Relationship between group velocity and symmetry of photonic crystals

Group velocity (GV) of eigenmode is a crucial parameter to explain the extraordinary phenomena about light propagation in photonic crystals (PhCs). To study relationships between group velocity and symmetry of PhCs, a new general expression of GV in PhCs made up of non-dispersive material is introduced. Based on this, the GVs of eigenmodes of PhCs, especially those of degenerate eigenmodes at highly symmetric points in the first Brillouin zone, are discussed. Some interesting results are obtained. For example, the summation of degenerate eigenmodes' GVs is invariant under the operations of wave vector ${{\bm K}}$-group $M_{{\bm K}} $. In addition, some numerical results are presented to verify them.     

纳秒级脉冲激光自动跟踪积分式测量方法

介绍了一种纳秒级脉冲激光光斑能量分布测量电路的设计方法,采用自动跟踪积分方式,根据预测先将脉冲光电流积分并保存,然后用速度较低的A/D芯片进行A/D转换,该方法避免了采用高速A/D芯片,且可以获得较高的采样分辨率,特别是在需要采集的通道数较多时具有明显优势。     

磁瓶式光电子能谱和速度成像光电子能谱对APS-(A=C14H10,蒽)的研究:电子结构,APS·的自旋轨道耦合和APS-的自旋偶极态

Gaseous dibenzo-7-phosphanorbornadiene P-sulfide anions APS^-(A=C₁₄H₁₀ or anthracene) were generated via electrospray ionization, and characterized by magnetic-bottle photoelectron spectroscopy, velocity-map imaging (VMI) photoelectron spectroscopy, and quantum chemical calculations. The electron affinity (EA) and spin-orbit (SO) splitting of the APS^· radical are determined from the photoelectron spectra and Franck-Condon factor simulations to be EA=(2.62±0.05) eV and SO splitting=(43±7) meV. VMI photoelectron images show strong and sharp peaks near the detachment threshold with an identical electron kinetic energy (eKE) of 17.9 meV at three different detachment wavelengths, which are therefore assigned to autodetachment from dipole-bound anion states. The B3LYP/6-31++G(d,p) calculations indicate APS^· has a dipole moment of 3.31 Debye, large enough to support a dipole-bound electron.     

Improved data analysis method of single-molecule experiments based on probability optimization

To extract the dynamic parameters from single molecule manipulation experiments, usually lots of data at different forces need to be recorded. But the measuring time of a single molecule is limited due to breakage of the tether or degradation of the molecule. Here we propose a data analysis method based on probability maximization of the recorded time trace to extract the dynamic parameters from a single measurement. The feasibility of this method was verified by dealing with the simulation data of a two-state system. We also applied this method to estimate the parameters of DNA hairpin folding and unfolding dynamics measured by a magnetic tweezers experiment.     

IMDD-OFDM系统的低开支、高准确度信道估计方法

提出一种应用于强度调制直接检测光正交频分复用(IMDD-OFDM)传输系统的低开支、高准确度的信道估计算法.该算法充分考虑系统噪声特性,利用梳状导频插入结构,结合符号间平均与子载波间频域线性插值的思想,在低开支导频条件下实现较高的估计准确度.仿真和理论推导结果表明:与传统平均算法和直接线性插值算法相比,基于梳状导频先平均后线性插值的算法估计出来的信道特性更能接近实际信道的.实验结果表明:在误码率为3.8×10~(-3)处,本文所提出的算法仅使用0.78%导频开支即可与使用20%导频开支的平均算法获得相同的接收灵敏度;同时,与传统估计算法相比,该算法与导频开支无关,能较好抗系统中的高斯噪声,获得与真实信道较为接近的估计性能.     

BBO，LBO，KDP晶体光参量啁啾脉冲放大特性的比较研究

 对BBO，LBO，KDP晶体I类非共线匹配下的光参量啁啾脉冲放大的相位匹配、参量范围、增益特性等进行了理论分析，重点对BBO和LBO的光参量啁啾脉冲放大特性进行了比较。结果表明对于以光参量啁啾脉冲放大系统代替800nm中心波长的Ti:sappire再生放大系统，用BBO晶体可获得更宽的增益带宽，而对1 053nm中心波长的种子光用LBO晶体更好。     

交叉分子束方法研究H+CH4和H+CD4反应:CH3/CD3的振动激发态产物通道

We study the H+CH₄/CD₄→H₂/HD+CH₃/CD₃ reactions using the time sliced velocity map ion imaging technique. Ion images of the CH₃/CD₃ products were measured by the (2+1) resonance enhanced multi-photon ionization (REMPI) detection method. Besides the CH₃/CD₃ products in the ground state, ion images of the vibrationally excited CH₃/CD₃ products were also observed at two collision energies of 0.72 and 1.06 eV. It is shown that the angular distribution of the products CH₃/CD₃ in vibrationally excited states gradually vary from backward scattering to sideways scattering as the collision energy increases. Compared to the CH₃/CD₃ products in the ground state, the CH₃/CD₃ products in vibrationally excited states tend to be more sideways scattered, indicating that larger impact parameters play a more important role in the vibrationally excited product channels.     

激发态Cs(5D)原子间碰撞能量转移

用激光二步激发Cs原子至8S态,从谱线的波长及强度可以确定Cs原子的辐射及碰撞过程,5D态主要是由8S→7P→5D跃迁布居的.在1016-1017Cs密度范围内,测量了碰撞能量合并5D 5D→nL 6S(nL=9D,11S,7F)速率系数,因5D→6P(3.0-3.6μm)处于红外本实验不能探测,利用一个已经测量过的过程(即6P 5D→6S 7D)作相对测量,对于9D,11S和7F态,其平均速率系数分别为(8.4±4.2)×10-10,(7.3±3.6)×10-10和(9.7±4.8)×10-10cm3s-1.讨论了碰撞转移过程11S 6S 7F 6S对速率系数的影响.     

激光诱导Ti等离子体电子温度的实验研究

室温,常压下,利用Nd∶YAG脉冲激光器产生的波长为1 064 nm, 脉宽12 ns,能量分别180, 230和280 mJ的脉冲激光冲击Ti靶,使用中阶梯光栅光谱仪检测了三种激光能量下对应的光谱。调节延时器DG645的延迟时间,检测了延迟0～500 ns时间范围内Ti等离子体对应激光能量下的发射光谱,分析光谱,可以得到了九条不同的的TiⅠ 和TiⅡ等离子体谱线,证明在该实验条件下,Ti靶能够充分吸收能量电离且离子谱线具有不同的演化速率,利用Saha-Boltzmann法计算并分析Ti等离子体电子温度,实验结果表明：相同的延迟时间,激光能量越大,谱线相对强度越大,电子温度越高,谱线相对强度的变化量随激光能量的变化量增大而增大;在延时0～150 ns内,三种激光能量下的等离子体电子温度和谱线的相对强度都随延迟时间的增加而快速下降,其中280 mJ激光能量下的等离子体电子温度和谱线强度下降速率较快;在150～250 ns范围内,电子温度和谱线强度均随延迟时间的增加有一个缓慢的上升,180 mJ激光能量下的等离子体电子温度和谱线强度的上升速率较快。250～500 ns范围内,三种激光能量下的电子温度和谱线强度均随延迟时间的增加而缓慢下降。     

预处理对355nm激光作用下熔石英损伤增长的影响

测试了经化学蚀刻、紫外激光预处理及其共同处理后的熔石英355 nm激光损伤阈值;研究了处理前后其损伤斑面积随激光辐照脉冲数的增长情况。结果表明,处理后熔石英355 nm激光损伤阈值得到了提高,且损伤斑面积增长变慢。利用CO2激光对熔石英表面损伤点进行了修复处理,修复后的损伤点R-on-1抗损伤阈值和基底阈值相当,损伤增长得到有效抑制。