Observation and assignment of the first photoelectron band of the CH3CO (XA) radical

HeI photoelectron spectra have been recorded for the reaction of fluorine atoms with acetaldehyde at different reaction times. A structured band associated with a short-lived primary reaction product was recorded at a reactant mixing distance of 6 mm above the photon beam. The vertical ionization energy was measured as (8.39 ± 0.05 eV), and regularly spaced vibrational structure was observed in this band with an average vibrational separation of (1605 ± 30 cm⁻¹). The band was assigned to ionization of the CH₃CO (X²A) radical on the basis of first vertical ionization energies computed for the two possible primary products, CH₃CO and CH₂CHO, using ab-initio calculations. The calculations carried out on CH₃CO (X²A), and its singlet ground cationic state, revealed that the observed vibrational structure can be assigned to excitation of the CO stretching mode in the ion. The measured adiabatic ionization energy, 7.21 ± 0.05 eV, is higher than the value expected (6.94 ± 0.03 eV) from evidence in the literature and calculated values in this work. This difference is assigned to poor Franck–Condon factors in the region of the band onset which means that the true adiabatic ionization energy was not observed.     

Energy Bounds for Static Spherically Symmetric Spacetime in f(R,G) Gravity

The main purpose of this paper is to investigate energy bounds in the context of f(R,G) gravity. To meet this aim, we choose static spherically symmetric spacetime in f(R,G) gravity to develop the field equations. We select three different models of f(R,G) gravity, which are thoroughly discussed in the literature. Firstly, the inequalities are formulated using energy bounds and then viability of the considered models are checked respectively. Graphical analysis show that specific f(R,G) gravity models are satisfied under suitable values of model parameters. It is shown that in a certain case energy bounds are satisfied expect SEC, which supports the late time acceleration expansion of unverse.     

基于零拍探测和压缩真空光输入增强Sagnac效应

利用量子技术增强Sagnac效应提高陀螺输出精度具有重要的研究意义, 是实现全自主导航的重要途径. 以相干态激光作为输入光源的光学陀螺因真空零点波动使其输出精度限制于散粒噪声极限而难以提高. 为减小真空波动的影响, 提出在激光输入的分束器的另一输入端输入压缩真空光并结合平衡零拍探测技术的方法增强Sagnac效应. 理论分析表明Sagnac效应性能得到有效提升: 干涉输出的灵敏度检测极限和动态范围均随着压缩程度的增加而呈指数级增长. 该方法只需对经典光学陀螺做少量改动就可实现, 是提高光学陀螺输出精度的一种新方法.     

甚高频激发容性耦合氩等离子体的电子能量分布函数的演变

甚高频激发的容性耦合等离子体由于离子通量和能量的相对独立可控而受到人们的关注. 本文采用朗缪尔探针诊断技术测量了40.68 MHz激发的容性耦合Ar等离子体的特性(如电子能量概率分布、电子温度和密度等)随宏观参量的演变情况. 实验结果表明, 电子能量概率分布随着气压的增加从双麦克斯韦分布逐步转变为单麦克斯韦分布并最终演变为Druyvesteyn分布, 而射频激发功率的增加促进了低能电子布居数的增强; 在从等离子体放电中心移向边界的过程中, 低能电子的布居数显著下降, 而高能电子的布居则有所上升; 放电极板间距的变化直接导致了等离子体中电子加热模式的转变. 另外, 我们也对等离子体中的高低能电子密度和温度的分配情况进行了讨论.     

LiBr分子基态光谱常数和分子常数研究

采用高精度的量子化学从头计算多参考组态相互作用方法和相关一致基, 计算了LiBr分子基态的光谱常数和势能曲线. 为获得更准确的结果, 计算中还考虑了二阶Douglas-Kroll-Hess相对论修正对LiBr分子基态的平衡键长、谐振频率和离解能影响. 将计算得到的势能曲线拟合为Murrell-Sorbie解析势能函数形式, 并进一步计算得到LiBr分子基态的其它光谱常数,ωeχe, αe, Be, D0. 比较发现它们与实验值符合的非常好. 通过求解核运动径向Schrodinger方程, 找到了LiBr分子基态的全部振动态. 还计算了每一个振动态的振动能级、经典转折点和惯性转动常数, 这些结果与已有的实验值一致.     

FP-1装置铝套筒内爆动力学过程的一维磁流体力学模拟

作为一种重要的柱面会聚冲击和准等熵压缩加载源,磁驱动固体套筒内爆技术已广泛应用于高能量密度物理实验研究.针对FP-1装置驱动的固体套筒内爆动力学过程,建立了含强度的一维磁流体力学模型,并对典型实验进行了模拟.计算获得的套筒内爆速度同实验结果较为相符.模拟结果显示,该装置在40 kV充压条件下,可以将直径3 cm,厚0.5 mm的铝套筒加速至1.1 km/s,内壁速度超过1.5 km/s,同时保持大部分材料为固体状态.内爆套筒与相同材料靶筒碰撞产生的冲击压力约9 GPa.改变靶筒内部填充气体的压力,可以获得不同的靶筒运动速度、轨迹以及反弹半径,以满足不同类型实验的研究需要.     

天光背景下混浊大气中成像质量的分析方法

调制传递函数(MTF)定量描述混浊介质对图像质量的影响,它是混浊介质的固有光学特性,利用等效原理可以获得MTF从低频到高频的完整特征.在实际应用中,混浊介质中的图像质量不仅取决于介质的MTF,还与图像的背景辐射密切相关.本文从混浊大气中图像退化机理出发,理论分析了空间频域中天光背景下图像质量的退化过程.参考等效原理,提出了一种考虑天光背景的表观MTF,得到了表观MTF与介质MTF和天光背景的定量关系,从而得到了一种分析背景辐射下混浊介质中图像质量的有效便捷方法.针对图像质量优化方法,从空间频域的角度提出了一种评价原则.     

Dimethyl sulfoxide/deep eutectic solvents mixtures as media in the reaction of 1‐fluoro‐2,4‐dinitrobenzene with piperidine: A solvent effect study

Aromatic nucleophilic substitution reaction of 1‐fluoro‐2,4‐dinitrobenzene with piperidine was kinetically investigated in ethylene glycol‐choline chloride and glycerol‐choline chloride as 2 deep eutectic solvents (DESs) mixed with dimethyl sulfoxide, in whole mole fractions, at room temperature. The investigation of the reaction in different concentrations of the piperidine shows that the reaction follows the base‐catalyzed mechanism. The measured rate coefficients of the reaction demonstrated a sharp decreasing in all mixtures with the increasing mole fraction of DESs. Linear free energy relationship investigations confirm that hydrogen bond donor ability in addition to polarity‐polarizability of the media has a major effect on the reaction rate. The decrease in the rate coefficient is attributed to not only hydrogen‐bonding donor interactions of the media with piperidine as both reactant and catalyst but also the preferential solvation of reactants by DES compared with the intermediate of the reaction.     

Commissioning of a multi‐beamline femtoslicing facility at SOLEIL

The investigation of ultrafast dynamics, taking place on the few to sub‐picosecond time scale, is today a very active research area pursued in a variety of scientific domains. With the recent advent of X‐ray free‐electron lasers (XFELs), providing very intense X‐ray pulses of duration as short as a few femtoseconds, this research field has gained further momentum. As a consequence, the demand for access strongly exceeds the capacity of the very few XFEL facilities existing worldwide. This situation motivates the development of alternative sub‐picosecond pulsed X‐ray sources among which femtoslicing facilities at synchrotron radiation storage rings are standing out due to their tunability over an extended photon energy range and their high stability. Following the success of the femtoslicing installations at ALS, BESSY‐II, SLS and UVSOR, SOLEIL decided to implement a femtoslicing facility. Several challenges were faced, including operation at the highest electron beam energy ever, and achievement of slice separation exclusively with the natural dispersion function of the storage ring. SOLEIL's setup also enables, for the first time, delivering sub‐picosecond pulses simultaneously to several beamlines. This last feature enlarges the experimental capabilities of the facility, which covers the soft and hard X‐ray photon energy range. In this paper, the commissioning of this original femtoslicing facility is reported. Furthermore, it is shown that the slicing‐induced THz signal can be used to derive a quantitative estimate for the degree of energy exchange between the femtosecond infrared laser pulse and the circulating electron bunch.     

两原子相干共振能量传递的单次与N次能量提取

两原子间隔一定距离且两原子跃迁频率接近时,两原子之间可发生能量传递.理论研究了供能原子和受能原子两共振原子的能量传递.求解薛定谔方程得出两原子共振能量传递效率.结果表明,供能原子在真空场中的激发态寿命在能量传递效率中起到十分重要的作用.能量传递效率与两原子间距离的负三次幂的正弦值的平方成正比,在一阶近似条件下,与两原子间距离的6次方成反比.以供能原子处于激发态时为初始时刻,能量从初始时刻随时间由供能原子向受能原子传递,对受能原子的单次能量提取的最大值大约在供能原子寿命的2/3时刻;对受能原子的连续N次能量提取的最大值,每次提取时间大约在供能原子寿命的1/2时刻.