky. Our result can be considered as an affine version of the isomorphism between the Drinfield/Jimbo and the Faddeev-Reshetikhin-Takhtajan constructions of the quantum algebra .     

The mm-wave dielectric measurements with an electric-field cross-correlation Fourier transform spectrometer

A method for measuring complex permittivity based on an electric-field cross-correlation Fourier transform spectrometer was proposed. Its principle can be extended over the whole microwave region. Two typical solid media, teflon and plexigrass, and a kind of sand were measured in 8mm-wave region by the method. The results show that this method has potentialities to perform accurate permittivity measurements.Supported by Foundation of Specialities Opened to Doctorate Study     

阿尔芬波加热托卡马克等离子体的能量平衡问题

本文用“剖面不变性”确定等效电子热导系数,研究了TCA装置上阿尔芬波加热的能量平衡,结果与实验符合很好。证明本文所用的方法对不同装置、不同加热方式都适用。     

Light induced microstructure transformation in a-Si：H films

A series of a-Si:H films are deposited by hot wire assisted microwave electron cyclotron resonant chemical vapour deposition (HW-MWECR-CVD), subsequently exposed under simulated illumination for three hours. This paper studies the microstructure change during illumination by Fourier Transformation Infrared (FTIR) spectra. There are two typical transformation tendencies of microstructure after illumination. It proposes a model of light induced structural change based on the experimental results. It is found that all samples follow the same mechanism during illumination, and intrinsic structure of samples affect the total H content.     

Structural phase transition of vanadium at 69 GPa

A phase transition was observed at 63-69 GPa and room temperature in vanadium with synchrotron x-ray diffraction. The transition is characterized as a rhombohedral lattice distortion of the body-centered-cubic vanadium without a discontinuity in the pressure-volume data, thus representing a novel type of transition that has never been observed in elements. Instead of driven by the conventional s-d electronic transition mechanism, the phase transition could be associated with the softening of C44 trigonal elasticity tensor that originates from the combination of Fermi surface nesting, band Jahn-Teller distortion, and electronic topological transition.     

5 TW/40 fs级台式钛宝石激光系统研究

在TSA-25系统输出35 mJ,800 nm啁啾脉冲的基础上,建立了以钛宝石作为增益介质的二级啁啾脉冲放大(CPA)系统。使用0.6 J和1.6 J,532 nm,10 Hz Nd∶YAG激光抽运,输出脉冲能量达到500 mJ,经压缩脉冲宽度为41 fs,压缩器的能量转换效率为63%,峰值功率可达7.6 TW。通过对放大器系统的钛宝石晶体、抽运密度以及多通结构通道数的选择等实验,有效地提高了能量放大器的萃取效率。其主放大器能量萃取效率达到32%,整个系统占用尺寸不到10 m2。     

掺杂对CH样品Rayleigh-Taylor不稳定性增长的影响

在神光II激光装置上进行了辐射驱动不同掺杂样品的单模Rayleigh-Taylor(RT)不稳定性实验.结果显示:与纯碳氢(CH)样品相比,掺Br的CH样品的扰动更早、更快地进入非线性区,产生二次谐波,并且掺Br比例越高,CH样品扰动进入非线性区的时间越早,相同时刻扰动的二次谐波的幅度越高.这是因为密度梯度效应抑制了二次谐波的产生,掺Br比例越高,密度梯度标长越小;同时密度梯度效应还抑制三次谐波对基模增长的负反馈,造成基模具有更大的线性增长,导致线性饱和幅值大于经典值0.1λ.     

Theoretical study of stereodynamics for the N+H2/D2/T2 reactions

The effects of isotopic variants on stereodynamic properties for the title reactions have been investigated using a quasi-classical trajectory method based on the first excited state NH2（I^2A＇） potential energy surface [Li Y Q and Varandas A J C 2010 J. Phys. Chem. A 114 9644]. The forward–backward symmetry scattering of the differential cross section can be observed, which demonstrates that all these reactions follow the insertion mechanism. Three angle distribution functions P（θr）, P（φr）, and P（θr, φr） with different collision energies and target molecules H2/D2/T2 are calculated. It is shown that the product rotational angular momentum is not only aligned, but also oriented along the direction perpendicular to the scattering plane. The title reaction is mainly governed by the ＂in-plane＂ mechanism through the calculated distribution function P（θr, φr）. The observable influences on the rotational polarization of the product by the isotopic substitution of H/D/T can be demonstrated.